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Similar articles for PubMed (Select 1998341)

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Intervention of somatic mutational events in vivo by a germline defect at the adenine phosphoribosyltransferase locus.

Hakoda M, Kamatani N, Kurumada S, Hirai Y, Sakamoto K, Yamanaka H, Terai C, Kashiwazaki S.

Hum Genet. 1997 Feb;99(2):164-70.

PMID:
9048914
4.

High frequency in vivo loss of heterozygosity is primarily a consequence of mitotic recombination.

Gupta PK, Sahota A, Boyadjiev SA, Bye S, Shao C, O'Neill JP, Hunter TC, Albertini RJ, Stambrook PJ, Tischfield JA.

Cancer Res. 1997 Mar 15;57(6):1188-93.

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Severe impairment in adenine metabolism with a partial deficiency of adenine phosphoribosyltransferase.

Kamatani N, Takeuchi F, Nishida Y, Yamanaka H, Nishioka K, Tatara K, Fujimori S, Kaneko K, Akaoka I, Tofuku Y.

Metabolism. 1985 Feb;34(2):164-8.

PMID:
3871499
10.

Genetic and clinical studies on 19 families with adenine phosphoribosyltransferase deficiencies.

Kamatani N, Terai C, Kuroshima S, Nishioka K, Mikanagi K.

Hum Genet. 1987 Feb;75(2):163-8.

PMID:
3817810
11.

Germline and somatic mutations leading to adenine phosphoribosyltransferase (APRT) deficiency.

Hakoda M, Kamatani N, Ohtsuka S, Kashiwazaki S.

Adv Exp Med Biol. 1991;309B:87-90. No abstract available.

PMID:
1781412
12.

Similarity of in vivo somatic mutations at an autosomal adenine phosphoribosyltransferase locus between T- and B-cells in human peripheral blood.

Hakoda M, Kamatani N, Terai C, Yamanaka H, Taniguchi A, Ueda H, Kashiwazaki S.

Mutat Res. 1996 Oct 25;357(1-2):107-13.

PMID:
8876686
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Detection of mutations in adenine phosphoribosyltransferase (APRT) deficiency using the LightCycler system.

Funato T, Nishiyama Y, Ioritani N, Matsuki R, Yoshida K, Kaku M, Sasaki T, Ideguchi H, Ono J.

J Clin Lab Anal. 2000;14(6):274-9.

PMID:
11138609
17.

Two families with compound heterozygosity for adenine phosphoribosyltransferase deficiency.

Iwaki T, Kusaka T, Ohashi I, Nishida T, Imai T, Itoh S.

Pediatr Nephrol. 2010 Jun;25(6):1173-6. doi: 10.1007/s00467-009-1430-4. Epub 2010 Jan 26.

PMID:
20101413
18.

Adenine phosphoribosyltransferase deficiency identified by urinary sediment analysis: cellular and molecular confirmation.

Terai C, Hakoda M, Yamanaka H, Kamatani N, Okai M, Takahashi F, Kashiwazaki S.

Clin Genet. 1995 Nov;48(5):246-50.

PMID:
8825602
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Identification of a 7-basepair deletion in the adenine phosphoribosyltransferase gene as a cause of 2,8-dihydroxyadenine urolithiasis.

Bye S, Mallmann R, Duley J, Simmonds HA, Chen J, Tischfield JA, Sahota A.

Clin Investig. 1994 Jul;72(7):550-3.

PMID:
7981585
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