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Journal Abstract Search

434 related items for PubMed ID: 7527413

  • 1. 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]

  • 2. 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]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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 14; 85(12):4799-805. PubMed ID: 11134146
    [Abstract] [Full Text] [Related]

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

  • 6. A case of male-limited precocious puberty caused by a point mutation in the second transmembrane domain of the luteinizing hormone choriogonadotropin receptor gene.
    Yano K, Kohn LD, Saji M, Kataoka N, Okuno A, Cutler GB.
    Biochem Biophys Res Commun; 1996 Mar 27; 220(3):1036-42. PubMed ID: 8607787
    [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 14; 92(6):1906-10. PubMed ID: 7892197
    [Abstract] [Full Text] [Related]

  • 8. 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 Mar 14; 57(12):1055-60. PubMed ID: 21060208
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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 14; 83(7):2435-40. PubMed ID: 9661624
    [Abstract] [Full Text] [Related]

  • 11. [Constitutively activating mutations in the luteinizing hormone receptor gene in cases of male-limited precocious puberty].
    Yano K, Okuno A.
    Nihon Rinsho; 1998 Jul 14; 56(7):1843-7. PubMed ID: 9702063
    [Abstract] [Full Text] [Related]

  • 12. 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, Shenker A.
    Hum Mol Genet; 1995 Feb 14; 4(2):183-8. PubMed ID: 7757065
    [Abstract] [Full Text] [Related]

  • 13. [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 14; 29(6):631-4. PubMed ID: 23225038
    [Abstract] [Full Text] [Related]

  • 14. A mutation in the first transmembrane domain of the lutropin receptor causes male precocious puberty.
    Gromoll J, Partsch CJ, Simoni M, Nordhoff V, Sippell WG, Nieschlag E, Saxena BB.
    J Clin Endocrinol Metab; 1998 Feb 14; 83(2):476-80. PubMed ID: 9467560
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  • 17. 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 14; 58(2):192-8. PubMed ID: 8812739
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  • 19. The regulation of the binding affinity of the luteinizing hormone/choriogonadotropin receptor by sodium ions is mediated by a highly conserved aspartate located in the second transmembrane domain of G protein-coupled receptors.
    Quintana J, Wang H, Ascoli M.
    Mol Endocrinol; 1993 Jun 14; 7(6):767-75. PubMed ID: 8395653
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