Kudoh J - Search Results

1

Screening of H-ras gene point mutations in 50 cases of bladder carcinoma.

Saito S, Hata M, Fukuyama R, Sakai K, Kudoh J, Tazaki H, Shimizu N. Saito S, et al. Among authors: kudoh j. Int J Urol. 1997 Mar;4(2):178-85. doi: 10.1111/j.1442-2042.1997.tb00167.x. Int J Urol. 1997. PMID: 9179693 Free article.

2

p53 gene mutation in recurrent superficial bladder cancer.

Yoshimura I, Kudoh J, Saito S, Tazaki H, Shimizu N. Yoshimura I, et al. Among authors: kudoh j. J Urol. 1995 May;153(5):1711-5. J Urol. 1995. PMID: 7715016

3

Molecular cloning and chromosomal mapping of a cDNA encoding human 80K-L protein: major substrate for protein kinase C.

Sakai K, Hirai M, Kudoh J, Minoshima S, Shimizu N. Sakai K, et al. Among authors: kudoh j. Genomics. 1992 Sep;14(1):175-8. doi: 10.1016/s0888-7543(05)80301-5. Genomics. 1992. PMID: 1427823

4

Methylation status of ribosomal RNA gene clusters in the flow-sorted human acrocentric chromosomes.

Kawasaki K, Minoshima S, Kudoh J, Fukuyama R, Shimizu N. Kawasaki K, et al. Among authors: kudoh j. Mamm Genome. 1992;3(3):173-8. doi: 10.1007/BF00352463. Mamm Genome. 1992. PMID: 1617224

5

Mitochondrial DNA analysis of Leber's hereditary optic neuropathy.

Hiida Y, Mashima Y, Oguchi Y, Uemura Y, Kudoh J, Sakai K, Shimizu N. Hiida Y, et al. Among authors: kudoh j. Jpn J Ophthalmol. 1991;35(1):102-6. Jpn J Ophthalmol. 1991. PMID: 1895564

6

DNA diagnosis of hydatidiform mole using the polymerase chain reaction.

Fukuyama R, Takata M, Kudoh J, Sakai K, Tamura S, Shimizu N. Fukuyama R, et al. Among authors: kudoh j. Hum Genet. 1991 Jun;87(2):216-8. doi: 10.1007/BF00204186. Hum Genet. 1991. PMID: 2066110

7

[DNA diagnosis of Leber's hereditary optic neuropathy].

Mashima Y, Oguchi Y, Uemura Y, Kudoh J, Sakai K, Shimizu N. Mashima Y, et al. Among authors: kudoh j. Nippon Ganka Gakkai Zasshi. 1990 Jul;94(7):683-7. Nippon Ganka Gakkai Zasshi. 1990. PMID: 2220506 Japanese.

8

Human ribosomal RNA gene cluster: identification of the proximal end containing a novel tandem repeat sequence.

Sakai K, Ohta T, Minoshima S, Kudoh J, Wang Y, de Jong PJ, Shimizu N. Sakai K, et al. Among authors: kudoh j. Genomics. 1995 Apr 10;26(3):521-6. doi: 10.1016/0888-7543(95)80170-q. Genomics. 1995. PMID: 7607675

9

Autosomal dominant retinitis pigmentosa. A mutation in codon 181 (Glu-->Lys) of the rhodopsin gene in a Japanese family.

Saga M, Mashima Y, Akeo K, Oguchi Y, Kudoh J, Shimizu N. Saga M, et al. Among authors: kudoh j. Ophthalmic Genet. 1994 Jun;15(2):61-7. doi: 10.3109/13816819409098865. Ophthalmic Genet. 1994. PMID: 7850270

10

High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy.

Mashima Y, Hiida Y, Oguchi Y, Kudoh J, Shimizu N. Mashima Y, et al. Among authors: kudoh j. Hum Genet. 1993 Aug;92(1):101-2. doi: 10.1007/BF00216156. Hum Genet. 1993. PMID: 8103501

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