Literature DB >> 3684585

Nucleotide sequence of the human APRT gene.

Y Hidaka1, S A Tarlé, T E O'Toole, W N Kelley, T D Palella.   

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Year:  1987        PMID： 3684585      PMCID： PMC306432          DOI： 10.1093/nar/15.21.9086

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  1 in total

1.  Comparative anatomy of the human APRT gene and enzyme: nucleotide sequence divergence and conservation of a nonrandom CpG dinucleotide arrangement.

Authors:  T P Broderick; D A Schaff; A M Bertino; M K Dush; J A Tischfield; P J Stambrook
Journal:  Proc Natl Acad Sci U S A       Date:  1987-05       Impact factor: 11.205
  1 in total
  20 in total

1.  Multiple dispersed spontaneous mutations: a novel pathway of mutation in a malignant human cell line.

Authors:  J Harwood; A Tachibana; M Meuth
Journal:  Mol Cell Biol       Date:  1991-06       Impact factor: 4.272

Review 2.  A reappraisal of non-consensus mRNA splice sites.

Authors:  I J Jackson
Journal:  Nucleic Acids Res       Date:  1991-07-25       Impact factor: 16.971

3.  Identification of DNA sequences required for mouse APRT gene expression.

Authors:  M K Dush; M R Briggs; M E Royce; D A Schaff; S A Khan; J A Tischfield; P J Stambrook
Journal:  Nucleic Acids Res       Date:  1988-09-12       Impact factor: 16.971

4.  Functional complementation by electroporation of human BACs into mammalian fibroblast cells.

Authors:  J A Hejna; P L Johnstone; S L Kohler; D A Bruun; C A Reifsteck; S B Olson; R E Moses
Journal:  Nucleic Acids Res       Date:  1998-02-15       Impact factor: 16.971

5.  The 5' splice site: phylogenetic evolution and variable geometry of association with U1RNA.

Authors:  M Jacob; H Gallinaro
Journal:  Nucleic Acids Res       Date:  1989-03-25       Impact factor: 16.971

6.  Identification of a compound heterozygote for adenine phosphoribosyltransferase deficiency (APRT*J/APART*Q0) leading to 2,8-dihydroxyadenine urolithiasis.

Authors:  N Kamatani; S Kuroshima; H Yamanaka; S Nakashe; H Take; M Hakoda
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

7.  Crossovers within a short DNA sequence indicate a long evolutionary history of the APRT*J mutation.

Authors:  N Kamatani; S Kuroshima; M Hakoda; T D Palella; Y Hidaka
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

8.  Human adenine phosphoribosyltransferase deficiency. Demonstration of a single mutant allele common to the Japanese.

Authors:  Y Hidaka; S A Tarlé; S Fujimori; N Kamatani; W N Kelley; T D Palella
Journal:  J Clin Invest       Date:  1988-03       Impact factor: 14.808

9.  Loss of heterozygosity and base substitution at the APRT locus in mismatch-repair-proficient and -deficient colorectal carcinoma cell lines.

Authors:  G Phear; N P Bhattacharyya; M Meuth
Journal:  Mol Cell Biol       Date:  1996-11       Impact factor: 4.272

Review 10.  Hereditary causes of kidney stones and chronic kidney disease.

Authors:  Vidar O Edvardsson; David S Goldfarb; John C Lieske; Lada Beara-Lasic; Franca Anglani; Dawn S Milliner; Runolfur Palsson
Journal:  Pediatr Nephrol       Date:  2013-01-20       Impact factor: 3.714
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