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Items: 1 to 20 of 122

2.
3.

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.

5.
6.

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
7.

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
9.

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
10.
11.

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
12.

Establishment and characterization of B cell lines from individuals with various types of adenine phosphoribosyltransferase deficiencies.

Nobori T, Kamatani N, Mikanagi K, Nishida Y, Nishioka K.

Biochem Biophys Res Commun. 1986 Jun 30;137(3):998-1005.

PMID:
3488062
13.

[Adenine phosphoribosyltransferase(APRT) deficiency].

Kamatani N.

Nihon Rinsho. 1996 Dec;54(12):3321-7. Review. Japanese.

PMID:
8976113
14.

The origin of the most common mutation of adenine phosphoribosyltransferase among Japanese goes back to a prehistoric era.

Kamatani N, Terai C, Kim SY, Chen CL, Yamanaka H, Hakoda M, Totokawa S, Kashiwazaki S.

Hum Genet. 1996 Nov;98(5):596-600.

PMID:
8882882
15.

Heritable alterations at the adenine phosphoribosyltransferase (APRT) locus in human lymphoblastoid cell lines.

Amundson SA, Fortunato JE, Liber HL.

Mutat Res. 1992 Dec 16;284(2):287-95.

PMID:
1281280
16.

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
17.

[Detection of mutant adenine phosphoribosyltransferase genes by polymerase chain reaction-single strand conformation polymorphism analysis].

Kaneko Y, Takeuchi H, Takenawa J, Yoshida O, Takano S, Fujita J.

Hinyokika Kiyo. 1992 Jun;38(6):641-5. Japanese.

18.

APRT: a versatile in vivo resident reporter of local mutation and loss of heterozygosity.

Stambrook PJ, Shao C, Stockelman M, Boivin G, Engle SJ, Tischfield JA.

Environ Mol Mutagen. 1996;28(4):471-82.

PMID:
8991080
19.

Identification of two novel mutations in adenine phosphoribosyltransferase gene in patients with 2,8-dihydroxyadenine urolithiasis.

Taniguchi A, Tsuchida S, Kuno S, Mita M, Machida T, Ioritani N, Terai C, Yamanaka H, Kamatani N.

Nucleosides Nucleotides Nucleic Acids. 2004 Oct;23(8-9):1141-5.

PMID:
15571218

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