نتایج جستجو برای: cockayne syndrome

تعداد نتایج: 621994  

Journal: :Cancer research 1979
A R Lehmann S Kirk-Bell L Mayne

Cells from patients with the hereditary disorder Cockayne's syndrome and from the sun-sensitive individual, 11961, are sensitive to the lethal effects of ultraviolet light (UV) but have no detectable defect in either excision- or postreplication repair after UV irradiation. In normal cells and in Cockayne heterozygotes, UV causes a depression in the rate of DNA-replicative synthesis followed by...

Journal: :Mechanisms of Ageing and Development 2013

Journal: :The American Journal of Human Genetics 2003

Journal: :Indian Journal of Dermatology, Venereology and Leprology 2008

Journal: :International Journal of Contemporary Pediatrics 2021

Journal: :Collegium antropologicum 2010
Lena Kotrulja Suzana Ozanić-Bulić Ines Sjerobabski-Masnec Mirna Situm Sanja Poduje

Photosensitivity in childhood is caused by a diverse group of diseases. A specific sensitivity of a child's skin to ultraviolet light is often the first manifestation or a clinical symptom of photodermatosis. It might indicate a serious underlying systemic disease such as lupus erythematosus or dermatomyositis, or a rare group of genetic skin disorders like Xeroderma pigmentosum, Cockayne syndr...

Journal: :American journal of medical genetics 2002
Adel A H Mahmoud George M Yousef Ibrahim Al-Hifzi Eleftherios P Diamandis

We report three sisters showing the clinical features and investigational findings of Cockayne syndrome (CS). In the rehabilitation unit of Northwest Armed Forces Hospital (N.W.A.F.H.), Tabuk, Saudi Arabia, there was a 12-year-old girl with typical features of CS. The girl had no apparent problems until the end of the first year when growth and developmental delay prompted medical evaluation. B...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2014
Yuming Wang Probir Chakravarty Michael Ranes Gavin Kelly Philip J Brooks Edward Neilan Aengus Stewart Giampietro Schiavo Jesper Q Svejstrup

Cockayne syndrome (CS) is a multisystem disorder with severe neurological symptoms. The majority of CS patients carry mutations in Cockayne syndrome group B (CSB), best known for its role in transcription-coupled nucleotide excision repair. Indeed, because various repair pathways are compromised in patient cells, CS is widely considered a genome instability syndrome. Here, we investigate the co...

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