Towards Retinoid Therapy for Alzheimers Disease

Control of Regulatory T Cell Development by the Transcription Factor <i>Foxp3</i>

Hori, S., Nomura, T., & Sakaguchi, S. (2003) · Science · doi:10.1126/science.1079490 · Cited by 8,187 · see citing works

Foxp3 programs the development and function of CD4+CD25+ regulatory T cells

Fontenot, J. D., Gavin, M. A., & Rudensky, A. Y. (2003) · Nature Immunology · doi:10.1038/ni904 · Cited by 7,745 · see citing works

Signaling by intrathymic cytokines, not T cell antigen receptors, specifies CD8 lineage choice and promotes the differentiation of cytotoxic-lineage T cells

Park, J., Adoro, S., Guinter, T. I., Erman, B., Alag, A., Catálfamo, M., Kimura, M. Y., Cui, Y., Lucas, P. J., Gress, R. E., et al. (2010) · Nature Immunology · doi:10.1038/ni.1840 · Cited by 5,835 · see citing works

Immunologic self-tolerance maintained by activated T cells expressing IL-2 receptor α-chains (CD25). Breakdown of a single mechanism of self-tolerance causes various autoimmune diseases

Sakaguchi, S., Sakaguchi, N., Asano, M., Itoh, M., & Toda, M. (1995) · The Journal of Immunology · doi:10.4049/jimmunol.155.3.1151 · Cited by 5,608 · see citing works

The Orphan Nuclear Receptor RORγt Directs the Differentiation Program of Proinflammatory IL-17+ T Helper Cells

Ivanov, I. I., McKenzie, B. S., Zhou, L., Tadokoro, C. E., Lepelley, A., Lafaille, J. J., Cua, D. J., & Littman, D. R. (2006) · Cell · doi:10.1016/j.cell.2006.07.035 · Cited by 5,145 · see citing works

Inflammation and Alzheimer’s disease

Akiyama, H. (2000) · Neurobiology of Aging · doi:10.1016/s0197-4580(00)00124-x · Cited by 4,514 · see citing works

A functionally specialized population of mucosal CD103+ DCs induces Foxp3+ regulatory T cells via a TGF-β– and retinoic acid–dependent mechanism

Coombes, J. L., Siddiqui, K. R. R., Arancibia-Cárcamo, C. V., Hall, J. A., Sun, C., Belkaid, Y., & Powrie, F. M. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070590 · Cited by 2,708 · see citing works

Reciprocal T _H 17 and Regulatory T Cell Differentiation Mediated by Retinoic Acid

Mucida, D., Park, Y., Kim, G., Turovskaya, O., Scott, I., Kronenberg, M., & Cheroutre, H. (2007) · Science · doi:10.1126/science.1145697 · Cited by 1,982 · see citing works

Small intestine lamina propria dendritic cells promote de novo generation of Foxp3 T reg cells via retinoic acid

Sun, C., Hall, J. A., Blank, R. B., Bouladoux, N. J., Oukka, M., Mora, J. R., & Belkaid, Y. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070602 · Cited by 1,880 · see citing works

Loss of Functional Suppression by CD4+CD25+ Regulatory T Cells in Patients with Multiple Sclerosis

Viglietta, V., Baecher‐Allan, C., Weiner, H. L., & Hafler, D. A. (2004) · The Journal of Experimental Medicine · doi:10.1084/jem.20031579 · Cited by 1,858 · see citing works

Human TH17 lymphocytes promote blood-brain barrier disruption and central nervous system inflammation

Kebir, H., Kreymborg, K., Ifergan, I., Dodelet-Devillers, A., Cayrol, R., Bernard, M., Giuliani, F., Arbour, N., Becher, B., & Prat, A. (2007) · Nature Medicine · doi:10.1038/nm1651 · Cited by 1,759 · see citing works

The Biological Functions of T Helper 17 Cell Effector Cytokines in Inflammation

Ouyang, W., Kolls, J. K., & Zheng, Y. (2008) · Immunity · doi:10.1016/j.immuni.2008.03.004 · Cited by 1,698 · see citing works

The induction of differentiation in teratocarcinoma stem cells by retinoic acid

Strickland, S., & Mahdavi, V. (1978) · Cell · doi:10.1016/0092-8674(78)90008-9 · Cited by 1,420 · see citing works

Acute promyelocytic leukemia: from highly fatal to highly curable

Wang, Z., & Chen, Z. (2008) · Blood · doi:10.1182/blood-2007-07-102798 · Cited by 1,283 · see citing works

The role of inflammation in CNS injury and disease

Lucas, S., Rothwell, N. J., & Gibson, R. M. (2006) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0706400 · Cited by 1,272 · see citing works

Alzheimer’s disease

Cummings, J. L. (2004) · New England Journal of Medicine · doi:10.1056/nejmra040223 · Cited by 1,152 · see citing works

Cleavage of proBDNF by tPA/Plasmin Is Essential for Long-Term Hippocampal Plasticity

Pang, P. T., Teng, H. K., Zaitsev, E., Woo, N. T., Sakata, K., Zhen, S., Teng, K. K., Yung, W.-H., Hempstead, B. L., & Lu, B. (2004) · Science · doi:10.1126/science.1100135 · Cited by 1,136 · see citing works

Pillars Article: Control of Regulatory T Cell Development by the Transcription Factor Foxp3 . Science 2003. 299: 1057–1061

Hori, S., Nomura, T., & Sakaguchi, S. (2017) · The Journal of Immunology · doi:10.1093/jimmunol/198.3.981 · Cited by 1,067 · see citing works

Gene expression regulation by retinoic acid

Balmer, J. E., & Blomhoff, R. (2002) · Journal of Lipid Research · doi:10.1194/jlr.r100015-jlr200 · Cited by 1,039 · see citing works

Systemic infections and inflammation affect chronic neurodegeneration

Perry, V. H., Cunningham, C., & Holmes, C. (2007) · Nature Reviews Immunology · doi:10.1038/nri2015 · Cited by 1,027 · see citing works

The Foxp3+ regulatory T cell: a jack of all trades, master of regulation

Tang, Q., & Bluestone, J. A. (2008) · Nature Immunology · doi:10.1038/ni1572 · Cited by 1,026 · see citing works

Increased hippocampal neurogenesis in Alzheimer's disease

Jin, K., Peel, A. L., Mao, X. O., Xie, L., Cottrell, B. A., Henshall, D. C., & Greenberg, D. A. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2634794100 · Cited by 971 · see citing works

Overview of retinoid metabolism and function

Blomhoff, R., & Blomhoff, H. K. (2006) · Journal of Neurobiology · doi:10.1002/neu.20242 · Cited by 948 · see citing works

Ccr2 deficiency impairs microglial accumulation and accelerates progression of Alzheimer-like disease

El Khoury, J., Toft, M., Hickman, S. E., Means, T. K., Terada, K., Geula, C., & Luster, A. D. (2007) · Nature Medicine · doi:10.1038/nm1555 · Cited by 915 · see citing works

Retinoic acid in the development, regeneration and maintenance of the nervous system

Maden, M. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2212 · Cited by 896 · see citing works

All-trans retinoic acid mediates enhanced T reg cell growth, differentiation, and gut homing in the face of high levels of co-stimulation

Benson, M. J., Pino-Lagos, K., Rosemblatt, M., & Noelle, R. J. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070719 · Cited by 847 · see citing works

Association of olfactory dysfunction with risk for future Parkinson's disease

Ross, G. W., Petrovitch, H., Abbott, R. D., Tanner, C. M., Popper, J. S., Masaki, K., Launer, L. J., & White, L. R. (2007) · Annals of Neurology · doi:10.1002/ana.21291 · Cited by 739 · see citing works

Th17 Cell Differentiation: The Long and Winding Road

McGeachy, M. J., & Cua, D. J. (2008) · Immunity · doi:10.1016/j.immuni.2008.03.001 · Cited by 700 · see citing works

Control of muscle and neuronal differentiation in a cultured embryonal carcinoma cell line

McBurney, M. W., Jones-Villeneuve, E., Edwards, M. K. S., & Anderson, P. J. (1982) · Nature · doi:10.1038/299165a0 · Cited by 665 · see citing works

100 Years and Counting: Prospects for Defeating Alzheimer's Disease

Roberson, E. D., & Mucke, L. (2006) · Science · doi:10.1126/science.1132813 · Cited by 550 · see citing works

Immunologic reactions in amyotrophic lateral sclerosis brain and spinal cord tissue.

Kawamata, T., Akiyama, H., Yamada, T., & McGeer, P. L. (1992) · PubMed Central · Cited by 546 · see citing works

Retinoic acid treatment abrogates elastase-induced pulmonary emphysema in rats

Massaro, G. D. C., & Massaro, D. J. (1997) · Nature Medicine · doi:10.1038/nm0697-675 · Cited by 536 · see citing works

RAR and RXR modulation in cancer and metabolic disease

Altucci, L., Leibowitz, M. D., Ogilvie, K. M., de Lera, A. R., & Gronemeyer, H. (2007) · Nature Reviews Drug Discovery · doi:10.1038/nrd2397 · Cited by 517 · see citing works

ALS-causing SOD1 mutants generate vascular changes prior to motor neuron degeneration

Zhong, Z., Deane, R., Ali, Z., Parisi, M., Shapovalov, Y., O'Banion, M. K., Stojanovic, K., Sagare, A., Boillee, S., Cleveland, D. W., et al. (2008) · Nature Neuroscience · doi:10.1038/nn2073 · Cited by 476 · see citing works

Why new neurons? Possible functions for adult hippocampal neurogenesis

Kempermann, G. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-03-00635.2002 · Cited by 469 · see citing works

CD4+ T cells support glial neuroprotection, slow disease progression, and modify glial morphology in an animal model of inherited ALS

Beers, D. R., Henkel-Tigges, J., Zhao, W., Wang, J., & Appel, S. H. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0807419105 · Cited by 468 · see citing works

A Hundred Years of Alzheimer's Disease Research

Hardy, J. (2006) · Neuron · doi:10.1016/j.neuron.2006.09.016 · Cited by 467 · see citing works

Retinoic acid inhibits Th17 polarization and enhances FoxP3 expression through a Stat-3/Stat-5 independent signaling pathway

Elias, K. M., Laurence, A. D. J., Davidson, T. S., Stephens, G. L., Kanno, Y., Shevach, E. M., & O’Shea, J. J. (2007) · Blood · doi:10.1182/blood-2007-06-096438 · Cited by 448 · see citing works

Serum insulin-like growth factor I regulates brain amyloid-β levels

Carro, E., Trejo, J. L., Gómez‐Isla, T., LeRoith, D., & Torres‐Alemán, I. (2002) · Nature Medicine · doi:10.1038/nm793 · Cited by 448 · see citing works

Serum insulin-like growth factor I regulates brain amyloid-β levels

Carro, E., Jl, T., Gómez‐Isla, T., LeRoith, D., & Torres‐Alemán, I. (2002) · Nature Medicine · doi:10.1038/nm1202-793 · Cited by 442 · see citing works

Functional defect of regulatory CD4+CD25+ T cells in the thymus of patients with autoimmune myasthenia gravis

Balandina, A., Lécart, S., Dartevelle, P., Saoudi, A., & Berrih‐Aknin, S. (2004) · Blood · doi:10.1182/blood-2003-11-3900 · Cited by 429 · see citing works

Neuroprotective activities of CD4+CD25+ regulatory T cells in an animal model of Parkinson’s disease

Reynolds, A. D., Banerjee, R., Liu, J., Gendelman, H. E., & Mosley, R. L. (2007) · Journal of Leukocyte Biology · doi:10.1189/jlb.0507296 · Cited by 422 · see citing works

Transthyretin sequesters amyloid beta protein and prevents amyloid formation.

Schwarzman, A. L., Gregori, L. L., Vitek, M. P., Lyubski, S., Strittmatter, W. J., Enghilde, J. J., Bhasin, R., Silverman, J. M., Weisgraber, K. H., & Coyle, P. K. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.18.8368 · Cited by 410 · see citing works

Neuroinflammatory processes in Parkinson's disease

Hunot, S., & Hirsch, É. C. (2003) · Annals of Neurology · doi:10.1002/ana.10481 · Cited by 399 · see citing works

International Union of Pharmacology. LX. Retinoic Acid Receptors

Germain, P., Chambon, P., Gregor Eichele, C., Evans, R. M., Lazar, M. A., Leid, M. E., de Lera, Á. R., Lotan, R., Mangelsdorf, D. J., & Gronemeyer, H. (2006) · Pharmacological Reviews · doi:10.1124/pr.58.4.4 · Cited by 398 · see citing works

Role of retinoid signalling in the adult brain

Lane, M. A., & Bailey, S. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.03.002 · Cited by 396 · see citing works

The olfactory vector hypothesis of neurodegenerative disease: Is it viable?

Doty, R. L. (2008) · Annals of Neurology · doi:10.1002/ana.21327 · Cited by 391 · see citing works

Immunology and immunotherapy of Alzheimer's disease

Weiner, H. L., & Frenkel, D. (2006) · Nature Reviews Immunology · doi:10.1038/nri1843 · Cited by 335 · see citing works

An Essential Role for Retinoid Receptors RARβ and RXRγ In Long-Term Potentiation and Depression

Chiang, M.-Y., Misner, D., Kempermann, G., Schikorski, T., Giguère, V., Sucov, H. M., Gage, F. H., Stevens, C. F., & Evans, R. M. (1998) · Neuron · doi:10.1016/s0896-6273(00)80654-6 · Cited by 323 · see citing works

PPARs in the brain

HENEKA, M., & LANDRETH, G. (2007) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2007.04.016 · Cited by 317 · see citing works

Vitamin A Metabolites Induce Gut-Homing FoxP3+ Regulatory T Cells

Kang, S. G., Lim, H. W., ANDRISANI, O. M., Broxmeyer, H. E., & Kim, C. H. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.6.3724 · Cited by 312 · see citing works

Neuroinflammatory processes in Parkinson's disease

Hirsch, É. C., Hunot, S., & Hartmann, A. (2005) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2004.10.013 · Cited by 298 · see citing works

Retinoic acids exert direct effects on T cells to suppress Th1 development and enhance Th2 development via retinoic acid receptors

Iwata, M. (2003) · International Immunology · doi:10.1093/intimm/dxg101 · Cited by 294 · see citing works

Design of selective nuclear receptor modulators: RAR and RXR as a case study

de Lera, Á. R., Bourguet, W., Altucci, L., & Gronemeyer, H. (2007) · Nature Reviews Drug Discovery · doi:10.1038/nrd2398 · Cited by 272 · see citing works

Retinoic Acid Attenuates β-Amyloid Deposition and Rescues Memory Deficits in an Alzheimer's Disease Transgenic Mouse Model

Ding, Y., Qiao, A., Wang, Z., Goodwin, J. S., Lee, E.-S., Block, M. L., Allsbrook, M., McDonald, M. P., & Fan, G.-H. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.3153-08.2008 · Cited by 269 · see citing works

Vitamin A deprivation results in reversible loss of hippocampal long-term synaptic plasticity

Misner, D., Jacobs, S. G. P. M., Shimizu, Y., de Urquiza, A. M., Solomin, L., Perlmann, T., Luca, L. M. D., Stevens, C. F., & Evans, R. M. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.191369798 · Cited by 261 · see citing works

Higher frequency of regulatory T cells in the elderly and increased suppressive activity in neurodegeneration

Rosenkranz, D., Weyer, S. W., Tolosa, E., Gaenslen, A., Berg, D., Leyhe, T., Gasser, T., & Stoltze, L. (2007) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2007.05.011 · Cited by 255 · see citing works

Retinoid treatment of experimental allergic encephalomyelitis. IL-4 production correlates with improved disease course.

Racke, M. K., Burnett, D., Pak, S. H., Albert, P. S., Cannella, B., Raine, C. S., McFarlin, D. E., & Scott, D. E. (1995) · The Journal of Immunology · doi:10.4049/jimmunol.154.1.450 · Cited by 252 · see citing works

A 10‐item smell identification scale related to risk for Alzheimer's disease

Tabert, M. H., Liu, X., Doty, R. L., Serby, M., Zamora, D., Pelton, G. H., Marder, K. S., Albers, M. W., Stern, Y., & Devanand, D. P. (2005) · Annals of Neurology · doi:10.1002/ana.20533 · Cited by 250 · see citing works

Differential expression of retinoid receptors in the adult mouse central nervous system

Krężel, W., Kastner, P., & Chambon, P. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00342-x · Cited by 238 · see citing works

Inflammatory Aspects of Alzheimer Disease and Other Neurodegenerative Disorders

Schwab, C., & McGeer, P. L. (2008) · Journal of Alzheimer s Disease · doi:10.3233/jad-2008-13402 · Cited by 234 · see citing works

Regulation of dopaminergic pathways by retinoids: Activation of the D2 receptor promoter by members of the retinoic acid receptor–retinoid X receptor family

Samad, T. A., Krężel, W., Chambon, P., & Borrelli, E. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.26.14349 · Cited by 219 · see citing works

Alleviation of a selective age-related relational memory deficit in mice by pharmacologically induced normalization of brain retinoid signaling

Etchamendy, N., Enderlin, V., Marighetto, A., Vouimba, R.-M., Pallet, V., Jaffard, R., & Higueret, P. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-16-06423.2001 · Cited by 207 · see citing works

Retinoic acid inhibits expression of TNF-? and iNOS in activated rat microglia

Dheen, S. T., Jun, Y., Yan, Z., Tay, S. S. W., & Ling, E. (2004) · Glia · doi:10.1002/glia.20153 · Cited by 200 · see citing works

The blood-brain barrier induces differentiation of migrating monocytes into Th17-polarizing dendritic cells

Ifergan, I., Kébir, H., Bernard, M., Wosik, K., Dodelet-Devillers, A., Cayrol, R., Arbour, N., & Prat, A. (2007) · Brain · doi:10.1093/brain/awm295 · Cited by 198 · see citing works

Activation of retinoic acid receptor‐α favours regulatory T cell induction at the expense of IL‐17‐secreting T helper cell differentiation

Schambach, F., Schupp, M., Lazar, M. A., & Reiner, S. L. (2007) · European Journal of Immunology · doi:10.1002/eji.200737621 · Cited by 198 · see citing works

Tissue plasminogen activator in central nervous system physiology and pathology

Melchor, J. P., & Strickland, S. (2005) · Thrombosis and Haemostasis · doi:10.1160/th04-12-0838 · Cited by 193 · see citing works

Disruption of the retinoid signalling pathway causes a deposition of amyloid β in the adult rat brain

Corcoran, J. P. T., So, P. L., & Maden, M. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03563.x · Cited by 190 · see citing works

Three independent lines of evidence suggest retinoids as causal to schizophrenia

Goodman, A. B. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.13.7240 · Cited by 190 · see citing works

Retinoic Acid: Its Biosynthesis and Metabolism

Napoli, J. L. (1999) · Progress in nucleic acid research and molecular biology · doi:10.1016/s0079-6603(08)60722-9 · Cited by 187 · see citing works

Trisomy eight in ES cells is a common potential problem in gene targeting and interferes with germ line transmission

Liu, X., Wu, H., Loring, J. M., Hormuzdi, S. G., Distèche, C. M., BORNSTEIN, P. K., & Jaenisch, R. (1997) · Developmental Dynamics · doi:10.1002/(sici)1097-0177(199705)209:1 · Cited by 187 · see citing works

Vitamin A deficiency and relational memory deficit in adult mice: relationships with changes in brain retinoid signalling

Etchamendy, N., Enderlin, V., Marighetto, A., Pallet, V., Higueret, P., & Jaffard, R. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(03)00099-8 · Cited by 185 · see citing works

Evidence for defective retinoid transport and function in late onset Alzheimer's disease

Goodman, A. B., & Pardee, A. B. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0437937100 · Cited by 184 · see citing works

Chemistry and Biology of Synthetic Retinoids

Dawson, M. I. (2018) · CRC Press eBooks · doi:10.1201/9781351070638 · Cited by 178 · see citing works

The transthyretin-retinol-binding protein complex

Monaco, H. L. (2000) · Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology · doi:10.1016/s0167-4838(00)00140-0 · Cited by 169 · see citing works

Virus-induced dysfunction of CD4+CD25+ T cells in patients with HTLV-I–associated neuroimmunological disease

Yamano, Y., Takenouchi, N., Li, H., Tomaru, U., Yao, K., Grant, C. W., Maric, D., & Jacobson, S. (2005) · Journal of Clinical Investigation · doi:10.1172/jci23913 · Cited by 168 · see citing works

Coordinated Up-regulation of Choline Acetyltransferase and Vesicular Acetylcholine Transporter Gene Expression by the Retinoic Acid Receptor α, cAMP, and Leukemia Inhibitory Factor/Ciliary Neurotrophic Factor Signaling Pathways in a Murine Septal Cell Line

Berse, B., & Blusztajn, J. K. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.38.22101 · Cited by 164 · see citing works

Cracking the cytokine code in psoriasis

Nickoloff, B. J. (2007) · Nature Medicine · doi:10.1038/nm0307-242 · Cited by 163 · see citing works

Retinoid production and catabolism: Role of diet in regulating retinol esterification and retinoic acid oxidation

Ross, A. C. (2003) · The Journal of Nutrition · doi:10.1093/jn/133.1.291s · Cited by 161 · see citing works

Chronic Inflammation and Amyloidogenesis in Alzheimer's Disease -- Role of Spirochetes

Miklossy, J. (2008) · Journal of Alzheimer's Disease · doi:10.3233/jad-2008-13404 · Cited by 156 · see citing works

Retinoic acid, a regeneration‐inducing molecule

Maden, M., & Hind, M. D. (2003) · Developmental Dynamics · doi:10.1002/dvdy.10222 · Cited by 152 · see citing works

STAT6 Inhibits TGF-β1-mediated Foxp3 Induction through Direct Binding to the Foxp3 Promoter, Which Is Reverted by Retinoic Acid Receptor

Takaki, H., Ichiyama, K., Koga, K., Chinen, T., Takaesu, G., Sugiyama, Y., Kato, S., Yoshimura, A., & Kobayashi, T. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m801123200 · Cited by 151 · see citing works

Autoantibodies to amyloid-? and Alzheimer's disease

Hyman, B. T., Smith, C. R., Buldyrev, I., Whelan, C. M., Brown, H., Tang, M., & Mayeux, R. P. (2001) · Annals of Neurology · doi:10.1002/ana.1061 · Cited by 144 · see citing works

Chlamydophila Pneumoniae and the Etiology of Late-Onset Alzheimer's Disease

Balin, B. J., Little, C. S., Hammond, C. J., Appelt, D. M., Whittum‐Hudson, J. A., Gérard, H. C., & Hudson, A. P. (2008) · Journal of Alzheimer s Disease · doi:10.3233/jad-2008-13403 · Cited by 144 · see citing works

Herpes Simplex Virus Type 1 in Alzheimer's Disease: The Enemy Within

Itzhaki, R. F., & Wozniak, M. A. (2008) · Journal of Alzheimer s Disease · doi:10.3233/jad-2008-13405 · Cited by 143 · see citing works

Nurr1-RXR heterodimers mediate RXR ligand-induced signaling in neuronal cellsPreprint

Wallén‐Mackenzie, Å., de Urquiza, A. M., Petersson, S., Rodríguez, F. J., Friling, S., Wagner, J., Ordentlich, P., Lengqvist, J., Heyman, R. A., Arenas, E., et al. (2003) · Genes & Development · doi:10.1101/gad.276003 · Cited by 138 · see citing works

Retinoid receptors, transporters, and metabolizers as therapeutic targets in late onset Alzheimer disease

Goodman, A. B. (2006) · Journal of Cellular Physiology · doi:10.1002/jcp.20784 · Cited by 137 · see citing works

Genomic structure and functional characterization of the human ADAM10 promoter

Prinzen, C., Müller, U., Endres, K., Fahrenholz, F., & Postina, R. (2005) · The FASEB Journal · doi:10.1096/fj.04-3619fje · Cited by 131 · see citing works

Identification of interleukin-6 (IL-6)-expressing neurons in the cerebellum and hippocampus of normal adult rats

Gadient, R. A., & Otten, U. (1994) · Neuroscience Letters · doi:10.1016/0304-3940(94)90807-9 · Cited by 128 · see citing works

Retinoic acid receptor β2 promotes functional regeneration of sensory axons in the spinal cord

Wong, L., Yip, P. K., Battaglia, A. A., Grist, J., Corcoran, J. P. T., Maden, M., Azzouz, M., Kingsman, S. M., Kingsman, A. J., Mazarakis, N. D., et al. (2005) · Nature Neuroscience · doi:10.1038/nn1622 · Cited by 124 · see citing works

Transthyretin: A key gene involved in the maintenance of memory capacities during aging

Brouillette, J., & Quirion, R. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.04.007 · Cited by 120 · see citing works

Retinoids: the biochemical and molecular basis of Vitamin A and retinoid action

Nau, H., & Blaner, W. S. (1999) · Handbook of experimental pharmacology · Cited by 116 · see citing works

Add Alzheimer's disease to the list of autoimmune diseases

D’Andrea, M. R. (2005) · Medical Hypotheses · doi:10.1016/j.mehy.2004.08.024 · Cited by 113 · see citing works

Apolipoprotein E, transthyretin and actin in the CSF of Alzheimer's patients: relation with the senile plaques and cytoskeleton biochemistry

Merched, A. J., Sérot, J., Visvikis‐Siest, S., Aguillon, D., Faure, G. C., & Siest, G. (1998) · FEBS Letters · doi:10.1016/s0014-5793(98)00234-8 · Cited by 111 · see citing works

Retinoids and spinal cord development.

Maden, M. (2006) · Journal of Neurobiology · doi:10.1002/neu.20248 · Cited by 111 · see citing works

Alpha-Secretase As a Therapeutic Target

Fahrenholz, F. (2007) · Current Alzheimer Research · doi:10.2174/156720507781788837 · Cited by 111 · see citing works

Retinoic Acid Signaling Affects Cortical Synchrony During Sleep

Maret, S., Franken, P., Dauvilliers, Y. A., Ghyselinck, N. B., Chambon, P., & Tafti, M. (2005) · Science · doi:10.1126/science.1117623 · Cited by 107 · see citing works

Retinoic acid receptor β2 and neurite outgrowth in the adult mouse spinal cord in vitro

Corcoran, J. P. T., So, P.-L., Barber, R. D., Vincent, K. J., Mazarakis, N. D., Mitrophanous, K. A., Kingsman, S. M., & Maden, M. (2002) · Journal of Cell Science · doi:10.1242/jcs.00046 · Cited by 107 · see citing works

Synthetic Retinoids: Recent Developments Concerning Structure and Clinical Utility

Kagechika, H., & Shudo, K. (2005) · Journal of Medicinal Chemistry · doi:10.1021/jm0581821 · Cited by 106 · see citing works

Lymphocytic infiltration in the spinal cord of patients with amyotrophic lateral sclerosis.

Troost, D., van den Oord, J. J., de Jong, J. M. B. V., & Swaab, D. F. (1989) · PubMed · Cited by 101 · see citing works

Retinoid Hyposignaling Contributes to Aging-Related Decline in Hippocampal Function in Short-Term/Working Memory Organization and Long-Term Declarative Memory Encoding in Mice

Mingaud, F., Mormède, C., Etchamendy, N., Mons, N. E., Niedergang, B., Wietrzych, M., Pallet, V., Jaffard, R., Krężel, W., Higueret, P., et al. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4065-07.2008 · Cited by 100 · see citing works

The immune system in aging: roles of cytokines, T cells and NK cells

Huang, H. W. (2005) · Frontiers in bioscience · doi:10.2741/1521 · Cited by 98 · see citing works

Nur77 and retinoid X receptors: crucial factors in dopamine-related neuroadaptation

Lévesque, D., & Rouillard, C. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.11.006 · Cited by 98 · see citing works

Oral tolerance: is it all retinoic acid?

von Boehmer, H. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20071251 · Cited by 97 · see citing works

Novel Synthetic Retinoids and Separation of the Pleiotropic Retinoidal Activities

Kagechika, H. (2002) · Current Medicinal Chemistry · doi:10.2174/0929867024606975 · Cited by 97 · see citing works

Cellular Retinoic Acid Bioavailability Determines Epithelial Integrity: Role of Retinoic Acid Receptor α Agonists in Colitis

Osanai, M., Nishikiori, N., Murata, M., Chiba, H., Kojima, T., & Sawada, N. (2006) · Molecular Pharmacology · doi:10.1124/mol.106.029579 · Cited by 97 · see citing works

Interleukins, Inflammation, and Mechanisms of Alzheimer's Disease

Weisman, D., Hakimian, E., & Ho, G. J. (2006) · Vitamins &amp; Hormones · doi:10.1016/s0083-6729(06)74020-1 · Cited by 95 · see citing works

Synthetic Retinoid Am80 Suppresses Smooth Muscle Phenotypic Modulation and In-Stent Neointima Formation by Inhibiting KLF5

Fujiu, K., Manabe, I., Ishihara, A., et al. (2005) · Circulation Research · doi:10.1161/01.res.0000190613.22565.13 · Cited by 95 · see citing works

Genetic polymorphisms in the cathespin D and interleukin-6 genes and the risk of Alzheimer's disease

Bhojak, T., DeKosky, S. T., Ganguli, M., & Kamboh, M. I. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(00)01185-x · Cited by 94 · see citing works

Induction of neural-like cells and acetylcholinesterase activity in cultures of F9 teratocarcinoma treated with retinoic acid and dibutyryl cyclic adenosine monophosphate

Kuff, E. L., & Fewell, J. W. (1980) · Developmental Biology · doi:10.1016/0012-1606(80)90459-5 · Cited by 88 · see citing works

New therapeutic target for CNS injury? The role of retinoic acid signaling after nerve lesions

Mey, J. (2006) · Journal of Neurobiology · doi:10.1002/neu.20238 · Cited by 84 · see citing works

Tamibarotene

Miwako, I., & Kagechika, H. (2007) · Drugs of today · doi:10.1358/dot.2007.43.8.1072615 · Cited by 84 · see citing works

Glial Cell–Derived Cytokines Attenuate the Breakdown of Vascular Integrity in Diabetic Retinopathy

Nishikiori, N., Osanai, M., Chiba, H., Kojima, T., Mitamura, Y., Ohguro, H., & Sawada, N. (2007) · Diabetes · doi:10.2337/db06-1431 · Cited by 82 · see citing works

Effect of IL‐6 polymorphism on risk of Alzheimer disease: Genotype‐phenotype association study in Japanese cases

Shibata, N., Ohnuma, T., Takahashi, T., Baba, H., Ishizuka, T., Ohtsuka, M., Ueki, A., Nagao, M., & Arai, H. (2002) · American Journal of Medical Genetics · doi:10.1002/ajmg.10417 · Cited by 80 · see citing works

All- trans -Retinoic Acid Limits Restenosis After Balloon Angioplasty in the Focally Atherosclerotic Rabbit

Wiegman, P., Barry, W. L., McPherson, J., et al. (2000) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.20.1.89 · Cited by 71 · see citing works

Retinoic acid normalizes nuclear receptor mediated hypo-expression of proteins involved in β-amyloid deposits in the cerebral cortex of vitamin A deprived rats

Husson, M., Enderlin, V., Delacourte, A., Ghenimi, N., Alfos, S., Pallet, V., & Higueret, P. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.01.008 · Cited by 67 · see citing works

Immune cells may fend off Alzheimer disease

Britschgi, M., & Wyss‐Coray, T. (2007) · Nature Medicine · doi:10.1038/nm0407-408 · Cited by 60 · see citing works

Retinoic acid synthesis by a population of NG2‐positive cells in the injured spinal cord

Mey, J., Morassutti, D. J., Brook, G. A., et al. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.03928.x · Cited by 60 · see citing works

C57BL/6 Mice Genetically Deficient in IL-12/IL-23 and IFN-γ Are Susceptible to Experimental Autoimmune Myasthenia Gravis, Suggesting a Pathogenic Role of Non-Th1 Cells

Wang, W., Milani, M., Ostlie, N. S., Okita, D. K., Agarwal, R. K., Caspi, R. R., & Conti‐Fine, B. M. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.11.7072 · Cited by 60 · see citing works

α-Secretase Activation – An Approach to Alzheimer’s Disease Therapy

Fahrenholz, F., & Postina, R. (2006) · Neurodegenerative Diseases · doi:10.1159/000095264 · Cited by 59 · see citing works

All‐trans‐ and 9‐cis‐Retinoic Acid Enhance the Cholinergic Properties of a Murine Septal Cell Line: Evidence that the Effects Are Mediated by Activation of Retinoic Acid Receptor‐α

Pedersen, W. A., Berse, B., Schüler, U., Wainer, B. H., & Blusztajn, J. K. (1995) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1995.65010050.x · Cited by 59 · see citing works

Retinoic Acid Induction of Human Tissue-type Plasminogen Activator Gene Expression via a Direct Repeat Element (DR5) Located at −7 Kilobases

Bulens, F., Ibáñez-Tallon, I., Acker, P. V., et al. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.13.7167 · Cited by 57 · see citing works

Selective Regulation of TrkA and TrkB Receptors by Retinoic Acid and Interferon-γ in Human Neuroblastoma Cell Lines

Lucarelli, E., Kaplan, D. R., & Thiele, C. J. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.42.24725 · Cited by 57 · see citing works

Proliferative Diseases

Sporn, M. B., & Harris, E. D. (1981) · The American Journal of Medicine · doi:10.1016/0002-9343(81)90832-9 · Cited by 54 · see citing works

Regulation of FoxP 3+ Regulatory T Cells and Th17 Cells by Retinoids

Kim, C. H. (2008) · Clinical and Developmental Immunology · doi:10.1155/2008/416910 · Cited by 54 · see citing works

Nerve growth factor induces adrenergic neuronal differentiation in F9 teratocarcinoma cells

Liesi, P., Rechardt, L., & Wartiovaara, J. (1983) · Nature · doi:10.1038/306265a0 · Cited by 53 · see citing works

Retinoic acid inhibition of IL-1-induced IL-6 production by human lung fibroblasts.

Zitnik, R. J., Kotloff, R. M., Latifpour, J., Zheng, T., Whiting, N. L., Schwalb, J. M., & Elias, J. A. (1994) · The Journal of Immunology · doi:10.4049/jimmunol.152.3.1419 · Cited by 51 · see citing works

Cholinergic differentiation of cultured sympathetic neurons induced by retinoic acid

Kobayashi, M., Matsuoka, I., & Kurihara, K. (1994) · FEBS Letters · doi:10.1016/0014-5793(94)80204-1 · Cited by 50 · see citing works

Regulation of retinoic acid receptors α, β and retinoid X receptor α after sciatic nerve injury

Zhelyaznik, N., & Mey, J. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.05.021 · Cited by 50 · see citing works

High frequency of systemic mycoplasmal infections in Gulf War veterans and civilians with Amyotrophic Lateral Sclerosis (ALS)

Nicolson, G. L., Nasralla, M. Y., Haier, J., et al. (2002) · Journal of Clinical Neuroscience · doi:10.1054/jocn.2001.1075 · Cited by 50 · see citing works

BEYOND AMYLOID: The Next Generation of Alzheimer's Disease Therapeutics

Seabrook, G. R., Ray, W. J., Shearman, M. S., & Hutton, M. L. (2007) · Molecular Interventions · doi:10.1124/mi.7.5.8 · Cited by 48 · see citing works

Insulin-like growth factor I and II expression and modulation in amoeboid microglial cells by lipopolysaccharide and retinoic acid

Kaur, C., Sivakumar, V., Dheen, S. T., & Ling, E. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.12.025 · Cited by 48 · see citing works

Effect of Am-80, a Synthetic Derivative of Retinoid, on Experimental Arthritis in Mice

Nagai, H., Matsuura, S., Bouda, K., Takaoka, Y., Wang, T., Niwa, S., & Shudo, K. (1999) · Pharmacology · doi:10.1159/000028272 · Cited by 47 · see citing works

Is the modulation of retinoid and retinoid‐associated signaling a future therapeutic strategy in neurological trauma and neurodegeneration?

Malaspina, A., & Michael-Titus, A. T. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.05071.x · Cited by 46 · see citing works

Synthetic Retinoids and Their Nuclear Receptors

Dawson, M. I. (2004) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/1568011043352975 · Cited by 46 · see citing works

A speculative essay on retinoic acid regulation of neural stem cells in the developing and aging olfactory system

Rawson, N. E., & LaMantia, A. (2006) · Experimental Gerontology · doi:10.1016/j.exger.2006.05.021 · Cited by 45 · see citing works

Three novel synthetic retinoids, Re 80, Am 580 and Am 80, all exhibit anti-angiogenic activity in vivo

Oikawa, T., Okayasu, I., Ashino, H., et al. (1993) · European Journal of Pharmacology · doi:10.1016/0014-2999(93)90669-9 · Cited by 45 · see citing works

Once and again: Retinoic acid signaling in the developing and regenerating olfactory pathway

Rawson, N. E., & LaMantia, A. (2006) · Journal of Neurobiology · doi:10.1002/neu.20236 · Cited by 44 · see citing works

Novel synthetic retinoic acid inhibits rat collagen arthritis and differentially affects serum immunoglobulin subclass levels

Kuwabara, K., Shudo, K., & Hori, Y. (1996) · FEBS Letters · doi:10.1016/0014-5793(95)01440-3 · Cited by 43 · see citing works

Early induction of interleukin-6 mRNA in the hippocampus and cortex of APPsw transgenic mice Tg2576

Tehranian, R., Hasanvan, H., Iverfeldt, K., Post, C., & Schultzberg, M. (2001) · Neuroscience Letters · doi:10.1016/s0304-3940(01)01592-0 · Cited by 43 · see citing works

Cognitive impairment and infectious burden in the elderly

STRANDBERG, T. E., PITKALA, K. H., LINNAVUORI, K., & TILVIS, R. S. (2004) · Archives of Gerontology and Geriatrics · doi:10.1016/j.archger.2004.04.053 · Cited by 43 · see citing works

Effects of inflammatory cytokines IL‐1β, IL‐6, and TNFα on the intracellular localization of retinoid receptors in Schwann cells

Mey, J., Schrage, K., Weßels, I., & Vollpracht‐Crijns, I. (2006) · Glia · doi:10.1002/glia.20444 · Cited by 39 · see citing works

Lack of involvement of retinoic acid receptor α in retinoid-induced skin irritation in hairless mice

Standeven, A. M., Teng, M., & Chandraratna, R. A. S. (1997) · Toxicology Letters · doi:10.1016/s0378-4274(97)00065-9 · Cited by 35 · see citing works

Retinoids: Fascinating Up‐and‐Coming Scenario

Sardana, K., & Sehgal, V. N. (2003) · The Journal of Dermatology · doi:10.1111/j.1346-8138.2003.tb00402.x · Cited by 34 · see citing works

The effect of Am-80, one of retinoids derivatives on experimental allergic encephalomyelitis in rats

Wang, T., Niwa, S., Bouda, K., Matsuura, S., Homma, T., Shudo, K., & Nagai, H. (2000) · Life Sciences · doi:10.1016/s0024-3205(00)00776-1 · Cited by 34 · see citing works

Inhibition of IL-1-Induced IL-6 Production by Synthetic Retinoids

Kagechika, H., Kawachi, E., Fukasawa, H., Saito, G., Iwanami, N., Umemiya, H., Hashimoto, Y., & Shudo, K. (1997) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1997.6087 · Cited by 32 · see citing works

Characterization of retinaldehyde dehydrogenase‐2 induction in NG2‐positive glia after spinal cord contusion injury

Kern, J., Schrage, K., Koopmans, G. C., Joosten, E. A. J., McCaffery, P. J. A., & Mey, J. (2007) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2006.11.006 · Cited by 30 · see citing works

A Synthetic Retinoid Am80 (Tamibarotene) Rescues the Memory Deficit Caused by Scopolamine in a Passive Avoidance Paradigm

Shudo, K., Kagechika, H., Yamazaki, N., Igarashi, M., & Tateda, C. (2004) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.27.1887 · Cited by 30 · see citing works

Effect of Synthetic Retinoid, TAC-101, on Experimental Autoimmune Disease

Miyagawa, N., Homma, T., Kagechika, H., et al. (2002) · Pharmacology · doi:10.1159/000066783 · Cited by 27 · see citing works

Functional studies of newly synthesized benzoic acid derivatives: Identification of highly potent retinoid‐like activity

Sato, M., Shudo, K., & Hiragun, A. (1988) · Journal of Cellular Physiology · doi:10.1002/jcp.1041350205 · Cited by 25 · see citing works

Role of Retinoic Acid Receptor Gamma in the Rhino Mouse and Rabbit Irritation Models of Retinoid Activity

Reczek, P. R., Ostrowski, J., Yu, K., et al. (2009) · Skin Pharmacology · doi:10.1159/000211360 · Cited by 23 · see citing works

CNS regeneration: A morphogen's tale

Vergara, M. N., Arsenijévic, Y., & Rio‐Tsonis, K. D. (2005) · Journal of Neurobiology · doi:10.1002/neu.20158 · Cited by 22 · see citing works

Marked resistance of RAR gamma-deficient mice to the toxic effects of retinoic acid

Look, J. J., Landwehr, J., Bauer, F. W., et al. (1995) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1995.269.1.e91 · Cited by 22 · see citing works

A review of the functional role and of the expression profile of retinoid signaling and of nuclear receptors in human spinal cord

Malaspina, A., & Turkheimer, F. (2006) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2006.10.032 · Cited by 17 · see citing works

Vitamin A and sleep regulation

Séi, H. (2008) · The Journal of Medical Investigation · doi:10.2152/jmi.55.1 · Cited by 16 · see citing works

The transcription factors Nur77 and retinoid X receptors participate in amphetamine-induced locomotor activities

Bourhis, E., Maheux, J., Paquet, B., et al. (2008) · Psychopharmacology · doi:10.1007/s00213-008-1343-0 · Cited by 15 · see citing works

Selective retinoic acid receptor ligands for rheumatoid arthritis.

Beehler, B. C., Brinckerhoff, C., & Ostrowski, J. (2004) · PubMed · Cited by 12 · see citing works

Oral Administration of Synthetic Retinoid Am80 Inhibits the Development of Type 1 Diabetes in Non-obese Diabetic (NOD) Mice

Ishido, M., & Shudo, K. (2009) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.32.157 · Cited by 11 · see citing works

The Transthyretin—Retinol-Binding Protein Complex

Monaco, H. L. (2009) · Springer eBooks · doi:10.1007/978-3-642-00646-3_8 · Cited by 11 · see citing works

Retinoid Therapy for Autoimmune Diseases

Fukasawa, H., Kagechika, H., & Shudo, K. (2006) · Japanese Journal of Clinical Immunology · doi:10.2177/jsci.29.114 · Cited by 9 · see citing works

Inhibitory Effects of Retinoic Acid Receptor Alpha Stimulants on Murine Cataractogenesis through Suppression of Deregulated Calpains

Nishikiori, N., Osanai, M., Chiba, H., et al. (2007) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.06-1222 · Cited by 8 · see citing works

Synthetic Retinoids: Recent Developments Concerning Structure and Clinical Utility

Kagechika, H., & Shudo, K. (2005) · ChemInform · doi:10.1002/chin.200552244 · Cited by 7 · see citing works

[Immunological aspects of amyotrophic lateral sclerosis].

Yoshino, H. (1994) · PubMed · Cited by 1 · see citing works

The Role of Antioxidants in the Interplay between Oxidative Stress and Senescence

Varesi, A., Chirumbolo, S., Campagnoli, L. I. M., Pierella, E., Piccini, G. B., Carrara, A., Ricevuti, G., Scassellati, C., Bonvicini, C., & Pascale, A. (2022) · Antioxidants · doi:10.3390/antiox11071224 · Cited by 145 · see citing works

A medicinal chemistry perspective of drug repositioning: Recent advances and challenges in drug discovery

Pillaiyar, T., Meenakshisundaram, S., Manickam, M., & Sankaranarayanan, M. (2020) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2020.112275 · Cited by 140 · see citing works

Tamibarotene: A Candidate Retinoid Drug for Alzheimer’s Disease

Fukasawa, H., Nakagomi, M., Yamagata, N., Katsuki, H., Kawahara, K., Kitaoka, K., Miki, T., & Shudo, K. (2012) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b12-00314 · Cited by 91 · see citing works

Molecular Signaling Mechanisms of Natural and Synthetic Retinoids for Inhibition of Pathogenesis in Alzheimer’s Disease

Chakrabarti, M., McDonald, A. J., Will Reed, J., Moss, M. A., Das, B. C., & Ray, S. K. (2016) · Journal of Alzheimer's Disease · doi:10.3233/jad-150450 · Cited by 57 · see citing works

Retinoids for treatment of Alzheimer’s disease

Lerner, A. J., Gustaw‐Rothenberg, K., Smyth, S., & Casadesus, G. (2012) · BioFactors · doi:10.1002/biof.196 · Cited by 44 · see citing works

The Retinoic Acid Receptor Agonist Am80 Increases Hippocampal ADAM10 in Aged SAMP8 Mice

Kitaoka, K., Shimizu, N., Ono, K., Chikahisa, S., Nakagomi, M., Shudo, K., Ishimura, K., Séi, H., & Yoshizaki, K. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.04.009 · Cited by 27 · see citing works

Teratogenesis by retinoic acid analogs positively correlates with elevation of retinoic acid receptor‐β2 mRNA levels in treated embryos

Jiang, H., Gyda, M., Harnish, D. C., Chandraratna, R. A. S., Soprano, K. J., Kochhar, D. M., & Soprano, D. R. (1994) · Teratology · doi:10.1002/tera.1420500106 · Cited by 36 · see citing works

A sustained elevation in retinoic acid receptor-β2 mRNA and protein occurs during retinoic acid-induced fetal dysmorphogenesis

Soprano, D. R., Gyda, M., Jiang, H., Harnish, D. C., Ugen, K., Satre, M. A., Chen, L., Soprano, K. J., & Kochhar, D. M. (1994) · Mechanisms of Development · doi:10.1016/0925-4773(94)90011-6 · Cited by 33 · see citing works

Quantitative axial profiles of retinoic acid in the embryonic mouse spinal cord: 9‐Cis retinoic acid only detected after all‐trans‐retinoic acid levels are super‐elevated experimentally

Ulven, S. M., Gundersen, T. E., Sakhi, A. K., Glover, J. C., & Blomhoff, R. (2001) · Developmental Dynamics · doi:10.1002/dvdy.1184 · Cited by 51 · see citing works

Retinoids and Epididymal Function

Orgebin‐Crist, M., Lareyre, J., Suzuki, K., Araki, Y., Fouchécourt, S., Matusik, R. J., & Ong, D. E. (2002) · Springer eBooks · doi:10.1007/978-1-4615-0679-9_19 · Cited by 13 · see citing works

Influences of retinoic acid and retinoid on skin metabolism

Raab, W. P. E., & Gmeiner, B. M. K. (1976) · Archives of Dermatological Research · doi:10.1007/bf00572489 · Cited by 6 · see citing works