Works matching DE "WERNER'S syndrome"
Results: 350
Cisplatin induces Sirt1 in association with histone deacetylation and increased Werner syndrome protein in the kidney.
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- Clinical & Experimental Nephrology, 2011, v. 15, n. 3, p. 363, doi. 10.1007/s10157-011-0421-5
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- Article
53. Werner Syndrome (includes Adult Progeria).
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- JNCI: Journal of the National Cancer Institute, 2008, n. 38, p. 89
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- Article
Update on ageing research initiative.
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- 2006
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- Journal Article
Retroperitoneal sarcomas: Anatomy, pathology and current trends in management'.
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- Pakistan Journal of Surgery, 2023, v. 39, n. 2, p. 76
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- Article
PROTAC-mediated conditional degradation of the WRN helicase as a potential strategy for selective killing of cancer cells with microsatellite instability.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-71160-5
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- Article
Characterization of Stress Responses in a Drosophila Model of Werner Syndrome.
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- Biomolecules (2218-273X), 2021, v. 11, n. 12, p. 1868, doi. 10.3390/biom11121868
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- Article
Wiedemann-Rautenstrauch Syndrome: Case Report.
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- Cumhuriyet Dental Journal, 2022, v. 25, n. 3, p. 282, doi. 10.7126/cumudj.1127344
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- Article
'Werner Syndrome foot'—A case series of four Irish Traveller siblings with Werner Syndrome, diabetes mellitus and complex foot disease.
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- Diabetic Medicine, 2024, v. 41, n. 9, p. 1, doi. 10.1111/dme.15390
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- Article
ELASTIC FIBRES IN UNUSUAL DERMATOSES.
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- British Journal of Dermatology, 1955, v. 67, n. 12, p. 460
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- Article
WERNER'S SYNDROME.
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- British Journal of Dermatology, 1953, v. 65, n. 5, p. 165, doi. 10.1111/j.1365-2133.1953.tb13193.x
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- Article
Werner's Syndrome: Understanding the Phenotype of Premature Aging—First Case Described in Colombia.
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- 2019
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- Case Study
Werner's syndrome: A case report and review of literature.
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- 2018
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- Case Study
WERNER SYNDROME: A NEW CASE REPORT.
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- 2013
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- Case Study
Roles of Caenorhabditis elegans WRN Helicase in DNA Damage Responses, and a Comparison with Its Mammalian Homolog: A Mini-Review.
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- 2016
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- journal article
Case Report: A novel WRN mutation in Werner syndrome patient with diabetic foot disease and myelodysplastic syndrome.
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- Frontiers in Endocrinology, 2022, v. 13, p. 1, doi. 10.3389/fendo.2022.918979
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- Article
Werner syndrome presenting as early‐onset diabetes: A case report.
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- Journal of Diabetes Investigation, 2022, v. 13, n. 3, p. 592, doi. 10.1111/jdi.13682
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- Article
HERLYN WERNER WUNDERLICH SYNDROME; AN UNUSUAL PRESENTATION. A CASE REPORT.
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- Professional Medical Journal, 2019, v. 26, n. 2, p. 368, doi. 10.29309/TPMJ/2019.26.02.3125
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- Article
Mutations Involved in Premature-Ageing Syndromes.
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- Application of Clinical Genetics, 2021, v. 14, p. 279, doi. 10.2147/TACG.S273525
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- Article
Physical and functional interaction of the Werner syndrome protein with poly-ADP ribosyl transferase
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- FEBS Letters, 2003, v. 554, n. 1/2, p. 55, doi. 10.1016/S0014-5793(03)01088-3
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- Article
Regulation of the Werner helicase through a direct interaction with a subunit of protein kinase A
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- FEBS Letters, 2002, v. 521, n. 1-3, p. 170, doi. 10.1016/S0014-5793(02)02868-5
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- Article
From old organisms to new molecules: integrative biology and therapeutic targets in accelerated human ageing.
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- Cellular & Molecular Life Sciences, 2007, v. 64, n. 19/20, p. 2620, doi. 10.1007/s00018-007-7123-x
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- Article
Human progeroid syndromes, aging and cancer: new genetic and epigenetic insights into old questions.
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- Cellular & Molecular Life Sciences, 2007, v. 64, n. 2, p. 155, doi. 10.1007/s00018-006-6349-3
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- Article
Human Genome and Diseases: A new series of reviews in CMLS¶Werner Syndrome: genetic and molecular basis of a premature aging disorder.
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- Cellular & Molecular Life Sciences, 2001, v. 58, n. 7, p. 857, doi. 10.1007/s00018-001-8398-y
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- Article
RecQ helicases and topoisomerases: components of a conserved complex for the regulation of genetic recombination.
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- Cellular & Molecular Life Sciences, 2001, v. 58, n. 7, p. 894, doi. 10.1007/PL00000909
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- Article
Helicases and aging.
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- Cellular & Molecular Life Sciences, 2000, v. 57, n. 5, p. 716, doi. 10.1007/s000180050036
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- Article
Recent Trends in WRN Gene Mutation Patterns in Individuals with Werner Syndrome.
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- Journal of the American Geriatrics Society, 2017, v. 65, n. 8, p. 1853, doi. 10.1111/jgs.14906
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- Article
Improved Glycemic Control and Vascular Function and Reduction of Abdominal Fat Accumulation with Liraglutide in a Case of Werner Syndrome with Diabetes Mellitus.
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- 2016
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- Letter to the Editor
Astaxanthin Improves Nonalcoholic Fatty Liver Disease in Werner Syndrome with Diabetes Mellitus.
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- 2015
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- Letter to the Editor
Endocrine and Metabolic Abnormalities in a Girl with Childhood Werner Syndrome: Case Report.
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- 2014
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- Publication type:
- Case Study
Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity.
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- EMBO Journal, 2001, v. 20, n. 20, p. 5791, doi. 10.1093/emboj/20.20.5791
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- Article
The Saccharomyces cerevisiae WRN homolog Sgs1p participates in telomere maintenance in cells lacking telomerase.
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- EMBO Journal, 2001, v. 20, n. 4, p. 905, doi. 10.1093/emboj/20.4.905
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- Article
rqh1<sup>+</sup>, a fission yeast gene related to the Bloom's and Werner's syndrome genes, is required for reversible S phase arrest.
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- EMBO Journal, 1997, v. 16, n. 10, p. 2682, doi. 10.1093/emboj/16.10.2682
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- Article
Vitamin C restores healthy aging in a mouse model for Werner syndrome.
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- FASEB Journal, 2010, v. 24, n. 1, p. 158, doi. 10.1096/fj.09-137133
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- Article
Werner syndrome cells escape hydrogen peroxide-induced cell proliferation arrest.
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- FASEB Journal, 2004, v. 18, n. 15, p. 1970, doi. 10.1096/fj.04-1895fje
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- Article
Werner Syndrome and Diabetes: Opportunities for Precision Medicine.
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- Diabetes Care, 2024, v. 47, n. 5, p. 785, doi. 10.2337/dci24-0005
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- Article
A Novel Variant in the WRN Gene Detected in a Case of Early-Onset Severe Insulin Resistance Displaying Some but Not All Hallmarks of Progeroid Werner Syndrome.
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- Diabetes Care, 2024, v. 47, n. 5, p. 798, doi. 10.2337/dc23-1479
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- Article
Sitagliptin Improves Postprandial Hyperglycemia by Inhibiting Glucagon Secretion in Werner Syndrome With Diabetes.
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- Diabetes Care, 2013, v. 36, n. 8, p. e119, doi. 10.2337/dc13-0709
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- Article
Sitagliptin Successfully Ameliorates Glycemic Control in Werner Syndrome With Diabetes.
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- Diabetes Care, 2012, v. 35, n. 12, p. e83, doi. 10.2337/dc12-1179
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- Article
The Werner's Syndrome RecQ Helicase/Exonuclease at the Nexus of Cancer and Aging.
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- Hawaii Medical Journal, 2011, v. 70, n. 3, p. 52
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- Article
XPG in the Nucleotide Excision Repair and Beyond: a study on the different functional aspects of XPG and its associated diseases.
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- Molecular Biology Reports, 2022, v. 49, n. 8, p. 7995, doi. 10.1007/s11033-022-07324-1
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- Article
GFT NMR based resonance assignment for the 21 kDa human protein UFC1.
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- Journal of Biomolecular NMR, 2005, v. 32, n. 3, p. 261, doi. 10.1007/s10858-005-7941-9
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- Article
Diabetes mellitus and cancer in Werner syndrome.
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- 2014
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- Letter
Japanese diabetic patients with Werner syndrome exhibit high incidence of cancer.
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- 2012
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- Publication type:
- Letter
The Werner Syndrome Protein Functions in Repair of Cr(VI)-Induced Replication-Associated DNA Damage.
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- Toxicological Sciences, 2009, v. 110, n. 2, p. 307, doi. 10.1093/toxsci/kfp104
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- Article
Spontaneous and X-ray-induced chromosomal aberrations in Werner syndrome cells detected by FISH using chromosome-specific painting probes.
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- Mutagenesis, 2000, v. 15, n. 4, p. 303, doi. 10.1093/mutage/15.4.303
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- Article
Werner's syndrome protein (WRN) migrates Holliday junctions and co-localizes with RPA upon replication arrest.
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- EMBO Reports, 2000, v. 1, n. 1, p. 80, doi. 10.1093/embo-reports/kvd004
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- Article
WRN modulates translation by influencing nuclear mRNA export in HeLa cancer cells.
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- BMC Molecular & Cell Biology, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12860-020-00315-9
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- Article
Ageing: Heterochromatin disorganization associated with premature ageing.
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- Nature Reviews Genetics, 2015, v. 16, n. 6, p. 318, doi. 10.1038/nrg3958
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- Article
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations.
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- Human Genetics, 2010, v. 128, n. 1, p. 103, doi. 10.1007/s00439-010-0832-5
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- Article
The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis.
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- Human Genetics, 2008, v. 124, n. 4, p. 369, doi. 10.1007/s00439-008-0562-0
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- Publication type:
- Article