Maternal Undernutrition Influences Placental-Fetal Development1

Developmental potential in the first 5 years for children in developing countries

Grantham-McGregor, S., Cheung, Y. B., Cueto, S., Glewwe, P., Richter, L., & Strupp, B. (2007) · The Lancet · doi:10.1016/s0140-6736(07)60032-4 · Cited by 3,630 · see citing works

Angiopoietin-2, a Natural Antagonist for Tie2 That Disrupts in vivo Angiogenesis

Maisonpierre, P. C., Suri, C., Jones, P. F., Bartunkova, S., Wiegand, S. J., Radziejewski, C., Compton, D., McClain, J., Aldrich, T. H., Papadopoulos, N., et al. (1997) · Science · doi:10.1126/science.277.5322.55 · Cited by 3,570 · see citing works

Trophic Action of Leptin on Hypothalamic Neurons That Regulate Feeding

Bouret, S. G., Draper, S. J., & Simerly, R. B. (2004) · Science · doi:10.1126/science.1095004 · Cited by 1,219 · see citing works

Dietary Protein Restriction of Pregnant Rats Induces and Folic Acid Supplementation Prevents Epigenetic Modification of Hepatic Gene Expression in the Offspring

Lillycrop, K. A., Phillips, E. S., Jackson, A. A., Hanson, M. A., & Burdge, G. C. (2005) · Journal of Nutrition · doi:10.1093/jn/135.6.1382 · Cited by 1,139 · see citing works

Maternal Nutrition and Fetal Development

Bazer, F. W., Spencer, T. E., Wu, G., Cudd, T. A., & Meininger, C. J. (2004) · The Journal of Nutrition · doi:10.1093/jn/134.9.2169 · Cited by 1,019 · see citing works

Differential Effects of Culture on Imprinted H19 Expression in the Preimplantation Mouse Embryo1

Doherty, A. S., Mann, M. R. W., Tremblay, K. D., Bartolomei, M. S., & Schultz, R. M. (2000) · Biology of Reproduction · doi:10.1095/biolreprod62.6.1526 · Cited by 723 · see citing works

Role of the placenta in fetal programming: underlying mechanisms and potential interventional approaches

Jansson, T., & Powell, T. L. (2007) · Clinical Science · doi:10.1042/cs20060339 · Cited by 542 · see citing works

Placental adaptive responses and fetal programming

Myatt, L. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.104968 · Cited by 536 · see citing works

Dexamethasone in the Last Week of Pregnancy Attenuates Hippocampal Glucocorticoid Receptor Gene Expression and Elevates Blood Pressure in the Adult Offspring in the Rat

Levitt, N. S., Lindsay, R. S., Holmes, M. C., & Seckl, J. R. (2008) · Neuroendocrinology · doi:10.1159/000127146 · Cited by 535 · see citing works

Intrauterine Programming of Physiological Systems: Causes and Consequences

Fowden, A. L., Giussani, D. A., & Forhead, A. J. (2006) · Physiology · doi:10.1152/physiol.00050.2005 · Cited by 511 · see citing works

The Risk of Maternal Nutritional Depletion and Poor Outcomes Increases in Early or Closely Spaced Pregnancies

King, J. C. (2003) · Journal of Nutrition · doi:10.1093/jn/133.5.1732s · Cited by 469 · see citing works

Fetal undernutrition and disease in later life

Barker, D. (1997) · Reviews of Reproduction · doi:10.1530/ror.0.0020105 · Cited by 457 · see citing works

Utero-placental vascular development and placental function

Reynolds, L. P., & Redmer, D. A. (1995) · Journal of Animal Science · doi:10.2527/1995.7361839x · Cited by 418 · see citing works

Nitric Oxide and Angiogenesis

Ziche, M., & Morbidelli, L. (2000) · Journal of Neuro-Oncology · doi:10.1023/a:1006431309841 · Cited by 391 · see citing works

Aspects of Human Fetoplacental Vasculogenesis and Angiogenesis. I. Molecular Regulation

Jones, D. S., Kaufmann, P., & Mayhew, T. M. (2003) · Placenta · doi:10.1016/j.placenta.2003.10.004 · Cited by 359 · see citing works

Angiogenesis in the female reproductive system

Reynolds, L. P., Killilea, S. D., & Redmer, D. A. (1992) · The FASEB Journal · doi:10.1096/fasebj.6.3.1371260 · Cited by 346 · see citing works

Inhibition of 11β‐hydroxysteroid dehydrogenase, the foeto‐placental barrier to maternal glucocorticoids, permanently programs amygdala GR mRNA expression and anxiety‐like behaviour in the offspring

Welberg, L., Seckl, J. R., & Holmes, M. C. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00958.x · Cited by 344 · see citing works

Angiogenesis in female reproductive system

Longjiang, Shao, S., Cheng, & Zhu (2001) · 中国科学通报：英文版 · Cited by 339 · see citing works

Programmed obesity in intrauterine growth-restricted newborns: modulation by newborn nutrition

Desai, M., Gayle, D. A., Babu, J., & Ross, M. G. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00340.2004 · Cited by 338 · see citing works

Placental-specific insulin-like growth factor 2 ( Igf2 ) regulates the diffusional exchange characteristics of the mouse placenta

Sibley, C. P., Coan, P. M., Ferguson‐Smith, A. C., Dean, W., Hughes, J., Smith, P., Reik, W., Burton, G. J., Fowden, A. L., & Constância, M. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402508101 · Cited by 299 · see citing works

Effect of nutrient intake during pregnancy on fetal and placental growth and vascular development

Redmer, D. A., Wallace, J. M., & Reynolds, L. P. (2004) · Domestic Animal Endocrinology · doi:10.1016/j.domaniend.2004.06.006 · Cited by 294 · see citing works

Regulation of adipocyte gene expression in differentiation and syndromes of obesity/diabetes.

Spiegelman, B. M., Choy, L., Hotamışlıgil, G. S., Graves, R. A., & Tontonoz, P. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)53107-0 · Cited by 275 · see citing works

Nutritional Epigenomics of Metabolic Syndrome

Gallou‐Kabani, C., & Junien, C. (2005) · Diabetes · doi:10.2337/diabetes.54.7.1899 · Cited by 273 · see citing works

The Placenta and Intrauterine Programming

Fowden, A. L., Forhead, A. J., Coan, P. M., & Burton, G. J. (2008) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2008.01663.x · Cited by 267 · see citing works

Down‐regulation of placental transport of amino acids precedes the development of intrauterine growth restriction in rats fed a low protein diet

Jansson, N., Pettersson, J., Haafiz, A., Ericsson, A., Palmberg, I., Tranberg, M., Ganapathy, V., Powell, T. L., & Jansson, T. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.550004 · Cited by 265 · see citing works

Umbilical amino acid concentrations in normal and growth-retarded fetuses sampled in utero by cordocentesis

Cetin, I., Corbetta, C., Sereni, L. P., Marconi, A. M., Bozzetti, P., Pardi, G., & Battaglia, F. C. (1990) · American Journal of Obstetrics and Gynecology · doi:10.1016/0002-9378(90)90860-a · Cited by 259 · see citing works

Placental Phenotypes of Intrauterine Growth

Sibley, C. P., Turner, M. A., Cetin, I., Ayuk, P. T.-Y., Boyd, C. A. R., D'Souza, S. W., Glazier, J. D., Greenwood, S. L., Jansson, T., & Powell, T. L. (2005) · Pediatric Research · doi:10.1203/01.pdr.0000181381.82856.23 · Cited by 250 · see citing works

Central Administration of Leptin to Ovariectomized Ewes Inhibits Food Intake without Affecting the Secretion of Hormones from the Pituitary Gland: Evidence for a Dissociation of Effects on Appetite and Neuroendocrine Function

Henry, B. A., Goding, J. W., Alexander, W. S., Tilbrook, A. J., Canny, B. J., Dunshea, F. R., Rao, A., Mansell, A. S., & Clarke, I. J. (1999) · Endocrinology · doi:10.1210/en.140.3.1175 · Cited by 238 · see citing works

Association of intrauterine fetal growth retardation and learning deficits at age 9 to 11 years

Low, J. A., Handley‐Derry, M., Burke, S. O., Peters, R. D., Pater, E. A., Killen, H. L., & Derrick, E. J. (1992) · American Journal of Obstetrics and Gynecology · doi:10.1016/0002-9378(92)91727-r · Cited by 218 · see citing works

Nutritional and Placental Determinants of Foetal Growth Rate in Sheep and Consequences for the Newborn Lamb

Mellor, D. J. (1983) · British Veterinary Journal · doi:10.1016/s0007-1935(17)30436-0 · Cited by 218 · see citing works

Possible mechanisms underlying pregnancy-induced changes in uterine artery endothelial function

Bird, I. M., Zhang, L., & Magness, R. R. (2003) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00108.2002 · Cited by 214 · see citing works

Triglyceride Hydrolase Activities and Expression of Fatty Acid Binding Proteins in the Human Placenta in Pregnancies Complicated by Intrauterine Growth Restriction and Diabetes

Magnusson, A., Waterman, I. J., Wennergren, M., Jansson, T., & Powell, T. L. (2004) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2003-032234 · Cited by 206 · see citing works

Adaptations in placental phenotype support fetal growth during undernutrition of pregnant mice: Undernutrition and placental phenotype

Coan, P. M., Vaughan, O. R., Sekita, Y., Finn, S. L., Burton, G. J., Constancia, M., & Fowden, A. L. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2009.181214 · Cited by 199 · see citing works

The effect of maternal undernutrition on ovine fetal growth

Osgerby, J., Wathes, D. C., Howard, D. J., & Gadd, T. (2002) · Journal of Endocrinology · doi:10.1677/joe.0.1730131 · Cited by 179 · see citing works

Imbilical amino acid concentrations in appropriate and small for gestational age infants: a biochemical difference present in utero

Cetin, I., Marconi, A. M., Bozzetti, P., Sereni, L. P., Corbetta, C., Pardi, G., & Battaglia, F. C. (1988) · American Journal of Obstetrics and Gynecology · doi:10.1016/0002-9378(88)90792-2 · Cited by 177 · see citing works

Influence of maternal nutrition on birth weight

Lechtig, A., Yarbrough, C., Delgado, H. L., Habicht, J., Martorell, R., & Klein, R. E. (1975) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/28.11.1223 · Cited by 174 · see citing works

Compensatory placental growth after restricted maternal nutrition in early pregnancy

Lunney, L. H. (1998) · Placenta · doi:10.1016/s0143-4004(98)90105-9 · Cited by 164 · see citing works

Maternal Protein Deficiency Causes Hypermethylation of DNA in the Livers of Rat Fetuses

Rees, W. D., Hay, S. M., Brown, D. S., Antipatis, C., & Palmer, R. M. (2000) · Journal of Nutrition · doi:10.1093/jn/130.7.1821 · Cited by 164 · see citing works

Central infusion of leptin into well-fed and undernourished ewe lambs: effects on feed intake and serum concentrations of growth hormone and luteinizing hormone

Morrison, C. D., Daniel, J. A., Holmberg, B., Djiane, J., Raver, N., Gertler, A., & Keisler, D. H. (2001) · Journal of Endocrinology · doi:10.1677/joe.0.1680317 · Cited by 162 · see citing works

Plasma amino acids in appropriate- and small-for-gestational-age fetuses

Economides, D. L., Nicolaides, K. H., Gahl, W. A., Bernardini, I. M., & Evans, M. I. (1989) · American Journal of Obstetrics and Gynecology · doi:10.1016/0002-9378(89)90670-4 · Cited by 161 · see citing works

Periconceptional Undernutrition in Sheep Accelerates Maturation of the Fetal Hypothalamic-Pituitary-Adrenal Axis in Late Gestation

Bloomfield, F. H., Oliver, M. H., Hawkins, P., Holloway, A. C., Campbell, M. E., Gluckman, P. D., Harding, J. E., & Challis, J. R. G. (2004) · Endocrinology · doi:10.1210/en.2004-0424 · Cited by 159 · see citing works

The Guinea-Pig Placenta

Kaufmann, P., & Davidoff, M. S. (1977) · Springer eBooks · doi:10.1007/978-3-642-66618-6 · Cited by 156 · see citing works

Central Administration of Leptin to Ovariectomized Ewes Inhibits Food Intake without Affecting the Secretion of Hormones from the Pituitary Gland: Evidence for a Dissociation of Effects on Appetite and Neuroendocrine Function*

Henry, B. A., Goding, J. W., Alexander, W. S., et al. (1999) · Endocrinology · doi:10.1210/endo.140.3.6604 · Cited by 156 · see citing works

Intrauterine Growth Restriction Is Associated with Changes in Polyunsaturated Fatty Acid Fetal-Maternal Relationships

Cetin, I., Giovannini, N., Alvino, G., Agostoni, C. V., Riva, E., Giovannini, M., & Pardi, G. (2002) · Pediatric Research · doi:10.1203/00006450-200211000-00023 · Cited by 155 · see citing works

Association of disproportionate growth of fetal rats in late gestation with raised systolic blood pressure in later life

Langley‐Evans, S. C., Gardner, D. S., & Jackson, A. A. (1996) · Reproduction · doi:10.1530/jrf.0.1060307 · Cited by 150 · see citing works

Effect of low-protein diet-induced intrauterine growth retardation on rat placental amino acid transport

Malandro, M. S., Beveridge, M. J., Kilberg, M. S., & Novak, D. (1996) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1996.271.1.c295 · Cited by 150 · see citing works

Nutrient transport across the placenta

Knipp, G. T., Audus, K. L., & Soares, M. J. (1999) · Advanced Drug Delivery Reviews · doi:10.1016/s0169-409x(99)00005-8 · Cited by 140 · see citing works

Intrauterine growth restriction

Maršál, K. (2002) · Current Opinion in Obstetrics & Gynecology · doi:10.1097/00001703-200204000-00005 · Cited by 134 · see citing works

The genetics of pre‐eclampsia: a feto‐placental or maternal problem?

Cross, J. C. (2003) · Clinical Genetics · doi:10.1034/j.1399-0004.2003.00127.x · Cited by 132 · see citing works

Insulin and Leptin Combine Additively to Reduce Food Intake and Body Weight in Rats

Air, E. L., Benoit, S. C., Clegg, D. J., Seeley, R. J., & Woods, S. C. (2002) · Endocrinology · doi:10.1210/endo.143.6.8948 · Cited by 131 · see citing works

High Serum Leptin Concentrations during Catch-Up Growth of Children Born with Intrauterine Growth Retardation1

Jaquet, D., Léger, J., Tabone, M., Czernichow, P., & Lévy‐Marchal, C. (1999) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.84.6.5744 · Cited by 126 · see citing works

Effects of leptin and orexin-A on food intake and feeding related hypothalamic neurons

Shiraishi, T., Oomura, Y., Sasaki, K., & Wayner, M. J. (2000) · Physiology & Behavior · doi:10.1016/s0031-9384(00)00341-3 · Cited by 125 · see citing works

Maternal Food Restriction Reduces the Exchange Surface Area and Increases the Barrier Thickness of the Placenta in the Guinea-pig

Roberts, C. T., Sohlström, A., Kind, K. L., Earl, R., Khong, T. Y., Robinson, J. S., Owens, P. C., & Owens, J. A. (2001) · Placenta · doi:10.1053/plac.2000.0602 · Cited by 124 · see citing works

MORPHOMETRY OF THE HUMAN PLACENT

Aherne, W., & Dunnill, M. S. (1966) · British Medical Bulletin · doi:10.1093/oxfordjournals.bmb.a070437 · Cited by 123 · see citing works

Circulating levels of IGF-I and IGF-binding protein-1 throughout pregnancy: relation to birthweight and maternal weight

Hills, F. A., English, J., & Chard, T. (1996) · Journal of Endocrinology · doi:10.1677/joe.0.1480303 · Cited by 121 · see citing works

Placental Glucose Transporter Expression Is Regulated by Glucocorticoids

Hahn, T. (1999) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.84.4.1445 · Cited by 119 · see citing works

Placental Glucose Transporter Expression Is Regulated by Glucocorticoids1

Hahn, T., Barth, S., Graf, R., Engelmann, M., Beslagic, D., Reul, J. M. H. M., Holsboer, F., Dohr, G., & Desoyé, G. (1999) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.84.4.5607 · Cited by 116 · see citing works

Influence of Restricted Maternal Nutrition in Early to Mid Gestation on Placental and Fetal Development at Term in Sheep

Heasman, L., Clarke, L., Firth, K., Stephenson, T. J., & Symonds, M. E. (1998) · Pediatric Research · doi:10.1203/00006450-199810000-00013 · Cited by 111 · see citing works

Maternal undernutrition during late gestation-induced intrauterine growth restriction in the rat is associated with impaired placental GLUT3 expression, but does not correlate with endogenous corticosterone levels

Lésage, J., Hahn, D., Léonhardt, M., Blondeau, B., Bréant, B., & Dupouy, J. (2002) · Journal of Endocrinology · doi:10.1677/joe.0.1740037 · Cited by 107 · see citing works

Maternal Dietary Protein Deficiency Decreases Nitric Oxide Synthase and Ornithine Decarboxylase Activities in Placenta and Endometrium of Pigs During Early Gestation

Wu, G., Pond, W. G., Flynn, S. P., OTT, T. L., & Bazer, F. W. (1998) · Journal of Nutrition · doi:10.1093/jn/128.12.2395 · Cited by 104 · see citing works

l ‐Arginine treatment for asymmetric fetal growth restriction

Xiao, X. M., & Li, L. P. (2004) · International Journal of Gynecology & Obstetrics · doi:10.1016/j.ijgo.2004.09.017 · Cited by 96 · see citing works

Time-dependent physiological regulation of rodent and ovine placental glucose transporter (GLUT-1) protein

Das, U. G., Sadiq, H. F., Soares, M. J., Hay, W. W., & Devaskar, S. U. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.274.2.r339 · Cited by 96 · see citing works

Enhanced placental GLUT1 and GLUT3 expression in dexamethasone-induced fetal growth retardation

LANGDOWN, M. L., & Sugden, M. C. (2001) · Molecular and Cellular Endocrinology · doi:10.1016/s0303-7207(01)00629-3 · Cited by 92 · see citing works

Fetal programming of insulin-like growth factor (IGF)-I and IGF-binding protein-3: evidence for an altered response to undernutrition in late gestation following exposure to periconceptual undernutrition in the sheep

Gallaher, B. W., Breier, B. H., Keven, C., Harding, J. E., & Gluckman, P. D. (1998) · Journal of Endocrinology · doi:10.1677/joe.0.1590501 · Cited by 87 · see citing works

Placental transporter activity and expression in relation to fetal growth

Sibley, C. P., Glazier, J. D., & D’Souza, S. W. (1997) · Experimental Physiology · doi:10.1113/expphysiol.1997.sp004034 · Cited by 86 · see citing works

Cortisol stimulates system A amino acid transport and SNAT2 expression in a human placental cell line (BeWo)

Jones, H. N., Ashworth, C. J., Page, K., & McArdle, H. J. (2006) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00359.2005 · Cited by 83 · see citing works

Down-regulation of transcription factor peroxisome proliferator-activated receptor in programmed hepatic lipid dysregulation and inflammation in intrauterine growth–restricted offspring

Magee, T. R., Han, G., Cherian, B., Khorram, O., Ross, M. G., & Desai, M. (2008) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2008.05.022 · Cited by 79 · see citing works

Glucocorticoids accelerate fetal maturation of the epidermal permeability barrier in the rat.

Aszterbaum, M., Feingold, K. R., Menon, G. K., & Williams, M. L. K. (1993) · Journal of Clinical Investigation · doi:10.1172/jci116509 · Cited by 78 · see citing works

Antenatal Dexamethasone Treatment Leads to Changes in Gene Expression in a Murine Late Placenta

Baisden, B. L., Sonne, S., Joshi, R., Ganapathy, V., & Shekhawat, P. (2007) · Placenta · doi:10.1016/j.placenta.2007.04.002 · Cited by 76 · see citing works

EG-VEGF and Bv8: a novel family of tissue-restricted angiogenic factors

Ferrara, N., LeCouter, J. E., Lin, R., & Peale, F. V., Jr. (2003) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2003.07.001 · Cited by 72 · see citing works

Chronic maternal feed restriction impairs growth but increases adiposity of the fetal guinea pig

Kind, K. L., Roberts, C. T., Sohlström, A., Katsman, A. I., Clifton, P. M., Robinson, J. S., & Owens, J. A. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00360.2004 · Cited by 69 · see citing works

Vasodilation to Vascular Endothelial Growth Factor in the Uterine Artery of the Pregnant Rat Is Blunted by Low Dietary Protein Intake

Itoh, S., Brawley, L., Wheeler, T., Anthony, F. W., Poston, L., & Hanson, M. A. (2002) · Pediatric Research · doi:10.1203/00006450-200204000-00014 · Cited by 56 · see citing works

α-Ketoglutarate treatment early in postnatal life improves bone density in lambs at slaughter

Harrison, A. P., Tygesen, M. P., Sawa-Wojtanowicz, B., Husted, S., & Tatara, M. R. (2004) · Bone · doi:10.1016/j.bone.2004.03.016 · Cited by 55 · see citing works

Maternal-Fetal Exchange During Protein Malnutrition in the Rat. Placental Transfer of Glucose and a Nonmetabolizable Glucose Analog

Rosso, P. (1977) · Journal of Nutrition · doi:10.1093/jn/107.11.2006 · Cited by 54 · see citing works

Effect of maternal food restriction on fetal rat lung lipid differentiation program

Karadag, A., Sakurai, R., Wang, Y., Guo, P., Desai, M., Ross, M. G., Torday, J. S., & Rehan, V. K. (2009) · Pediatric Pulmonology · doi:10.1002/ppul.21030 · Cited by 49 · see citing works

Nutrient Restriction In Utero Induces Remodeling of the Vascular Extracellular Matrix in Rat Offspring

Khorram, O., Momeni, M., Desai, M., & Ross, M. G. (2007) · Reproductive Sciences · doi:10.1177/1933719106298215 · Cited by 47 · see citing works

Supplementation of a restricted maternal diet with protein or carbohydrate alone prevents a reduction in fetal muscle fibre number in the guinea-pig

Dwyer, C. M., & Stickland, N. C. (1994) · British Journal Of Nutrition · doi:10.1079/bjn19940022 · Cited by 46 · see citing works

Ovine feto‐placental metabolism

Ward, J. W., Wooding, F. B. P., & Fowden, A. L. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.054577 · Cited by 45 · see citing works

Glucocorticoid effects on rabbit fetal lung maturation in vivo: An ultrastructural morphometric study

Snyder, J. M., Rodgers, H. F., O'Brien, J. A., Mahli, N., Magliato, S. A., & Durham, P. L. (1992) · The Anatomical Record · doi:10.1002/ar.1092320115 · Cited by 40 · see citing works

Increased Placental Apoptosis in Maternal Food Restricted Gestations: Role of the Fas Pathway

Belkacemi, L., Chen, C. H., Ross, M. G., & Desai, M. (2009) · Placenta · doi:10.1016/j.placenta.2009.06.003 · Cited by 39 · see citing works

Decrease in voluntary feed intake and pulsatile luteinizing hormone secretion after intracerebroventricular infusion of recombinant bovine leptin in mature male sheep

Blache, D., Celi, P., Blackberry, M. A., Dynes, R. A., & Martin, G. B. (2001) · Reproduction Fertility and Development · doi:10.1071/rd00102 · Cited by 37 · see citing works

Control of growth hormone receptor and insulin‐like growth factor‐I expression by cortisol in ovine fetal skeletal muscle

Li, J., Forhead, A. J., Dauncey, M. J., Gilmour, R. S., & Fowden, A. L. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2002.016402 · Cited by 37 · see citing works

Altered Placental Structure Induced by Maternal Food Restriction in Guinea Pigs: A Role for Circulating IGF-II and IGFBP-2 in the Mother?

Roberts, C. T., Sohlström, A., Kind, K. L., Grant, P. A., Earl, R., Robinson, J. S., Khong, T. Y., Owens, P. C., & Owens, J. A. (2001) · Placenta · doi:10.1053/plac.2001.0643 · Cited by 36 · see citing works

The fatty acid composition of placenta in intrauterine growth retardation

Percy, P., Vilbergsson, G., Percy, A. K., Månsson, J., Wennergren, M., & Svennerholm, L. T. (1991) · Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism · doi:10.1016/0005-2760(91)90217-6 · Cited by 31 · see citing works

Single intracerebroventricular bolus injection of a recombinant adenovirus expressing leptin results in reduction of food intake and body weight in both lean and obese Zucker fa/fa rats

Muzzin, P., Cusin, I., Charnay, Y., & Rohner-Jeanrenaud, F. (2000) · Regulatory Peptides · doi:10.1016/s0167-0115(00)00150-6 · Cited by 29 · see citing works

Metabolic Crisis: Hyperemesis Gravidarum

Snell, L. H., Haughey, B. P., Buck, G., & Marecki, M. (1998) · The Journal of Perinatal & Neonatal Nursing · doi:10.1097/00005237-199809000-00004 · Cited by 26 · see citing works

Regulation of Insulin-Like Growth Factor I Messenger Ribonucleic Acid Levels by Serum in Cultured Rat Fibroblasts*

Lowe, W. L., KUMMER, M., Karpen, C. W., & Wu, X. (1990) · Endocrinology · doi:10.1210/endo-127-6-2854 · Cited by 25 · see citing works

Low-protein diet impairs vascular relaxation in virgin and pregnant rats

KOUMENTAKI, A., Anthony, F. W., Poston, L., & Wheeler, T. (2002) · Clinical Science · doi:10.1042/cs20010252 · Cited by 25 · see citing works

Proceedings of the Australian Physiological and Pharmacological Society Symposium: The Hypothalamus LEPTIN AND THE REGULATION OF FOOD INTAKE AND THE NEUROENDOCRINE AXIS IN SHEEP

Clarke, I. J., Henry, B. A., Iqbal, J., & Goding, J. W. (2001) · Clinical and Experimental Pharmacology and Physiology · doi:10.1046/j.1440-1681.2001.03410.x · Cited by 20 · see citing works

Angiogenesis in female reproductive system

Shao, L., & Zhu, C. (2001) · Chinese Science Bulletin · doi:10.1007/bf02900588 · Cited by 13 · see citing works

Serum leptin levels of premature and full-term newborns in early infancy: metabolic catch-up of premature babies.

Toprak, D., Gökalp, A. S., Hatun, Ş., Zengin, E., Arısoy, A. E., & Yumuk, Z. (2004) · PubMed · Cited by 12 · see citing works

Purification and endocrine evaluation of bovine binucleate trophoblastic cells

Myers, D. A., & Reimers, T. J. (1988) · Methods in Cell Science · doi:10.1007/bf01404137 · Cited by 11 · see citing works

Magnesium regulates hypoxia-stimulated apoptosis in the human placenta

Gude, N. M., Stevenson, J. L., Moses, E. K., & KING, R. G. (2000) · Clinical Science · doi:10.1042/cs0980375 · Cited by 10 · see citing works

[Modification of the lipid profile of human placenta by moderate maternal undernutrition].

Araya, J., Soto, C. A., Aguilera, A. M., Bosco, C., & Monlina, R. (1995) · PubMed · Cited by 8 · see citing works

Maternal malnutrition, perinatal mortality and foetal pathology--a clinicopathological study.

Mitra, K., & Chowdhury, M. (2002) · PubMed · Cited by 2 · see citing works

Maternal malnutrition, low birthweight and related phenomena in man

Wehmer, F., & Hafez, E. S. E. (1975) · European Journal of Obstetrics & Gynecology and Reproductive Biology · doi:10.1016/0028-2243(75)90024-6 · Cited by 1 · see citing works

Placental Origins of Chronic Disease

Burton, G. J., Fowden, A. L., & Thornburg, K. L. (2016) · Physiological Reviews · doi:10.1152/physrev.00029.2015 · Cited by 717 · see citing works

Stress during pregnancy alters temporal and spatial dynamics of the maternal and offspring microbiome in a sex-specific manner

Jašarević, E., Howard, C. D., Misic, A. M., Beiting, D. P., & Bale, T. L. (2017) · Scientific Reports · doi:10.1038/srep44182 · Cited by 262 · see citing works

Association of maternal thyroid function with birthweight: a systematic review and individual-participant data meta-analysis

Derakhshan, A., Peeters, R. P., Taylor, P. N., Bliddal, S., Carty, D., Meems, M., Vaidya, B., Chen, L., Knight, B., Ghafoor, F., et al. (2020) · The Lancet Diabetes & Endocrinology · doi:10.1016/s2213-8587(20)30061-9 · Cited by 253 · see citing works

Developmental Programming, a Pathway to Disease

Padmanabhan, V., Cardoso, R. C., & Puttabyatappa, M. (2016) · Endocrinology · doi:10.1210/en.2016-1003 · Cited by 234 · see citing works

Maternal Thyroid Hormone Parameters during Early Pregnancy and Birth Weight: The Generation R Study

Medici, M., Timmermans, S., Visser, W. E., Keizer‐Schrama, S. M. P. F. D. M., Jaddoe, V. W. W., Albert Hofman, D., Hooijkaas, H., de Rijke, Y. B., Tiemeier, H. W., Bongers‐Schokking, J. J., et al. (2012) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2012-2420 · Cited by 226 · see citing works

The influence of maternal prenatal and early childhood nutrition and maternal prenatal stress on offspring immune system development and neurodevelopmental disorders

Marques, A. H., O'Connor, T. G., Roth, C., Susser, E., & Bjørke-Monsen, A.-L. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00120 · Cited by 226 · see citing works

A Review of the Impact of Dietary Intakes in Human Pregnancy on Infant Birthweight

Grieger, J. A., & Clifton, V. L. (2014) · Nutrients · doi:10.3390/nu7010153 · Cited by 202 · see citing works

Priming for Life: Early Life Nutrition and the Microbiota-Gut-Brain Axis

Ratsika, A., Codagnone, M. G., O’Mahony, S. M., Stanton, C., & Cryan, J. F. (2021) · Nutrients · doi:10.3390/nu13020423 · Cited by 184 · see citing works

Maternal stress, nutrition and physical activity: Impact on immune function, CNS development and psychopathology

Marques, A. H., Bjørke-Monsen, A.-L., Teixeira, A. L., & Silverman, M. N. (2015) · Brain Research · doi:10.1016/j.brainres.2014.10.051 · Cited by 166 · see citing works

The Role of Placental Nutrient Sensing in Maternal-Fetal Resource Allocation1

Díaz, P., Powell, T. L., & Jansson, T. (2014) · Biology of Reproduction · doi:10.1095/biolreprod.114.121798 · Cited by 158 · see citing works

The Pivotal Role of the Placenta in Normal and Pathological Pregnancies: A Focus on Preeclampsia, Fetal Growth Restriction, and Maternal Chronic Venous Disease

Ortega, M. A., Fraile‐Μartinez, O., Montero, C. G., Sáez, M. A., Álvarez-Mon, M. Á., Torres‐Carranza, D., Álvarez‐Mon, M., Buján, J., García‐Honduvilla, N., Bravo, C., et al. (2022) · Cells · doi:10.3390/cells11030568 · Cited by 156 · see citing works

Puberty: Normal physiology (brief overview)

Wood, C. L., Lane, L. C., & Cheetham, T. D. (2019) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2019.03.001 · Cited by 151 · see citing works

Melatonin supplementation alters uteroplacental hemodynamics and fetal development in an ovine model of intrauterine growth restriction

Lemley, C. O., Meyer, A. M., Camacho, L. E., Neville, T. L. L., Newman, D. J., Caton, J. S. S., & Vonnahme, K. A. (2011) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00407.2011 · Cited by 144 · see citing works

Nutritional programming of insulin resistance: causes and consequences

Duque-Guimaraes, D. E., & Ozanne, S. E. (2013) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2013.05.006 · Cited by 137 · see citing works

Can Nutritional Modulation of Maternal Intestinal Microbiota Influence the Development of the Infant Gastrointestinal Tract?,

Thum, C., Cookson, A. L., Otter, D. E., McNabb, W. C., Hodgkinson, A. J., Dyer, J. M., & Roy, N. C. (2012) · Journal of Nutrition · doi:10.3945/jn.112.166231 · Cited by 135 · see citing works

Placental transport in response to altered maternal nutrition

Gaccioli, F., Lager, S., Powell, T. L., & Jansson, T. (2013) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s2040174412000529 · Cited by 129 · see citing works

Hypoxia: From Placental Development to Fetal Programming

Fajersztajn, L., & Veras, M. M. (2017) · Birth Defects Research · doi:10.1002/bdr2.1142 · Cited by 109 · see citing works

Fetal and neonatal programming of postnatal growth and feed efficiency in swine

Ji, Y. S., Wu, Z., Dai, Z., Wang, X., Li, J., Wang, B., & Wu, G. (2017) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-017-0173-5 · Cited by 109 · see citing works

Understanding Sex Differences in Childhood Undernutrition: A Narrative Review

Thurstans, S., Opondo, C., Seal, A., Wells, J. C. K., Khara, T., Dolan, C. M., Briend, A., Myatt, M. A., Garenne, M., Mertens, A., et al. (2022) · Nutrients · doi:10.3390/nu14050948 · Cited by 105 · see citing works

Impact of maternal under nutrition on obstetric outcomes

Triunfo, S., & Lanzone, A. (2014) · Journal of Endocrinological Investigation · doi:10.1007/s40618-014-0168-4 · Cited by 98 · see citing works

Improving amino acid nutrition to prevent intrauterine growth restriction in mammals

Lin, G., Wang, X., Wu, G., Feng, C., Zhou, H., Li, D., & Wang, J. (2014) · Amino Acids · doi:10.1007/s00726-014-1725-z · Cited by 98 · see citing works

Low Birth Weight in Children Born to Mothers with Hyperthyroidism and High Birth Weight in Hypothyroidism, whereas Preterm Birth Is Common in Both Conditions: A Danish National Hospital Register Study

Andersen, S. L., Olsen, J., Wu, C. S., & Laurberg, P. (2013) · European Thyroid Journal · doi:10.1159/000350513 · Cited by 98 · see citing works

Plasmodium falciparum parasitaemia in the first half of pregnancy, uterine and umbilical artery blood flow, and foetal growth: a longitudinal Doppler ultrasound study

Griffin, J. B., Lokomba, V., Landis, S. H., Thorp, J. M., Herring, A. H., Tshefu, A. K., Rogerson, S. J., & Meshnick, S. R. (2012) · Malaria Journal · doi:10.1186/1475-2875-11-319 · Cited by 97 · see citing works

Neuronal Control of Metabolism through Nutrient-Dependent Modulation of Tracheal Branching

Linneweber, G. A., Jacobson, J., Busch, K. E., Hudry, B., Christov, C. P., Dormann, D., Yuan, M., Otani, T., Knust, E., de Bono, M., et al. (2014) · Cell · doi:10.1016/j.cell.2013.12.008 · Cited by 95 · see citing works

Maternal western diet primes non‐alcoholic fatty liver disease in adult mouse offspring

Pruis, M., Lendvai, Á., Bloks, V., Zwier, M., Baller, J., de Bruin, A., Groen, A. K., & Plösch, T. (2014) · Acta Physiologica · doi:10.1111/apha.12197 · Cited by 98 · see citing works

Lipid-based nutrient supplements for maternal, birth, and infant developmental outcomes

Das, J. K., Hoodbhoy, Z. A., Salam, R. A., Bhutta, Z. A., Valenzuela‐Rubio, N. G., Prinzo, Z. W., & Bhutta, Z. A. (2018) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd012610.pub2 · Cited by 89 · see citing works

Nutritional epigenetics with a focus on amino acids: implications for the development and treatment of metabolic syndrome

Ji, Y. S., Wu, Z., Dai, Z., Sun, K., Wang, J., & Wu, G. (2015) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2015.08.003 · Cited by 82 · see citing works

Placental Lactogen as a Marker of Maternal Obesity, Diabetes, and Fetal Growth Abnormalities: Current Knowledge and Clinical Perspectives

Sibiak, R., Jankowski, M., Gutaj, P., Mozdziak, P. E., Kempisty, B., & Wender-Ożegowska, E. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9041142 · Cited by 83 · see citing works

Gestational diabetes mellitus alters apoptotic and inflammatory gene expression of trophobasts from human term placenta

Magee, T. R., Ross, M. G., WEDEKIND, L. E., Desai, M., Kjos, S. L., & Belkacemi, L. (2014) · Journal of Diabetes and its Complications · doi:10.1016/j.jdiacomp.2014.03.010 · Cited by 80 · see citing works

Maternal Heme Oxygenase 1 Regulates Placental Vasculature Development via Angiogenic Factors in Mice1

Zhao, H. F., Azuma, J., Kalish, F. S., Wong, R. J., & Stevenson, D. K. (2011) · Biology of Reproduction · doi:10.1095/biolreprod.111.093039 · Cited by 70 · see citing works

Cell dynamics in human villous trophoblast

Aplin, J., & Jones, C. J. P. (2021) · Human Reproduction Update · doi:10.1093/humupd/dmab015 · Cited by 68 · see citing works

The Expression and Function of Fatty Acid Transport Protein-2 and -4 in the Murine Placenta

Mishima, T., Miner, J. H., Morizane, M., Stahl, A., & Sadovsky, Y. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025865 · Cited by 68 · see citing works

Maternal calorie restriction modulates placental mitochondrial biogenesis and bioenergetic efficiency: putative involvement in fetoplacental growth defects in rats

Mayeur, S., Lancel, S., Theys, N., Lukaszewski, M., Duban‐Deweer, S., Bastide, B., Hachani, J., Cecchelli, R., Breton, C., Gabory, A., et al. (2012) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00332.2012 · Cited by 65 · see citing works

Caloric restriction in female reproduction: is it beneficial or detrimental?

Sun, J., Shen, X., Liu, H., Lu, S., Peng, J., & Kuang, H. (2021) · Reproductive Biology and Endocrinology · doi:10.1186/s12958-020-00681-1 · Cited by 64 · see citing works

Factors controlling nutrient availability to the developing fetus in ruminants

Dunlap, K. A., Brown, J. D., Keith, A. B., & Satterfield, M. C. (2015) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-015-0012-5 · Cited by 60 · see citing works

ACSL1 Is Associated With Fetal Programming of Insulin Sensitivity and Cellular Lipid Content

Joseph, R., Poschmann, J., Sukarieh, R., Too, P. G., Julien, S. G., Xu, F., Teh, A. L., Holbrook, J. D., Ng, K. L., Chong, Y. S., et al. (2015) · Molecular Endocrinology · doi:10.1210/me.2015-1020 · Cited by 60 · see citing works

Maternal Nutrition and Offspring Stress Response—Implications for Future Development of Non-Communicable Disease: A Perspective From India

Krishnaveni, G. V., & Srinivasan, K. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00795 · Cited by 56 · see citing works

High Folate, Perturbed One-Carbon Metabolism and Gestational Diabetes Mellitus

Williamson, J. M., Arthurs, A. L., Smith, M. D., Roberts, C. T., & Jankovic-Karasoulos, T. (2022) · Nutrients · doi:10.3390/nu14193930 · Cited by 56 · see citing works

Maternal micronutrients and brain global methylation patterns in the offspring

Sable, P., Randhir, K., Kale, A. A., Chavan, P., & Joshi, S. (2013) · Nutritional Neuroscience · doi:10.1179/1476830513y.0000000097 · Cited by 56 · see citing works

Maternal Dietary Quality and Dietary Inflammation Associations with Offspring Growth, Placental Development, and DNA Methylation

Lecorguillé, M., Teo, S. M., & Phillips, C. M. (2021) · Nutrients · doi:10.3390/nu13093130 · Cited by 56 · see citing works

The effect of maternal prenatal smoking and alcohol consumption on the placenta-to-birth weight ratio

Wang, N., Tikellis, G., Sun, C., Pezic, A., Wang, L., Wells, J. C. K., Cochrane, J., Ponsonby, A., & Dwyer, T. (2014) · Placenta · doi:10.1016/j.placenta.2014.04.006 · Cited by 53 · see citing works

Prenatal maternal depression is associated with low birth weight through shorter gestational age in term infants in Korea

Chang, H. Y., Keyes, K. M., Lee, K., Choi, I. A., Kim, S. J., Kim, K. W., Shin, Y. H., Ahn, K. M., Hong, S., & Shin, Y. (2013) · Early Human Development · doi:10.1016/j.earlhumdev.2013.11.006 · Cited by 54 · see citing works

Influence of pre- and peri-natal nutrition on skeletal acquisition and maintenance

Devlin, M. J., & Bouxsein, M. (2011) · Bone · doi:10.1016/j.bone.2011.06.019 · Cited by 52 · see citing works

Perinatal outcomes of infants born to mothers with hyperemesis gravidarum: A systematic review and meta-analysis

Jansen, L. A. W., Nijsten, K., Limpens, J., van EEKELEN, R., Koot, M. H., Grooten, I. J., Roseboom, T. J., & Painter, R. C. (2023) · European Journal of Obstetrics & Gynecology and Reproductive Biology · doi:10.1016/j.ejogrb.2023.03.004 · Cited by 52 · see citing works

Maternal malnutrition impacts placental morphology and transporter expression: an origin for poor offspring growth

Connor, K. L., Kibschull, M., Matysiak‐Zablocki, E., Nguyen, T. T.-T. N., Matthews, S. G., Lye, S. J., & Bloise, E. (2020) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2019.108329 · Cited by 52 · see citing works

Country characteristics and acute diarrhea in children from developing nations: a multilevel study

Pinzón-Rondón, Á. M., Zárate-Ardila, C., Hoyos-Martínez, A., Ruiz-Sternberg, Á. M., & Vélez-van-Meerbeke, A. (2015) · BMC Public Health · doi:10.1186/s12889-015-2120-8 · Cited by 53 · see citing works

Effects of Maternal Nutritional Supplements and Dietary Interventions on Placental Complications: An Umbrella Review, Meta-Analysis and Evidence Map

Kinshella, M. W., Omar, S., Scherbinsky, K., Vidler, M., Magee, L. A., von Dadelszen, P., Moore, S. E., Elango, R., & The PRECISE Conceptual Framework Working Group (2021) · Nutrients · doi:10.3390/nu13020472 · Cited by 52 · see citing works

Maternal fats and pregnancy complications: Implications for long-term health

Khaire, A. A., Wadhwani, N. S., Madiwale, S. D., & Joshi, S. (2020) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2020.102098 · Cited by 49 · see citing works

Altered thyroid hormone profile in offspring after exposure to high estradiol environment during the first trimester of pregnancy: a cross-sectional study

Lv, P., Ye, M., Lv, M., Feng, C., Liu, Y., Li, J., Yu, D.-Q., Shen, Y., Hu, X., Gao, Q., et al. (2014) · BMC Medicine · doi:10.1186/s12916-014-0240-0 · Cited by 48 · see citing works

Role of Maternal Dietary Protein and Amino Acids on Fetal Programming, Early Neonatal Development, and Lactation in Swine

Zhang, S., Heng, J., Song, H., Zhang, Y., Lin, X., Tian, M., Chen, F., & Guan, W. (2019) · Animals · doi:10.3390/ani9010019 · Cited by 48 · see citing works

Fetal undernutrition, placental insufficiency, and pancreatic β-cell development programming in utero

Mohan, R., Baumann, D. C., & Alejandro, E. U. (2018) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00072.2018 · Cited by 48 · see citing works

Maternal Protein Malnutrition: Current and Future Perspectives of Spirulina Supplementation in Neuroprotection

Sinha, S., Patro, N., & Patro, I. K. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00966 · Cited by 49 · see citing works

Maternal nutrition influences angiogenesis in the placenta through peroxisome proliferator activated receptors: A novel hypothesis

Meher, A. P., Sundrani, D. P., & Joshi, S. (2015) · Molecular Reproduction and Development · doi:10.1002/mrd.22518 · Cited by 45 · see citing works

Maternal Nutrient Restriction in Guinea Pigs as an Animal Model for Inducing Fetal Growth Restriction

Elias, A., Ghaly, A., Matushewski, B. J., Regnault, T. R. H., & Richardson, B. S. (2015) · Reproductive Sciences · doi:10.1177/1933719115602773 · Cited by 43 · see citing works

The role of maternal nutrition, metabolic function and the placenta in developmental programming of renal dysfunction

Richter, V., Briffa, J. F., Moritz, K. M., Wlodek, M. E., & Hryciw, D. H. (2015) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.12505 · Cited by 42 · see citing works

Undernutrition and malaria in pregnancy – a dangerous dyad?

Unger, H. W., Ashorn, P., Cates, J., Dewey, K. G., & Rogerson, S. J. (2016) · BMC Medicine · doi:10.1186/s12916-016-0695-2 · Cited by 43 · see citing works

Colony-stimulating factor 2 acts from days 5 to 7 of development to modify programming of the bovine conceptus at day 86 of gestation†

Siqueira, L. G. B., Tríbulo, P., Chen, Z., Denicol, A. C., Ortega, M. S., Negrón‐Pérez, V. M., Kannampuzha‐Francis, J., Pohler, K. G., Rivera, R. M., & Hansen, P. J. (2017) · Biology of Reproduction · doi:10.1093/biolre/iox018 · Cited by 42 · see citing works

2011 AND 2012 EARLY CAREERS ACHIEVEMENT AWARDS: Placental programming: How the maternal environment can impact placental function1,2

Vonnahme, K. A., Lemley, C. O., Shukla, P., & O'Rourke, S. T. (2013) · Journal of Animal Science · doi:10.2527/jas.2012-5929 · Cited by 40 · see citing works

The human placenta and its role in reproductive outcomes revisited

Aye, I. L. M. H., Tong, S., Jones, D. S., & Smith, G. C. S. (2025) · Physiological Reviews · doi:10.1152/physrev.00039.2024 · Cited by 45 · see citing works

Malnutrition Among Children Under Five Years in Uganda

Mawa, R. (2018) · American Journal of Health Research · doi:10.11648/j.ajhr.20180602.14 · Cited by 40 · see citing works

The GLP-1 analog, liraglutide prevents the increase of proinflammatory mediators in the hippocampus of male rat pups submitted to maternal perinatal food restriction

Diz-Chaves, Y., Toba, L., Fandiño, J., González-Matías, L. C., García‐Segura, L. M., & Mallo, F. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1370-7 · Cited by 39 · see citing works

Effect of maternal supplement beverage with and without probiotics during pregnancy and lactation on maternal and infant health: a randomized controlled trial in the Philippines

Mantaring, J. B., Benyacoub, J., Destura, R. V., Pecquet, S., Vidal, K., Volger, S., & Guinto, V. T. (2018) · BMC Pregnancy and Childbirth · doi:10.1186/s12884-018-1828-8 · Cited by 37 · see citing works

Down-regulation of the transcription factor snail in the placentas of patients with preeclampsia and in a rat model of preeclampsia

Fedorova, L. V., Gatto-Weis, C. M., Smaili, S., Khurshid, N., Shapiro, J. I., Malhotra, D. K., & Horrigan, T. J. (2012) · Reproductive Biology and Endocrinology · doi:10.1186/1477-7827-10-15 · Cited by 37 · see citing works

Placental dysfunction is associated with altered microRNA expression in pregnant women with low folate status

Baker, B., Mackie, F. L., Lean, S. C., Greenwood, S. L., Heazell, A. E. P., Forbes, K. A., & Jones, R. L. (2017) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201600646 · Cited by 37 · see citing works

The effects of gestational transient thyrotoxicosis on the perinatal outcomes: a case–control study

Kinomoto, S., Umehara, N., SATO, S. T., Ogawa, K., Fujiwara, T., Arata, N., & Sago, H. (2016) · Archives of Gynecology and Obstetrics · doi:10.1007/s00404-016-4219-2 · Cited by 36 · see citing works

Maternal nutrient restriction in guinea pigs leads to fetal growth restriction with evidence for chronic hypoxia

Elias, A., Maki, Y., Matushewski, B. J., Nygard, K. L., Regnault, T. R. H., & Richardson, B. S. (2017) · Pediatric Research · doi:10.1038/pr.2017.92 · Cited by 34 · see citing works

Placental Vascular Defects in Compromised Pregnancies: Effects of Assisted Reproductive Technologies and Other Maternal Stressors

Reynolds, L. P., Borowicz, P. P., Palmieri, C., & Grazul‐Bilska, A. T. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-1-4939-1031-1_17 · Cited by 34 · see citing works

Long-term impacts of late-gestation maternal heat stress on growth performance, blood hormones and metabolites of newborn calves independent of maternal reduced feed intake

Almoosavi, S. M. M. S., Ghoorchi, T., Naserian, A. A., Ramezanpor, S. S., & Ghaffari, M. H. (2020) · Domestic Animal Endocrinology · doi:10.1016/j.domaniend.2019.106433 · Cited by 35 · see citing works

Dynamic Proteomic Profiles of In Vivo- and In Vitro-Produced Mouse Postimplantation Extraembryonic Tissues and Placentas1

Sui, L., An, L., Tan, K., Wang, Z., Wang, S., Miao, K., Ren, L., Li, T., He, S.-Z., Yu, Y., et al. (2014) · Biology of Reproduction · doi:10.1095/biolreprod.114.124248 · Cited by 32 · see citing works

Maternal supplementation with uridine influences fatty acid and amino acid constituents of offspring in a sow–piglet model

Gao, L., Liu, Y., Zhou, X., Zhang, Y., Wu, X., & Yin, Y. (2020) · British Journal Of Nutrition · doi:10.1017/s0007114520003165 · Cited by 32 · see citing works

Effects of maternal low‐protein diet on parameters of locomotor activity in a rat model of cerebral palsy

da Silva, K. O. G., Pereira, S. D. C., Portovedo, M., Milanski, M., Galindo, L. C. M., Guzmán‐Quevedo, O., Manhães‐de‐Castro, R., & Toscano, A. E. (2016) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2016.05.002 · Cited by 30 · see citing works

Maternal Calorie Restriction Causing Uteroplacental Insufficiency Differentially Affects Mammalian Placental Glucose and Leucine Transport Molecular Mechanisms

Ganguly, A., Touma, M., Thamotharan, S., Vivo, D. C. D., & Devaskar, S. U. (2016) · Endocrinology · doi:10.1210/en.2016-1259 · Cited by 30 · see citing works

Foetal growth restriction in mice modifies postnatal airway responsiveness in an age and sex-dependent manner

Wang, K. C. W., Larcombe, A. N., Berry, L. J., Morton, J. S., Davidge, S. T., James, A. L., & Noble, P. B. (2017) · Clinical Science · doi:10.1042/cs20171554 · Cited by 30 · see citing works

Low Birth Weight, Blood Pressure and Renal Susceptibility

Coats, L. E., Davis, G. K., Newsome, A. D., Ojeda, N. B., & Alexander, B. T. (2019) · Current Hypertension Reports · doi:10.1007/s11906-019-0969-0 · Cited by 29 · see citing works

The Effect of Gestational Age on Angiogenic Gene Expression in the Rat Placenta

Vaswani, K., Hum, M., Chan, H., Ryan, J., Wood‐Bradley, R. J., Nitert, M. D., Mitchell, M. D., Armitage, J. A., & Rice, G. E. (2013) · PLoS ONE · doi:10.1371/journal.pone.0083762 · Cited by 29 · see citing works

Association of brain-derived neurotrophic factor and tyrosine kinase B receptor in pregnancy

Dhobale, M. V., Mehendale, S. S., Pisal, H., D’Souza, V., & Joshi, S. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.04.016 · Cited by 29 · see citing works

Competition for Materno-Fetal Resource Partitioning in a Rabbit Model of Undernourished Pregnancy

López‐Tello, J., Arias‐Álvarez, M., Martínez, M. D. L. Á. J., García-García, R. M., Rodríguez, M., Lorenzo, P. L., Bermejo‐Poza, R., Gonzalez‐Bulnes, A., & Rebollar, P. G. (2017) · PLoS ONE · doi:10.1371/journal.pone.0169194 · Cited by 28 · see citing works

Intermittent Fasting: Potential Utility in the Treatment of Chronic Pain across the Clinical Spectrum

Caron, J. P., Kreher, M. A., Mickle, A. M., Wu, S., Przkora, R., Estores, I. M., & Sibille, K. T. (2022) · Nutrients · doi:10.3390/nu14122536 · Cited by 27 · see citing works

Diet choice in frugivorous bats: gourmets or operational pragmatists?

Orr, T. J., Ortega, J., Medellín, R. A., Sánchez, C. D., & Hammond, K. A. (2016) · Journal of Mammalogy · doi:10.1093/jmammal/gyw122 · Cited by 27 · see citing works

Maternal propionate supplementation ameliorates glucose and lipid metabolic disturbance in hypoxia-induced fetal growth restriction

Chen, D., Wang, Y., Li, S.-P., Zhao, H., Jiang, F., Wu, Y., Tong, Y., & Pang, Q. (2022) · Food & Function · doi:10.1039/d2fo01481e · Cited by 26 · see citing works

Maternal body mass index impacts fetal-placental size at birth and umbilical cord oxygen values with implications for regulatory mechanisms

Richardson, B. S., Ruttinger, S., Brown, H. K., Regnault, T. R. H., & de Vrijer, B. (2017) · Early Human Development · doi:10.1016/j.earlhumdev.2017.06.009 · Cited by 27 · see citing works

Pregnancy after Bariatric Surgery: A Nested Case-Control Study of Risk Factors for Small for Gestational Age Babies in AURORA

Akhter, Z., Heslehurst, N., Ceulemans, D., Rankin, J. M., Ackroyd, R., & Devlieger, R. (2021) · Nutrients · doi:10.3390/nu13051699 · Cited by 25 · see citing works

Maternal Underweight and Obesity Are Associated with Placental Pathologies in Human Pregnancy

Scott, H., Grynspan, D., Anderson, L. N., & Connor, K. L. (2022) · Reproductive Sciences · doi:10.1007/s43032-022-00983-2 · Cited by 28 · see citing works

Regional changes of placental vascularization in preeclampsia: A review

Sahay, A. S., Sundrani, D. P., & Joshi, S. (2015) · IUBMB Life · doi:10.1002/iub.1407 · Cited by 25 · see citing works

Maternal supplementation with citrulline or arginine during gestation impacts fetal amino acid availability in a model of intrauterine growth restriction (IUGR)

Bourdon, A., Hannigsberg, J., Misbert, E., Tran, T. N., Amarger, V., Ferchaud‐Roucher, V., Winer, N., & Darmaun, D. (2020) · Clinical Nutrition · doi:10.1016/j.clnu.2020.03.036 · Cited by 23 · see citing works

Does low birth weight share common genetic or environmental risk with childhood disruptive disorders?

Ficks, C. A., Lahey, B. B., & Waldman, I. D. (2013) · Journal of Abnormal Psychology · doi:10.1037/a0033079 · Cited by 24 · see citing works

Maternal Perceived Stress during Pregnancy Increases Risk for Low Neonatal Iron at Delivery and Depletion of Storage Iron at One Year

Rendina, D. N., Blohowiak, S. E., Coe, C. L., & Kling, P. J. (2018) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2018.04.040 · Cited by 25 · see citing works

Effects of Dietary L-arginine Supplementation from Conception to Post- Weaning in Piglets

Che, D., Adams, S., Zhao, B. X., Qin, G., & Jiang, H. (2019) · Current Protein and Peptide Science · doi:10.2174/1389203720666190125104959 · Cited by 24 · see citing works

Associations between Nutrients in One-Carbon Metabolism and Fetal DNA Methylation in Pregnancies with or without Gestational Diabetes Mellitus

Kadam, I., Dalloul, M., Hausser, J., Huntley, M., Hoepner, L., Fordjour, L., Hittelman, J., Saxena, A., Liu, J., Futterman, I. D., et al. (2023) · Clinical Epigenetics · doi:10.1186/s13148-023-01554-1 · Cited by 23 · see citing works

How should the welfare of fetal and neurologically immature postnatal animals be protected?

Campbell, M., Mellor, D. J., & Sandøe, P. (2014) · Animal Welfare · doi:10.7120/09627286.23.4.369 · Cited by 24 · see citing works

Better Diet Quality before Pregnancy Is Associated with Reduced Risk of Gastroschisis in Hispanic Women

Feldkamp, M. L., Krikov, S. V., Botto, L. D., Shaw, G. M., & Carmichael, S. L. (2014) · Journal of Nutrition · doi:10.3945/jn.114.201376 · Cited by 23 · see citing works

Perinatal undernutrition associated to experimental model of cerebral palsy increases adverse effects on chewing in young rats

Lacerda, D. C., Ferraz‐Pereira, K. N., Visco, D. B., Pontes, P. B., Chaves, W. F., Guzmán‐Quevedo, O., Manhães‐de‐Castro, R., & Toscano, A. E. (2017) · Physiology & Behavior · doi:10.1016/j.physbeh.2017.01.043 · Cited by 23 · see citing works

Eating disorders are associated with adverse obstetric and perinatal outcomes: a systematic review

das Neves, M. D. C. L., Teixeira, A. A., Garcia, F. M., Rennó, J., da Silva, A. G., Cantilino, A., Rosa, C. E., Ribeiro, J. D. A. M., Rocha, R., Lobo, H. R., et al. (2021) · Brazilian Journal of Psychiatry · doi:10.1590/1516-4446-2020-1449 · Cited by 22 · see citing works

Meta-analysis of morphometric parameters of late-gestation fetal sheep developed under natural and artificial constraints1

Gootwine, E. (2013) · Journal of Animal Science · doi:10.2527/jas.2013-5363 · Cited by 22 · see citing works

Effect of paternal folate deficiency on placental folate content and folate receptor α expression in rats

Kim, H. W., Choi, Y. J., Kim, K. N., Tamura, T., & Chang, N. (2011) · Nutrition Research and Practice · doi:10.4162/nrp.2011.5.2.112 · Cited by 22 · see citing works

Morphometric analysis of the placenta in the New World mouse Necromys lasiurus (Rodentia, Cricetidae): a comparison of placental development in cricetids and murids

Favaron, P. O., Mess, A., de Oliveira, M. F., Gabory, A., Miglino, M. A., Chavatte‐Palmer, P., & Couturier‐Tarrade, A. (2013) · Reproductive Biology and Endocrinology · doi:10.1186/1477-7827-11-10 · Cited by 22 · see citing works

The Revised WIC Food Package and Child Development: A Quasi-Experimental Study

Guan, A., Hamad, R., Batra, A., Bush, N. R., Tylavsky, F. A., & LeWinn, K. Z. (2021) · PEDIATRICS · doi:10.1542/peds.2020-1853 · Cited by 21 · see citing works

Altered metabolic homeostasis between vitamin D and long chain polyunsaturated fatty acids in preeclampsia

Nandi, A. A., Wadhwani, N. S., & Joshi, S. (2017) · Medical Hypotheses · doi:10.1016/j.mehy.2017.01.009 · Cited by 21 · see citing works

Exploring the role of oxidative stress, fatty acids and neurotrophins in gestational diabetes mellitus

Jadhav, A. T., Khaire, A. A., & Joshi, S. (2020) · Growth Factors · doi:10.1080/08977194.2021.1895143 · Cited by 22 · see citing works

Recapitulation of characteristics of human placental vascular insufficiency in a novel mouse model

Habli, M. A., Jones, H. N., Aronow, B. J., Omar, K., & Crombleholme, T. M. (2013) · Placenta · doi:10.1016/j.placenta.2013.09.011 · Cited by 20 · see citing works

Effect of nutrient intake during pregnancy on fetal and placental growth and vascular development

Redmer, D. A., Wallace, J. M., & Reynolds, L. P. (2004) · Domestic Animal Endocrinology · doi:10.1016/j.domaniend.2004.06.006 · Cited by 294 · see citing works

Maternal Micronutrients, Placental Growth, and Fetal Outcome

Duttaroy, A. K., & Basak, S. (2015) · CRC Press eBooks · doi:10.1201/b19151-15

Nutrition, placental growth and pregnancy outcome

Wallace, J. M. (2008)

Maternal nutrition, nutrient exchange, and fetal growth.

Rosso, P. (1977) · PubMed · Cited by 18 · see citing works

Nutrition in Pregnancy: Volume I

Morrison, J. L., & Regnault, T. R. H. (n.d.) · Directory of Open access Books (OAPEN Foundation)