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Items: 3

Select item 41919381.

Cell-Autonomous Progeroid Changes in Conditional Mouse Models for Repair Endonuclease XPG Deficiency

Sander Barnhoorn, Lieneke M. Uittenboogaard, Dick Jaarsma, Wilbert P. Vermeij, Maria Tresini, Michael Weymaere, Hervé Menoni, Renata M. C. Brandt, Monique C. de Waard, Sander M. Botter, Altaf H. Sarker, Nicolaas G. J. Jaspers, Gijsbertus T. J. van der Horst, Priscilla K. Cooper, Jan H. J. Hoeijmakers, Ingrid van der Pluijm

PLoS Genet. 2014 Oct; 10(10): e1004686. Published online 2014 Oct 9. doi: 10.1371/journal.pgen.1004686

PMCID:: PMC4191938

Article PDF–4.9M

Select item 12881892.

Manitoba Aboriginal Kindred with Original Cerebro-Oculo-Facio-Skeletal Syndrome Has a Mutation in the Cockayne Syndrome Group B (CSB) Gene

Lisiane B. Meira, John M. Graham, Jr., Cheryl R. Greenberg, David B. Busch, Ana T. B. Doughty, Deborah W. Ziffer, Donna M. Coleman, Isabelle Savre-Train, Errol C. Friedberg

Am J Hum Genet. 2000 Apr; 66(4): 1221–1228. Published online 2000 Mar 15. doi: 10.1086/302867