Lifespan extension by dietary intervention in a mouse model of Cockayne Syndrome uncouples early postnatal development from segmental progeria

Aging Cell

Volumn 12, Issue 6, 2013, Pages 1144-1147

  Brace, Lear E ^a   Vose, Sarah C ^a   Vargas, Dorathy F ^a   Zhao, Shuangyun ^b   Wang, Xiu Ping ^b   Mitchell, James R ^a  

^a HARVARD SCHOOL OF PUBLIC HEALTH   (United States)

^b HARVARD SCHOOL OF DENTAL MEDICINE   (United States)

Author keywords

Cockayne syndrome; CSA; DNA repair; Lifespan; Segmental progeria; XPA

Indexed keywords

GLUCOSE; TRIACYLGLYCEROL;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BROWN ADIPOSE TISSUE; COCKAYNE SYNDROME; CONTROLLED STUDY; DIET THERAPY; DNA REPAIR; FAT CONTENT; GLUCOSE BLOOD LEVEL; LIFE EXTENSION; LIFESPAN; LIPODYSTROPHY; MACRONUTRIENT; MOUSE; NEUROLOGIC DISEASE; NONHUMAN; OBESITY; PENETRANCE; PERINATAL PERIOD; POSTNATAL DEVELOPMENT; PREMATURE AGING; PRIORITY JOURNAL; PROGERIA; SURVIVAL; TRIACYLGLYCEROL BLOOD LEVEL; WEANING;

COCKAYNE SYNDROME; CSA; DNA REPAIR; LIFESPAN; SEGMENTAL PROGERIA; XPA;

ANIMALS; ANIMALS, NEWBORN; COCKAYNE SYNDROME; DIET; DISEASE MODELS, ANIMAL; DISEASE PROGRESSION; LIPODYSTROPHY; LONGEVITY; MICE; MICE, INBRED C57BL; PROGERIA; WEANING;

EID: 84888135733     PISSN: 14749718     EISSN: 14749726     Source Type: Journal    
DOI: 10.1111/acel.12142     Document Type: Article

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