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 *

131 related articles for article (PubMed ID: 8812454)

  • 1. Glomerular-specific imprinting of the mouse gsalpha gene: how does this relate to hormone resistance in albright hereditary osteodystrophy?
    Williamson CM; Schofield J; Dutton ER; Seymour A; Beechey CV; Edwards YH; Peters J
    Genomics; 1996 Sep; 36(2):280-7. PubMed ID: 8812454
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2.
    Peters J; Wroe SF; Wells CA; Miller HJ; Bodle D; Beechey CV; Williamson CM; Kelsey G
    Proc Natl Acad Sci U S A; 1999 Mar; 96(7):3830-5. PubMed ID: 10097123
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Protective protein for beta-galactosidase, Ppgb, maps to the distal imprinting region of mouse chromosome 2 but is not imprinted.
    Williamson CM; Dutton ER; Beechey CV; Peters J
    Genomics; 1994 Jul; 22(1):240-2. PubMed ID: 7959780
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Endocrine manifestations of stimulatory G protein alpha-subunit mutations and the role of genomic imprinting.
    Weinstein LS; Yu S; Warner DR; Liu J
    Endocr Rev; 2001 Oct; 22(5):675-705. PubMed ID: 11588148
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Variable and tissue-specific hormone resistance in heterotrimeric Gs protein alpha-subunit (Gsalpha) knockout mice is due to tissue-specific imprinting of the gsalpha gene.
    Yu S; Yu D; Lee E; Eckhaus M; Lee R; Corria Z; Accili D; Westphal H; Weinstein LS
    Proc Natl Acad Sci U S A; 1998 Jul; 95(15):8715-20. PubMed ID: 9671744
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A mouse model of albright hereditary osteodystrophy generated by targeted disruption of exon 1 of the Gnas gene.
    Germain-Lee EL; Schwindinger W; Crane JL; Zewdu R; Zweifel LS; Wand G; Huso DL; Saji M; Ringel MD; Levine MA
    Endocrinology; 2005 Nov; 146(11):4697-709. PubMed ID: 16099856
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic and functional analysis of neuronatin in mice with maternal or paternal duplication of distal Chr 2.
    Kikyo N; Williamson CM; John RM; Barton SC; Beechey CV; Ball ST; Cattanach BM; Surani MA; Peters J
    Dev Biol; 1997 Oct; 190(1):66-77. PubMed ID: 9331332
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pseudohypoparathyroidism type Ia from maternal but not paternal transmission of a Gsalpha gene mutation.
    Nakamoto JM; Sandstrom AT; Brickman AS; Christenson RA; Van Dop C
    Am J Med Genet; 1998 May; 77(4):261-7. PubMed ID: 9600732
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A disruptive mutation in exon 3 of the GNAS gene with albright hereditary osteodystrophy, normocalcemic pseudohypoparathyroidism, and selective long transcript variant Gsalpha-L deficiency.
    Thiele S; Werner R; Ahrens W; Hoppe U; Marschke C; Staedt P; Hiort O
    J Clin Endocrinol Metab; 2007 May; 92(5):1764-8. PubMed ID: 17299070
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Tissue-specific expression of antisense and sense transcripts at the imprinted Gnas locus.
    Li T; Vu TH; Zeng ZL; Nguyen BT; Hayward BE; Bonthron DT; Hu JF; Hoffman AR
    Genomics; 2000 Nov; 69(3):295-304. PubMed ID: 11056047
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins.
    Hayward BE; Kamiya M; Strain L; Moran V; Campbell R; Hayashizaki Y; Bonthron DT
    Proc Natl Acad Sci U S A; 1998 Aug; 95(17):10038-43. PubMed ID: 9707596
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Minireview: GNAS: normal and abnormal functions.
    Weinstein LS; Liu J; Sakamoto A; Xie T; Chen M
    Endocrinology; 2004 Dec; 145(12):5459-64. PubMed ID: 15331575
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Embryological and molecular investigations of parental imprinting on mouse chromosome 7.
    Ferguson-Smith AC; Cattanach BM; Barton SC; Beechey CV; Surani MA
    Nature; 1991 Jun; 351(6328):667-70. PubMed ID: 2052093
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteins.
    Hayward BE; Moran V; Strain L; Bonthron DT
    Proc Natl Acad Sci U S A; 1998 Dec; 95(26):15475-80. PubMed ID: 9860993
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Distinct patterns of abnormal GNAS imprinting in familial and sporadic pseudohypoparathyroidism type IB.
    Liu J; Nealon JG; Weinstein LS
    Hum Mol Genet; 2005 Jan; 14(1):95-102. PubMed ID: 15537666
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Pseudopseudohypoparathyroidism and genomic imprinting].
    Minagawa M
    Clin Calcium; 2007 Aug; 17(8):1229-33. PubMed ID: 17660620
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Paternal uniparental isodisomy of chromosome 20q--and the resulting changes in GNAS1 methylation--as a plausible cause of pseudohypoparathyroidism.
    Bastepe M; Lane AH; Jüppner H
    Am J Hum Genet; 2001 May; 68(5):1283-9. PubMed ID: 11294659
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Pseudohypoparathyroidism type I b and genomic imprinting].
    Fukumoto S
    Clin Calcium; 2007 Aug; 17(8):1222-7. PubMed ID: 17660619
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Imprinting on chromosome 20: tissue-specific imprinting and imprinting mutations in the GNAS locus.
    Kelsey G
    Am J Med Genet C Semin Med Genet; 2010 Aug; 154C(3):377-86. PubMed ID: 20803660
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.