BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 10943739)

  • 21. Characterization of GH-1 mutations in children with isolated growth hormone deficiency in the Turkish population.
    Coker A; Cetinkaya E; Dundar B; Siklar Z; Buyukgebiz A; Arman A
    J Pediatr Endocrinol Metab; 2009 Oct; 22(10):937-46. PubMed ID: 20020582
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Isolated growth hormone deficiency in two siblings because of paternal mosaicism for a mutation in the GH1 gene.
    Tsubahara M; Hayashi Y; Niijima S; Yamamoto M; Kamijo T; Murata Y; Haruna H; Okumura A; Shimizu T
    Clin Endocrinol (Oxf); 2012 Mar; 76(3):420-4. PubMed ID: 21933221
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Clinical and molecular characterization of Brazilian patients with growth hormone gene deletions.
    Arnhold IJ; Osorio MG; Oliveira SB; Estefan V; Kamijo T; Krishnamani MR; Cogan JD; Phillips JA; Mendonca BB
    Braz J Med Biol Res; 1998 Apr; 31(4):491-7. PubMed ID: 9698799
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Adult height in patients with permanent growth hormone deficiency with and without multiple pituitary hormone deficiencies.
    Maghnie M; Ambrosini L; Cappa M; Pozzobon G; Ghizzoni L; Ubertini MG; di Iorgi N; Tinelli C; Pilia S; Chiumello G; Lorini R; Loche S
    J Clin Endocrinol Metab; 2006 Aug; 91(8):2900-5. PubMed ID: 16684828
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Growth hormone (GH) insensitivity syndrome with high serum GH-binding protein levels caused by a heterozygous splice site mutation of the GH receptor gene producing a lack of intracellular domain.
    Iida K; Takahashi Y; Kaji H; Nose O; Okimura Y; Abe H; Chihara K
    J Clin Endocrinol Metab; 1998 Feb; 83(2):531-7. PubMed ID: 9467570
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Absence of GH-releasing hormone (GHRH) mutations in selected patients with isolated GH deficiency.
    França MM; Jorge AA; Alatzoglou KS; Carvalho LR; Mendonca BB; Audi L; Carrascosa A; Dattani MT; Arnhold IJ
    J Clin Endocrinol Metab; 2011 Sep; 96(9):E1457-60. PubMed ID: 21715545
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Autosomal-dominant isolated growth hormone deficiency (IGHD type II) with normal GH-1 gene.
    Fintini D; Salvatori R; Salemi S; Otten B; Ubertini G; Cambiaso P; Mullis PE
    Horm Res; 2006; 65(2):76-82. PubMed ID: 16424673
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A novel GH1 mutation in a family with isolated growth hormone deficiency type II.
    Gucev Z; Tasic V; Saranac L; Stobbe H; Kratzsch J; Klammt J; Pfäffle R
    Horm Res Paediatr; 2012; 77(3):200-4. PubMed ID: 22188748
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Novel compound heterozygous mutations of growth hormone (GH) receptor gene in a patient with GH insensitivity syndrome.
    Kaji H; Nose O; Tajiri H; Takahashi Y; Iida K; Takahashi T; Okimura Y; Abe H; Chihara K
    J Clin Endocrinol Metab; 1997 Nov; 82(11):3705-9. PubMed ID: 9360529
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Isolated GH deficiency: mutation screening and copy number analysis of HMGA2 and CDK6 genes.
    Gorbenko del Blanco D; de Graaff LC; Posthouwer D; Visser TJ; Hokken-Koelega AC
    Eur J Endocrinol; 2011 Oct; 165(4):537-44. PubMed ID: 21803798
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mutations in GH1 gene and isolated growth hormone deficiency (IGHD): A familial case of IGHD type I and systematic review.
    Li Q; Xu Z; Zhang M; Zhao Z; Sun B; Yang L; Lu W; Luo F; Sun C
    Growth Horm IGF Res; 2021; 60-61():101423. PubMed ID: 34375817
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Type IA isolated growth hormone deficiency (IGHD) consistent with compound heterozygous deletions of 6.7 and 7.6 Kb at the GH1 gene locus.
    Keselman A; Scaglia PA; Rodríguez Prieto MS; Ballerini MG; Rodríguez ME; Ropelato MG; Bergadá I; Jasper HG; Domené HM
    Arq Bras Endocrinol Metabol; 2012 Nov; 56(8):558-63. PubMed ID: 23295298
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel deletion in the GH1 gene including the IVS3 branch site responsible for autosomal dominant isolated growth hormone deficiency.
    Vivenza D; Guazzarotti L; Godi M; Frasca D; di Natale B; Momigliano-Richiardi P; Bona G; Giordano M
    J Clin Endocrinol Metab; 2006 Mar; 91(3):980-6. PubMed ID: 16368751
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Structural analysis of human growth hormone with respect to the dominant expression of growth hormone (GH) mutations in isolated GH deficiency type II.
    Iliev DI; Wittekindt NE; Ranke MB; Binder G
    Endocrinology; 2005 Mar; 146(3):1411-7. PubMed ID: 15591149
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Short stature in carriers of recessive mutation causing familial isolated growth hormone deficiency.
    Leiberman E; Pesler D; Parvari R; Elbedour K; Abdul-Latif H; Brown MR; Parks JS; Carmi R
    Am J Med Genet; 2000 Jan; 90(3):188-92. PubMed ID: 10678654
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Short stature and decreased insulin-like growth factor I (IGF-I)/growth hormone (GH)-ratio in an adult GH-deficient patient pointing to additional partial GH insensitivity due to a R179C mutation of the growth hormone receptor.
    Meyer S; Ipek M; Keth A; Minnemann T; von Mach MA; Weise A; Ittner JR; Nawroth PP; Plöckinger U; Stalla GK; Tuschy U; Weber MM; Kann PH; ;
    Growth Horm IGF Res; 2007 Aug; 17(4):307-14. PubMed ID: 17462934
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Partial growth-hormone insensitivity: the role of growth-hormone receptor mutations in idiopathic short stature.
    Goddard AD; Dowd P; Chernausek S; Geffner M; Gertner J; Hintz R; Hopwood N; Kaplan S; Plotnick L; Rogol A; Rosenfield R; Saenger P; Mauras N; Hershkopf R; Angulo M; Attie K
    J Pediatr; 1997 Jul; 131(1 Pt 2):S51-5. PubMed ID: 9255229
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.