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 *

119 related articles for article (PubMed ID: 8004104)

  • 1. A point mutation responsible for human erythrocyte AMP deaminase deficiency.
    Yamada Y; Goto H; Ogasawara N
    Hum Mol Genet; 1994 Feb; 3(2):331-4. PubMed ID: 8004104
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Gene mutations for human erythrocyte AMP deaminase deficiency.
    Yamada Y; Goto H; Murase T; Ogasawara N
    Adv Exp Med Biol; 1994; 370():703-6. PubMed ID: 7661002
    [No Abstract]   [Full Text] [Related]  

  • 3. Gene mutations responsible for human erythrocyte AMP deaminase deficiency in Poles.
    Yamada Y; Makarewicz W; Goto H; Nomura N; Kitoh H; Ogasawara N
    Adv Exp Med Biol; 1998; 431():347-50. PubMed ID: 9598089
    [No Abstract]   [Full Text] [Related]  

  • 4. Deficiency of AMP deaminase in erythrocytes.
    Ogasawara N; Goto H; Yamada Y; Nishigaki I; Itoh T; Hasegawa I; Park KS
    Hum Genet; 1987 Jan; 75(1):15-8. PubMed ID: 3804327
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular basis for human erythrocyte AMP deaminase deficiency: screening for the major point mutation and identification of other mutations.
    Yamada Y; Goto H; Murase T; Ogasawara N
    Hum Mol Genet; 1994 Dec; 3(12):2243-5. PubMed ID: 7881427
    [No Abstract]   [Full Text] [Related]  

  • 6. Erythrocyte amp deaminase deficiency in Japanese: a compound heterozygote responsible for the complete deficiency.
    Yamada Y; Goto H; Ogasawara N
    Adv Exp Med Biol; 2000; 486():71-4. PubMed ID: 11783530
    [No Abstract]   [Full Text] [Related]  

  • 7. Molecular biology of AMP deaminase deficiency.
    Gross M
    Pharm World Sci; 1994 Apr; 16(2):55-61. PubMed ID: 8032342
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular basis of AMP deaminase deficiency in skeletal muscle.
    Morisaki T; Gross M; Morisaki H; Pongratz D; Zöllner N; Holmes EW
    Proc Natl Acad Sci U S A; 1992 Jul; 89(14):6457-61. PubMed ID: 1631143
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cloning of human AMP deaminase isoform E cDNAs. Evidence for a third AMPD gene exhibiting alternatively spliced 5'-exons.
    Mahnke-Zizelman DK; Sabina RL
    J Biol Chem; 1992 Oct; 267(29):20866-77. PubMed ID: 1400401
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cloning and expression of cDNA encoding heart-type isoform of AMP deaminase.
    Wang X; Morisaki H; Sermsuvitayawong K; Mineo I; Toyama K; Ogasawara N; Mukai T; Morisaki T
    Gene; 1997 Apr; 188(2):285-90. PubMed ID: 9133604
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cloning and nucleotide sequence of the cDNA encoding human erythrocyte-specific AMP deaminase.
    Yamada Y; Goto H; Ogasawara N
    Biochim Biophys Acta; 1992 Nov; 1171(1):125-8. PubMed ID: 1420359
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian population.
    Gross M; Rötzer E; Kölle P; Mortier W; Reichmann H; Goebel HH; Lochmüller H; Pongratz D; Mahnke-Zizelman DK; Sabina RL
    Neuromuscul Disord; 2002 Aug; 12(6):558-65. PubMed ID: 12117480
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A rare case of complete human erythrocyte AMP deaminase deficiency due to two novel missense mutations in AMPD3.
    Yamada Y; Goto H; Wakamatsu N; Ogasawara N
    Hum Mutat; 2001; 17(1):78. PubMed ID: 11139257
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Inherited AMP-deaminase deficiency--molecular basis of the defect].
    Kaletha K; Gross M
    Postepy Biochem; 1995; 41(3):183-7. PubMed ID: 7491357
    [No Abstract]   [Full Text] [Related]  

  • 15. Adenylate deaminase deficiency in a mutant murine T cell lymphoma cell line.
    Hanson S; McCartan K; Sabina RL; Holmes EW; Ullman B
    J Biol Chem; 1990 Jul; 265(20):11474-81. PubMed ID: 2365681
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical heterogeneity and molecular mechanisms in inborn muscle AMP deaminase deficiency.
    Gross M
    J Inherit Metab Dis; 1997 Jun; 20(2):186-92. PubMed ID: 9211191
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [AMP deaminase (AMPD)].
    Yamada Y
    Nihon Rinsho; 2003 Jan; 61 Suppl 1():103-8. PubMed ID: 12629700
    [No Abstract]   [Full Text] [Related]  

  • 18. AMP deaminase deficiency in skeletal muscle is unlikely to be of clinical relevance.
    Hanisch F; Joshi P; Zierz S
    J Neurol; 2008 Mar; 255(3):318-22. PubMed ID: 18338202
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Kinetic and immunologic evidence for a complete gene block in myoadenylate deaminase deficiency.
    Fishbein WN; Davis JI; Foellmer JW
    J Exp Pathol; 1983; 1(1):7-25. PubMed ID: 6086015
    [TBL] [Abstract][Full Text] [Related]  

  • 20. New method for detection of C34-T mutation in the AMPD1 gene causing myoadenylate deaminase deficiency.
    Gross M
    Ann Rheum Dis; 1994 May; 53(5):353-4. PubMed ID: 8017994
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.