Tsukamoto K - Search Results

1

A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family.

Okubo A, Miyoshi O, Baba K, Takagi M, Tsukamoto K, Kinoshita A, Yoshiura K, Kishino T, Ohta T, Niikawa N, Matsumoto N. Okubo A, et al. Among authors: tsukamoto k. J Med Genet. 2004 Jul;41(7):e97. doi: 10.1136/jmg.2004.018895. J Med Genet. 2004. PMID: 15235040 Free PMC article. No abstract available.

2

Chromosome-band-specific painting: chromosome in situ suppression hybridization using PCR products from a microdissected chromosome band as a probe pool.

Deng HX, Yoshiura K, Dirks RW, Harada N, Hirota T, Tsukamoto K, Jinno Y, Niikawa N. Deng HX, et al. Among authors: tsukamoto k. Hum Genet. 1992 Apr;89(1):13-7. doi: 10.1007/BF00207034. Hum Genet. 1992. PMID: 1577461

3

[Gene responsible for Waardenburg syndrome type I].

Tsukamoto K, Niikawa N. Tsukamoto K, et al. Tanpakushitsu Kakusan Koso. 1993 Feb;38(3):361-5. Tanpakushitsu Kakusan Koso. 1993. PMID: 8098159 Review. Japanese. No abstract available.

4

Three novel PAX3 mutations observed in patients with Waardenburg syndrome type 1.

Soejima H, Fujimoto M, Tsukamoto K, Matsumoto N, Yoshiura KI, Fukushima Y, Jinno Y, Niikawa N. Soejima H, et al. Among authors: tsukamoto k. Hum Mutat. 1997;9(2):177-80. doi: 10.1002/(SICI)1098-1004(1997)9:2<177::AID-HUMU11>3.0.CO;2-#. Hum Mutat. 1997. PMID: 9067759 No abstract available.

5

A simple and efficient amplification method of DNA with unknown sequences and its application to microdissection/microcloning.

Jinno Y, Harada N, Yoshiura K, Ohta T, Tohma T, Hirota T, Tsukamoto K, Deng HX, Oshimura M, Niikawa N. Jinno Y, et al. Among authors: tsukamoto k. J Biochem. 1992 Jul;112(1):75-80. doi: 10.1093/oxfordjournals.jbchem.a123869. J Biochem. 1992. PMID: 1429512 Free article.

6

Microdissection of human chromosomal regions 8q23.3-q24.11 and 2q33-qter: construction of DNA libraries and isolation of their clones.

Hirota T, Tsukamoto K, Deng HX, Yoshiura K, Ohta T, Tohma T, Kibe T, Harada N, Jinno Y, Niikawa N. Hirota T, et al. Among authors: tsukamoto k. Genomics. 1992 Jun;13(2):349-54. doi: 10.1016/0888-7543(92)90252-n. Genomics. 1992. PMID: 1612593

7

Isolation of two isoforms of the PAX3 gene transcripts and their tissue-specific alternative expression in human adult tissues.

Tsukamoto K, Nakamura Y, Niikawa N. Tsukamoto K, et al. Hum Genet. 1994 Mar;93(3):270-4. doi: 10.1007/BF00212021. Hum Genet. 1994. PMID: 7545913

8

Isolation of 2 novel RFLP markers and their localization at 2q35 by microdissection and subsequent enzymatic amplification.

Kibe T, Tsukamoto K, Hirota T, Yoshiura K, Ohta T, Tohma T, Tamura T, Jinno Y, Niikawa N. Kibe T, et al. Among authors: tsukamoto k. Jpn J Hum Genet. 1992 Dec;37(4):263-70. doi: 10.1007/BF01883317. Jpn J Hum Genet. 1992. PMID: 1284292

9

Cloning and characterization of the inversion breakpoint at chromosome 2q35 in a patient with Waardenburg syndrome type I.

Tsukamoto K, Tohma T, Ohta T, Yamakawa K, Fukushima Y, Nakamura Y, Niikawa N. Tsukamoto K, et al. Hum Mol Genet. 1992 Aug;1(5):315-7. doi: 10.1093/hmg/1.5.315. Hum Mol Genet. 1992. PMID: 1303207

10

Cosmid clones from microdissected human chromosomal region 15q11-q13.

Tohma T, Tamura T, Ohta T, Soejima H, Kubota T, Jinno Y, Tsukamoto K, Nakamura Y, Naritomi K, Niikawa N. Tohma T, et al. Among authors: tsukamoto k. Jpn J Hum Genet. 1993 Sep;38(3):267-75. doi: 10.1007/BF01874137. Jpn J Hum Genet. 1993. PMID: 8260719

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