Clonal chromosomal defects in the molecular pathogenesis of refractory hyperparathyroidism of uremia

Journal of the American Society of Nephrology

Volumn 13, Issue 6, 2002, Pages 1490-1498

  Imanishi, Yasuo ^a   Tahara, Hideki ^a   Palanisamy, Nallasivam ^a   Spitalny, Sarah ^a   Salusky, Isidro B ^a   Goodman, William ^a   Brandi, Maria Luisa ^a   Düeke, Tilman B ^a   Sarfati, Emile ^a   Ureña, Pablo ^a   Chaganti, R S K ^a   Arnold, Andrew ^a  

^a UNIVERSITY OF CONNECTICUT SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ALLELISM; ARTICLE; CHROMOSOME 11; CHROMOSOME 7; CHROMOSOME ABERRATION; CHROMOSOME LOSS; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; GENE INACTIVATION; HUMAN; HUMAN TISSUE; PARATHYROID ADENOMA; PARATHYROID TUMOR; PATHOGENESIS; PRIORITY JOURNAL; SECONDARY HYPERPARATHYROIDISM; UREMIA; X CHROMOSOME INACTIVATION; ALLELE; GENETICS; HETEROZYGOSITY LOSS; HYPERPARATHYROIDISM; MIDDLE AGED;

MEN1 PROTEIN, HUMAN; ONCOPROTEIN; TUMOR PROTEIN;

ADULT; AGED; ALLELES; CHROMOSOME ABERRATIONS; HUMANS; HYPERPARATHYROIDISM; LOSS OF HETEROZYGOSITY; MIDDLE AGED; NEOPLASM PROTEINS; PROTO-ONCOGENE PROTEINS; UREMIA;

EID: 0036014931     PISSN: 10466673     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.ASN.0000018148.50109.C0     Document Type: Article

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