老年病・寿命関連遺伝子について

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Published in日本老年医学会雑誌 Vol. 42; no. 2; pp. 155 - 157
Main Author 三木, 哲郎
Format Journal Article
LanguageJapanese
Published 一般社団法人 日本老年医学会 2005
Subjects
Online AccessGet full text
ISSN0300-9173
DOI10.3143/geriatrics.42.155

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Author 三木, 哲郎
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References 4) 新井康通, 広瀬信義: 百寿者の多面的検討-医学的側面から Aging and Health 2004; 13: 38-41.
5) Geesaman BJ, Benson E, Brewster SJ, Kunkel LM, Blanche H, Thomas G, et al.: Haplotype-based identification of a microsomal transfser protein marker associated with the human lifespan. Proc Natl Acad Sci USA 2003; 100: 14115-141120.
2) Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, et al.: Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome. Nature 2003; 423: 293-298.
1) Chen L, Oshima J: Werner Syndrome. J Biomed Biotechnol 2002; 2: 46-54.
3) Goldman RD, Shumaker DK, Erdos MR, Eriksson M, Goldman AE, Gordon LB, et al.: Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome. Proc Natl Acad Sci USA 2004; 101: 8963-8968.
References_xml – reference: 2) Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, et al.: Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome. Nature 2003; 423: 293-298.
– reference: 4) 新井康通, 広瀬信義: 百寿者の多面的検討-医学的側面から Aging and Health 2004; 13: 38-41.
– reference: 1) Chen L, Oshima J: Werner Syndrome. J Biomed Biotechnol 2002; 2: 46-54.
– reference: 3) Goldman RD, Shumaker DK, Erdos MR, Eriksson M, Goldman AE, Gordon LB, et al.: Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome. Proc Natl Acad Sci USA 2004; 101: 8963-8968.
– reference: 5) Geesaman BJ, Benson E, Brewster SJ, Kunkel LM, Blanche H, Thomas G, et al.: Haplotype-based identification of a microsomal transfser protein marker associated with the human lifespan. Proc Natl Acad Sci USA 2003; 100: 14115-141120.
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StartPage 155
SubjectTerms 寿命関連遺伝子
老年病
Title 老年病・寿命関連遺伝子について
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Volume 42
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