Mechanism of alcohol-induced impairment in renal development: Could it be reduced by retinoic acid?

Clinical and Experimental Pharmacology and Physiology

Volumn 39, Issue 9, 2012, Pages 807-813

  Gray, Stephen P ^a   Cullen Mcewen, Luise A ^a   Bertram, John F ^a   Moritz, Karen M ^b  

^a MONASH UNIVERSITY   (Australia)

^b UNIVERSITY OF QUEENSLAND   (Australia)

Author keywords

Fetal alcohol exposure; Kidney development; Metanephric culture; Nephron number; Ureteric branching

Indexed keywords

ALCOHOL; RETINOIC ACID;

ALCOHOL METABOLISM; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRANCHING MORPHOGENESIS; COCULTURE; CONTROLLED STUDY; EMBRYO; FEMALE; GENE EXPRESSION PROFILING; GENETIC ANALYSIS; GLOMERULUS; IN VITRO STUDY; KIDNEY CELL CULTURE; KIDNEY DEVELOPMENT; NONHUMAN; PROTEIN EXPRESSION; RAT; URETER;

ANIMALS; ETHANOL; FEMALE; FETAL ALCOHOL SYNDROME; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GLIAL CELL LINE-DERIVED NEUROTROPHIC FACTOR; KIDNEY; KIDNEY GLOMERULUS; ORGAN CULTURE TECHNIQUES; ORGANOGENESIS; OSMOLAR CONCENTRATION; PREGNANCY; PROTECTIVE AGENTS; PROTO-ONCOGENE PROTEINS C-RET; RANDOM ALLOCATION; RATS; RATS, SPRAGUE-DAWLEY; RENAL INSUFFICIENCY; RETINOID X RECEPTOR ALPHA; TERATOGENS; TRETINOIN;

EID: 84865603966     PISSN: 03051870     EISSN: 14401681     Source Type: Journal    
DOI: 10.1111/j.1440-1681.2011.05597.x     Document Type: Article

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