Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 79

Similar articles for PubMed (Select 21691974)

1.

Leydig cell hypoplasia due to inactivating luteinizing hormone/chorionic gonadotropin receptor gene mutation presenting as a 46,XY DSD.

Sinha SK, Bhangoo A, Ten S, Gromoll J.

Adv Exp Med Biol. 2011;707:147-8. doi: 10.1007/978-1-4419-8002-1_32. No abstract available.

PMID:
21691974
2.

Aberrant transcription of the LHCGR gene caused by a mutation in exon 6A leads to Leydig cell hypoplasia type II.

Kossack N, Troppmann B, Richter-Unruh A, Kleinau G, Gromoll J.

Mol Cell Endocrinol. 2013 Feb 5;366(1):59-67. doi: 10.1016/j.mce.2012.11.018. Epub 2012 Dec 8.

PMID:
23232123
3.

A novel missense homozygous inactivating mutation in the fourth transmembrane helix of the luteinizing hormone receptor in leydig cell hypoplasia.

Leung MY, Al-Muslim O, Wu SM, Aziz A, Inam S, Awadh M, Rennert OM, Chan WY.

Am J Med Genet A. 2004 Oct 1;130A(2):146-53.

PMID:
15372531
4.

Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene.

Kremer H, Kraaij R, Toledo SP, Post M, Fridman JB, Hayashida CY, van Reen M, Milgrom E, Ropers HH, Mariman E, et al.

Nat Genet. 1995 Feb;9(2):160-4.

PMID:
7719343
5.

[Leydig cell hypoplasia(agenesis)].

Koyama S, Arisaka O.

Nihon Rinsho. 2004 Feb;62(2):357-60. Review. Japanese.

PMID:
14968545
6.

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. doi: 10.1007/s10815-014-0241-0. Epub 2014 May 3. No abstract available.

7.

Luteinizing hormone receptor mutations and sex differentiation.

Themmen AP, Brunner HG.

Eur J Endocrinol. 1996 May;134(5):533-40. Review.

PMID:
8664969
8.

[Leydig cell hypoplasia (Leydig cell aplasia)].

Arisaka O, Koyama S.

Nihon Rinsho. 2006 Jun 28;Suppl 2:545-9. Review. Japanese. No abstract available.

PMID:
16817462
9.

Mutant luteinizing hormone receptors in a compound heterozygous patient with complete Leydig cell hypoplasia: abnormal processing causes signaling deficiency.

Martens JW, Lumbroso S, Verhoef-Post M, Georget V, Richter-Unruh A, Szarras-Czapnik M, Romer TE, Brunner HG, Themmen AP, Sultan Ch.

J Clin Endocrinol Metab. 2002 Jun;87(6):2506-13.

PMID:
12050206
10.

Inactivating mutations in the LH receptor-as rare as "a hen with teeth"or as frequent as polycystic ovary syndrome?

Toledo SP, Marino F.

Fertil Steril. 2000 Mar;73(3):655. No abstract available. Erratum in: Fertil Steril 2000 Jun;73(6):1268. Toledo SF [corrected to Toledo SP].

PMID:
10733310
11.
12.

Inactivation of the luteinizing hormone/chorionic gonadotropin receptor by an insertional mutation in Leydig cell hypoplasia.

Wu SM, Hallermeier KM, Laue L, Brain C, Berry AC, Grant DB, Griffin JE, Wilson JD, Cutler GB Jr, Chan WY.

Mol Endocrinol. 1998 Nov;12(11):1651-60.

PMID:
9817592
13.

A missense mutation of the Dhh gene is associated with male pseudohermaphroditic rats showing impaired Leydig cell development.

Kawai Y, Noguchi J, Akiyama K, Takeno Y, Fujiwara Y, Kajita S, Tsuji T, Kikuchi K, Kaneko H, Kunieda T.

Reproduction. 2011 Feb;141(2):217-25. doi: 10.1530/REP-10-0006. Epub 2010 Nov 9.

14.
15.

Luteinizing hormone resistance syndromes.

Tsigos C, Latronico C, Chrousos GP.

Ann N Y Acad Sci. 1997 Jun 17;816:263-73.

PMID:
9238276
16.

Leydig cell hypoplasia: absent luteinizing hormone receptor cell surface expression caused by a novel homozygous mutation in the extracellular domain.

Richter-Unruh A, Verhoef-Post M, Malak S, Homoki J, Hauffa BP, Themmen AP.

J Clin Endocrinol Metab. 2004 Oct;89(10):5161-7.

PMID:
15472221
17.

A novel inactivating mutation of the LH/chorionic gonadotrophin receptor with impaired membrane trafficking leading to Leydig cell hypoplasia type 1.

Rivero-Müller A, Potorac I, Pintiaux A, Daly AF, Thiry A, Rydlewski C, Nisolle M, Parent AS, Huhtaniemi I, Beckers A.

Eur J Endocrinol. 2015 Jun;172(6):K27-36. doi: 10.1530/EJE-14-1095. Epub 2015 Mar 20.

PMID:
25795638
18.

Mutations in a novel, cryptic exon of the luteinizing hormone/chorionic gonadotropin receptor gene cause male pseudohermaphroditism.

Kossack N, Simoni M, Richter-Unruh A, Themmen AP, Gromoll J.

PLoS Med. 2008 Apr 22;5(4):e88. doi: 10.1371/journal.pmed.0050088.

19.

A nonsense mutation of the human luteinizing hormone receptor gene in Leydig cell hypoplasia.

Laue L, Wu SM, Kudo M, Hsueh AJ, Cutler GB Jr, Griffin JE, Wilson JD, Brain C, Berry AC, Grant DB, et al.

Hum Mol Genet. 1995 Aug;4(8):1429-33.

PMID:
7581384
20.
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk