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 *

103 related articles for article (PubMed ID: 10689634)

  • 1. Growth hormone deficiency type IB caused by cryptic splicing of the GH-1 gene.
    Abdul-Latif H; Leiberman E; Brown MR; Carmi R; Parks JS
    J Pediatr Endocrinol Metab; 2000 Jan; 13(1):21-8. PubMed ID: 10689634
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel IVS2 -2A>T splicing mutation in the GH-1 gene in familial isolated growth hormone deficiency type II in the spectrum of other splicing mutations in the Russian population.
    Fofanova OV; Evgrafov OV; Polyakov AV; Poltaraus AB; Peterkova VA; Dedov II
    J Clin Endocrinol Metab; 2003 Feb; 88(2):820-6. PubMed ID: 12574219
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mechanisms responsible for dominant expression of human growth hormone gene mutations.
    Binder G; Brown M; Parks JS
    J Clin Endocrinol Metab; 1996 Nov; 81(11):4047-50. PubMed ID: 8923859
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Screening for growth hormone (GH) gene splice-site mutations in sporadic cases with severe isolated GH deficiency using ectopic transcript analysis.
    Binder G; Ranke MB
    J Clin Endocrinol Metab; 1995 Apr; 80(4):1247-52. PubMed ID: 7714096
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel and de novo splice-donor site mutation in intron 3 of the GH-1 gene in a patient with isolated growth hormone deficiency.
    Katsumata N; Matsuo S; Sato N; Tanaka T
    Growth Horm IGF Res; 2001 Dec; 11(6):378-83. PubMed ID: 11914025
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Isolated GH deficiency with dominant inheritance: new mutations, new insights.
    Binder G; Keller E; Mix M; Massa GG; Stokvis-Brantsma WH; Wit JM; Ranke MB
    J Clin Endocrinol Metab; 2001 Aug; 86(8):3877-81. PubMed ID: 11502827
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel mutation at the donor splice site of intron 3 of the GH-I gene in a patient with isolated growth hormone deficiency.
    Hayashi Y; Kamijo T; Yamamoto M; Ohmori S; Phillips JA; Ogawa M; Igarashi Y; Seo H
    Growth Horm IGF Res; 1999 Dec; 9(6):434-7. PubMed ID: 10629163
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Three new mutations in the gene for the growth hormone (gh)-releasing hormone receptor in familial isolated gh deficiency type ib.
    Salvatori R; Fan X; Phillips JA; Espigares-Martin R; Martin De Lara I; Freeman KL; Plotnick L; Al-Ashwal A; Levine MA
    J Clin Endocrinol Metab; 2001 Jan; 86(1):273-9. PubMed ID: 11232012
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Complex alternative splicing of the GH-V gene in the human testis.
    Untergasser G; Hermann M; Rumpold H; Berger P
    Eur J Endocrinol; 1998 Oct; 139(4):424-7. PubMed ID: 9820620
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort.
    Lido AC; França MM; Correa FA; Otto AP; Carvalho LR; Quedas EP; Nishi MY; Mendonca BB; Arnhold IJ; Jorge AA
    Growth Horm IGF Res; 2014 Oct; 24(5):180-6. PubMed ID: 25116472
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial growth hormone deficiency: a model of dominant and recessive mutations affecting a monomeric protein.
    Cogan JD; Phillips JA; Schenkman SS; Milner RD; Sakati N
    J Clin Endocrinol Metab; 1994 Nov; 79(5):1261-5. PubMed ID: 7962317
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An exonic mutation of the GH-1 gene causing familial isolated growth hormone deficiency type II.
    Takahashi I; Takahashi T; Komatsu M; Sato T; Takada G
    Clin Genet; 2002 Mar; 61(3):222-5. PubMed ID: 12000366
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of an intron splice enhancer that regulates alternative splicing of human GH pre-mRNA.
    McCarthy EM; Phillips JA
    Hum Mol Genet; 1998 Sep; 7(9):1491-6. PubMed ID: 9700205
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Isolated autosomal dominant growth hormone deficiency: stimulating mutant GH-1 gene expression drives GH-1 splice-site selection, cell proliferation, and apoptosis.
    Salemi S; Yousefi S; Lochmatter D; Eblé A; Deladoëy J; Robinson IC; Simon HU; Mullis PE
    Endocrinology; 2007 Jan; 148(1):45-53. PubMed ID: 17038549
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary isolated growth hormone deficiency caused by GH1 gene mutations in Japanese patients.
    Kamijo T; Hayashi Y; Seo H; Ogawa M
    Growth Horm IGF Res; 1999 Jun; 9 Suppl B():31-4; discussion 35-6. PubMed ID: 10549303
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Two different 5' splice site mutations in the growth hormone gene causing autosomal dominant growth hormone deficiency.
    Missarelli C; Herrera L; Mericq V; Carvallo P
    Hum Genet; 1997 Nov; 101(1):113-7. PubMed ID: 9385381
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An exon splice enhancer mutation causes autosomal dominant GH deficiency.
    Moseley CT; Mullis PE; Prince MA; Phillips JA
    J Clin Endocrinol Metab; 2002 Feb; 87(2):847-52. PubMed ID: 11836331
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations in intron 3 of GH-1 gene associated with isolated GH deficiency type II in three Japanese families.
    Kamijo T; Hayashi Y; Shimatsu A; Kinoshita E; Yoshimoto M; Ogawa M; Seo H
    Clin Endocrinol (Oxf); 1999 Sep; 51(3):355-60. PubMed ID: 10469016
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel mechanism of aberrant pre-mRNA splicing in humans.
    Cogan JD; Prince MA; Lekhakula S; Bundey S; Futrakul A; McCarthy EM; Phillips JA
    Hum Mol Genet; 1997 Jun; 6(6):909-12. PubMed ID: 9175738
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Variable phenotypes in familial isolated growth hormone deficiency caused by a G6664A mutation in the GH-1 gene.
    Hess O; Hujeirat Y; Wajnrajch MP; Allon-Shalev S; Zadik Z; Lavi I; Tenenbaum-Rakover Y
    J Clin Endocrinol Metab; 2007 Nov; 92(11):4387-93. PubMed ID: 17785368
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.