Matsunaga J - Search Results

1

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: matsunaga j. 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

2

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: matsunaga j. J Dermatol Sci. 2002 Feb;28(2):102-5. doi: 10.1016/s0923-1811(01)00141-4. J Dermatol Sci. 2002. PMID: 11858948

3

Six novel P gene mutations and oculocutaneous albinism type 2 frequency in Japanese albino patients.

Suzuki T, Miyamura Y, Matsunaga J, Shimizu H, Kawachi Y, Ohyama N, Ishikawa O, Ishikawa T, Terao H, Tomita Y. Suzuki T, et al. Among authors: matsunaga j. J Invest Dermatol. 2003 May;120(5):781-3. doi: 10.1046/j.1523-1747.2003.12127.x. J Invest Dermatol. 2003. PMID: 12713581 Free article.

4

Molecular bases of tyrosinase-negative oculocutaneous albinism: a single base insertion or a missense point mutation in the tyrosinase gene.

Tomita Y, Takeda A, Matsunaga J, Okinaga S, Shibahara S, Tagami H. Tomita Y, et al. Among authors: matsunaga j. Pigment Cell Res. 1992;Suppl 2:96-100. doi: 10.1111/j.1600-0749.1990.tb00356.x. Pigment Cell Res. 1992. PMID: 1409445

5

Sequence analysis of the human tyrosinase promoter from a patient with tyrosinase-negative oculocutaneous albinism.

Matsunaga J, Dakeishi M, Miyamura Y, Tomita Y. Matsunaga J, et al. Pigment Cell Res. 1997 Feb-Apr;10(1-2):64-7. doi: 10.1111/j.1600-0749.1997.tb00468.x. Pigment Cell Res. 1997. PMID: 9170165

6

Sequence-based diagnosis of tyrosinase-related oculocutaneous albinism: successful sequence analysis of the tyrosinase gene from blood spots dried on filter paper.

Matsunaga J, Dakeishi-Hara M, Miyamura Y, Nakamura E, Tanita M, Satomura K, Tomita Y. Matsunaga J, et al. Dermatology. 1998;196(2):189-93. doi: 10.1159/000017897. Dermatology. 1998. PMID: 9568405

7

A splicing mutation of the tyrosinase gene causes yellow oculocutaneous albinism in a Japanese patient with a pigmented phenotype.

Matsunaga J, Dakeishi-Hara M, Tanita M, Nindl M, Nagata Y, Nakamura E, Miyamura Y, Kikuchi K, Furue M, Tomita Y. Matsunaga J, et al. Dermatology. 1999;199(2):124-9. doi: 10.1159/000018218. Dermatology. 1999. PMID: 10559577

8

Electron microscopic DOPA reaction test for oculocutaneous albinism.

Takizawa Y, Kato S, Matsunaga J, Aozaki R, Tomita Y, Nishikawa T, Shimizu H. Takizawa Y, et al. Among authors: matsunaga j. Arch Dermatol Res. 2000 Jun;292(6):301-5. doi: 10.1007/s004030000133. Arch Dermatol Res. 2000. PMID: 10929771

9

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: matsunaga j. J Hum Genet. 2002;47(1):1-6. doi: 10.1007/s10038-002-8648-3. J Hum Genet. 2002. PMID: 11829136

10

Cloning and sequence analysis of the tyrosinase gene from a patient with tyrosinase-positive oculocutaneous albinism.

Matsunaga J, Takeda A, Tomita Y, Hara M, Shibahara S, Tagami H. Matsunaga J, et al. J Dermatol Sci. 1992 May;3(3):181-5. doi: 10.1016/0923-1811(92)90033-8. J Dermatol Sci. 1992. PMID: 1498098

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