Severe hypertension caused by alleles from normotensive Lewis for a quantitative trait locus on chromosome 2

Physiological Genomics

Volumn 22, Issue , 2005, Pages 70-75

  Eliopoulos, Vasiliki ^a   Dutil, Julie ^a   Deng, Yishu ^b   Grondin, Myrian ^a   Deng, Alan Y ^a  

^a CENTRE HOSPITALIER DE L UNIVERSITÉ DE MONTRÉAL   (Canada)

^b Third People's Hospital of Kunming   (China)

Author keywords

Blood pressure; Comparative congenics; Fine mapping; Functional genomics

Indexed keywords

ANGIOTENSIN 1B RECEPTOR; ANGIOTENSIN 2 RECEPTOR; UNCLASSIFIED DRUG;

ALLELISM; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BLOOD PRESSURE REGULATION; CHROMOSOME 2; CONTROLLED STUDY; GENE FUNCTION; GENE MAPPING; GENETIC LINKAGE; HYPERTENSION; MALE; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; QUANTITATIVE TRAIT LOCUS; RAT; RAT STRAIN; SEQUENCE HOMOLOGY;

ALLELES; ANIMALS; ANIMALS, CONGENIC; BLOOD PRESSURE; CHROMOSOME MAPPING; CHROMOSOMES, MAMMALIAN; HUMANS; HYPERTENSION; MICE; QUANTITATIVE TRAIT LOCI; RATS; RATS, INBRED DAHL; RATS, INBRED LEW; SEQUENCE HOMOLOGY, NUCLEIC ACID;

ANIMALIA;

EID: 25144452252     PISSN: 15312267     EISSN: None     Source Type: Journal    
DOI: 10.1152/physiolgenomics.00019.2005     Document Type: Article

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