These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
124 related articles for article (PubMed ID: 38927643)
1. FANCM Gene Variants in a Male Diagnosed with Sertoli Cell-Only Syndrome and Diffuse Astrocytoma. Klarić ML; Marić T; Žunić L; Trgovec-Greif L; Rokić F; Fiolić A; Šorgić AM; Ježek D; Vugrek O; Jakovčević A; Barbalić M; Belužić R; Katušić Bojanac A Genes (Basel); 2024 May; 15(6):. PubMed ID: 38927643 [TBL] [Abstract][Full Text] [Related]
2. Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia. Kasak L; Punab M; Nagirnaja L; Grigorova M; Minajeva A; Lopes AM; Punab AM; Aston KI; Carvalho F; Laasik E; Smith LB; ; Conrad DF; Laan M Am J Hum Genet; 2018 Aug; 103(2):200-212. PubMed ID: 30075111 [TBL] [Abstract][Full Text] [Related]
3. Identification and Functional Investigation of Novel Heterozygous Murtaza G; Yang L; Khan I; Unar A; Khan M; Huan Z; Khan R; Shi Q Genet Test Mol Biomarkers; 2021 Oct; 25(10):654-659. PubMed ID: 34672775 [No Abstract] [Full Text] [Related]
4. Testis cell pyroptosis mediated by CASP1 and CASP4: possible sertoli cell-only syndrome pathogenesis. Liu W; Li X; Ma Q; Zhu Y; Zhao W; Yang Y; Xiao W; Huang D; Cai F; Chan DYL; Zhao S; Chu Q Reprod Biol Endocrinol; 2023 Jun; 21(1):53. PubMed ID: 37296437 [TBL] [Abstract][Full Text] [Related]
5. Sertoli cell-only syndrome: advances, challenges, and perspectives in genetics and mechanisms. Wang X; Liu X; Qu M; Li H Cell Mol Life Sci; 2023 Feb; 80(3):67. PubMed ID: 36814036 [TBL] [Abstract][Full Text] [Related]
6. Novel Bi-Allelic Variants of Zhang Y; Li P; Liu N; Jing T; Ji Z; Yang C; Zhao L; Tian R; Chen H; Huang Y; Zhi E; Ou N; Bai H; Zhou Y; Li Z; Yao C Front Genet; 2021; 12():799886. PubMed ID: 34976027 [TBL] [Abstract][Full Text] [Related]
7. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest. Riera-Escamilla A; Enguita-Marruedo A; Moreno-Mendoza D; Chianese C; Sleddens-Linkels E; Contini E; Benelli M; Natali A; Colpi GM; Ruiz-Castañé E; Maggi M; Baarends WM; Krausz C Hum Reprod; 2019 Jun; 34(6):978-988. PubMed ID: 31125047 [TBL] [Abstract][Full Text] [Related]
8. Whole-exome sequencing in patients with maturation arrest: a potential additional diagnostic tool for prevention of recurrent negative testicular sperm extraction outcomes. Ghieh F; Barbotin AL; Swierkowski-Blanchard N; Leroy C; Fortemps J; Gerault C; Hue C; Mambu Mambueni H; Jaillard S; Albert M; Bailly M; Izard V; Molina-Gomes D; Marcelli F; Prasivoravong J; Serazin V; Dieudonne MN; Delcroix M; Garchon HJ; Louboutin A; Mandon-Pepin B; Ferlicot S; Vialard F Hum Reprod; 2022 May; 37(6):1334-1350. PubMed ID: 35413094 [TBL] [Abstract][Full Text] [Related]
9. A homozygous FANCM frameshift pathogenic variant causes male infertility. Yin H; Ma H; Hussain S; Zhang H; Xie X; Jiang L; Jiang X; Iqbal F; Bukhari I; Jiang H; Ali A; Zhong L; Li T; Fan S; Zhang B; Gao J; Li Y; Nazish J; Khan T; Khan M; Zubair M; Hao Q; Fang H; Huang J; Huleihel M; Sha J; Pandita TK; Zhang Y; Shi Q Genet Med; 2019 Jan; 21(1):62-70. PubMed ID: 29895858 [TBL] [Abstract][Full Text] [Related]
10. From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia. Krausz C; Riera-Escamilla A; Chianese C; Moreno-Mendoza D; Ars E; Rajmil O; Pujol R; Bogliolo M; Blanco I; Rodríguez I; Badell I; Ruiz-Castañé E; Surrallés J Genet Med; 2019 Jan; 21(1):189-194. PubMed ID: 29904161 [TBL] [Abstract][Full Text] [Related]
11. HnRNPL as a key factor in spermatogenesis: Lesson from functional proteomic studies of azoospermia patients with sertoli cell only syndrome. Li J; Guo W; Li F; He J; Yu Q; Wu X; Li J; Mao X J Proteomics; 2012 Jun; 75(10):2879-91. PubMed ID: 22245417 [TBL] [Abstract][Full Text] [Related]
12. Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome. Tüttelmann F; Simoni M; Kliesch S; Ledig S; Dworniczak B; Wieacker P; Röpke A PLoS One; 2011 Apr; 6(4):e19426. PubMed ID: 21559371 [TBL] [Abstract][Full Text] [Related]
13. SIN3A mutations are rare in men with azoospermia. Miyamoto T; Koh E; Tsujimura A; Miyagawa Y; Minase G; Ueda Y; Namiki M; Sengoku K Andrologia; 2015 Nov; 47(9):1083-5. PubMed ID: 25395209 [TBL] [Abstract][Full Text] [Related]
14. Up-regulation of SOX9 in sertoli cells from testiculopathic patients accounts for increasing anti-mullerian hormone expression via impaired androgen receptor signaling. Lan KC; Chen YT; Chang C; Chang YC; Lin HJ; Huang KE; Kang HY PLoS One; 2013; 8(10):e76303. PubMed ID: 24098470 [TBL] [Abstract][Full Text] [Related]
16. Genetic variants in the ETV5 gene in fertile and infertile men with nonobstructive azoospermia associated with Sertoli cell-only syndrome. O'Bryan MK; Grealy A; Stahl PJ; Schlegel PN; McLachlan RI; Jamsai D Fertil Steril; 2012 Oct; 98(4):827-35.e1-3. PubMed ID: 22771031 [TBL] [Abstract][Full Text] [Related]
17. Study of trinucleotide expansions and expression of androgen receptor in infertile men with abnormal spermogram referred to Royan institute. Borjian Boroujeni P; Firouzi V; Zari Moradi S; Mokhtari P; Dehghankhalili F; Mollaahmadi F; Gourabi H; Sadighi-Gilani MA; Sabbaghian M; Mohseni-Meybodi A Andrologia; 2018 Dec; 50(10):e13121. PubMed ID: 30156032 [TBL] [Abstract][Full Text] [Related]
18. Mutation in TDRD9 causes non-obstructive azoospermia in infertile men. Arafat M; Har-Vardi I; Harlev A; Levitas E; Zeadna A; Abofoul-Azab M; Dyomin V; Sheffield VC; Lunenfeld E; Huleihel M; Parvari R J Med Genet; 2017 Sep; 54(9):633-639. PubMed ID: 28536242 [TBL] [Abstract][Full Text] [Related]
19. The poly(A) polymerase beta gene may not be associated with azoospermia caused by Sertoli-cell-only syndrome in Japanese patients by comparing patients and normal controls. Miyamoto T; Shin T; Iijima M; Minase G; Okada H; Saijo Y; Sengoku K J Obstet Gynaecol; 2019 Apr; 39(3):434-436. PubMed ID: 30744435 [TBL] [Abstract][Full Text] [Related]
20. A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review. Sha Y; Zheng L; Ji Z; Mei L; Ding L; Lin S; Wang X; Yang X; Li P BMC Med Genet; 2018 Apr; 19(1):63. PubMed ID: 29661171 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]