Artykuły w czasopismach na temat „Nr5a1”
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Shi, Boyang, Huijie Lu, Lihong Zhang i 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.
Pełny tekst źródłaKUO, Ming-Wei, John POSTLETHWAIT, Wen-Chih LEE, Show-Wan LOU, Woon-Khiong CHAN i 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.
Pełny tekst źródłaSuyama, Atsuhito, Nahoko Iwata, Yoshiaki Soejima, Yasuhiro Nakano, Koichiro Yamamoto, Takahiro Nada i 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 (1.05.2021): A768. http://dx.doi.org/10.1210/jendso/bvab048.1562.
Pełny tekst źródłaSuzuki, Taiga, Megumi Kasahara, Hidefumi Yoshioka, Ken-ichirou Morohashi i 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 (1.01.2003): 238–49. http://dx.doi.org/10.1128/mcb.23.1.238-249.2003.
Pełny tekst źródłaMartin, Luc J., i 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 (1.07.2008): 165–75. http://dx.doi.org/10.1677/jme-07-0145.
Pełny tekst źródłaEmura, Natsuko, Chiung-Min Wang, William Harry Yang i 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.
Pełny tekst źródłaMorohashi, Ken-ichirou, Miki Inoue i 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.
Pełny tekst źródłaLuppino, Giovanni, Malgorzata Wasniewska, Roberto Coco, Giorgia Pepe, Letteria Anna Morabito, Alessandra Li Pomi, Domenico Corica i Tommaso Aversa. "Role of NR5A1 Gene Mutations in Disorders of Sex Development: Molecular and Clinical Features". Current Issues in Molecular Biology 46, nr 5 (9.05.2024): 4519–32. http://dx.doi.org/10.3390/cimb46050274.
Pełny tekst źródłaDomenice, Sorahia, Aline Zamboni Machado, Frederico Moraes Ferreira, Bruno Ferraz‐de‐Souza, Antonio Marcondes Lerario, Lin Lin, Mirian Yumie Nishi i in. "Wide spectrum of NR5A1‐related phenotypes in 46,XY and 46,XX individuals". Birth Defects Research Part C: Embryo Today: Reviews 108, nr 4 (grudzień 2016): 309–20. http://dx.doi.org/10.1002/bdrc.21145.
Pełny tekst źródłaShima, Yuichi, Kanako Miyabayashi, Takami Mori, Koji Ono, Mizuki Kajimoto, Hae Lim Cho, Hitomi Tsuchida i in. "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.
Pełny tekst źródłaMartínez de LaPiscina, Idoia, Rana AA Mahmoud, Kay-Sara Sauter, Isabel Esteva, Milagros Alonso, Ines Costa, Jose Manuel Rial-Rodriguez i in. "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.
Pełny tekst źródłaTanaka, Tomoko, Chikao Aoyagi, Toshihiko Yanase i 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 (1.11.2022): A60. http://dx.doi.org/10.1210/jendso/bvac150.124.
Pełny tekst źródłaTantawy, Sally, Inas Mazen, Hala Soliman, Ghada Anwar, Abeer Atef, Mona El-Gammal, Ahmed El-Kotoury i in. "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 (maj 2014): 759–67. http://dx.doi.org/10.1530/eje-13-0965.
Pełny tekst źródłaFaienza, Maria F., Mariangela Chiarito, Fulvia Baldinotti, Domenico Canale, Carmela Savino, Guglielmo Paradies, Domenico Corica i in. "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.
Pełny tekst źródłaSakai, Noriko, Hiromi Terami, Shinobu Suzuki, Megumi Haga, Ken Nomoto, Nobuko Tsuchida, Ken-ichirou Morohashi i in. "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.
Pełny tekst źródłaMartinez de Lapiscina, Idoia, Chrysanthi Kouri, Josu Aurrekoetxea, Mirian Sanchez, Rawda Naamneh Elzenaty, Kay-Sara Sauter, Núria Camats i in. "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.
Pełny tekst źródłaCamats, N., A. V. Pandey, M. Fernández-Cancio, P. Andaluz, M. Janner, N. Torán, F. Moreno i in. "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 (1.07.2012): E1294—E1306. http://dx.doi.org/10.1210/jc.2011-3169.
Pełny tekst źródłaKato, Tomoko, Michiyo Esaki, Ayami Matsuzawa i Yayoi Ikeda. "NR5A1 is required for functional maturation of Sertoli cells during postnatal development". REPRODUCTION 143, nr 5 (maj 2012): 663–72. http://dx.doi.org/10.1530/rep-11-0365.
Pełny tekst źródłaKöhler, Birgit, Lin Lin, Inas Mazen, Cigdem Cetindag, Heike Biebermann, Ilker Akkurt, Rainer Rossi, Olaf Hiort, Annette Grüters i 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 (sierpień 2009): 237–42. http://dx.doi.org/10.1530/eje-09-0067.
Pełny tekst źródłaKherouatou-Chaoui, Naouel, Djalila Chellat-Rezgoune, Mohamed Larbi Rezgoune, Ken Mc Elreavey, Laaldja Souhem Touabti, Noreddine Abadi i 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.
Pełny tekst źródłaOrekhova, Anna S., Natalia Kalinchenko, Ivan A. Morozov, Evgeny V. Vasilyev, Petr M. Rubtsov, Ivan I. Dedov i 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.
Pełny tekst źródłaPiprek, Rafal P., Izabela Rams-Pociecha, Robert Zdanowski, Malgorzata Kloc i Jacek Z. Kubiak. "Desmoplakin (Dsp) conditional knockout in NR5A1+ somatic cells affects germ cell survival in developing mouse gonads". Reproduction 163, nr 4 (1.04.2022): 199–207. http://dx.doi.org/10.1530/rep-21-0295.
Pełny tekst źródłaHattori, Atsushi, i 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.
Pełny tekst źródłaMeinsohn, Marie-Charlotte, Olivia E. Smith, Kalyne Bertolin i 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 (1.04.2019): 1249–79. http://dx.doi.org/10.1152/physrev.00019.2018.
Pełny tekst źródłaWei, Xianzhen, Shan Li i 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.
Pełny tekst źródłaMinh Duc, Bui, Luong Thi Lan Anh, Nong Van Hai i Nguyen Thuy Duong. "Association study of NR5A1 rs1110061 with infertile male in 401 Vietnamese individuals". Vietnam Journal of Biotechnology 19, nr 4 (3.05.2022): 625–31. http://dx.doi.org/10.15625/1811-4989/16358.
Pełny tekst źródłaMönig, Isabel, Julia Schneidewind, Trine H. Johannsen, Anders Juul, Ralf Werner, Ralf Lünstedt, Wiebke Birnbaum, Louise Marshall, Lutz Wünsch i Olaf Hiort. "Pubertal development in 46,XY patients with NR5A1 mutations". Endocrine 75, nr 2 (6.10.2021): 601–13. http://dx.doi.org/10.1007/s12020-021-02883-y.
Pełny tekst źródłaKelly, Victoria R., Bin Xu, Rork Kuick, Ronald J. Koenig i Gary D. Hammer. "Dax1 Up-Regulates Oct4 Expression in Mouse Embryonic Stem Cells via LRH-1 and SRA". Molecular Endocrinology 24, nr 12 (1.12.2010): 2281–91. http://dx.doi.org/10.1210/me.2010-0133.
Pełny tekst źródłaLin, Lin, Pascal Philibert, Bruno Ferraz-de-Souza, Daniel Kelberman, Tessa Homfray, Assunta Albanese, Veruska Molini i in. "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 (1.03.2007): 991–99. http://dx.doi.org/10.1210/jc.2006-1672.
Pełny tekst źródłaFan, Jinjiang, Enrico Campioli, Andrew Midzak, Martine Culty i 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.
Pełny tekst źródłaGuzmán, Adrian, Camilla H. K. Hughes i Bruce D. Murphy. "Orphan nuclear receptors in angiogenesis and follicular development". Reproduction 162, nr 3 (1.09.2021): R35—R54. http://dx.doi.org/10.1530/rep-21-0118.
Pełny tekst źródłaAbisad, Daniela Aguilar, Andrea Montano Ballesteros i 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 (1.11.2022): A709—A710. http://dx.doi.org/10.1210/jendso/bvac150.1462.
Pełny tekst źródłaLourenço, Diana, Raja Brauner, Lin Lin, Arantzazu De Perdigo, Georges Weryha, Mihaela Muresan, Radia Boudjenah i in. "Mutations in NR5A1 Associated With Ovarian Insufficiency". Obstetrical & Gynecological Survey 64, nr 10 (październik 2009): 665–66. http://dx.doi.org/10.1097/01.ogx.0000359268.91477.36.
Pełny tekst źródłade 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 i 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.
Pełny tekst źródłaMello, Maricilda Palandi de, Emerson Salvador de Souza França, Helena Campos Fabbri, Andréa Trevas Maciel-Guerra i Gil Guerra-Júnior. "Multifunctional role of steroidogenic factor 1 and disorders of sex development". Arquivos Brasileiros de Endocrinologia & Metabologia 55, nr 8 (listopad 2011): 607–12. http://dx.doi.org/10.1590/s0004-27302011000800015.
Pełny tekst źródłaKalinchenko, Natalia Yur'evna, Tatiana Aleksandrovna Anosova, Vitaliy Alekseevich Ioutsi i 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.
Pełny tekst źródłaMorales-Miranda, A., F. Vilchis, B. Chávez, C. Chan, G. Robles-Díaz i V. Díaz-Sánchez. "EXPRESSION OF NR5A1/SF-1, NR5A2/SF-2, CYP11A1 (P450SCC) AND STAR PROTEIN IN NORMAL HUMAN PANCREAS." Pancreas 29, nr 4 (listopad 2004): 346. http://dx.doi.org/10.1097/00006676-200411000-00085.
Pełny tekst źródłaKalinchenko, Natalia Yu, Anna A. Kolodkina, Nadezda Y. Raygorodskaya i 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.
Pełny tekst źródłaZheng, Weiming, Jingying Yang, Qiaorong Jiang, Zhibin He i Lisa M. Halvorson. "Liver receptor homologue-1 regulates gonadotrope function". Journal of Molecular Endocrinology 38, nr 2 (luty 2007): 207–19. http://dx.doi.org/10.1677/jme-06-0001.
Pełny tekst źródłaShi, Boyang, Huijie Lu, Lihong Zhang i 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 (styczeń 2018): 85–93. http://dx.doi.org/10.1016/j.mce.2017.07.008.
Pełny tekst źródłaFerraz-de-Souza, Bruno, Lin Lin i John C. Achermann. "Steroidogenic factor-1 (SF-1, NR5A1) and human disease". Molecular and Cellular Endocrinology 336, nr 1-2 (kwiecień 2011): 198–205. http://dx.doi.org/10.1016/j.mce.2010.11.006.
Pełny tekst źródłaWerner, Ralf, Isabel Mönig, Ralf Lünstedt, Lutz Wünsch, Christoph Thorns, Benedikt Reiz, Alexandra Krause i in. "New NR5A1 mutations and phenotypic variations of gonadal dysgenesis". PLOS ONE 12, nr 5 (1.05.2017): e0176720. http://dx.doi.org/10.1371/journal.pone.0176720.
Pełny tekst źródłaZhu, Zhengya, Zhongyuan He, Tao Tang, Fuan Wang, Hongkun Chen, Baoliang Li, Guoliang Chen i in. "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.
Pełny tekst źródłaLalli, Enzo. "Adrenocortical development and cancer: focus on SF-1". Journal of Molecular Endocrinology 44, nr 6 (3.03.2010): 301–7. http://dx.doi.org/10.1677/jme-09-0143.
Pełny tekst źródłaHu, S. C., J. Ye, A. K. Fathi, X. Fu, S. Huang, Q. Ning i 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.
Pełny tekst źródłaBashamboo, A., i K. McElreavey. "NR5A1/SF-1 and development and function of the ovary". Annales d'Endocrinologie 71, nr 3 (maj 2010): 177–82. http://dx.doi.org/10.1016/j.ando.2010.02.013.
Pełny tekst źródłaMétivier, Raphaël, Yves Le Dréan, Gilles Salbert i Farzad Pakdel. "Interplay between liganded and orphan nuclear receptors controls reproductive pathways". Biochemistry and Cell Biology 78, nr 3 (2.04.2000): 345–58. http://dx.doi.org/10.1139/o00-057.
Pełny tekst źródłaWhitby, Richard J., Jozef Stec, Raymond D. Blind, Sally Dixon, Lisa M. Leesnitzer, Lisa A. Orband-Miller, Shawn P. Williams i in. "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.
Pełny tekst źródłaZhang, Lingling, Lijun Ding, Yifan Li, Fangxi Zhang, Yanhong Xu, Hongjie Pan, Xiaofeng Wan, Guijun Yan, Fei Yu i Runsheng Li. "EHD3 positively regulated by NR5A1 participates in testosterone synthesis via endocytosis". Life Sciences 278 (sierpień 2021): 119570. http://dx.doi.org/10.1016/j.lfs.2021.119570.
Pełny tekst źródłaWang, Chiung-Min, Runhua Liu, Lizhong Wang i 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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