Accumulation of allelic changes at chromosomes 7p, 18q, and 2 in parathyroid lesions of uremic patients

Laboratory Investigation

Volumn 81, Issue 4, 2001, Pages 527-533

  Nagy, Anetta ^a   Chudek, Jerzy ^b   Kovacs, Gyula ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b MEDICAL UNIVERSITY OF SILESIA   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

CALCITRIOL;

ADULT; AGED; ALLELE; ARTICLE; CHROMOSOME 18Q; CHROMOSOME 2; CHROMOSOME 7P; CHROMOSOME ABERRATION; CLINICAL ARTICLE; FEMALE; HUMAN; HUMAN TISSUE; HYPERPARATHYROIDISM; KIDNEY FAILURE; MALE; PRIORITY JOURNAL; SECONDARY HYPERPARATHYROIDISM; UREMIA; X CHROMOSOME; X CHROMOSOME INACTIVATION; Y CHROMOSOME;

EID: 0035044510     PISSN: 00236837     EISSN: None     Source Type: Journal    
DOI: 10.1038/labinvest.3780261     Document Type: Article

References (22)

1. Monoclonality of parathyroid tumors in chronic renal failure and in primary parathyroid hyperplasia
2. Molecular mechanisms of parathyroid hyperplasia and neoplasia
3. Analysis of the RAD54 gene on chromosome 1p as a potential tumor-suppressor gene in parathyroid adenomas
4. No evidence for mutations in the calcium-sensing receptor gene in sporadic parathyroid adenomas
5. Deletion mapping of endocrine tumors localizes a second tumor suppressor gene on chromosome band 11q13
6. Genetic abnormalities in parathyroid nodules of uremic patients
7. Frequent loss of chromosome arm 1p DNA in parathyroid adenomas
8. Point mutations of the human parathyroid calcium receptor gene are not responsible for non-suppressible renal hyperparathyroidism
9. Alternative genetic pathways in parathyroid tumorigenesis
10. Cell biology of parathyroid hyperplasia in uraemia
11. 3receptor density is associated with a more severe form of parathyroid hyperplasia in chronic uremic patients
12. Parathyroid hyperplasia in tertiary hyperparathyroidism: A pathological and immunohistochemical reappraisal
13. Somatic mutation of the MEN1 gene in parathyroid tumours
14. 2+-sensing receptor gene in human parathyroid tumors
15. Microsatellite instability and loss of heterozygosity in primary and secondary proliferative lesions of the parathyroid gland
16. Apoptosis and growth factors in parathyroid adenomas
17. Sex identification by polymerase chain reaction by using X-Y homologous primer
18. Novel chromosomal abnormalities identified by comparative genomic hybridization in parathyroid adenomas
19. The role of the parathyroid glands in the uremic syndrome
20. Rearrangement and overexpression of D11S287E, a candidate oncogene on chromosome 11q13 in benign parathyroid tumors
21. Genomic localization of novel candidate tumor suppressor gene loci in human parathyroid adenomas
22. Parathyroid tumor suppressor on 1p: Analysis of the p18 cyclin-dependent kinase inhibitor gene as a candidate