Complete mutation scan of the human Fas ligand gene: Linkage studies in type I diabetes mellitus families

Diabetologia

Volumn 45, Issue 1, 2002, Pages 134-139

  Nolsoe R L ^a   Kristiansen, O P ^a   Larsen, Z M ^a   Johannesen, J ^a   Pociot, F ^a   Mandrup Poulsen, T ^a  

^a STENO DIABETES CENTER   (Denmark)

Author keywords

Apoptosis; Candidate gene; Genetics; Immune regulation; Microsatellite; SP 1, NF B; T cells; Tolerance

Indexed keywords

FAS LIGAND;

ADULT; APOPTOSIS; ARTICLE; CHROMOSOME 1Q; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENETIC LINKAGE; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; HAPLOTYPE; HETERODUPLEX ANALYSIS; HUMAN; IMMUNE RESPONSE; IMMUNOREGULATION; INSULIN DEPENDENT DIABETES MELLITUS; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; PANCREAS ISLET BETA CELL; PATHOGENESIS; PRIORITY JOURNAL; PROMOTER REGION; SINGLE STRAND CONFORMATION POLYMORPHISM; T LYMPHOCYTE;

AMINO ACID SUBSTITUTION; BASE SEQUENCE; DENMARK; DIABETES MELLITUS, TYPE 1; DNA PRIMERS; EUROPEAN CONTINENTAL ANCESTRY GROUP; EXONS; FAS LIGAND PROTEIN; FEMALE; HAPLOTYPES; HUMANS; INTRONS; LINKAGE (GENETICS); MALE; MEMBRANE GLYCOPROTEINS; MOLECULAR SEQUENCE DATA; NUCLEAR FAMILY; NUCLEIC ACID HETERODUPLEXES; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROMOTER REGIONS (GENETICS); REFERENCE VALUES;

EID: 18244383561     PISSN: 0012186X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s125-002-8254-7     Document Type: Article

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