Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 151


Recombine and Associate to Prevent Genomic Instability and Premature Aging.

Poot M.

Mol Syndromol. 2017 Jan;8(1):1-3. doi: 10.1159/000452784. Epub 2016 Nov 17. No abstract available.


Different non-synonymous polymorphisms modulate the interaction of the WRN protein to its protein partners and its enzymatic activities.

Gagné JP, Lachapelle S, Garand C, Tsofack SP, Coulombe Y, Caron MC, Poirier GG, Masson JY, Lebel M.

Oncotarget. 2016 Dec 27;7(52):85680-85696. doi: 10.18632/oncotarget.13341.


Human RECQ Helicase Pathogenic Variants, Population Variation and "Missing" Diseases.

Fu W, Ligabue A, Rogers KJ, Akey JM, Monnat RJ Jr.

Hum Mutat. 2017 Feb;38(2):193-203. doi: 10.1002/humu.23148. Epub 2016 Dec 9.


Use of p38 MAPK Inhibitors for the Treatment of Werner Syndrome.

Bagley MC, Davis T, Murziani PG, Widdowson CS, Kipling D.

Pharmaceuticals (Basel). 2010 Jun 4;3(6):1842-1872. Review.


Werner syndrome through the lens of tissue and tumour genomics.

Tokita M, Kennedy SR, Risques RA, Chun SG, Pritchard C, Oshima J, Liu Y, Bryant-Greenwood PK, Welcsh P, Monnat RJ.

Sci Rep. 2016 Aug 25;6:32038. doi: 10.1038/srep32038.


DNA Damage: A Main Determinant of Vascular Aging.

Bautista-Niño PK, Portilla-Fernandez E, Vaughan DE, Danser AH, Roks AJ.

Int J Mol Sci. 2016 May 18;17(5). pii: E748. doi: 10.3390/ijms17050748. Review.


Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions.

Oshima J, Sidorova JM, Monnat RJ Jr.

Ageing Res Rev. 2017 Jan;33:105-114. doi: 10.1016/j.arr.2016.03.002. Epub 2016 Mar 15. Review.


The Werner syndrome RECQ helicase targets G4 DNA in human cells to modulate transcription.

Tang W, Robles AI, Beyer RP, Gray LT, Nguyen GH, Oshima J, Maizels N, Harris CC, Monnat RJ Jr.

Hum Mol Genet. 2016 May 15;25(10):2060-2069. Epub 2016 Mar 16.


Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome Rearrangements.

Poot M, Haaf T.

Mol Syndromol. 2015 Sep;6(3):110-34. doi: 10.1159/000438812. Epub 2015 Aug 15. Review.


Relationships between putative G-quadruplex-forming sequences, RecQ helicases, and transcription.

Smestad JA, Maher LJ 3rd.

BMC Med Genet. 2015 Oct 8;16:91. doi: 10.1186/s12881-015-0236-4.


Metabolic and Phenotypic Differences between Mice Producing a Werner Syndrome Helicase Mutant Protein and Wrn Null Mice.

Aumailley L, Garand C, Dubois MJ, Johnson FB, Marette A, Lebel M.

PLoS One. 2015 Oct 8;10(10):e0140292. doi: 10.1371/journal.pone.0140292. eCollection 2015.


Gene Fusion due to Chromosome Misconnection May Seriously Affect Your Health.

Poot M.

Mol Syndromol. 2015 Jul;6(2):55-7. doi: 10.1159/000381081. Epub 2015 Mar 26. No abstract available.


Genetics of primary ovarian insufficiency: new developments and opportunities.

Qin Y, Jiao X, Simpson JL, Chen ZJ.

Hum Reprod Update. 2015 Nov-Dec;21(6):787-808. doi: 10.1093/humupd/dmv036. Epub 2015 Aug 4. Review.


The Werner Protein Acts as a Coactivator of Nuclear Factor κB (NF-κB) on HIV-1 and Interleukin-8 (IL-8) Promoters.

Mizutani T, Ishizaka A, Furuichi Y.

J Biol Chem. 2015 Jul 24;290(30):18391-9. doi: 10.1074/jbc.M115.657155. Epub 2015 Jun 2.


A novel Werner Syndrome mutation: pharmacological treatment by read-through of nonsense mutations and epigenetic therapies.

Agrelo R, Sutz MA, Setien F, Aldunate F, Esteller M, Da Costa V, Achenbach R.

Epigenetics. 2015;10(4):329-41. doi: 10.1080/15592294.2015.1027853.


"...Rewritten in the skin": clues to skin biology and aging from inherited disease.

Monnat RJ Jr.

J Invest Dermatol. 2015 Jun;135(6):1484-90. doi: 10.1038/jid.2015.88. Epub 2015 Mar 26. Review.


Cellular senescence: from growth arrest to immunogenic conversion.

Burton DG, Faragher RG.

Age (Dordr). 2015;37(2):27. doi: 10.1007/s11357-015-9764-2. Epub 2015 Mar 20. Review.


The nuclease FAN1 is involved in DNA crosslink repair in Arabidopsis thaliana independently of the nuclease MUS81.

Herrmann NJ, Knoll A, Puchta H.

Nucleic Acids Res. 2015 Apr 20;43(7):3653-66. doi: 10.1093/nar/gkv208. Epub 2015 Mar 16.


Werner Syndrome-specific induced pluripotent stem cells: recovery of telomere function by reprogramming.

Shimamoto A, Yokote K, Tahara H.

Front Genet. 2015 Jan 29;6:10. doi: 10.3389/fgene.2015.00010. eCollection 2015. Review.


Supplemental Content

Support Center