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354 related items for 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
    [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
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  • 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
    [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
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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
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  • 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 14; 92(6):1906-10. PubMed ID: 7892197
    [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 14; 80(8):2490-4. PubMed ID: 7629248
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  • 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 Aug 14; 57(12):1055-60. PubMed ID: 21060208
    [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 14; 53(5):609-13. PubMed ID: 11106922
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  • 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 14; 12(12):1857-69. PubMed ID: 9849960
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  • 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 14; 82(8):2586-91. PubMed ID: 9253338
    [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 14; 80(11):3168-72. PubMed ID: 7593421
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  • 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 14; 365(6447):652-4. PubMed ID: 7692306
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  • 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 14; 15(6):972-84. PubMed ID: 11376115
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  • 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 14; 49(12):1024-7. PubMed ID: 21211360
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