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 *

81 related articles for article (PubMed ID: 8595432)

  • 1. A deletion hot-spot in exon 7 of the Gs alpha gene (GNAS1) in patients with Albright hereditary osteodystrophy.
    Yu S; Yu D; Hainline BE; Brener JL; Wilson KA; Wilson LC; Oude-Luttikhuis ME; Trembath RC; Weinstein LS
    Hum Mol Genet; 1995 Oct; 4(10):2001-2. PubMed ID: 8595432
    [No Abstract]   [Full Text] [Related]  

  • 2. Characterization of a de novo 43-bp deletion of the Gs alpha gene (GNAS1) in Albright hereditary osteodystrophy.
    Luttikhuis ME; Wilson LC; Leonard JV; Trembath RC
    Genomics; 1994 May; 21(2):455-7. PubMed ID: 8088846
    [No Abstract]   [Full Text] [Related]  

  • 3. A heterozygous 4-bp deletion mutation in the Gs alpha gene (GNAS1) in a patient with Albright hereditary osteodystrophy.
    Weinstein LS; Gejman PV; de Mazancourt P; American N; Spiegel AM
    Genomics; 1992 Aug; 13(4):1319-21. PubMed ID: 1505964
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Heterogeneous mutations in the gene encoding the alpha-subunit of the stimulatory G protein of adenylyl cyclase in Albright hereditary osteodystrophy.
    Miric A; Vechio JD; Levine MA
    J Clin Endocrinol Metab; 1993 Jun; 76(6):1560-8. PubMed ID: 8388883
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pseudohypoparathyroidism type Ia: two new heterozygous frameshift mutations in exons 5 and 10 of the Gs alpha gene.
    Shapira H; Mouallem M; Shapiro MS; Weisman Y; Farfel Z
    Hum Genet; 1996 Jan; 97(1):73-5. PubMed ID: 8557265
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of two novel deletion mutations within the Gs alpha gene (GNAS1) in Albright hereditary osteodystrophy.
    Yu D; Yu S; Schuster V; Kruse K; Clericuzio CL; Weinstein LS
    J Clin Endocrinol Metab; 1999 Sep; 84(9):3254-9. PubMed ID: 10487696
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis.
    Weinstein LS; Gejman PV; Friedman E; Kadowaki T; Collins RM; Gershon ES; Spiegel AM
    Proc Natl Acad Sci U S A; 1990 Nov; 87(21):8287-90. PubMed ID: 2122458
    [TBL] [Abstract][Full Text] [Related]  

  • 8. GNAS1 mutation and Cbfa1 misexpression in a child with severe congenital platelike osteoma cutis.
    Yeh GL; Mathur S; Wivel A; Li M; Gannon FH; Ulied A; Audi L; Olmstead EA; Kaplan FS; Shore EM
    J Bone Miner Res; 2000 Nov; 15(11):2063-73. PubMed ID: 11092389
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Study of the multiple endocrine neoplasia type 1, growth hormone-releasing hormone receptor, Gs alpha, and Gi2 alpha genes in isolated familial acromegaly.
    Jorge BH; Agarwal SK; Lando VS; Salvatori R; Barbero RR; Abelin N; Levine MA; Marx SJ; Toledo SP
    J Clin Endocrinol Metab; 2001 Feb; 86(2):542-4. PubMed ID: 11158006
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy.
    Patten JL; Johns DR; Valle D; Eil C; Gruppuso PA; Steele G; Smallwood PM; Levine MA
    N Engl J Med; 1990 May; 322(20):1412-9. PubMed ID: 2109828
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophy.
    Wilson LC; Oude Luttikhuis ME; Clayton PT; Fraser WD; Trembath RC
    J Med Genet; 1994 Nov; 31(11):835-9. PubMed ID: 7853365
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of the GNAS1 gene in Albright's hereditary osteodystrophy.
    Ahrens W; Hiort O; Staedt P; Kirschner T; Marschke C; Kruse K
    J Clin Endocrinol Metab; 2001 Oct; 86(10):4630-4. PubMed ID: 11600516
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Paternally inherited inactivating mutations of the GNAS1 gene in progressive osseous heteroplasia.
    Shore EM; Ahn J; Jan de Beur S; Li M; Xu M; Gardner RJ; Zasloff MA; Whyte MP; Levine MA; Kaplan FS
    N Engl J Med; 2002 Jan; 346(2):99-106. PubMed ID: 11784876
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Activating mutations of the stimulatory G protein in the McCune-Albright syndrome.
    Weinstein LS; Shenker A; Gejman PV; Merino MJ; Friedman E; Spiegel AM
    N Engl J Med; 1991 Dec; 325(24):1688-95. PubMed ID: 1944469
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Albright hereditary osteodystrophy: identification of a novel mutation in a family].
    Bastida Eizaguirre M; Iturbe Ortiz De Urbina R; Arto Urzainqui M; Ezquerra Larreina R; Escalada San Martín J
    An Esp Pediatr; 2001 Jun; 54(6):598-600. PubMed ID: 11412411
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Localization of the rat stimulatory G-protein alpha subunit (GNPAS) gene to rat chromosome 3 by linkage analysis.
    Kato N; Bihoreau M; Lathrop GM; Rapp JP
    Mamm Genome; 1996 Aug; 7(8):628-9. PubMed ID: 8679006
    [No Abstract]   [Full Text] [Related]  

  • 17. Mutational analysis of GNAS1 in patients with pseudohypoparathyroidism: identification of two novel mutations.
    Mantovani G; Romoli R; Weber G; Brunelli V; De Menis E; Beccio S; Beck-Peccoz P; Spada A
    J Clin Endocrinol Metab; 2000 Nov; 85(11):4243-8. PubMed ID: 11095461
    [TBL] [Abstract][Full Text] [Related]  

  • 18. SSCP polymorphism in exon 8B of the human G protein alpha O2 subunit (GNA01) gene.
    Drews RT; Lagacé G; Gravel RA; Collu R
    Hum Mol Genet; 1993 Aug; 2(8):1333. PubMed ID: 8401528
    [No Abstract]   [Full Text] [Related]  

  • 19. Parental origin of transcription from the human GNAS1 gene.
    Campbell R; Gosden CM; Bonthron DT
    J Med Genet; 1994 Aug; 31(8):607-14. PubMed ID: 7815417
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A GNAS1 imprinting defect in pseudohypoparathyroidism type IB.
    Liu J; Litman D; Rosenberg MJ; Yu S; Biesecker LG; Weinstein LS
    J Clin Invest; 2000 Nov; 106(9):1167-74. PubMed ID: 11067869
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.