New areas of focus at workshop on human diseases involving DNA repair deficiency and premature aging

Mechanisms of Ageing and Development

Volumn 128, Issue 2, 2007, Pages 229-235

  Kraemer, Kenneth H ^a   Sander, Miriam ^b   Bohr, Vilhelm A ^c  

^a NATIONAL CANCER INSTITUTE   (United States)

^b Page One Editorial Services   (United States)

^c NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

Cockayne syndrome; DNA repair; Mitochondria; Oxidative stress; Trichothiodystrophy; Werner syndrome; Xeroderma pigmentosum

Indexed keywords

DERMATOLOGICAL AGENT; DIMERICINE; UNCLASSIFIED DRUG;

CLINICAL FEATURE; COCKAYNE SYNDROME; CONFERENCE PAPER; DISORDERS OF DNA SYNTHESIS AND REPAIR; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DNA REPAIR; EYE MALFORMATION; FAMILY; GENOTYPE; GRAY MATTER; HUMAN; NEUROLOGIC DISEASE; NONHUMAN; OXIDATIVE STRESS; PHENOTYPE; PREMATURE AGING; PRIORITY JOURNAL; TRICHOTHIODYSTROPHY; WERNER SYNDROME; WHITE MATTER; XERODERMA PIGMENTOSUM;

AGING; AGING, PREMATURE; COCKAYNE SYNDROME; DNA REPAIR-DEFICIENCY DISORDERS; HAIR DISEASES; HUMANS; OXIDATIVE STRESS; PREVALENCE; XERODERMA PIGMENTOSUM;

EID: 33846219516     PISSN: 00476374     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mad.2006.11.028     Document Type: Conference Paper

References (0)