Редактирование: Aging genes 30-39 (раздел)

==WRN==

* {{medline-title
|title=The Impact of Vitamin C on Different System Models of Werner Syndrome.
|date=17.11.2020
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/33202145
|full-text-url=https://sci-hub.do/10.1089/ars.2020.8147
}}
* {{medline-title
|title=[[WRN]] modulates translation by influencing nuclear mRNA export in HeLa cancer cells.
|date=14.10.2020
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/33054770
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7557079
}}
* {{medline-title
|title=[[MIB1]]-mediated degradation of [[WRN]] promotes cellular senescence in response to camptothecin treatment.
|date=09.2020
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/32652764
|full-text-url=https://sci-hub.do/10.1096/fj.202000268RRR
}}
* {{medline-title
|title=A Case Report of Werner's Syndrome With a Novel Mutation From India.
|date=08.05.2020
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/32528764
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282380
}}
* {{medline-title
|title=Evidence for premature aging in a Drosophila model of Werner syndrome.
|date=11.2019
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/31518666
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6935377
}}
* {{medline-title
|title=Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes.
|date=10.2019
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/31259468
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718529
}}
* {{medline-title
|title=Studying Werner syndrome to elucidate mechanisms and therapeutics of human aging and age-related diseases.
|date=06.2019
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/30666569
|full-text-url=https://sci-hub.do/10.1007/s10522-019-09798-2
}}
* {{medline-title
|title=Werner Syndrome Protein and DNA Replication.
|date=02.11.2018
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/30400178
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274846
}}
* {{medline-title
|title=A case report of Werner's syndrome with bilateral juvenile cataracts.
|date=14.08.2018
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/30107835
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092780
}}
* {{medline-title
|title=Genomic instability and DNA replication defects in progeroid syndromes.
|date=31.12.2018
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29936894
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000143
}}
* {{medline-title
|title=Nonfunctional mutant Wrn protein leads to neurological deficits, neuronal stress, microglial alteration, and immune imbalance in a mouse model of Werner syndrome.
|date=10.2018
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29908963
|full-text-url=https://sci-hub.do/10.1016/j.bbi.2018.06.007
}}
* {{medline-title
|title=Acidic domain of [[WRN]]p is critical for autophagy and up-regulates age associated proteins.
|date=08.2018
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29800817
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6338341
}}
* {{medline-title
|title=RECQ helicase disease and related progeroid syndromes: RECQ2018 meeting.
|date=07.2018
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29752965
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217841
}}
* {{medline-title
|title=Differential stem cell aging kinetics in Hutchinson-Gilford progeria syndrome and Werner syndrome.
|date=04.2018
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29476423
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876188
}}
* {{medline-title
|title=Serum vitamin C levels modulate the lifespan and endoplasmic reticulum stress response pathways in mice synthesizing a nonfunctional mutant [[WRN]] protein.
|date=07.2018
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29452565
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998970
}}
* {{medline-title
|title=Werner syndrome ([[WRN]]) gene variants and their association with altered function and age-associated diseases.
|date=01.2018
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29146545
|full-text-url=https://sci-hub.do/10.1016/j.arr.2017.11.003
}}
* {{medline-title
|title=Human RecQL4 helicase plays multifaceted roles in the genomic stability of normal and cancer cells.
|date=28.01.2018
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29080750
|full-text-url=https://sci-hub.do/10.1016/j.canlet.2017.10.021
}}
* {{medline-title
|title=Recent Advances in Understanding Werner Syndrome.
|date=2017
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29043077
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5621106
}}
* {{medline-title
|title=Systematic analysis of DNA crosslink repair pathways during development and aging in Caenorhabditis elegans.
|date=19.09.2017
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/28934497
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766164
}}
* {{medline-title
|title=The Werner Syndrome Helicase Coordinates Sequential Strand Displacement and [[FEN1]]-Mediated Flap Cleavage during Polymerase δ Elongation.
|date=01.02.2017
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/27849570
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5247617
}}
* {{medline-title
|title=Vitamin C alleviates aging defects in a stem cell model for Werner syndrome.
|date=07.2016
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/27271327
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930768
}}
* {{medline-title
|title=Bloom's syndrome: Why not premature aging?: A comparison of the [[BLM]] and [[WRN]] helicases.
|date=01.2017
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/27238185
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5124422
}}
* {{medline-title
|title=Understanding Vascular Diseases: Lessons From Premature Aging Syndromes.
|date=05.2016
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/26948039
|full-text-url=https://sci-hub.do/10.1016/j.cjca.2015.12.003
}}
* {{medline-title
|title=Stem Cell Depletion by Global Disorganization of the H3K9me3 Epigenetic Marker in Aging.
|date=08.2015
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/26160351
|full-text-url=https://sci-hub.do/10.1089/rej.2015.1742
}}
* {{medline-title
|title=The Werner Protein Acts as a Coactivator of Nuclear Factor κB (NF-κB) on HIV-1 and Interleukin-8 (IL-8) Promoters.
|date=24.07.2015
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/26037922
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4513100
}}
* {{medline-title
|title=Aging stem cells. A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging.
|date=05.06.2015
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/25931448
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4494668
}}
* {{medline-title
|title=Werner Syndrome-specific induced pluripotent stem cells: recovery of telomere function by reprogramming.
|date=2015
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/25688260
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310323
}}
* {{medline-title
|title=Transient overexpression of Werner protein rescues starvation induced autophagy in Werner syndrome cells.
|date=12.2014
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/25257404
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5582615
}}
* {{medline-title
|title=Senescence induced by [[RECQL4]] dysfunction contributes to Rothmund-Thomson syndrome features in mice.
|date=15.05.2014
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/24832598
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4047874
}}
* {{medline-title
|title=Search and insights into novel genetic alterations leading to classical and atypical Werner syndrome.
|date=2014
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/24401204
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3997596
}}
* {{medline-title
|title=Hydrogen sulfide restores a normal morphological phenotype in Werner syndrome fibroblasts, attenuates oxidative damage and modulates mTOR pathway.
|date=08.2013
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/23702336
|full-text-url=https://sci-hub.do/10.1016/j.phrs.2013.04.011
}}
* {{medline-title
|title=Copy number variations of DNA repair genes and the age-related cataract: Jiangsu Eye Study.
|date=01.02.2013
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/23329665
|full-text-url=https://sci-hub.do/10.1167/iovs.12-10948
}}
* {{medline-title
|title=The associations between single nucleotide polymorphisms of DNA repair genes, DNA damage, and age-related cataract: Jiangsu Eye Study.
|date=01.02.2013
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/23322570
|full-text-url=https://sci-hub.do/10.1167/iovs.12-10940
}}
* {{medline-title
|title=Aberrant DNA methylation profiles in the premature aging disorders Hutchinson-Gilford Progeria and Werner syndrome.
|date=01.2013
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/23257959
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549877
}}