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 *

113 related articles for article (PubMed ID: 8504252)

  • 1. Lessons from lethal albino mice.
    Kelsey G; Schütz G
    Curr Opin Genet Dev; 1993 Apr; 3(2):259-64. PubMed ID: 8504252
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rescue of mice homozygous for lethal albino deletions: implications for an animal model for the human liver disease tyrosinemia type 1.
    Kelsey G; Ruppert S; Beermann F; Grund C; Tanguay RM; Schütz G
    Genes Dev; 1993 Dec; 7(12A):2285-97. PubMed ID: 8253377
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Loss of fumarylacetoacetate hydrolase is responsible for the neonatal hepatic dysfunction phenotype of lethal albino mice.
    Grompe M; al-Dhalimy M; Finegold M; Ou CN; Burlingame T; Kennaway NG; Soriano P
    Genes Dev; 1993 Dec; 7(12A):2298-307. PubMed ID: 8253378
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Multiple effects on liver-specific gene expression in albino lethal mice caused by deficiency of an enzyme in tyrosine metabolism.
    Kelsey G; Ruppert S; Schedl A; Schmid E; Thies E; Schütz G
    J Cell Sci Suppl; 1992; 16():117-22. PubMed ID: 1297646
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic control of morphogenetic and biochemical differentiation: lethal albino deletions in the mouse.
    Gluecksohn-Waelsch S
    Cell; 1979 Feb; 16(2):225-37. PubMed ID: 36985
    [No Abstract]   [Full Text] [Related]  

  • 6. Deficiency of an enzyme of tyrosine metabolism underlies altered gene expression in newborn liver of lethal albino mice.
    Ruppert S; Kelsey G; Schedl A; Schmid E; Thies E; Schütz G
    Genes Dev; 1992 Aug; 6(8):1430-43. PubMed ID: 1644288
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Isolation and characterization of mouse hepatocyte lines carrying a lethal albino deletion.
    Chou JY; Ruppert S; Shelly LL; Pan CJ
    J Biol Chem; 1991 Mar; 266(9):5716-22. PubMed ID: 1848557
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mouse albino-deletions: from genetics to genes in development.
    Holdener-Kenny B; Sharan SK; Magnuson T
    Bioessays; 1992 Dec; 14(12):831-9. PubMed ID: 1365899
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Microclones derived from the mouse chromosome 7 D-E bands map within the proximal region of the c14CoS deletion in albino mutant mice.
    Tönjes RR; Weith A; Rinchik EM; Winking H; Carnwath JW; Kaliner B; Paul D
    Genomics; 1991 Jul; 10(3):686-91. PubMed ID: 1889814
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Selective loss of a DNase I hypersensitive site upstream of the tyrosine aminotransferase gene in mice homozygous for lethal albino deletions.
    Zaret KS; Milos P; Lia M; Bali D; Gluecksohn-Waelsch S
    Proc Natl Acad Sci U S A; 1992 Jul; 89(14):6540-4. PubMed ID: 1378630
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Perinatal activation of a tyrosine aminotransferase fusion gene does not occur in albino lethal mice.
    Beermann F; Hummler E; Schmid E; Schütz G
    Mech Dev; 1993 Jul; 42(1-2):59-65. PubMed ID: 8103668
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Metabolic studies in a mouse model of hepatorenal tyrosinemia: absence of perinatal abnormalities.
    Collins JC; Buchanan DN; Thoene JG; Erickson RP; Brooks SS; Gluecksohn-Waelsch S
    Biochem Biophys Res Commun; 1992 Aug; 187(1):340-6. PubMed ID: 1520318
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Murine fumarylacetoacetate hydrolase (Fah) gene is disrupted by a neonatally lethal albino deletion that defines the hepatocyte-specific developmental regulation 1 (hsdr-1) locus.
    Klebig ML; Russell LB; Rinchik EM
    Proc Natl Acad Sci U S A; 1992 Feb; 89(4):1363-7. PubMed ID: 1741389
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Studies of a spontaneous lethal mutation at the albino locus in SELH/Bc mice.
    Juriloff DM; Harris MJ; Wong V; Miller JE
    Genome; 1992 Apr; 35(2):342-6. PubMed ID: 1618394
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Three spontaneous mutations at the albino locus in SELH/Bc mice.
    Juriloff DM; Porter SD; Harris MJ
    Genome; 1994 Apr; 37(2):190-7. PubMed ID: 8200511
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Physical analysis of murine albino deletions that disrupt liver-specific gene regulation or mesoderm development.
    Klebig ML; Kwon BS; Rinchik EM
    Mamm Genome; 1992; 2(1):51-63. PubMed ID: 1543902
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular analysis of radiation-induced albino (c)-locus mutations that cause death at preimplantation stages of development.
    Rinchik EM; Tönjes RR; Paul D; Potter MD
    Genetics; 1993 Dec; 135(4):1107-16. PubMed ID: 8307326
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Analysis of the albino-locus region of the mouse: IV. Characterization of 34 deficiencies.
    Russell LB; Montgomery CS; Raymer GD
    Genetics; 1982 Mar; 100(3):427-53. PubMed ID: 7117820
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Metallothionein mRNA expression in mice homozygous for chromosomal deletions around the albino locus.
    DeFranco D; Morris SM; Leonard CM; Gluecksohn-Waelsch S
    Proc Natl Acad Sci U S A; 1988 Feb; 85(4):1161-4. PubMed ID: 3422486
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Localization of cloned mouse chromosome 7-specific DNA to lethal albino deletions.
    Disteche CM; Adler D
    Somat Cell Mol Genet; 1984 May; 10(3):211-5. PubMed ID: 6585968
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.