Genetic analysis of lithium-associated parathyroid tumors

European Journal of Endocrinology

Volumn 146, Issue 5, 2002, Pages 619-627

  Dwight, T ^a   Kytola S ^a   Teh, B T ^a   Theodosopoulos, G ^a   Richardson, A L ^a   Philips, J ^a   Twigg, S ^a   Delbridge, L ^a   Marsh, D J ^a   Nelson, A E ^a   Larsson, C ^a   Robinson, B G ^a  

^a ROYAL NORTH SHORE HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

LITHIUM;

ADULT; AGED; ARTICLE; CARCINOGENESIS; CHROMOSOME 11; CHROMOSOME 15Q; CHROMOSOME 1P; CHROMOSOME 22Q; CHROMOSOME ABERRATION; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; DISEASE ASSOCIATION; FEMALE; FISHER EXACT TEST; GENE MUTATION; GENETIC ANALYSIS; HETEROZYGOSITY LOSS; HUMAN; HYPERPARATHYROIDISM; MALE; MULTIPLE ENDOCRINE NEOPLASIA; NUCLEOTIDE SEQUENCE; PARATHYROID TUMOR; PREVALENCE; PRIORITY JOURNAL; X CHROMOSOME;

EID: 0036106464     PISSN: 08044643     EISSN: None     Source Type: Journal    
DOI: 10.1530/eje.0.1460619     Document Type: Article

References (42)

1. Hyperparathyroidism associated with treatment of manic-depressive disorders by lithium
2. Lithium-induced alterations in parathyroid cell function: Insight into the pathogenesis of lithium-associated hyperparathyroidism
3. Hypothyroidism and hyperparathyroidism associated with lithium
4. Lithium-induced parathyroid dysfunction: A case report and review of the literature
5. Pathology and outcome of surgical treatment for lithium-associated hyperparathyroidism
6. Endocrine effects of lithium: II. Primary hyperparathyroidism
7. Hyperparathyroidism, hypothyroidism, and impaired renal function after 10 to 20 years of lithium treatment
8. Primary hyperparathyroidism
9. Regulation of signal transduction pathways and gene expression by mood stabilizers and antidepressants
10. Lithium stimulates gene expression through the AP-1 transcription factor pathway
11. Identification of somatic mutations of the MEN1 gene in sporadic endocrine tumours
12. Loss of heterozygosity in sporadic parathyroid tumours: Involvement of chromosome 1 and the MEN1 gene locus in 11q13
13. Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism
14. Identification of MEN1 gene mutations in families with MEN 1 and related disorders
15. Criteria for mutation analysis in MEN 1-suspected patients: MEN 1 case-finding
16. Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: A clinically and genetically distinct syndrome
17. Hereditary hyperparathyroidism jaw tumor syndrome - The endocrine tumor gene HRPT2 maps to chromosome 1q21-q31
18. Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease - Linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas
19. A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome
20. Frequent loss of chromosome arm 1p DNA in parathyroid adenomas
21. Genomic localization of novel candidate tumor suppressor gene loci in human parathyroid adenomas
22. Differential loss of heterozygosity in familial, sporadic, and uremic hyperparathyroidism
23. Comparative genomic hybridization analysis of human parathyroid tumors
24. Novel chromosomal abnormalities identified by comparative genomic hybridization in parathyroid adenomas
25. Familial isolated hyperparathyroidism maps to the hyperparathyroidism - Jaw tumor locus in 1q21-q32 in a subset of families
26. Alternative genetic pathways in parathyroid tumorigenesis
27. Patterns of chromosomal imbalances in parathyroid carcinomas
28. Morphology, DNA ploidy and allele losses on chromosome 11 in sporadic hyperparathyroidism and that associated with multiple neoplasia, type 1
29. Deletion of genes on chromosome 1 in endocrine neoplasia
30. Comprehensive genetic map of the human genome based on 5,264 microsatellites
31. Eighteen new polymorphic markers in the multiple endocrine neoplasia type 1 (men1) region
32. Positional cloning of the gene for multiple endocrine neoplasia-type 1
33. Monoclonality of parathyroid tumors in chronic renal failure and in primary parathyroid hyperplasia
34. Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1
35. Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11
36. Allelic loss from chromosome 11 in parathyroid tumors
37. Localisation of a gene causing endocrine neoplasia to a 4 cM region on chromosome 1p35-p36
38. Characterization of the mouse men1 gene and its expression during development
39. Structure and distribution of rat menin mRNA
40. Bipolar affective disorder
41. Lithium induces abnormal calcium-regulated PTH release in dispersed bovine parathyroid cells
42. The normal parathyroid gland