193 related articles for article (PubMed ID: 30444213)
21. Diseases associated with mutations of the human lutropin receptor.
Segaloff DL
Prog Mol Biol Transl Sci; 2009; 89():97-114. PubMed ID: 20374734
[TBL] [Abstract][Full Text] [Related]
22. Inactivating mutations of the human luteinizing hormone receptor in both sexes.
Latronico AC; Arnhold IJ
Semin Reprod Med; 2012 Oct; 30(5):382-6. PubMed ID: 23044874
[TBL] [Abstract][Full Text] [Related]
23. Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type II.
Hassan HA; Mazen I; Elaidy A; Kamel AK; Eissa NR; Essawi ML
Hormones (Athens); 2024 Mar; ():. PubMed ID: 38526829
[TBL] [Abstract][Full Text] [Related]
24. Novel NR5A1 mutations found in Chinese patients with 46, XY disorders of sex development.
Yu B; Liu Z; Gao Y; Mao J; Wang X; Hao M; Ma W; Huang Q; Zhang R; Nie M; Wu X
Clin Endocrinol (Oxf); 2018 Nov; 89(5):613-620. PubMed ID: 30103258
[TBL] [Abstract][Full Text] [Related]
25. Novel homozygous nonsense mutations in the luteinizing hormone receptor (LHCGR) gene associated with 46,XY primary amenorrhea.
Ben Hadj Hmida I; Mougou-Zerelli S; Hadded A; Dimassi S; Kammoun M; Bignon-Topalovic J; Bibi M; Saad A; Bashamboo A; McElreavey K
Fertil Steril; 2016 Jul; 106(1):225-229.e11. PubMed ID: 27016457
[TBL] [Abstract][Full Text] [Related]
26. Molecular study and genotype-phenotype in Chinese female patients with 46, XY disorders of sex development.
Xia J; Wu J; Chen C; Zhao Z; Xie Y; Bai Z; Kong X
Gynecol Endocrinol; 2021 Oct; 37(10):934-940. PubMed ID: 34338568
[TBL] [Abstract][Full Text] [Related]
27. Successful testicular sperm recovery and IVF treatment in a man with Leydig cell hypoplasia.
Bakircioglu ME; Tulay P; Findikli N; Erzik B; Gultomruk M; Bahceci M
J Assist Reprod Genet; 2014 Jul; 31(7):817-21. PubMed ID: 24792890
[No Abstract] [Full Text] [Related]
28. [Analysis of a family affected with familial male-limited precocious puberty due to a Ala568Val mutation in LHCGR gene].
Chen RM; Zhang Y; Yang XH; Lin XQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec; 29(6):631-4. PubMed ID: 23225038
[TBL] [Abstract][Full Text] [Related]
29. Diseases caused by mutations in luteinizing hormone/chorionic gonadotropin receptor.
Qiao J; Han B
Prog Mol Biol Transl Sci; 2019; 161():69-89. PubMed ID: 30711030
[TBL] [Abstract][Full Text] [Related]
30. Genetic evidence of 'genuine' empty follicle syndrome: a novel effective mutation in the LHCGR gene and review of the literature.
Yuan P; He Z; Zheng L; Wang W; Li Y; Zhao H; Zhang VW; Zhang Q; Yang D
Hum Reprod; 2017 Apr; 32(4):944-953. PubMed ID: 28175319
[TBL] [Abstract][Full Text] [Related]
31. Male pseudohermaphroditism due to inactivating luteinizing hormone receptor mutations.
Wu SM; Chan WY
Arch Med Res; 1999; 30(6):495-500. PubMed ID: 10714363
[TBL] [Abstract][Full Text] [Related]
32. MYRF haploinsufficiency causes 46,XY and 46,XX disorders of sex development: bioinformatics consideration.
Hamanaka K; Takata A; Uchiyama Y; Miyatake S; Miyake N; Mitsuhashi S; Iwama K; Fujita A; Imagawa E; Alkanaq AN; Koshimizu E; Azuma Y; Nakashima M; Mizuguchi T; Saitsu H; Wada Y; Minami S; Katoh-Fukui Y; Masunaga Y; Fukami M; Hasegawa T; Ogata T; Matsumoto N
Hum Mol Genet; 2019 Jul; 28(14):2319-2329. PubMed ID: 30985895
[TBL] [Abstract][Full Text] [Related]
33. Disruption of Zebrafish Follicle-Stimulating Hormone Receptor (fshr) But Not Luteinizing Hormone Receptor (lhcgr) Gene by TALEN Leads to Failed Follicle Activation in Females Followed by Sexual Reversal to Males.
Zhang Z; Lau SW; Zhang L; Ge W
Endocrinology; 2015 Oct; 156(10):3747-62. PubMed ID: 25993524
[TBL] [Abstract][Full Text] [Related]
34. Novel C617Y mutation in the 7th transmembrane segment of luteinizing hormone/choriogonadotropin receptor in a Japanese boy with peripheral precocious puberty.
Nagasaki K; Katsumata N; Ogawa Y; Kikuchi T; Uchiyama M
Endocr J; 2010; 57(12):1055-60. PubMed ID: 21060208
[TBL] [Abstract][Full Text] [Related]
35. Leydig cell hypoplasia: cases with new mutations, new polymorphisms and cases without mutations in the luteinizing hormone receptor gene.
Richter-Unruh A; Martens JW; Verhoef-Post M; Wessels HT; Kors WA; Sinnecker GH; Boehmer A; Drop SL; Toledo SP; Brunner HG; Themmen AP
Clin Endocrinol (Oxf); 2002 Jan; 56(1):103-12. PubMed ID: 11849253
[TBL] [Abstract][Full Text] [Related]
36. Mutational and functional studies on NR5A1 gene in 46,XY disorders of sex development: identification of six novel loss of function mutations.
Rocca MS; Ortolano R; Menabò S; Baronio F; Cassio A; Russo G; Balsamo A; Ferlin A; Baldazzi L
Fertil Steril; 2018 Jun; 109(6):1105-1113. PubMed ID: 29935645
[TBL] [Abstract][Full Text] [Related]
37. A novel compound heterozygous mutation of the luteinizing hormone receptor -implications for fertility.
Mitri F; Bentov Y; Behan LA; Esfandiari N; Casper RF
J Assist Reprod Genet; 2014 Jul; 31(7):787-94. PubMed ID: 24849377
[TBL] [Abstract][Full Text] [Related]
38. Novel compound heterozygous missense variants in TOE1 gene associated with pontocerebellar hypoplasia type 7.
Wang C; Ge Y; Li R; He G; Lin Y
Gene; 2023 Apr; 862():147250. PubMed ID: 36738896
[TBL] [Abstract][Full Text] [Related]
39. Genetic Evidence of the Association of DEAH-Box Helicase 37 Defects With 46,XY Gonadal Dysgenesis Spectrum.
da Silva TE; Gomes NL; Lerário AM; Keegan CE; Nishi MY; Carvalho FM; Vilain E; Barseghyan H; Martinez-Aguayo A; Forclaz MV; Papazian R; Pedroso de Paula LC; Costa EC; Carvalho LR; Jorge AAL; Elias FM; Mitchell R; Costa EMF; Mendonca BB; Domenice S
J Clin Endocrinol Metab; 2019 Dec; 104(12):5923-5934. PubMed ID: 31287541
[TBL] [Abstract][Full Text] [Related]
40. Luteinizing hormone resistance syndromes.
Tsigos C; Latronico C; Chrousos GP
Ann N Y Acad Sci; 1997 Jun; 816():263-73. PubMed ID: 9238276
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
