Genomic organization and polymorphism of human angiotensin II type 2 receptor: No evidence for its gene mutation in two families of human premature ovarian failure syndrome

Molecular and Cellular Endocrinology

Volumn 127, Issue 2, 1997, Pages 221-228

  Katsuya, Tomohiro ^a   Horiuchi, Masatsugu ^a   Minami, Sawako ^b   Koike, George ^a   Santoro, Nanetto F ^b   Hsueh, Aaron J W ^b   Dzau, Victor J ^a  

^a HARVARD MEDICAL SCHOOL   (United States)

^b NONE

Author keywords

AT2 receptor; Chromosome X; Genetics; Premature ovarian failure; Renin angiotensin system

Indexed keywords

ANGIOTENSIN 2 RECEPTOR; COMPLEMENTARY DNA; DNA;

ADULT; ARTICLE; CASE REPORT; CONTROLLED STUDY; DNA POLYMORPHISM; EXON; FEMALE; GENE MAPPING; GENE MUTATION; GENE STRUCTURE; HUMAN; HUMAN CELL; INTRON; MOLECULAR CLONING; OVARY INSUFFICIENCY; PRIORITY JOURNAL; RECEPTOR GENE; START CODON; TATA BOX; TRANSCRIPTION INITIATION; X CHROMOSOME;

BASE SEQUENCE; CLONING, MOLECULAR; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; GENES; GENETIC MARKERS; HUMANS; INTRONS; MOLECULAR SEQUENCE DATA; MUTATION; OVARIAN FAILURE, PREMATURE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; RECEPTOR, ANGIOTENSIN, TYPE 2; RECEPTORS, ANGIOTENSIN; RESTRICTION MAPPING; TRANSCRIPTION, GENETIC;

EID: 0030891355     PISSN: 03037207     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0303-7207(97)04011-2     Document Type: Article

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