Mitochondria: A central target for sex differences in pathologies

ROS function in redox signaling and oxidative stress

Schieber, M., & Chandel, N. S. (2014) · Current Biology · doi:10.1016/j.cub.2014.03.034 · Cited by 6,931 · see citing works

Extension of murine life span by overexpression of catalase targeted to mitochondria

Schriner, S. E., Linford, N. J., Martin, G. M., Treuting, P., Ogburn, C. E., Emond, M., Coskun, P. E., Ladiges, W., Wolf, N., Van Remmen, H., et al. (2005) · Science · doi:10.1126/science.1106653 · Cited by 1,724 · see citing works

PGC-1α, SIRT1 and AMPK, an energy sensing network that controls energy expenditure

Cantó, C., & Auwerx, J. (2009) · Current Opinion in Lipidology · doi:10.1097/mol.0b013e328328d0a4 · Cited by 1,624 · see citing works

Sex Differences in Stroke Epidemiology

Appelros, P., Stegmayr, B., & Terént, A. (2009) · Stroke · doi:10.1161/strokeaha.108.540781 · Cited by 1,034 · see citing works

Clinical epidemiology of Alzheimer’s disease: assessing sex and gender differences

Mielke, M., Vemuri, P., & Rocca, W. (2014) · Clinical Epidemiology · doi:10.2147/clep.s37929 · Cited by 1,021 · see citing works

Transcriptional control of mitochondrial biogenesis: the central role of PGC-1

Ventura-Clapier, R., Garnier, A., & Veksler, V. (2008) · Cardiovascular Research · doi:10.1093/cvr/cvn098 · Cited by 932 · see citing works

PGC-1 α, A Potential Therapeutic Target for Early Intervention in Parkinson’s Disease

Zheng, B., Liao, Z., Locascio, J. J., Lesniak, K. A., Roderick, S. S., Watt, M. L., Eklund, A. C., Zhang‐James, Y., Kim, P. D., Hauser, M. A., et al. (2010) · Science Translational Medicine · doi:10.1126/scitranslmed.3001059 · Cited by 854 · see citing works

Sex-specific genetic architecture of human disease

Ober, C., Loisel, D. A., & Gilad, Y. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2415 · Cited by 787 · see citing works

Gender in cardiovascular diseases: impact on clinical manifestations, management, and outcomes

Regitz‐Zagrosek, V., Oertelt‐Prigione, S., Prescott, E., Franconi, F., Gerdts, E., Foryst‐Ludwig, A., Maas, A. H. E. M., Kautzky‐Willer, A., Knappe-Wegner, D., Kintscher, U., et al. (2015) · European Heart Journal · doi:10.1093/eurheartj/ehv598 · Cited by 744 · see citing works

Animal models of diabetes mellitus

Rees, A., & Alcolado, J. C. (2005) · Diabetic Medicine · doi:10.1111/j.1464-5491.2005.01499.x · Cited by 735 · see citing works

Natural history of amyotrophic lateral sclerosis in a database population Validation of a scoring system and a model for survival prediction

Haverkamp, L. J., Appel, V., & Appel, S. H. (1995) · Brain · doi:10.1093/brain/118.3.707 · Cited by 697 · see citing works

Mitochondria from females exhibit higher antioxidant gene expression and lower oxidative damage than males

Borrás, C., Sastre, J., García-Sala, D., Lloret, A., Pallardó, F. V., & Viña, J. (2003) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(02)01356-4 · Cited by 654 · see citing works

The Mitochondrial Proteome and Human Disease

Calvo, S. E., & Mootha, V. K. (2010) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-082509-141720 · Cited by 590 · see citing works

Sex and gender differences in health: Science & Society Series on Sex and Science

Regitz‐Zagrosek, V. (2012) · The EMBO Reports · doi:10.1038/embor.2012.87 · Cited by 572 · see citing works

Mitochondrial localization of estrogen receptor β

Yang, S.-H., Liu, R., Perez, E., Wen, Y., Stevens, S. M., Valencia, T. G., Brun‐Zinkernagel, A., Prókai, L., Will, Y., Dykens, J. A., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0306948101 · Cited by 501 · see citing works

The mitochondrial permeability transition pore: Molecular nature and role as a target in cardioprotection

Bernardi, P., & Lisa, F. D. (2014) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2014.09.023 · Cited by 499 · see citing works

Energy metabolism in heart failure

Ventura‐Clapier, R., Garnier, A., & Veksler, V. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.055095 · Cited by 499 · see citing works

Sex differences in Parkinson’s disease

Gillies, G. E., Pienaar, I. S., Vohra, S., & Qamhawi, Z. (2014) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.02.002 · Cited by 495 · see citing works

Relationship Between Testosterone Levels, Insulin Sensitivity, and Mitochondrial Function in Men

Pitteloud, N., Mootha, V. K., Dwyer, A. A., Hardin, M., Lee, H., Eriksson, K.-F., Tripathy, D., Yialamas, M., Groop, L., Elahi, D., et al. (2005) · Diabetes Care · doi:10.2337/diacare.28.7.1636 · Cited by 472 · see citing works

Gender differences in the metabolic syndrome and their role for cardiovascular disease

Regitz‐Zagrosek, V., Lehmkuhl, E., & Weickert, M. O. (2006) · Clinical Research in Cardiology · doi:10.1007/s00392-006-0351-5 · Cited by 457 · see citing works

Influence of endurance exercise training and sex on intramyocellular lipid and mitochondrial ultrastructure, substrate use, and mitochondrial enzyme activity

Tarnopolsky, M. A., Rennie, C. D., Robertshaw, H. A., Fedak-Tarnopolsky, S. N., Devries, M. C., & Hamadeh, M. J. (2007) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00472.2006 · Cited by 457 · see citing works

Why Women Have More Alzheimer's Disease Than Men: Gender and Mitochondrial Toxicity of Amyloid-β Peptide

Viña, J., & Lloret, A. (2010) · Journal of Alzheimer's Disease · doi:10.3233/jad-2010-100501 · Cited by 447 · see citing works

A gender-related defect in lipid metabolism and glucose homeostasis in peroxisome proliferator- activated receptor alpha- deficient mice.

Djouadi, F., Weinheimer, C. J., Saffitz, J. E., Pitchford, C., Bastin, J., Gonzalez, F. J., & Kelly, D. P. (1998) · Journal of Clinical Investigation · doi:10.1172/jci3949 · Cited by 410 · see citing works

New insights into doxorubicin-induced cardiotoxicity: The critical role of cellular energetics

Tokarska-Schlattner, M., Zaugg, M., Zuppinger, C., Wallimann, T., & Schlattner, U. (2006) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2006.06.009 · Cited by 353 · see citing works

Sex Differences in the Phosphorylation of Mitochondrial Proteins Result in Reduced Production of Reactive Oxygen Species and Cardioprotection in Females

Lagranha, C. J., Deschamps, A. M., Aponte, A. M., Steenbergen, C., & Murphy, E. (2010) · Circulation Research · doi:10.1161/circresaha.109.213645 · Cited by 328 · see citing works

Estrogenic control of mitochondrial function and biogenesis

Klinge, C. M. (2008) · Journal of Cellular Biochemistry · doi:10.1002/jcb.21936 · Cited by 320 · see citing works

Estrogen Increases Mitochondrial Efficiency and Reduces Oxidative Stress in Cerebral Blood Vessels

Stirone, C., Duckles, S. P., Krause, D. N., & Procaccio, V. (2005) · Molecular Pharmacology · doi:10.1124/mol.105.014662 · Cited by 315 · see citing works

Threshold Effect and Tissue Specificity

Rossignol, R., Malgat, M., Mazat, J.-P., & Letellier, T. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.47.33426 · Cited by 288 · see citing works

Incidence and prevalence of ALS in Ireland, 1995–1997

Traynor, B. J., Codd, M., Corr, B., Forde, C., Frost, E., & Hardiman, O. M. (1999) · Neurology · doi:10.1212/wnl.52.3.504 · Cited by 287 · see citing works

Why females live longer than males? Importance of the upregulation of longevity‐associated genes by oestrogenic compounds

Viña, J., Borrás, C., Gambini, J., Sastre, J., & Pallardó, F. V. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.03.090 · Cited by 271 · see citing works

Defects in Mitochondrial Dynamics and Metabolomic Signatures of Evolving Energetic Stress in Mouse Models of Familial Alzheimer's Disease

Trushina, E. V., Nemutlu, E., Zhang, S., Christensen, T. A., Camp, J. J., Mesa, J., Siddiqui, A., Tamura, Y., Sesaki, H., Wengenack, T. M., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032737 · Cited by 268 · see citing works

Regulation of mitochondrial respiratory chain biogenesis by estrogens/estrogen receptors and physiological, pathological and pharmacological implications

Chen, J., Cammarata, P. R., Baines, C. P., & Yager, J. D. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2009.06.001 · Cited by 266 · see citing works

Neural mitochondrial Ca 2+ capacity impairment precedes the onset of motor symptoms in G93A Cu/Zn‐superoxide dismutase mutant mice

Damiano, M. G., Starkov, A. A., Petri, S., Kipiani, K., Kiaei, M., Mattiazzi, M., Beal, M. F., & Manfredi, G. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03619.x · Cited by 247 · see citing works

Estradiol stimulates transcription of nuclear respiratory factor-1 and increases mitochondrial biogenesis

Mattingly, K. A., Ivanova, M. M., Riggs, K. A., Wickramasinghe, N. S., Barch, M. J., & Klinge, C. M. (2008) · Molecular Endocrinology · doi:10.1210/me.2007-0029 · Cited by 243 · see citing works

Mitochondrial dynamics in the adult cardiomyocytes: which roles for a highly specialized cell?

Piquereau, J., Caffin, F., Novotová, M., Lemaire, C., Veksler, V., Garnier, A., Ventura‐Clapier, R., & Joubert, F. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00102 · Cited by 235 · see citing works

Bioenergetics of the failing heart

Ventura‐Clapier, R., Garnier, A., Veksler, V., & Joubert, F. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2010.09.006 · Cited by 233 · see citing works

Sex and gender differences in symptoms of myocardial ischaemia

Regitz‐Zagrosek, V. (2011) · European Heart Journal · doi:10.1093/eurheartj/ehr272 · Cited by 232 · see citing works

Modulation of Estrogen Receptor-α Transcriptional Activity by the Coactivator PGC-1

Tcherepanova, I. Y., Puigserver, P., Norris, J. D., Spiegelman, B. M., & McDonnell, D. P. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m001364200 · Cited by 218 · see citing works

Sex-dependent Thermogenesis, Differences in Mitochondrial Morphology and Function, and Adrenergic Response in Brown Adipose Tissue

Rodrı́guez-Cuenca, S., Pujol, E., Justo, R., Frontera, M., Oliver, J., Gianotti, M., & Roca, P. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m207229200 · Cited by 206 · see citing works

Mitochondrial mechanisms of estrogen neuroprotection

Simpkins, J. W., Yi, K. D., Yang, S., & Dykens, J. A. (2009) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2009.11.013 · Cited by 205 · see citing works

Starving Neurons Show Sex Difference in Autophagy

Du, L., Hickey, R. W., Bayir, H., Watkins, S. C., Tyurin, V. A., Guo, F., Kochanek, P. M., Jenkins, L. W., Ren, J., Gibson, G., et al. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m804396200 · Cited by 204 · see citing works

Estrogen: An Emerging Regulator of Insulin Action and Mitochondrial Function

Gupte, A. A., Pownall, H. J., & Hamilton, D. J. (2015) · Journal of Diabetes Research · doi:10.1155/2015/916585 · Cited by 200 · see citing works

Novel quantitative phenotypes of exercise training in mouse models

De Bono, J. P., Adlam, D., Paterson, D. J., & Channon, K. M. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00694.2005 · Cited by 197 · see citing works

Tissue-specific differences in mitochondrial activity and biogenesis

Fernández‐Vizarra, E., Enrı́quez, J. A., Martos, A. P., Montoya, J., & Fernández‐Silva, P. (2010) · Mitochondrion · doi:10.1016/j.mito.2010.09.011 · Cited by 195 · see citing works

Sex and Gender Differences in Myocardial Hypertrophy and Heart Failure

Regitz‐Zagrosek, V., Oertelt‐Prigione, S., Seeland, U., & Hetzer, R. (2010) · Circulation Journal · doi:10.1253/circj.cj-10-0196 · Cited by 193 · see citing works

Sex differences in mitochondrial (dys)function: Implications for neuroprotection

Demarest, T. G., & McCarthy, M. M. (2015) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-014-9583-7 · Cited by 192 · see citing works

Estrogen protects neuronal cells from amyloid beta-induced apoptosis via regulation of mitochondrial proteins and function

Nilsen, J., Chen, S., Irwin, R. W., Iwamoto, S. J., & Brinton, R. D. (2006) · BMC Neuroscience · doi:10.1186/1471-2202-7-74 · Cited by 175 · see citing works

Sex and Gender Differences in Central Nervous System-Related Disorders

Zagni, E., Simoni, L., & Colombo, D. (2016) · Neuroscience Journal · doi:10.1155/2016/2827090 · Cited by 173 · see citing works

Caloric restriction and gender modulate cardiac muscle mitochondrial H2O2 production and oxidative damage

Colom, B., Oliver, J., Roca, P., & García-Palmer, F. (2007) · Cardiovascular Research · doi:10.1016/j.cardiores.2007.02.001 · Cited by 170 · see citing works

Roles of mitochondria in human disease

Duchen, M. R., & Szabadkai, G. (2010) · Essays in Biochemistry · doi:10.1042/bse0470115 · Cited by 167 · see citing works

Estrogen Receptors α and β Mediate Distinct Pathways of Vascular Gene Expression, Including Genes Involved in Mitochondrial Electron Transport and Generation of Reactive Oxygen Species

O’Lone, R., Knorr, K., Jaffe, I., Schaffer, M., Martini, P., Karas, R., Bienkowska, J., Mendelsohn, M., & Hansen, U. (2007) · Molecular Endocrinology · doi:10.1210/me.2006-0497 · Cited by 161 · see citing works

Mitochondrial Effects of Estrogen Are Mediated by Estrogen Receptor α in Brain Endothelial Cells

Razmara, A., Sunday, L., Stirone, C., Wang, X. B., Krause, D. N., Duckles, S. P., & Procaccio, V. (2008) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.107.134072 · Cited by 161 · see citing works

Sex-specific pathways in early cardiac response to pressure overload in mice

Witt, H., Schubert, C., Jaekel, J., Fliegner, D., Penkalla, A., Tiemann, K., Stypmann, J., Roepcke, S., Brokat, S., Mahmoodzadeh, S., et al. (2008) · Journal of Molecular Medicine · doi:10.1007/s00109-008-0385-4 · Cited by 159 · see citing works

Effect of Sex Differences on Brain Mitochondrial Function and Its Suppression by Ovariectomy and in Aged Mice

Gaignard, P., Savouroux, S., Liere, P., Pianos, A., Thérond, P., Schumacher, M., Slama, A., & Guennoun, R. (2015) · Endocrinology · doi:10.1210/en.2014-1913 · Cited by 150 · see citing works

Sexual Dimorphism of Doxorubicin-Mediated Cardiotoxicity

Moulin, M., Piquereau, J., Matéo, P., Fortin, D., Rücker‐Martin, C., Gressette, M., Lefebvre, F., Grešíková, M., Solgadi, A., Veksler, V., et al. (2014) · Circulation Heart Failure · doi:10.1161/circheartfailure.114.001180 · Cited by 147 · see citing works

Sex and Gender Aspects in Clinical Medicine

Franconi, F., Straface, E., Chessa, R., Rosano, G., & Sanna, M. (2011) · Springer eBooks · doi:10.1007/978-0-85729-832-4 · Cited by 140 · see citing works

Sex and Life Expectancy

Seifarth, J., McGowan, C. L. M., & Milne, K. J. (2012) · Gender Medicine · doi:10.1016/j.genm.2012.10.001 · Cited by 139 · see citing works

Gender Differences in Cardiac Ischemic Injury and Protection—Experimental Aspects

Ostadal, B., Netuka, I., Malý, J., Bešík, J., & Ostadalova, I. (2009) · Experimental Biology and Medicine · doi:10.3181/0812-mr-362 · Cited by 135 · see citing works

Gender dimorphism in rat liver mitochondrial oxidative metabolism and biogenesis

Justo, R., Boada, J., Frontera, M., Oliver, J., Bermúdez, J., & Gianotti, M. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00035.2005 · Cited by 133 · see citing works

Cardiac adaptation to chronic high-altitude hypoxia: Beneficial and adverse effects

Ošťádal, B., & Kolář, F. (2007) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2007.03.005 · Cited by 130 · see citing works

Beneficial effects of endurance training on cardiac and skeletal muscle energy metabolism in heart failure

Ventura‐Clapier, R., Mettauer, B., & Bigard, X. A. (2006) · Cardiovascular Research · doi:10.1016/j.cardiores.2006.09.003 · Cited by 130 · see citing works

Testosterone regulation of Alzheimer-like neuropathology in male 3xTg-AD mice involves both estrogen and androgen pathways

Rosario, E. R., Carroll, J. C., & Pike, C. J. (2010) · Brain Research · doi:10.1016/j.brainres.2010.08.068 · Cited by 126 · see citing works

Sex-specific regulation of aging and apoptosis

Tower, J. (2006) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2006.05.001 · Cited by 125 · see citing works

The connection between inner membrane topology and mitochondrial function

Mannella, C. A., Lederer, W. J., & Jafri, M. S. (2013) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2013.05.001 · Cited by 123 · see citing works

Adipose Tissue Resting Energy Expenditure and Expression of Genes Involved in Mitochondrial Function Are Higher in Women than in Men

Nookaew, I., Svensson, P., Jacobson, P., Jernås, M., Taube, M., Larsson, I., Andersson‐Assarsson, J. C., Sjöström, L., Froguel, P., Walley, A. J., et al. (2012) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2012-2764 · Cited by 122 · see citing works

Effects of estrogen on lifespan and motor functions in female hSOD1 G93A transgenic mice

Choi, C., Lee, Y., Gwag, B. J., Cho, S. I., Kim, S., & Suh‐Kim, H. (2007) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2007.10.024 · Cited by 119 · see citing works

ALS clinical trials

Chiò, A., Canosa, A., Gallo, S., Cammarosano, S., Moglia, C., Fuda, G., Calvo, A., Gabriele, M., & For the PARALS group (2011) · Neurology · doi:10.1212/wnl.0b013e318232ab9b · Cited by 114 · see citing works

Gender and myocardial salvage after reperfusion treatment in acute myocardial infarction

Mehilli, J., Ndrepepa, G., Kastrati, A., Nekolla, S. G., Markwardt, C., Bollwein, H., Pache, J., Martinoff, S. A., Dirschinger, J., Schwaiger, M., et al. (2005) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2004.11.054 · Cited by 113 · see citing works

From ATP to PTP and Back

Bernardi, P., Lisa, F. D., Fogolari, F., & Lippe, G. (2015) · Circulation Research · doi:10.1161/circresaha.115.306557 · Cited by 113 · see citing works

Gender-specific proteomic alterations in glycolytic and mitochondrial pathways in aging monkey hearts

YAN, L., GE, H., LI, H., LIEBER, S., NATIVIDAD, F., RESUELLO, R., KIM, S., AKEJU, S., SUN, A., & LOO, K. (2004) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2004.06.012 · Cited by 111 · see citing works

Alzheimer, mitochondria and gender

Grimm, A., Mensah‐Nyagan, A. G., & Eckert, A. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.04.012 · Cited by 107 · see citing works

Redox Features of the Cell: A Gender Perspective

Malorni, W., Campesi, I., Straface, E., Vella, S., & Franconi, F. (2007) · Antioxidants and Redox Signaling · doi:10.1089/ars.2007.1596 · Cited by 103 · see citing works

Testosterone-mediated sexual dimorphism of the rodent heart. Ventricular lysosomes, mitochondria, and cell growth are modulated by androgens.

Koenig, H., Goldstone, A. D., & Lu, C. Y. (1982) · Circulation Research · doi:10.1161/01.res.50.6.782 · Cited by 97 · see citing works

Sexual dimorphism in liver mitochondrial oxidative capacity is conserved under caloric restriction conditions

Valle, A., Guevara, R., García-Palmer, F., Roca, P., & Oliver, J. (2007) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00203.2007 · Cited by 96 · see citing works

Mitochondrial and sex steroid hormone crosstalk during aging

Velarde, M. C. (2014) · Longevity & Healthspan · doi:10.1186/2046-2395-3-2 · Cited by 96 · see citing works

Estrogen and Mitochondria: A New Paradigm for Vascular Protection?

DUCKLES, S. P. (2006) · Molecular Interventions · doi:10.1124/mi.6.1.6 · Cited by 95 · see citing works

PGC-1α activity in nigral dopamine neurons determines vulnerability to α-synuclein

Ciron, C., Zheng, L., Bobela, W., Knott, G. W., Leone, T. C., Kelly, D. P., & Schneider, B. L. (2015) · Acta Neuropathologica Communications · doi:10.1186/s40478-015-0200-8 · Cited by 95 · see citing works

Sex differences in myocardial infarct size are abolished by sarcolemmal KATPchannel blockade in rat

Johnson, M. S., Moore, R. L., & Brown, D. A. (2006) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01291.2005 · Cited by 93 · see citing works

Redox state and gender differences in vascular smooth muscle cells

Malorni, W., Straface, E., Matarrese, P., Ascione, B., Coinu, R., Canu, S., Galluzzo, P., Marino, M., & Franconi, F. (2008) · FEBS Letters · doi:10.1016/j.febslet.2008.01.034 · Cited by 91 · see citing works

Are the available experimental models of type 2 diabetes appropriate for a gender perspective?

Franconi, F., Seghieri, G., Canu, S., Straface, E., Campesi, I., & Malorni, W. (2007) · Pharmacological Research · doi:10.1016/j.phrs.2007.11.007 · Cited by 91 · see citing works

Skeletal muscle of female rats exhibit higher mitochondrial mass and oxidative-phosphorylative capacities compared to males

Colom, B., Alcolea, M., Valle, A., Oliver, J., Roca, P., & García-Palmer, F. (2007) · Cellular Physiology and Biochemistry · doi:10.1159/000099208 · Cited by 89 · see citing works

Significant role of estrogen in maintaining cardiac mitochondrial functions

Rattanasopa, C., Phungphong, S., Wattanapermpool, J., & Bupha‐Intr, T. (2014) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2014.11.009 · Cited by 88 · see citing works

Sex/Gender Medicine The Biological Basis for Personalized Care in Cardiovascular Medicine

Arain, F. A., Kuniyoshi, F. H. S., Abdalrhim, A. D., & Miller, V. M. (2009) · Circulation Journal · doi:10.1253/circj.cj-09-0588 · Cited by 84 · see citing works

Pgc-1 upregulation Via estrogen receptors: A common mechanism of salutary effects of estrogen and flutamide on heart function after trauma-hemorrhage

Hsieh, Y.-C., Yang, S., Choudhry, M. A., Yu, H.-P., Rue, L. W., Bland, K. I., & Chaudry, I. H. (2005) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00682.2005 · Cited by 84 · see citing works

Mammalian cardiolipin biosynthesis

Mejia, E. M., Nguyen, H., & Hatch, G. M. (2013) · Chemistry and Physics of Lipids · doi:10.1016/j.chemphyslip.2013.10.001 · Cited by 82 · see citing works

Sex differences in physiological cardiac hypertrophy are associated with exercise-mediated changes in energy substrate availability

Foryst‐Ludwig, A., Kreissl, M. C., Sprang, C., Thalke, B., Böhm, C., Benz, V., Gürgen, D., Dragun, D., Schubert, C., Mai, K., et al. (2011) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01222.2010 · Cited by 82 · see citing works

Estradiol stimulates mitochondrial biogenesis and adiponectin expression in skeletal muscle

Capllonch-Amer, G., Sbert-Roig, M., Galmés-Pascual, B. M., Proenza, A. M., Lladó, I., Gianotti, M., & García-Palmer, F. (2014) · Journal of Endocrinology · doi:10.1530/joe-14-0008 · Cited by 81 · see citing works

Sexual Dimorphism in the Expression of Mitochondria-Related Genes in Rat Heart at Different Ages

Vijay, V., Han, T., Moland, C. L., Kwekel, J. C., Fuscoe, J. C., & Desai, V. G. (2015) · PLoS ONE · doi:10.1371/journal.pone.0117047 · Cited by 80 · see citing works

Gender modulation of Ca2+ uptake in cardiac mitochondria

ARIELI, Y. (2004) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2004.04.023 · Cited by 72 · see citing works

Long-term High-fat-diet Feeding Impairs Mitochondrial Biogenesis in Liver of Male and Female Rats

Nadal-Casellas, A., Amengual-Cladera, E., Proenza, A. M., Lladó, I., & Gianotti, M. (2010) · Cellular Physiology and Biochemistry · doi:10.1159/000320552 · Cited by 71 · see citing works

Evolutionary origin and consequences of uniparental mitochondrial inheritance

Hoekstra, R. F. (2000) · Human Reproduction · doi:10.1093/humrep/15.suppl_2.102 · Cited by 68 · see citing works

Opposite effects of 17-Β estradiol and testosterone on mitochondrial biogenesis and adiponectin synthesis in white adipocytes

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Proteomic insights into chronic anthracycline cardiotoxicity

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