Zeitschriftenartikel zum Thema „Nr5a1“
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Shi, Boyang, Huijie Lu, Lihong Zhang und Weimin Zhang. „Nr5a1b promotes and Nr5a2 inhibits transcription of lhb in the orange-spotted grouper, Epinephelus coioides†“. Biology of Reproduction 101, Nr. 4 (17.07.2019): 800–812. http://dx.doi.org/10.1093/biolre/ioz121.
Der volle Inhalt der QuelleKUO, Ming-Wei, John POSTLETHWAIT, Wen-Chih LEE, Show-Wan LOU, Woon-Khiong CHAN und Bon-chu CHUNG. „Gene duplication, gene loss and evolution of expression domains in the vertebrate nuclear receptor NR5A (Ftz-F1) family“. Biochemical Journal 389, Nr. 1 (21.06.2005): 19–26. http://dx.doi.org/10.1042/bj20050005.
Der volle Inhalt der QuelleSuyama, Atsuhito, Nahoko Iwata, Yoshiaki Soejima, Yasuhiro Nakano, Koichiro Yamamoto, Takahiro Nada und Fumio Otsuka. „Involvement of NR5A1 and NR5A2 in the Regulation of Steroidogenesis by Clock Gene and BMPs by Human Granulosa Cells“. Journal of the Endocrine Society 5, Supplement_1 (01.05.2021): A768. http://dx.doi.org/10.1210/jendso/bvab048.1562.
Der volle Inhalt der QuelleSuzuki, Taiga, Megumi Kasahara, Hidefumi Yoshioka, Ken-ichirou Morohashi und Kazuhiko Umesono. „LXXLL-Related Motifs in Dax-1 Have Target Specificity for the Orphan Nuclear Receptors Ad4BP/SF-1 and LRH-1“. Molecular and Cellular Biology 23, Nr. 1 (01.01.2003): 238–49. http://dx.doi.org/10.1128/mcb.23.1.238-249.2003.
Der volle Inhalt der QuelleMartin, Luc J., und Jacques J. Tremblay. „Glucocorticoids antagonize cAMP-induced Star transcription in Leydig cells through the orphan nuclear receptor NR4A1“. Journal of Molecular Endocrinology 41, Nr. 3 (01.07.2008): 165–75. http://dx.doi.org/10.1677/jme-07-0145.
Der volle Inhalt der QuelleEmura, Natsuko, Chiung-Min Wang, William Harry Yang und Wei-Hsiung Yang. „Steroidogenic Factor 1 (NR5A1) Activates ATF3 Transcriptional Activity“. International Journal of Molecular Sciences 21, Nr. 4 (20.02.2020): 1429. http://dx.doi.org/10.3390/ijms21041429.
Der volle Inhalt der QuelleMorohashi, Ken-ichirou, Miki Inoue und Takashi Baba. „Coordination of Multiple Cellular Processes by NR5A1/Nr5a1“. Endocrinology and Metabolism 35, Nr. 4 (31.12.2020): 756–64. http://dx.doi.org/10.3803/enm.2020.402.
Der volle Inhalt der QuelleLuppino, Giovanni, Malgorzata Wasniewska, Roberto Coco, Giorgia Pepe, Letteria Anna Morabito, Alessandra Li Pomi, Domenico Corica und Tommaso Aversa. „Role of NR5A1 Gene Mutations in Disorders of Sex Development: Molecular and Clinical Features“. Current Issues in Molecular Biology 46, Nr. 5 (09.05.2024): 4519–32. http://dx.doi.org/10.3390/cimb46050274.
Der volle Inhalt der QuelleDomenice, Sorahia, Aline Zamboni Machado, Frederico Moraes Ferreira, Bruno Ferraz‐de‐Souza, Antonio Marcondes Lerario, Lin Lin, Mirian Yumie Nishi et al. „Wide spectrum of NR5A1‐related phenotypes in 46,XY and 46,XX individuals“. Birth Defects Research Part C: Embryo Today: Reviews 108, Nr. 4 (Dezember 2016): 309–20. http://dx.doi.org/10.1002/bdrc.21145.
Der volle Inhalt der QuelleShima, Yuichi, Kanako Miyabayashi, Takami Mori, Koji Ono, Mizuki Kajimoto, Hae Lim Cho, Hitomi Tsuchida et al. „Intronic Enhancer Is Essential for Nr5a1 Expression in The Pituitary Gonadotrope and for Postnatal Development of Male Reproductive Organs in a Mouse Model“. International Journal of Molecular Sciences 24, Nr. 1 (22.12.2022): 192. http://dx.doi.org/10.3390/ijms24010192.
Der volle Inhalt der QuelleMartínez de LaPiscina, Idoia, Rana AA Mahmoud, Kay-Sara Sauter, Isabel Esteva, Milagros Alonso, Ines Costa, Jose Manuel Rial-Rodriguez et al. „Variants of STAR, AMH and ZFPM2/FOG2 May Contribute towards the Broad Phenotype Observed in 46,XY DSD Patients with Heterozygous Variants of NR5A1“. International Journal of Molecular Sciences 21, Nr. 22 (13.11.2020): 8554. http://dx.doi.org/10.3390/ijms21228554.
Der volle Inhalt der QuelleTanaka, Tomoko, Chikao Aoyagi, Toshihiko Yanase und Shohta Kodama. „ODP045 Implantation of Steroidogenic Cells Derived from Human Adipose-derived Stem Cells Extends Survival in a Mouse Model of Adrenal Insufficiency“. Journal of the Endocrine Society 6, Supplement_1 (01.11.2022): A60. http://dx.doi.org/10.1210/jendso/bvac150.124.
Der volle Inhalt der QuelleTantawy, Sally, Inas Mazen, Hala Soliman, Ghada Anwar, Abeer Atef, Mona El-Gammal, Ahmed El-Kotoury et al. „Analysis of the gene coding for steroidogenic factor 1 (SF1, NR5A1) in a cohort of 50 Egyptian patients with 46,XY disorders of sex development“. European Journal of Endocrinology 170, Nr. 5 (Mai 2014): 759–67. http://dx.doi.org/10.1530/eje-13-0965.
Der volle Inhalt der QuelleFaienza, Maria F., Mariangela Chiarito, Fulvia Baldinotti, Domenico Canale, Carmela Savino, Guglielmo Paradies, Domenico Corica et al. „NR5A1 Gene Variants: Variable Phenotypes, New Variants, Different Outcomes“. Sexual Development 13, Nr. 5-6 (2019): 258–63. http://dx.doi.org/10.1159/000507411.
Der volle Inhalt der QuelleSakai, Noriko, Hiromi Terami, Shinobu Suzuki, Megumi Haga, Ken Nomoto, Nobuko Tsuchida, Ken-ichirou Morohashi et al. „Identification of NR5A1 (SF-1/AD4BP) gene expression modulators by large-scale gain and loss of function studies“. Journal of Endocrinology 198, Nr. 3 (25.06.2008): 489–97. http://dx.doi.org/10.1677/joe-08-0027.
Der volle Inhalt der QuelleMartinez de Lapiscina, Idoia, Chrysanthi Kouri, Josu Aurrekoetxea, Mirian Sanchez, Rawda Naamneh Elzenaty, Kay-Sara Sauter, Núria Camats et al. „Genetic reanalysis of patients with a difference of sex development carrying the NR5A1/SF-1 variant p.Gly146Ala has discovered other likely disease-causing variations“. PLOS ONE 18, Nr. 7 (11.07.2023): e0287515. http://dx.doi.org/10.1371/journal.pone.0287515.
Der volle Inhalt der QuelleCamats, N., A. V. Pandey, M. Fernández-Cancio, P. Andaluz, M. Janner, N. Torán, F. Moreno et al. „Ten Novel Mutations in the NR5A1 Gene Cause Disordered Sex Development in 46,XY and Ovarian Insufficiency in 46,XX Individuals“. Journal of Clinical Endocrinology & Metabolism 97, Nr. 7 (01.07.2012): E1294—E1306. http://dx.doi.org/10.1210/jc.2011-3169.
Der volle Inhalt der QuelleKato, Tomoko, Michiyo Esaki, Ayami Matsuzawa und Yayoi Ikeda. „NR5A1 is required for functional maturation of Sertoli cells during postnatal development“. REPRODUCTION 143, Nr. 5 (Mai 2012): 663–72. http://dx.doi.org/10.1530/rep-11-0365.
Der volle Inhalt der QuelleKöhler, Birgit, Lin Lin, Inas Mazen, Cigdem Cetindag, Heike Biebermann, Ilker Akkurt, Rainer Rossi, Olaf Hiort, Annette Grüters und John C. Achermann. „The spectrum of phenotypes associated with mutations in steroidogenic factor 1 (SF-1, NR5A1, Ad4BP) includes severe penoscrotal hypospadias in 46,XY males without adrenal insufficiency“. European Journal of Endocrinology 161, Nr. 2 (August 2009): 237–42. http://dx.doi.org/10.1530/eje-09-0067.
Der volle Inhalt der QuelleKherouatou-Chaoui, Naouel, Djalila Chellat-Rezgoune, Mohamed Larbi Rezgoune, Ken Mc Elreavey, Laaldja Souhem Touabti, Noreddine Abadi und Dalila Satta. „SRY and NR5A1 gene mutation in Algerian children and adolescents with DSD and testicular dysgenesis“. African Health Sciences 21, Nr. 3 (27.09.2021): 1491–97. http://dx.doi.org/10.4314/ahs.v21i3.61.
Der volle Inhalt der QuelleOrekhova, Anna S., Natalia Kalinchenko, Ivan A. Morozov, Evgeny V. Vasilyev, Petr M. Rubtsov, Ivan I. Dedov und Anatoly Tiulpakov. „A Novel Mutation in the Critical P-Box Residue of Steroidogenic Factor-1 Presenting with XY Sex Reversal and Transient Adrenal Failure“. Hormone Research in Paediatrics 89, Nr. 6 (17.11.2017): 450–54. http://dx.doi.org/10.1159/000481776.
Der volle Inhalt der QuellePiprek, Rafal P., Izabela Rams-Pociecha, Robert Zdanowski, Malgorzata Kloc und Jacek Z. Kubiak. „Desmoplakin (Dsp) conditional knockout in NR5A1+ somatic cells affects germ cell survival in developing mouse gonads“. Reproduction 163, Nr. 4 (01.04.2022): 199–207. http://dx.doi.org/10.1530/rep-21-0295.
Der volle Inhalt der QuelleHattori, Atsushi, und Maki Fukami. „Nuclear Receptor Gene Variants Underlying Disorders/Differences of Sex Development through Abnormal Testicular Development“. Biomolecules 13, Nr. 4 (19.04.2023): 691. http://dx.doi.org/10.3390/biom13040691.
Der volle Inhalt der QuelleMeinsohn, Marie-Charlotte, Olivia E. Smith, Kalyne Bertolin und Bruce D. Murphy. „The Orphan Nuclear Receptors Steroidogenic Factor-1 and Liver Receptor Homolog-1: Structure, Regulation, and Essential Roles in Mammalian Reproduction“. Physiological Reviews 99, Nr. 2 (01.04.2019): 1249–79. http://dx.doi.org/10.1152/physrev.00019.2018.
Der volle Inhalt der QuelleWei, Xianzhen, Shan Li und Yu He. „NR5A1-related 46,XY partial gonadal dysgenesis: A case report and literature review“. Medicine 102, Nr. 52 (29.12.2023): e36725. http://dx.doi.org/10.1097/md.0000000000036725.
Der volle Inhalt der QuelleMinh Duc, Bui, Luong Thi Lan Anh, Nong Van Hai und Nguyen Thuy Duong. „Association study of NR5A1 rs1110061 with infertile male in 401 Vietnamese individuals“. Vietnam Journal of Biotechnology 19, Nr. 4 (03.05.2022): 625–31. http://dx.doi.org/10.15625/1811-4989/16358.
Der volle Inhalt der QuelleMönig, Isabel, Julia Schneidewind, Trine H. Johannsen, Anders Juul, Ralf Werner, Ralf Lünstedt, Wiebke Birnbaum, Louise Marshall, Lutz Wünsch und Olaf Hiort. „Pubertal development in 46,XY patients with NR5A1 mutations“. Endocrine 75, Nr. 2 (06.10.2021): 601–13. http://dx.doi.org/10.1007/s12020-021-02883-y.
Der volle Inhalt der QuelleKelly, Victoria R., Bin Xu, Rork Kuick, Ronald J. Koenig und Gary D. Hammer. „Dax1 Up-Regulates Oct4 Expression in Mouse Embryonic Stem Cells via LRH-1 and SRA“. Molecular Endocrinology 24, Nr. 12 (01.12.2010): 2281–91. http://dx.doi.org/10.1210/me.2010-0133.
Der volle Inhalt der QuelleLin, Lin, Pascal Philibert, Bruno Ferraz-de-Souza, Daniel Kelberman, Tessa Homfray, Assunta Albanese, Veruska Molini et al. „Heterozygous Missense Mutations in Steroidogenic Factor 1 (SF1/Ad4BP, NR5A1) Are Associated with 46,XY Disorders of Sex Development with Normal Adrenal Function“. Journal of Clinical Endocrinology & Metabolism 92, Nr. 3 (01.03.2007): 991–99. http://dx.doi.org/10.1210/jc.2006-1672.
Der volle Inhalt der QuelleFan, Jinjiang, Enrico Campioli, Andrew Midzak, Martine Culty und Vassilios Papadopoulos. „Conditional steroidogenic cell-targeted deletion of TSPO unveils a crucial role in viability and hormone-dependent steroid formation“. Proceedings of the National Academy of Sciences 112, Nr. 23 (26.05.2015): 7261–66. http://dx.doi.org/10.1073/pnas.1502670112.
Der volle Inhalt der QuelleGuzmán, Adrian, Camilla H. K. Hughes und Bruce D. Murphy. „Orphan nuclear receptors in angiogenesis and follicular development“. Reproduction 162, Nr. 3 (01.09.2021): R35—R54. http://dx.doi.org/10.1530/rep-21-0118.
Der volle Inhalt der QuelleAbisad, Daniela Aguilar, Andrea Montano Ballesteros und Alejandro Diaz. „RF02 | PMON309 Two Siblings with p.Arg92Trp Variant in NR5A1 Presenting with Testicular Disorder of Sexual Differentiation“. Journal of the Endocrine Society 6, Supplement_1 (01.11.2022): A709—A710. http://dx.doi.org/10.1210/jendso/bvac150.1462.
Der volle Inhalt der QuelleLourenço, Diana, Raja Brauner, Lin Lin, Arantzazu De Perdigo, Georges Weryha, Mihaela Muresan, Radia Boudjenah et al. „Mutations in NR5A1 Associated With Ovarian Insufficiency“. Obstetrical & Gynecological Survey 64, Nr. 10 (Oktober 2009): 665–66. http://dx.doi.org/10.1097/01.ogx.0000359268.91477.36.
Der volle Inhalt der Quellede Oliveira, Felipe Rodrigues, Taís Nitsch Mazzola, Maricilda Palandi de Mello, Ana Paula Francese-Santos, Sofia Helena V. de Lemos-Marini, Andrea Trevas Maciel-Guerra, Olaf Hiort, Ralf Werner, Gil Guerra-Junior und Helena Fabbri-Scallet. „DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis“. Life 13, Nr. 5 (27.04.2023): 1093. http://dx.doi.org/10.3390/life13051093.
Der volle Inhalt der QuelleMello, Maricilda Palandi de, Emerson Salvador de Souza França, Helena Campos Fabbri, Andréa Trevas Maciel-Guerra und Gil Guerra-Júnior. „Multifunctional role of steroidogenic factor 1 and disorders of sex development“. Arquivos Brasileiros de Endocrinologia & Metabologia 55, Nr. 8 (November 2011): 607–12. http://dx.doi.org/10.1590/s0004-27302011000800015.
Der volle Inhalt der QuelleKalinchenko, Natalia Yur'evna, Tatiana Aleksandrovna Anosova, Vitaliy Alekseevich Ioutsi und Anatoly Nikolaevich Tiulpakov. „The first clinical presentation of disorders of sex development 46 XY due to mutation in Steroidogenic factor 1 (SF1) in Russian Literature“. Problems of Endocrinology 62, Nr. 1 (13.01.2016): 55–59. http://dx.doi.org/10.14341/probl201662155-59.
Der volle Inhalt der QuelleMorales-Miranda, A., F. Vilchis, B. Chávez, C. Chan, G. Robles-Díaz und V. Díaz-Sánchez. „EXPRESSION OF NR5A1/SF-1, NR5A2/SF-2, CYP11A1 (P450SCC) AND STAR PROTEIN IN NORMAL HUMAN PANCREAS.“ Pancreas 29, Nr. 4 (November 2004): 346. http://dx.doi.org/10.1097/00006676-200411000-00085.
Der volle Inhalt der QuelleKalinchenko, Natalia Yu, Anna A. Kolodkina, Nadezda Y. Raygorodskaya und Anatoly N. Tiulpakov. „Clinical and molecular characteristics of patients with 46,XY DSD due to NR5A1 gene mutations“. Problems of Endocrinology 66, Nr. 3 (16.09.2020): 62–69. http://dx.doi.org/10.14341/probl12445.
Der volle Inhalt der QuelleZheng, Weiming, Jingying Yang, Qiaorong Jiang, Zhibin He und Lisa M. Halvorson. „Liver receptor homologue-1 regulates gonadotrope function“. Journal of Molecular Endocrinology 38, Nr. 2 (Februar 2007): 207–19. http://dx.doi.org/10.1677/jme-06-0001.
Der volle Inhalt der QuelleShi, Boyang, Huijie Lu, Lihong Zhang und Weimin Zhang. „A homologue of Nr5a1 activates cyp19a1a transcription additively with Nr5a2 in ovarian follicular cells of the orange-spotted grouper“. Molecular and Cellular Endocrinology 460 (Januar 2018): 85–93. http://dx.doi.org/10.1016/j.mce.2017.07.008.
Der volle Inhalt der QuelleFerraz-de-Souza, Bruno, Lin Lin und John C. Achermann. „Steroidogenic factor-1 (SF-1, NR5A1) and human disease“. Molecular and Cellular Endocrinology 336, Nr. 1-2 (April 2011): 198–205. http://dx.doi.org/10.1016/j.mce.2010.11.006.
Der volle Inhalt der QuelleWerner, Ralf, Isabel Mönig, Ralf Lünstedt, Lutz Wünsch, Christoph Thorns, Benedikt Reiz, Alexandra Krause et al. „New NR5A1 mutations and phenotypic variations of gonadal dysgenesis“. PLOS ONE 12, Nr. 5 (01.05.2017): e0176720. http://dx.doi.org/10.1371/journal.pone.0176720.
Der volle Inhalt der QuelleZhu, Zhengya, Zhongyuan He, Tao Tang, Fuan Wang, Hongkun Chen, Baoliang Li, Guoliang Chen et al. „Integrative Bioinformatics Analysis Revealed Mitochondrial Dysfunction-Related Genes Underlying Intervertebral Disc Degeneration“. Oxidative Medicine and Cellular Longevity 2022 (11.10.2022): 1–35. http://dx.doi.org/10.1155/2022/1372483.
Der volle Inhalt der QuelleLalli, Enzo. „Adrenocortical development and cancer: focus on SF-1“. Journal of Molecular Endocrinology 44, Nr. 6 (03.03.2010): 301–7. http://dx.doi.org/10.1677/jme-09-0143.
Der volle Inhalt der QuelleHu, S. C., J. Ye, A. K. Fathi, X. Fu, S. Huang, Q. Ning und X. P. Luo. „Mutations in NR5A1 and PIN1 associated with idiopathic hypogonadotropic hypogonadism“. Genetics and Molecular Research 11, Nr. 4 (2012): 4575–84. http://dx.doi.org/10.4238/2012.october.9.6.
Der volle Inhalt der QuelleBashamboo, A., und K. McElreavey. „NR5A1/SF-1 and development and function of the ovary“. Annales d'Endocrinologie 71, Nr. 3 (Mai 2010): 177–82. http://dx.doi.org/10.1016/j.ando.2010.02.013.
Der volle Inhalt der QuelleMétivier, Raphaël, Yves Le Dréan, Gilles Salbert und Farzad Pakdel. „Interplay between liganded and orphan nuclear receptors controls reproductive pathways“. Biochemistry and Cell Biology 78, Nr. 3 (02.04.2000): 345–58. http://dx.doi.org/10.1139/o00-057.
Der volle Inhalt der QuelleWhitby, Richard J., Jozef Stec, Raymond D. Blind, Sally Dixon, Lisa M. Leesnitzer, Lisa A. Orband-Miller, Shawn P. Williams et al. „Small Molecule Agonists of the Orphan Nuclear Receptors Steroidogenic Factor-1 (SF-1, NR5A1) and Liver Receptor Homologue-1 (LRH-1, NR5A2)“. Journal of Medicinal Chemistry 54, Nr. 7 (14.04.2011): 2266–81. http://dx.doi.org/10.1021/jm1014296.
Der volle Inhalt der QuelleZhang, Lingling, Lijun Ding, Yifan Li, Fangxi Zhang, Yanhong Xu, Hongjie Pan, Xiaofeng Wan, Guijun Yan, Fei Yu und Runsheng Li. „EHD3 positively regulated by NR5A1 participates in testosterone synthesis via endocytosis“. Life Sciences 278 (August 2021): 119570. http://dx.doi.org/10.1016/j.lfs.2021.119570.
Der volle Inhalt der QuelleWang, Chiung-Min, Runhua Liu, Lizhong Wang und Wei-Hsiung Yang. „Acidic Residue Glu199 Increases SUMOylation Level of Nuclear Hormone Receptor NR5A1“. International Journal of Molecular Sciences 14, Nr. 11 (13.11.2013): 22331–45. http://dx.doi.org/10.3390/ijms141122331.
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