Works matching DE "WERNER'S syndrome"

Results: 355

No SIRT6.

Published in:

Nature Structural & Molecular Biology, 2008, v. 15, n. 4, p. 336, doi. 10.1038/nsmb0408-336

By:

Lall, Sabbi

Publication type:

Article

WRN exonuclease structure and molecular mechanism imply an editing role in DNA end processing.

Published in:

Nature Structural & Molecular Biology, 2006, v. 13, n. 5, p. 414, doi. 10.1038/nsmb1088

By:

Perry, J Jefferson P;
Yannone, Steven M;
Holden, Lauren G;
Hitomi, Chiharu;
Asaithamby, Aroumougame;
Han, Seungil;
Cooper, Priscilla K;
Chen, David J;
Tainer, John A

Publication type:

Article

Molecular biology of Werner syndrome.

Published in:

International Journal of Clinical Oncology, 2004, v. 9, n. 4, p. 288, doi. 10.1007/s10147-004-0426-0

By:

Shimamoto, Akira;
Sugimoto, Masanobu;
Furuichi, Yasuhiro

Publication type:

Article

Systemic sclerosis and scleroderma-like syndromes.

Published in:

Rheumatology Forum, 2024, v. 10, n. 3, p. 110, doi. 10.5603/rf.99299

By:

Bajor, Anna;
Kotyla, Przemysław

Publication type:

Article

Ageing: Heterochromatin disorganization associated with premature ageing.

Published in:

Nature Reviews Genetics, 2015, v. 16, n. 6, p. 318, doi. 10.1038/nrg3958

By:

Jones, Bryony

Publication type:

Article

'Werner Syndrome foot'—A case series of four Irish Traveller siblings with Werner Syndrome, diabetes mellitus and complex foot disease.

Published in:

Diabetic Medicine, 2024, v. 41, n. 9, p. 1, doi. 10.1111/dme.15390

By:

McGrath, Aisling;
Lockhart, Michael;
Griffin, Tomas;
Lynch, Sally Ann;
Dinneen, Sean F.

Publication type:

Article

RETINITIS PIGMENTOSA, HYPERTENSION AND URAEMIA IN WERNER'S SYNDROME.

Published in:: British Journal of Dermatology, 1962, v. 74, n. 4, p. 159
Publication type:: Article

ELASTIC FIBRES IN UNUSUAL DERMATOSES.

Published in:

British Journal of Dermatology, 1955, v. 67, n. 12, p. 460

By:

J. K.

Publication type:

Article

WERNER'S SYNDROME.

Published in:

British Journal of Dermatology, 1953, v. 65, n. 5, p. 165, doi. 10.1111/j.1365-2133.1953.tb13193.x

By:

Reed, R.;
Seville, R. H.;
Tattersall, R. N.

Publication type:

Article

SUBJECT INDEX.

Published in:: 1980
Publication type:: Other

Immunological studies on Werner's syndrome.

Published in:

Clinical & Experimental Immunology, 1980, v. 42, n. 1, p. 10

By:

Nakao, Y.;
Hattori, T.;
Takatsuki, K.;
Kuroda, Y.;
Nakaji, T.;
Fujiwara, Y.;
Kishihara, M.;
Baba, Y.;
Fujita, T.

Publication type:

Article

A novel mutation of the WRN gene in a Chinese patient with Werner syndrome.

Published in:

Clinical & Experimental Dermatology, 2008, v. 33, n. 3, p. 278, doi. 10.1111/j.1365-2230.2007.02641.x

By:

Zhao, N.;
Hao, F.;
Qu, T.;
Zuo, Y.-G.;
Wang, B-X.

Publication type:

Article

A brother and sister with Werner's syndrome demonstrating extensive tendon calcification and sacroiliitis.

Published in:

Clinical & Experimental Dermatology, 2006, v. 31, n. 4, p. 615, doi. 10.1111/j.1365-2230.2006.02130.x

By:

Özturk, M.;
Akdeniz, N.;
Ayakta^1, H.;
Kösem, M.

Publication type:

Article

Diagnosis of Werner syndrome by immunoblot analysis.

Published in:

Clinical & Experimental Dermatology, 2002, v. 27, n. 2, p. 157, doi. 10.1046/j.1365-2230.2002.00996.x

By:

Shimizu, T;
Tateishi, Y;
Furuichi, Y;
Sugimoto, M;
Kawabe, T;
Matsumoto, T;
Shimizu, H

Publication type:

Article

Research on Werner Syndrome: Trends from Past to Present and Future Prospects.

Published in:

Genes, 2022, v. 13, n. 10, p. N.PAG, doi. 10.3390/genes13101802

By:

Tsuge, Kyoshiro;
Shimamoto, Akira

Publication type:

Article

Genetic Mutations and Variants in the Susceptibility of Familial Non-Medullary Thyroid Cancer.

Published in:

Genes, 2020, v. 11, n. 11, p. 1364, doi. 10.3390/genes11111364

By:

Miasaki, Fabíola Yukiko;
Fuziwara, Cesar Seigi;
Carvalho, Gisah Amaral de;
Kimura, Edna Teruko

Publication type:

Article

Current Knowledge of Germline Genetic Risk Factors for the Development of Non-Medullary Thyroid Cancer.

Published in:

Genes, 2019, v. 10, n. 7, p. 482, doi. 10.3390/genes10070482

By:

Hińcza, Kinga;
Kowalik, Artur;
Kowalska, Aldona

Publication type:

Article

Computational image analysis of nuclear morphology associated with various nuclear-specific aging disorders.

Published in:

Nucleus (1949-1034), 2011, v. 2, n. 6, p. 1, doi. 10.4161/nucl.2.6.17798

By:

Choi, Siwon;
Wang, Wei;
Ribeiro, Alexandrew J.S.;
Kalinowski, Agnieszka;
Gregg, Siobhan Q.;
Opresko, Patricia L.;
Niedernhofer, Laura J.;
Rohde, Gustavo K.;
Dahl, Kris Noel

Publication type:

Article

Nailfold scleroderma-like capillary abnormalities in Werner syndrome (adult progeria).

Published in:

2017

By:

Ingegnoli, Francesca;
Crotti, Chiara

Publication type:

Case Study

Multiple primary malignancies in osteosarcoma patients. Incidence and predictive value of osteosarcoma subtype for cancer syndromes related with osteosarcoma.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 8, p. 611, doi. 10.1038/sj.ejhg.5201012

By:

Hauben, E I;
Arends, J;
Vandenbroucke, J P;
van Asperen, C J;
Van Marck, E;
Hogendoorn, P C W

Publication type:

Article

A high-throughput screen to identify novel small molecule inhibitors of the Werner Syndrome Helicase-Nuclease (WRN).

Published in:

PLoS ONE, 2019, v. 14, n. 01, p. 1, doi. 10.1371/journal.pone.0210525

By:

Sommers, Joshua A.;
Kulikowicz, Tomasz;
Croteau, Deborah L.;
Dexheimer, Thomas;
Dorjsuren, Dorjbal;
Jadhav, Ajit;
Maloney, David J.;
Simeonov, Anton;
Bohr, Vilhelm A.;
Jr.Brosh, Robert M.

Publication type:

Article

Vitamin C alters the amount of specific endoplasmic reticulum associated proteins involved in lipid metabolism in the liver of mice synthesizing a nonfunctional Werner syndrome (Wrn) mutant protein.

Published in:

PLoS ONE, 2018, v. 13, n. 3, p. 1, doi. 10.1371/journal.pone.0193170

By:

Aumailley, Lucie;
Roux-Dalvai, Florence;
Kelly, Isabelle;
Droit, Arnaud;
Lebel, Michel

Publication type:

Article

Aortic valve replacement with annular patch enlargement for a patient with Werner's syndrome and severe aortic stenosis.

Published in:

2020

By:

Handa, Kazuma;
Fukui, Shinya;
Shirakawa, Yukitoshi;
Sakamoto, Tomohiko;
Kitahara, Mutsunori;
Kakizawa, Yumi;
Nishi, Hiroyuki

Publication type:

journal article

Heterochromatin and human aging.

Published in:

Nature Genetics, 2015, v. 47, n. 6, p. 568, doi. 10.1038/ng.3325

By:

Faial, Tiago

Publication type:

Article

Modeling NOTCH1 haploinsufficiency.

Published in:

Nature Genetics, 2015, v. 47, n. 6, p. 568, doi. 10.1038/ng.3328

By:

Niemitz, Emily

Publication type:

Article

Essential role of limiting telomeres in the pathogenesis of Werner syndrome.

Published in:

Nature Genetics, 2004, v. 36, n. 8, p. 877, doi. 10.1038/ng1389

By:

Sandy Chang;
Multani, Asha S.;
Cabrera, Noelia G.;
Naylor, Maria L.;
Laud, Purnima;
Lombard, David;
Pathak, Sen;
Guarente, Leonard;
DePinho, Ronald A.

Publication type:

Article

SGS1, the Saccharomyces cerevisiae homologue of BLM and WRN, suppresses genome instability and homeologous recombination.

Published in:

Nature Genetics, 2001, v. 27, n. 1, p. 113, doi. 10.1038/83673

By:

Myung, Kyungjae;
Datta, Abhijit;
Chen, Clark;
Kolodner, Richard D.

Publication type:

Article

A radical solution to death.

Published in:

Nature Genetics, 2000, v. 25, n. 2, p. 132, doi. 10.1038/75957

By:

Klein, Hannah L

Publication type:

Article

Telomerase prevents the accelerated cell ageing of Werner syndrome fibroblasts.

Published in:

Nature Genetics, 2000, v. 24, n. 1, p. 16, doi. 10.1038/71630

By:

Wyllie, Fiona S.;
Jones, Christopher J.;
Skinner, Julia W.;
Haughton, Michele F.;
Wallis, Corrin;
Wynford-Thomas, David;
Faragher, Richard G.A.;
Kipling, David

Publication type:

Article

The premature ageing syndrome protein, WRN, is a 3′→5′ exonuclease.

Published in:

Nature Genetics, 1998, v. 20, n. 2, p. 114, doi. 10.1038/2410

By:

Huang, Shurong;
Li, Baomin;
Gray, Matthew D.;
Oshima, Junko;
Mian, I. Saira;
Campisi, Judith

Publication type:

Article

The three faces of the WS helicase.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 308, doi. 10.1038/1188

By:

Fry, Michael;
Loeb, Lawrence A

Publication type:

Article

Association of impaired phosphatidylinositol 3-kinase activity in GLUT1-containing vesicles with malinsertion of glucose transporters into the plasma membrane of fibroblasts from a patient with severe insulin resistance and clinical features of Werner syndrome.

Published in:

2000

By:

Kausch, C;
Hamann, A;
Uphues, I;
Niendorf, A;
Müller-Wieland, D;
Joost, H G;
Algenstaedt, P;
Dreyer, M;
Rüdiger, H W;
Häring, H U;
Eckel, J;
Matthaei, S

Publication type:

journal article

A case report of Werner's syndrome with bilateral juvenile cataracts.

Published in:

2018

By:

Chen, Chun-li;
Yang, Jia-song;
Zhang, Xiang;
Tian, Tian;
Zeng, Rui;
Zhang, Guan-hong;
Jia, Xin-guo

Publication type:

journal article

Expression profiling of mouse embryonicfibroblasts with a deletion in the helicase domainof the Werner Syndrome gene homologuetreated with hydrogen peroxide.

Published in:

BMC Genomics, 2010, v. 11, p. 127, doi. 10.1186/1471-2164-11-127

By:

Labbé, Adam;
Turaga, Ramachander V. N.;
Paquet, Éric R.;
Garand, Chantal;
Lebel, Michel

Publication type:

Article

Neurological complications of Werner's syndrome.

Published in:

Journal of Neurology, 2003, v. 250, n. 10, p. 1174, doi. 10.1007/s00415-003-0168-3

By:

Neil E. Anderson;
Lindsay F. Haas

Publication type:

Article

Werner's syndrome.

Published in:

2012

By:

Keen, Abid;
Hassan, Iffat

Publication type:

Case Study

The Werner's Syndrome RecQ Helicase/Exonuclease at the Nexus of Cancer and Aging.

Published in:

Hawaii Medical Journal, 2011, v. 70, n. 3, p. 52

By:

Chun, Stephen G.;
Shaeffer, David S.;
Bryant-Greenwood, Peter K.

Publication type:

Article

Werner's Syndrome as a Cause of Chronic Leg Ulcers.

Published in:

Journal of Dermatologic Surgery & Oncology, 1982, v. 8, n. 4, p. 293, doi. 10.1111/j.1524-4725.1982.tb00283.x

By:

Sternberg, Nathan;
Golan, Jacob;
Sternberg, Ido;
Ben-Hur, Nahum

Publication type:

Article

Senescence, regulators of alternative splicing and effects of trametinib treatment in progeroid syndromes.

Published in:

GeroScience, 2024, v. 46, n. 2, p. 1861, doi. 10.1007/s11357-023-00933-z

By:

Bramwell, Laura R.;
Harries, Lorna W.

Publication type:

Article

George M. Martin: tribute and personal remembrance.

Published in:

GeroScience, 2023, v. 45, n. 3, p. 2085, doi. 10.1007/s11357-023-00747-z

By:

Austad, Steven N.

Publication type:

Article

Replication protein A promotes 5′→3′ end processing during homology-dependent DNA double-strand break repair.

Published in:

Journal of Cell Biology, 2011, v. 192, n. 2, p. 251, doi. 10.1083/jcb.201005110

By:

Hong Yan;
Toczylowski, Thomas;
McCane, Jill;
Chinyi Chen;
Shuren Liao

Publication type:

Article

Replication fork stalling in WRN-deficient cells is overcome by prompt activation of a MUS81-dependent pathway.

Published in:

Journal of Cell Biology, 2008, v. 183, n. 2, p. 241, doi. 10.1083/jcb.200803173

By:

Franchitto, Annapaola;
Pirzio, Livia Maria;
Prosperi, Ennio;
Sapora, Orazio;
Bignami, Margherita;
Pichierri, Pietro

Publication type:

Article

Werner syndrome helicase activity is essential in maintaining fragile site stability.

Published in:

Journal of Cell Biology, 2008, v. 180, n. 2, p. 305, doi. 10.1083/jcb.200705126

By:

Pirzio, Livia Maria;
Pichierri, Pietro;
Bignami, Margherita;
Franchitto, Annapaola

Publication type:

Article

Longevity mutation in SCH9 prevents recombination errors and premature genomic instability in a Werner/Bloom model system.

Published in:

Journal of Cell Biology, 2008, v. 180, n. 1, p. 67, doi. 10.1083/jcb.200707154

By:

Madia, Federica;
Gattazzo, Cristina;
Wei, Min;
Fabrizio, Paola;
Galbani, Abdoulaye;
Smith, Jesse R.;
Nguyen, Christopher;
Huey, Selina;
Longo, Valter D.;
Burhans, William C.;
Weinberger, Martin;
Comai, Lucio

Publication type:

Article

Analysis of the Xenopus Werner syndrome protein in DNA double-strand break repair.

Published in:

Journal of Cell Biology, 2005, v. 171, n. 2, p. 217, doi. 10.1083/jcb.200502077

By:

Yan, Hong;
McCane, Jill;
Toczylowski, Thomas;
Chen, Chinyi

Publication type:

Article

C. elegans orthologs MUT-7/CeWRN-1 of Werner syndrome protein regulate neuronal plasticity.

Published in:

eLife, 2021, p. 1, doi. 10.7554/eLife.62449

By:

Tsung-Yuan Hsu;
Bo Zhang;
L'Etoile, Noelle D.;
Bi-Tzen Juang

Publication type:

Article

Increased susceptibility to oxidative stress- and ultraviolet A-induced apoptosis in fibroblasts in atypical progeroid syndrome/atypical Werner syndrome with LMNA mutation.

Published in:

Experimental Dermatology, 2016, v. 25, p. 20, doi. 10.1111/exd.13086

By:

Motegi, Sei‐ichiro;
Uchiyama, Akihiko;
Yamada, Kazuya;
Ogino, Sachiko;
Yokoyama, Yoko;
Perera, Buddhini;
Takeuchi, Yuko;
Ishikawa, Osamu

Publication type:

Article

Werner's syndrome.

Published in:

1989

By:

Dootson, G. M.;
Anderson, J. A. R.

Publication type:

Abstract

Cytogenetic studies in a patient with porokeratosis of Mibelli, multiple cancers and a <em>forme fruste</em> of Werner's syndrome.

Published in:

British Journal of Dermatology, 1984, v. 111, n. 5, p. 579, doi. 10.1111/j.1365-2133.1984.tb06628.x

By:

Machino, H.;
Miki, Y.;
Teramoto, T.;
Shiraishi, S.;
Sasaki, M. S.

Publication type:

Article

Cricotracheostomy in a patient with severe kyphosis: A case report.

Published in:

ENT: Ear, Nose & Throat Journal, 2024, v. 103, n. 11, p. NP633, doi. 10.1177/01455613221077596

By:

Kasahara, Ken;
Nishiyama, Takanori;
Shigetomi, Seiji;
Ikari, Yuichi;
Matsui, Yuki;
Ozawa, Hiroyuki

Publication type:

Article