A twenty strain survey and backcross localization of the erythrocytic GTP concentration determining locus Gtpc on mouse chromosome 9.

No abstract is available for this paper.

• Publication year

  1999

• Venue

  Genome

• Publication date

  1999-06-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1139/G98-150PMID 10382292
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• RI manager, a microcomputer program for analysis of data from recombinant inbred strains

  2006cited by this paper
• Point mutations at the purine nucleoside phosphorylase locus impair thymocyte differentiation in the mouse.

  1997cited by this paper
• The degree of lateralization of paw usage (handedness) in the mouse is defined by three major phenotypes

  1996cited by this paper
• Simultaneous detection of nucleotides, nucleosides and oxidative metabolites in myocardial biopsies.

  1996cited by this paper
• Characterization of Mouse and Human GTP Cyclohydrolase I Genes

  1995cited by this paper
• Analytical evaluation of high energy phosphate determination by high performance liquid chromatography in myocardial tissue.

  1994cited by this paper
• Assignment of a gene that determines erythrocytic guanosine-5'-triphosphate concentration (Gtpc) to mouse chromosome 9.

  1994cited by this paper
• Brain Purines in a Genetic Mouse Model of Lesch‐Nyhan Disease

  1993cited by this paper
• Genetic variation in paw preference (handedness) in the mouse.

  1993cited by this paper
• A simplified HPLC method for simultaneously quantifying ribonucleotides and deoxyribonucleotides in cell extracts or frozen tissues

  1993cited by this paper
• Simplified mammalian DNA isolation procedure.

  1991cited by this paper
• hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesis.

  1988cited by this paper
• Altered erythrocyte nucleotide patterns are characteristic of inherited disorders of purine or pyrimidine metabolism.

  1988cited by this paper
• A potential animal model for Lesch–Nyhan syndrome through introduction of HPRT mutations into mice

  1987cited by this paper
• Central nervous system dysfunction and erythrocyte guanosine triphosphate depletion in purine nucleoside phosphorylase deficiency.

  1987cited by this paper
• Biosynthesis and metabolism of tetrahydrobiopterin and molybdopterin.

  1985cited by this paper
• Variation in erythrocyte purine metabolism among mouse strains.

  1983cited by this paper
• GTP depletion and other erythrocyte abnormalities in inherited PNP deficiency.

  1982cited by this paper
• Additional data from two kindreds with genetically induced deficiencies of erythrocyte pyrimidine nucleotidase.

  1980cited by this paper
• Changes in nucleotide concentrations in the erythrocytes of man, rabbit and rat during short-term storage.

  1978cited by this paper
• Enzyme Defect Associated with a Sex-Linked Human Neurological Disorder and Excessive Purine Synthesis

  1967cited by this paper

• Flow cytometry for real-time measurement of guanine nucleotide binding and exchange by Ras-like GTPases.

  2008cites this paper
• cDNA sequence of five mouse guanine deaminase (Gda) alleles and mapping to mouse chromosome 19.

  2002cites this paper
• A mouse phenome project

  2000cites this paper