«Werner Syndrome

Below is an extended Werner Syndrome research listing. Click here to return to the Werner Syndrome main in depth entry.

Recent Publications on Werner Syndrome:
The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis. Werner syndrome (WS) is an adult onset segmental progeroid syndrome caused... Direct Link		19th November, 2008	Laboratory of Molecular Gerontology, National Institute on Aging, NIH,
Clinical outcome and mechanism of soft tissue calcification in Werner syndrome. Werner syndrome (WS) is an autosomal recessive progeroid disorder caused... Direct Link		19th November, 2008	Department of Clinical Cell Biology and Medicine, Chiba University
Familial thyroid carcinoma: a diagnostic algorithm. Thyroid carcinomas derived from follicular cells are the most common... Direct Link		15th November, 2008	Department of Pathology, Brigham and Women's Hospital, Harvard Medical
Replication fork stalling in WRN-deficient cells is overcome by prompt activation of a MUS81-dependent pathway. Failure to stabilize and properly process stalled replication forks... Direct Link		14th November, 2008	Section of Experimental and Computational Carcinogenesis, Istituto
[The atypical of Werner syndrome: effect of laminopathy]		31st October, 2008
Meningioma associated with Werner syndrome--case report--.		25th October, 2008	Department of Neurosurgery, Institute of Clinical Medicine, University of
Familial Non-Medullary Thyroid Carcinoma: An Update. Familial thyroid cancer can arise from follicular cells (familial... Direct Link		22nd October, 2008	Department of Pathology, Brigham and Women's Hospital, 75 Francis Street,
Assessing the role of stress signalling via p38 MAP kinase in the premature senescence of Ataxia Telangiectasia and Werner syndrome fibroblasts. The premature ageing Ataxia Telangiectasia (AT) and Werner syndromes (WS)... Direct Link		3rd October, 2008	Department of Pathology, School of Medicine, Cardiff University, Heath
Identification of the Xenopus DNA2 protein as a major nuclease for the 5'->3' strand-specific processing of DNA ends. The first step of homology-dependent DNA double-strand break (DSB) repair... Direct Link		30th September, 2008	Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA 19111, USA.
WRN protects against topo I but not topo II inhibitors by preventing DNA break formation. The Werner syndrome helicase/3'-exonuclease (WRN) is a major component of... Direct Link		23rd September, 2008	Department of Toxicology, University of Mainz, Obere Zahlbacher Strasse
Intrinsic ssDNA annealing activity in the C-terminal region of WRN. Werner syndrome (WS) is a rare autosomal recessive disorder in humans... Direct Link		6th September, 2008	Laboratory of Molecular Gerontology, National Institute on Aging, National
Werner syndrome, aging and cancer. Werner syndrome (WS) is a rare autosomal recessive genetic... Direct Link		30th August, 2008	The Joseph Gottstein Memorial Cancer Research Laboratory, Department of
Roles of the Werner syndrome RecQ helicase in DNA replication. Congenital deficiency in the WRN protein, a member of the human RecQ... Direct Link		30th August, 2008	Department of Pathology, University of Washington, Seattle, WA 98195-7705,
RecQ family helicases in genome stability: lessons from gene disruption studies in DT40 cells.		23rd August, 2008	Molecular Cell Biology Laboratory, Graduate School of Pharmaceutical
WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brazil. Werner syndrome (WS) is a premature aging disorder characterized by early... Direct Link		2nd August, 2008	Human Genetics Laboratory, Federal University of Piaui, Av. Sao Sebastiao

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