Nakatsu Y - Search Results

1

The p locus is closely linked to the mouse homolog of a gene from the Prader-Willi chromosomal region.

Nakatsu Y, Gondo Y, Brilliant MH. Nakatsu Y, et al. Mamm Genome. 1992;2(1):69-71. doi: 10.1007/BF00570442. Mamm Genome. 1992. PMID: 1347469 No abstract available.

2

The mouse pink-eyed dilution gene: association with human Prader-Willi and Angelman syndromes.

Gardner JM, Nakatsu Y, Gondo Y, Lee S, Lyon MF, King RA, Brilliant MH. Gardner JM, et al. Among authors: nakatsu y. Science. 1992 Aug 21;257(5073):1121-4. doi: 10.1126/science.257.5073.1121. Science. 1992. PMID: 1509264

3

The mouse pink-eyed dilution gene: association with hypopigmentation in Prader-Willi and Angelman syndromes and with human OCA2.

Brilliant MH, King R, Francke U, Schuffenhauer S, Meitinger T, Gardner JM, Durham-Pierre D, Nakatsu Y. Brilliant MH, et al. Among authors: nakatsu y. Pigment Cell Res. 1994 Dec;7(6):398-402. doi: 10.1111/j.1600-0749.1994.tb00068.x. Pigment Cell Res. 1994. PMID: 7761348

4

The original pink-eyed dilution mutation (p) arose in Asiatic mice: implications for the H4 minor histocompatibility antigen, Myod1 regulation and the origin of inbred strains.

Brilliant MH, Ching A, Nakatsu Y, Eicher EM. Brilliant MH, et al. Among authors: nakatsu y. Genetics. 1994 Sep;138(1):203-11. doi: 10.1093/genetics/138.1.203. Genetics. 1994. PMID: 8001787 Free PMC article.

5

High-frequency genetic reversion mediated by a DNA duplication: the mouse pink-eyed unstable mutation.

Gondo Y, Gardner JM, Nakatsu Y, Durham-Pierre D, Deveau SA, Kuper C, Brilliant MH. Gondo Y, et al. Among authors: nakatsu y. Proc Natl Acad Sci U S A. 1993 Jan 1;90(1):297-301. doi: 10.1073/pnas.90.1.297. Proc Natl Acad Sci U S A. 1993. PMID: 8419934 Free PMC article.

6

Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouse.

Lyon MF, King TR, Gondo Y, Gardner JM, Nakatsu Y, Eicher EM, Brilliant MH. Lyon MF, et al. Among authors: nakatsu y. Proc Natl Acad Sci U S A. 1992 Aug 1;89(15):6968-72. doi: 10.1073/pnas.89.15.6968. Proc Natl Acad Sci U S A. 1992. PMID: 1495987 Free PMC article.

7

African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism.

Durham-Pierre D, Gardner JM, Nakatsu Y, King RA, Francke U, Ching A, Aquaron R, del Marmol V, Brilliant MH. Durham-Pierre D, et al. Among authors: nakatsu y. Nat Genet. 1994 Jun;7(2):176-9. doi: 10.1038/ng0694-176. Nat Genet. 1994. PMID: 7920637

8

A very large protein with diverse functional motifs is deficient in rjs (runty, jerky, sterile) mice.

Lehman AL, Nakatsu Y, Ching A, Bronson RT, Oakey RJ, Keiper-Hrynko N, Finger JN, Durham-Pierre D, Horton DB, Newton JM, Lyon MF, Brilliant MH. Lehman AL, et al. Among authors: nakatsu y. Proc Natl Acad Sci U S A. 1998 Aug 4;95(16):9436-41. doi: 10.1073/pnas.95.16.9436. Proc Natl Acad Sci U S A. 1998. PMID: 9689098 Free PMC article.

9

Identification of a melanosomal membrane protein encoded by the pink-eyed dilution (type II oculocutaneous albinism) gene.

Rosemblat S, Durham-Pierre D, Gardner JM, Nakatsu Y, Brilliant MH, Orlow SJ. Rosemblat S, et al. Among authors: nakatsu y. Proc Natl Acad Sci U S A. 1994 Dec 6;91(25):12071-75. doi: 10.1073/pnas.91.25.12071. Proc Natl Acad Sci U S A. 1994. PMID: 7991586 Free PMC article.

10

Studies of in vivo mutations in rpsL transgene in UVB-irradiated epidermis of XPA-deficient mice.

Murai H, Takeuchi S, Nakatsu Y, Ichikawa M, Yoshino M, Gondo Y, Katsuki M, Tanaka K. Murai H, et al. Among authors: nakatsu y. Mutat Res. 2000 May 30;450(1-2):181-92. doi: 10.1016/s0027-5107(00)00024-5. Mutat Res. 2000. PMID: 10838142

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