沃纳综合征；衰老的缩影。一种用于研究退行性疾病的遗传模型。 - Suppr

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超能文献

Werner's syndrome; caricature of aging. A genetic model for the study of degenerative diseases.

作者信息

Epstein C J, Martin G M, Motulsky A G

出版信息

Trans Assoc Am Physicians. 1965;78:73-81.

PMID:5864984

Abstract

摘要

相似文献

Werner's syndrome; caricature of aging. A genetic model for the study of degenerative diseases.沃纳综合征；衰老的缩影。一种用于研究退行性疾病的遗传模型。

Trans Assoc Am Physicians. 1965;78:73-81.

Elevation of urinary hyaluronic acid in Werner's syndrome and progeria.沃纳综合征和早老症中尿透明质酸水平升高。

Biochem Med Metab Biol. 1986 Dec;36(3):276-82. doi: 10.1016/0885-4505(86)90136-2.

[Werner's syndrome as a caricature of aging].[沃纳综合征：衰老的缩影]

Pol Tyg Lek. 1982 Oct 25;37(40):1215-7.

Progeria and Werner's syndrome as models for the study of normal human aging.

J Am Geriatr Soc. 1971 May;19(5):369-75. doi: 10.1111/j.1532-5415.1971.tb03230.x.

[WERNER'S SYNDROME. CLINICAL COMPARISONS IN HISTOLOGICAL PICTURE OF SKIN CHANGES].

Sb Lek. 1964 Feb;66:55-60.

Looking for disease being a model of human aging.寻找作为人类衰老模型的疾病。

Acta Myol. 2007 Oct;26(2):101-4.

Increased procoagulant activity in cultured fibroblasts from progeria and Werner's syndromes of premature ageing.早老症和沃纳早衰综合征患者培养成纤维细胞中促凝血活性增加。

Nature. 1976 Apr 22;260(5553):711-3. doi: 10.1038/260711a0.

Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process.维尔纳综合征：对其症状学、自然史、病理特征、遗传学以及与自然衰老过程关系的综述。

Medicine (Baltimore). 1966 May;45(3):177-221. doi: 10.1097/00005792-196605000-00001.

[Werner's syndrome. Presentation of a new case].[韦纳综合征。一例新病例报告]

Rev Clin Esp. 1983 Dec 15;171(5):365-8.

[Progeria of adults (Werner's syndrome)].[成人早老症（沃纳综合征）]

Ter Arkh. 1975;47(1):99-102.

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Nucleolar and Ribosomal Dysfunction-A Common Pathomechanism in Childhood Progerias?核仁与核糖体功能障碍——儿童早老症的共同发病机制？

Cells. 2019 Jun 4;8(6):534. doi: 10.3390/cells8060534.

Sporadic premature aging in a Japanese monkey: a primate model for progeria.一只日本猕猴的散发性早衰：一种早衰症的灵长类动物模型。

PLoS One. 2014 Nov 3;9(11):e111867. doi: 10.1371/journal.pone.0111867. eCollection 2014.

[Werner syndrome. A prototypical form of segmental progeria.].[沃纳综合征。节段性早衰的典型形式。]

Med Genet. 2012 Dec;24(4):262-267. doi: 10.1007/s11825-012-0360-x.

Resolution of complex ends by Nonhomologous end joining - better to be lucky than good?通过非同源末端连接解决复杂末端——靠运气比靠能力更好？

Genome Integr. 2012 Dec 31;3(1):10. doi: 10.1186/2041-9414-3-10.

[Reversal of aging and lifespan elongation. Current biomedical key publications and the implications for geriatrics].[衰老逆转与寿命延长。当前生物医学重要出版物及其对老年医学的影响]

Z Gerontol Geriatr. 2013 Aug;46(6):563-8. doi: 10.1007/s00391-012-0415-2.

Roles of RECQ helicases in recombination based DNA repair, genomic stability and aging.RECQ解旋酶在基于重组的DNA修复、基因组稳定性和衰老中的作用。

Biogerontology. 2009 Jun;10(3):235-52. doi: 10.1007/s10522-008-9205-z. Epub 2008 Dec 15.

Progeria: a cell culture study on aging.早衰症：一项关于衰老的细胞培养研究。

J Clin Invest. 1971 Sep;50(9):2000-3. doi: 10.1172/JCI106692.

Werner's syndrome and acute myeloid leukemia.沃纳综合征与急性髓系白血病。

Can Med Assoc J. 1971 Nov;105(9):951 passim.

Fibroblast culture in Werner's syndrome.

Humangenetik. 1971;13(3):244-6. doi: 10.1007/BF00326950.

Progeria: a cell culture study and clinical report of familial incidence.早老症：一项细胞培养研究及家族发病率的临床报告。

Eur J Pediatr. 1977 Jan 26;124(2):101-11. doi: 10.1007/BF00477545.

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