Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 145

1.

Precocious puberty and Leydig cell hyperplasia in male mice with a gain of function mutation in the LH receptor gene.

McGee SR, Narayan P.

Endocrinology. 2013 Oct;154(10):3900-13. doi: 10.1210/en.2012-2179. Epub 2013 Jul 16.

2.

Mutation analysis of the LH receptor gene in Leydig cell adenoma and hyperplasia and functional and biochemical studies of activating mutations of the LH receptor gene.

Boot AM, Lumbroso S, Verhoef-Post M, Richter-Unruh A, Looijenga LH, Funaro A, Beishuizen A, van Marle A, Drop SL, Themmen AP.

J Clin Endocrinol Metab. 2011 Jul;96(7):E1197-205. doi: 10.1210/jc.2010-3031. Epub 2011 Apr 13.

3.

Infertility in Female Mice with a Gain-of-Function Mutation in the Luteinizing Hormone Receptor Is Due to Irregular Estrous Cyclicity, Anovulation, Hormonal Alterations, and Polycystic Ovaries.

Hai L, McGee SR, Rabideau AC, Paquet M, Narayan P.

Biol Reprod. 2015 Jul;93(1):16. doi: 10.1095/biolreprod.115.129072. Epub 2015 Jun 3.

4.

A sporadic case of male-limited precocious puberty has the same constitutively activating point mutation in luteinizing hormone/choriogonadotropin receptor gene as familial cases.

Yano K, Hidaka A, Saji M, Polymeropoulos MH, Okuno A, Kohn LD, Cutler GB Jr.

J Clin Endocrinol Metab. 1994 Dec;79(6):1818-23.

PMID:
7527413
5.

A constitutively activating mutation of the luteinizing hormone receptor in familial male precocious puberty.

Shenker A, Laue L, Kosugi S, Merendino JJ Jr, Minegishi T, Cutler GB Jr.

Nature. 1993 Oct 14;365(6447):652-4.

PMID:
7692306
6.
7.

A new constitutively activating point mutation in the luteinizing hormone/choriogonadotropin receptor gene in cases of male-limited precocious puberty.

Yano K, Saji M, Hidaka A, Moriya N, Okuno A, Kohn LD, Cutler GB Jr.

J Clin Endocrinol Metab. 1995 Apr;80(4):1162-8.

PMID:
7714085
8.

Venous sampling can be crucial in identifying the testicular origin of idiopathic male luteinising hormone-independent sexual precocity.

Richter-Unruh A, Jorch N, Wessels HT, Weber EA, Hauffa BP.

Eur J Pediatr. 2002 Dec;161(12):668-71. Epub 2002 Nov 6.

PMID:
12447668
9.

Characterization of heterogeneous mutations causing constitutive activation of the luteinizing hormone receptor in familial male precocious puberty.

Kosugi S, Van Dop C, Geffner ME, Rabl W, Carel JC, Chaussain JL, Mori T, Merendino JJ Jr, Shenker A.

Hum Mol Genet. 1995 Feb;4(2):183-8.

PMID:
7757065
10.

Activating mutations in the luteinizing hormone receptor gene: a human model of non-follicle-stimulating hormone-dependent inhibin production and germ cell maturation.

Soriano-Guillen L, Mitchell V, Carel JC, Barbet P, Roger M, Lahlou N.

J Clin Endocrinol Metab. 2006 Aug;91(8):3041-7. Epub 2006 May 9.

PMID:
16684832
11.

A novel mutation of the luteinizing hormone receptor gene causing male gonadotropin-independent precocious puberty.

Latronico AC, Anasti J, Arnhold IJ, Mendonça BB, Domenice S, Albano MC, Zachman K, Wajchenberg BL, Tsigos C.

J Clin Endocrinol Metab. 1995 Aug;80(8):2490-4.

PMID:
7629248
12.

Activating mutations of the lutropin choriogonadotropin receptor in precocious puberty.

Shenker A.

Receptors Channels. 2002;8(1):3-18. Review.

PMID:
12408104
14.

Nodular Leydig cell hyperplasia in a boy with familial male-limited precocious puberty.

Leschek EW, Chan WY, Diamond DA, Kaefer M, Jones J, Barnes KM, Cutler GB Jr.

J Pediatr. 2001 Jun;138(6):949-51.

PMID:
11391350
15.

Gonadotropin-independent precocious puberty due to luteinizing hormone receptor mutations in Brazilian boys: a novel constitutively activating mutation in the first transmembrane helix.

Latronico AC, Shinozaki H, Guerra G Jr, Pereira MA, Lemos Marini SH, Baptista MT, Arnhold IJ, Fanelli F, Mendonca BB, Segaloff DL.

J Clin Endocrinol Metab. 2000 Dec;85(12):4799-805.

PMID:
11134146
16.

Peripheral precocious puberty in a male caused by Leydig cell adenoma harboring a somatic mutation of the LHR gene: report of a case.

Sangkhathat S, Kanngurn S, Jaruratanasirikul S, Tubtawee T, Chaiyapan W, Patrapinyokul S, Chiengkriwate P.

J Med Assoc Thai. 2010 Sep;93(9):1093-7.

PMID:
20873084
17.

Disorders of sexual development caused by luteinizing hormone receptor mutations.

Chan WY.

Beijing Da Xue Xue Bao Yi Xue Ban. 2005 Feb 18;37(1):32-8.

18.

[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. doi: 10.3760/cma.j.issn.1003-9406.2012.06.002. Chinese.

PMID:
23225038

Supplemental Content

Support Center