These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 15711023)

  • 1. Distinct mechanisms of cAMP induction by constitutively activating LH receptor and wild-type LH receptor activated by hCG.
    Lee C; Ji I; Ji TH
    Endocrine; 2004 Nov; 25(2):111-5. PubMed ID: 15711023
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

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

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. The luteinizing hormone receptor activates phospholipase C via preferential coupling to Gi2.
    Kühn B; Gudermann T
    Biochemistry; 1999 Sep; 38(38):12490-8. PubMed ID: 10493819
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Absence of exon 10 of the human luteinizing hormone (LH) receptor impairs LH, but not human chorionic gonadotropin action.
    Müller T; Gromoll J; Simoni M
    J Clin Endocrinol Metab; 2003 May; 88(5):2242-9. PubMed ID: 12727981
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mechanisms for luteinizing hormone induction of growth hormone gene transcription in fish model: crosstalk of the cAMP/PKA pathway with MAPK-and PI3K-dependent cascades.
    Sun C; He M; Ko WK; Wong AO
    Mol Cell Endocrinol; 2014 Feb; 382(2):835-50. PubMed ID: 24161589
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. 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]  

  • 16. 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]  

  • 17. A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male LH-independent precocious puberty.
    Kremer H; Martens JW; van Reen M; Verhoef-Post M; Wit JM; Otten BJ; Drop SL; Delemarre-van de Waal HA; Pombo-Arias M; De Luca F; Potau N; Buckler JM; Jansen M; Parks JS; Latif HA; Moll GW; Epping W; Saggese G; Mariman EC; Themmen AP; Brunner HG
    J Clin Endocrinol Metab; 1999 Mar; 84(3):1136-40. PubMed ID: 10084607
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 220(3):1036-42. PubMed ID: 8607787
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of Key Receptor Residues Discriminating Human Chorionic Gonadotropin (hCG)- and Luteinizing Hormone (LH)-Specific Signaling.
    Lazzaretti C; Secco V; Paradiso E; Sperduti S; Rutz C; Kreuchwig A; Krause G; Simoni M; Casarini L
    Int J Mol Sci; 2020 Dec; 22(1):. PubMed ID: 33375708
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Specificity of cognate ligand-receptor interactions: fusion proteins of human chorionic gonadotropin and the heptahelical receptors for human luteinizing hormone, thyroid-stimulating hormone, and follicle-stimulating hormone.
    Schubert RL; Narayan P; Puett D
    Endocrinology; 2003 Jan; 144(1):129-37. PubMed ID: 12488338
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.