Kono M - Search Results

1

Interval sentinel lymph nodes in patients with cutaneous melanoma: a single-institution study in Japan.

Matsumoto T, Shibata S, Yasue S, Sakakibara A, Yokota K, Sawada M, Kono M, Kato K, Shimoyama Y, Tomita Y. Matsumoto T, et al. Among authors: kono m. J Dermatol. 2010 Jul;37(7):629-34. doi: 10.1111/j.1346-8138.2010.00856.x. J Dermatol. 2010. PMID: 20629829

2

Exclusion of linkage between dyschromatosis symmetrica hereditaria and chromosome 9.

Kono M, Miyamura Y, Matsunaga J, Tomita Y. Kono M, et al. J Dermatol Sci. 2000 Feb;22(2):88-95. doi: 10.1016/s0923-1811(99)00050-x. J Dermatol Sci. 2000. PMID: 10674821

3

Molecular bases of congenital hypopigmentary disorders in humans and oculocutaneous albinism 1 in Japan.

Tomita Y, Miyamura Y, Kono M, Nakamura R, Matsunaga J. Tomita Y, et al. Among authors: kono m. Pigment Cell Res. 2000;13 Suppl 8:130-4. doi: 10.1034/j.1600-0749.13.s8.23.x. Pigment Cell Res. 2000. PMID: 11041370

4

Polymorphic sequences of the tyrosinase gene: allele analysis on 16 OCA1 patients in Japan indicate that three polymorphic sequences in the tyrosinase gene promoter could be powerful markers for indirect gene diagnosis.

Tanita M, Matsunaga J, Miyamura Y, Dakeishi M, Nakamura E, Kono M, Shimizu H, Tagami H, Tomita Y. Tanita M, et al. Among authors: kono m. J Hum Genet. 2002;47(1):1-6. doi: 10.1007/s10038-002-8648-3. J Hum Genet. 2002. PMID: 11829136

5

A novel mutation of the tyrosinase gene causing oculocutaneous albinism type 1 (OCA1).

Nakamura E, Miyamura Y, Matsunaga J, Kano Y, Dakeishi-Hara M, Tanita M, Kono M, Tomita Y. Nakamura E, et al. Among authors: kono m. J Dermatol Sci. 2002 Feb;28(2):102-5. doi: 10.1016/s0923-1811(01)00141-4. J Dermatol Sci. 2002. PMID: 11858948

6

Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria.

Miyamura Y, Suzuki T, Kono M, Inagaki K, Ito S, Suzuki N, Tomita Y. Miyamura Y, et al. Among authors: kono m. Am J Hum Genet. 2003 Sep;73(3):693-9. doi: 10.1086/378209. Epub 2003 Aug 11. Am J Hum Genet. 2003. PMID: 12916015 Free PMC article.

7

Establishment of tyrosinase sequence database in normally pigmented Indians and Japanese for rapid determination of novel mutations.

Miyamura Y, Verma IC, Saxena R, Murase A, Kono M, Suzuki T, Yasue S, Shibata S, Sakakibara A, Tomita Y. Miyamura Y, et al. Among authors: kono m. J Dermatol Sci. 2005 Sep;39(3):167-73. doi: 10.1016/j.jdermsci.2005.03.004. J Dermatol Sci. 2005. PMID: 15885985

8

Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis.

Suzuki N, Suzuki T, Inagaki K, Ito S, Kono M, Fukai K, Takama H, Sato K, Ishikawa O, Abe M, Shimizu H, Kawai M, Horikawa T, Yoshida K, Matsumoto K, Terui T, Tsujioka K, Tomita Y. Suzuki N, et al. Among authors: kono m. J Invest Dermatol. 2005 Jun;124(6):1186-92. doi: 10.1111/j.0022-202X.2005.23732.x. J Invest Dermatol. 2005. PMID: 15955093 Free article.

9

Five novel mutations in tyrosinase gene of Japanese and Indian patients with oculocutaneous albinism type I (OCA1).

Miyamura Y, Verma IC, Saxena R, Hoshi M, Murase A, Nakamura E, Kono M, Suzuki T, Yasue S, Shibata S, Sakakibara A, Tomita Y. Miyamura Y, et al. Among authors: kono m. J Invest Dermatol. 2005 Aug;125(2):397-8. doi: 10.1111/j.0022-202X.2005.23815.x. J Invest Dermatol. 2005. PMID: 16098056 Free article. No abstract available.

10

Ten novel mutations of the ADAR1 gene in Japanese patients with dyschromatosis symmetrica hereditaria.

Suzuki N, Suzuki T, Inagaki K, Ito S, Kono M, Horikawa T, Fujiwara S, Ishiko A, Matsunaga K, Aoyama Y, Tosaki-Ichikawa H, Tomita Y. Suzuki N, et al. Among authors: kono m. J Invest Dermatol. 2007 Feb;127(2):309-11. doi: 10.1038/sj.jid.5700528. Epub 2006 Aug 17. J Invest Dermatol. 2007. PMID: 16917490 Free article.

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