Molecular pathology of parathyroid tumors (Q31889854)

4 July 2017

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title

Molecular pathology of parathyroid tumors (English)

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4 July 2017

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Carling T

1

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4 July 2017

publication date

1 March 2001

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Trends in Endocrinology and Metabolism

4 July 2017

published in

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4 July 2017

volume

12

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4 July 2017

issue

2

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4 July 2017

page(s)

53-58

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Population-based screening for primary hyperparathyroidism with serum calcium and parathyroid hormone values in menopausal women

4 July 2017

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Decreased 1,25-dihydroxyvitamin D3 receptor density is associated with a more severe form of parathyroid hyperplasia in chronic uremic patients.

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Regulation of parathyroid hormone release and cytosolic calcium by extracellular calcium in dispersed and cultured bovine and pathological human parathyroid cells

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Vitamin D receptor (VDR) and parathyroid hormone messenger ribonucleic acid levels correspond to polymorphic VDR alleles in human parathyroid tumors

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Vitamin D receptors and hyperparathyroidism

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Vitamin D receptor genotype is associated with cortical bone loss in Japanese patients with primary hyperparathyroidism

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Differences in vitamin D receptor genotype and geographical variation in osteoporosis

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7 January 2021

Monoclonality and abnormal parathyroid hormone genes in parathyroid adenomas

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Monoclonality of parathyroid tumors in chronic renal failure and in primary parathyroid hyperplasia

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Loss of the retinoblastoma tumor-suppressor gene in parathyroid carcinoma

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7 January 2021

Molecular cloning and chromosomal mapping of DNA rearranged with the parathyroid hormone gene in a parathyroid adenoma

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A novel cyclin encoded by a bcl1-linked candidate oncogene

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Cyclin D1/PRAD1 as a central target in oncogenesis

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7 January 2021

Cyclin D1/PRAD1 expression in parathyroid adenomas: an immunohistochemical study

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Function of a human cyclin gene as an oncogene

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Novel Chromosomal Abnormalities Identified by Comparative Genomic Hybridization in Parathyroid Adenomas

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7 January 2021

Somatic mutation of the MEN1 gene in parathyroid tumours

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7 January 2021

Parathyroid Tumor Suppressor on 1p: Analysis of the p18 Cyclin-Dependent Kinase Inhibitor Gene As a Candidate

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7 January 2021

RAD51 as a candidate parathyroid tumour suppressor gene on chromosome 15q: absence of somatic mutations

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7 January 2021

Analysis of theRAD54 gene on chromosome 1p as a potential tumor-suppressor gene in parathyroid adenomas

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7 January 2021

Functional collaboration between different cyclin-dependent kinase inhibitors suppresses tumor growth with distinct tissue specificity

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7 January 2021

RB-mediated suppression of spontaneous multiple neuroendocrine neoplasia and lung metastases in Rb+/- mice

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7 January 2021

Loss of heterozygosity studies at the retinoblastoma and breast cancer susceptibility (BRCA2) loci in pituitary, parathyroid, pancreatic and carcinoid tumours

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7 January 2021

Comparative genomic hybridization analysis of human parathyroid tumors

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7 January 2021

Positional cloning of the gene for multiple endocrine neoplasia-type 1

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7 January 2021

Menin, the product of the MEN1 gene, is a nuclear protein

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7 January 2021

Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription

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7 January 2021

Primary hyperparathyroidism in multiple endocrine neoplasia type IIa: retrospective French multicentric study. Groupe d'Etude des Tumeurs á Calcitonine (GETC, French Calcitonin Tumors Study Group), French Association of Endocrine Surgeons

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7 January 2021

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

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7 January 2021

Genetic studies of a family with hereditary hyperparathyroidism-jaw tumour syndrome.

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7 January 2021

Familial hyperparathyroidism without multiple endocrine neoplasia

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7 January 2021

A family with isolated hyperparathyroidism segregating a missense MEN1 mutation and showing loss of the wild-type alleles in the parathyroid tumors

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7 January 2021

Familial isolated hyperparathyroidism as a variant of multiple endocrine neoplasia type 1 in a large Danish pedigree

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7 January 2021

Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

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7 January 2021

Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13

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7 January 2021

Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptor

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7 January 2021

10.1016/S1043-2760(00)00345-3

Identifiers

DOI

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4 July 2017

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