357 related articles for article (PubMed ID: 11134146)
1. 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; 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. PubMed ID: 11134146
[TBL] [Abstract][Full Text] [Related]
2. A unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious puberty.
Latronico AC; Abell AN; Arnhold IJ; Liu X; Lins TS; Brito VN; Billerbeck AE; Segaloff DL; Mendonca BB
J Clin Endocrinol Metab; 1998 Jul; 83(7):2435-40. PubMed ID: 9661624
[TBL] [Abstract][Full Text] [Related]
3. 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
J Clin Endocrinol Metab; 1994 Dec; 79(6):1818-23. PubMed ID: 7527413
[TBL] [Abstract][Full Text] [Related]
4. 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
J Clin Endocrinol Metab; 1995 Apr; 80(4):1162-8. PubMed ID: 7714085
[TBL] [Abstract][Full Text] [Related]
5. A novel luteinizing hormone receptor mutation in a patient with familial male-limited precocious puberty: effect of the size of a critical amino acid on receptor activity.
Wu SM; Leschek EW; Brain C; Chan WY
Mol Genet Metab; 1999 Jan; 66(1):68-73. PubMed ID: 9973550
[TBL] [Abstract][Full Text] [Related]
6. Heterogeneity of activating mutations of the human luteinizing hormone receptor in male-limited precocious puberty.
Laue L; Wu SM; Kudo M; Hsueh AJ; Cutler GB; Jelly DH; Diamond FB; Chan WY
Biochem Mol Med; 1996 Aug; 58(2):192-8. PubMed ID: 8812739
[TBL] [Abstract][Full Text] [Related]
7. Genetic heterogeneity of constitutively activating mutations of the human luteinizing hormone receptor in familial male-limited precocious puberty.
Laue L; Chan WY; Hsueh AJ; Kudo M; Hsu SY; Wu SM; Blomberg L; Cutler GB
Proc Natl Acad Sci U S A; 1995 Mar; 92(6):1906-10. PubMed ID: 7892197
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 7629248
[TBL] [Abstract][Full Text] [Related]
9. Insights learned from L457(3.43)R, an activating mutant of the human lutropin receptor.
Latronico AC; Segaloff DL
Mol Cell Endocrinol; 2007 Jan; 260-262():287-93. PubMed ID: 17055147
[TBL] [Abstract][Full Text] [Related]
10. A homozygous microdeletion in helix 7 of the luteinizing hormone receptor associated with familial testicular and ovarian resistance is due to both decreased cell surface expression and impaired effector activation by the cell surface receptor.
Latronico AC; Chai Y; Arnhold IJ; Liu X; Mendonca BB; Segaloff DL
Mol Endocrinol; 1998 Mar; 12(3):442-50. PubMed ID: 9514160
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The effect of distinct activating mutations of the luteinizing hormone receptor gene on the pituitary-gonadal axis in both sexes.
Latronico AC; Lins TS; Brito VN; Arnhold IJ; Mendonca BB
Clin Endocrinol (Oxf); 2000 Nov; 53(5):609-13. PubMed ID: 11106922
[TBL] [Abstract][Full Text] [Related]
13. Desensitization of Gs-coupled receptor signaling by constitutively active mutants of the human lutropin/choriogonadotropin receptor.
Shinozaki H; Butnev V; Tao YX; Ang KL; Conti M; Segaloff DL
J Clin Endocrinol Metab; 2003 Mar; 88(3):1194-204. PubMed ID: 12629106
[TBL] [Abstract][Full Text] [Related]
14. Certain activating mutations within helix 6 of the human luteinizing hormone receptor may be explained by alterations that allow transmembrane regions to activate Gs.
Abell AN; McCormick DJ; Segaloff DL
Mol Endocrinol; 1998 Dec; 12(12):1857-69. PubMed ID: 9849960
[TBL] [Abstract][Full Text] [Related]
15. Phe576 plays an important role in the secondary structure and intracellular signaling of the human luteinizing hormone/chorionic gonadotropin receptor.
Yano K; Kohn LD; Saji M; Okuno A; Cutler GB
J Clin Endocrinol Metab; 1997 Aug; 82(8):2586-91. PubMed ID: 9253338
[TBL] [Abstract][Full Text] [Related]
16. A missense mutation in the second transmembrane segment of the luteinizing hormone receptor causes familial male-limited precocious puberty.
Kraaij R; Post M; Kremer H; Milgrom E; Epping W; Brunner HG; Grootegoed JA; Themmen AP
J Clin Endocrinol Metab; 1995 Nov; 80(11):3168-72. PubMed ID: 7593421
[TBL] [Abstract][Full Text] [Related]
17. A constitutively activating mutation of the luteinizing hormone receptor in familial male precocious puberty.
Shenker A; Laue L; Kosugi S; Merendino JJ; Minegishi T; Cutler GB
Nature; 1993 Oct; 365(6447):652-4. PubMed ID: 7692306
[TBL] [Abstract][Full Text] [Related]
18. Pleiotropic effects of substitutions of a highly conserved leucine in transmembrane helix III of the human lutropin/choriogonadotropin receptor with respect to constitutive activation and hormone responsiveness.
Shinozaki H; Fanelli F; Liu X; Jaquette J; Nakamura K; Segaloff DL
Mol Endocrinol; 2001 Jun; 15(6):972-84. PubMed ID: 11376115
[TBL] [Abstract][Full Text] [Related]
19. [Constitutively activating mutations in the luteinizing hormone receptor gene in cases of male-limited precocious puberty].
Yano K; Okuno A
Nihon Rinsho; 1998 Jul; 56(7):1843-7. PubMed ID: 9702063
[TBL] [Abstract][Full Text] [Related]
20. [A report of familial male-limited precocious puberty caused by a germ-line heterozygous mutation (M398T) in luteinizing hormone receptor gene].
Mao JF; Wu XY; Nie M; Lu SY; Gong FY; Dai YF
Zhonghua Nei Ke Za Zhi; 2010 Dec; 49(12):1024-7. PubMed ID: 21211360
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
