(Q34437592)

2 August 2017

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title

Molecular mechanisms of primary hyperparathyroidism (English)

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2 August 2017

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Hendy GN

1

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2 August 2017

1 November 2000

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Reviews in Endocrine and Metabolic Disorders

2 August 2017

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2 August 2017

1

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2 August 2017

297-305

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2 August 2017

4

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https://scigraph.springernature.com/pub.10.1023/a:1026518502081

2 August 2017

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cites work

p53 abnormalities in human parathyroid carcinoma

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic abnormalities in sporadic parathyroid adenomas

1 reference

12 December 2020

Mechanism of cyclin D1 (CCND1, PRAD1) overexpression in human cancer cells: analysis of allele-specific expression

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families

1 reference

12 December 2020

Frequent loss of chromosome arm 1p DNA in parathyroid adenomas

1 reference

12 December 2020

Mutation analysis of glial cell line-derived neurotrophic factor, a ligand for an RET/coreceptor complex, in multiple endocrine neoplasia type 2 and sporadic neuroendocrine tumors

1 reference

12 December 2020

Role of p53 mutations in endocrine tumorigenesis: mutation detection by polymerase chain reaction-single strand conformation polymorphism

1 reference

12 December 2020

Loss of chromosome arm 9p DNA and analysis of the p16 and p15 cyclin-dependent kinase inhibitor genes in human parathyroid adenomas

1 reference

12 December 2020

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.

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12 December 2020

Parathyroid adenoma with t(1;5)(p22;q32) as the sole clonal chromosome abnormality

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12 December 2020

Probable clonal origin of aldosteronomas versus multicellular origin of parathyroid "adenomas"

1 reference

12 December 2020

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

1 reference

12 December 2020

Parathyroid tumor suppressor on 1p: analysis of the p18 cyclin-dependent kinase inhibitor gene as a candidate

1 reference

12 December 2020

Localisation of a gene causing endocrine neoplasia to a 4 cM region on chromosome 1p35-p36.

1 reference

12 December 2020

Structural analysis of gene marker loci on chromosomes 10 and 11 in primary and secondary uraemic hyperparathyroidism

1 reference

12 December 2020

Genetic abnormalities in sporadic parathyroid adenomas: loss of heterozygosity for chromosome 3q markers flanking the calcium receptor locus

1 reference

12 December 2020

Loss of the retinoblastoma tumor-suppressor gene in parathyroid carcinoma

1 reference

12 December 2020

Genomic localization of novel candidate tumor suppressor gene loci in human parathyroid adenomas

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12 December 2020

The hypocalciuric or benign variant of familial hypercalcemia: clinical and biochemical features in fifteen kindreds

1 reference

12 December 2020

Novel Chromosomal Abnormalities Identified by Comparative Genomic Hybridization in Parathyroid Adenomas1

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12 December 2020

Allelic loss on chromosome 11 is uncommon in parathyroid glands of patients with hypercalcaemic secondary hyperparathyroidism

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12 December 2020

Alternative genetic pathways in parathyroid tumorigenesis

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12 December 2020

Expression of cyclin D1 in parathyroid carcinomas, adenomas, and hyperplasias: a paraffin immunohistochemical study

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12 December 2020

Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic basis of endocrine disease 5. Molecular genetics of parathyroid gland neoplasia

1 reference

12 December 2020

Analysis of the RAD54 gene on chromosome 1p as a potential tumor-suppressor gene in parathyroid adenomas

1 reference

12 December 2020

Expression of PRAD1/cyclin D1, retinoblastoma gene products, and Ki67 in parathyroid hyperplasia caused by chronic renal failure versus primary adenoma

1 reference

12 December 2020

Multicellular origin of parathyroid "adenomas"

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12 December 2020

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

1 reference

12 December 2020

Reduced immunostaining for the extracellular Ca2+-sensing receptor in primary and uremic secondary hyperparathyroidism

1 reference

12 December 2020

Multiple endocrine neoplasia type 1: clinical and genetic features of the hereditary endocrine neoplasias.

1 reference

12 December 2020

Familial isolated primary hyperparathyroidism.

1 reference

12 December 2020

Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype

1 reference

12 December 2020

Nucleotide sequence of cloned cDNAs encoding human preproparathyroid hormone

1 reference

12 December 2020

Mapping of the calcium-sensing receptor gene (CASR) to human chromosome 3q13.3-21 by fluorescence in situ hybridization, and localization to rat chromosome 11 and mouse chromosome 16.

1 reference

12 December 2020

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

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12 December 2020

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

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12 December 2020

Stable overexpression of MEN1 suppresses tumorigenicity of RAS.

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12 December 2020

Nucleotide sequence of the human parathyroid hormone gene

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12 December 2020

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

1 reference

12 December 2020

Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31

1 reference

12 December 2020

Multiple endocrine neoplasia type 1.

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12 December 2020

Cell cycle regulation of menin expression

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12 December 2020

Hypercalcemia and ectopic secretion of parathyroid hormone by an ovarian carcinoma with rearrangement of the gene for parathyroid hormone

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12 December 2020

No evidence for mutations in the calcium-sensing receptor gene in sporadic parathyroid adenomas.

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12 December 2020

Depressed expression of calcium receptor in parathyroid gland tissue of patients with hyperparathyroidism.

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12 December 2020

Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma.

1 reference

12 December 2020

Ectopic production of parathyroid hormone by small cell lung cancer in a patient with hypercalcemia

1 reference

12 December 2020

Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1

1 reference

12 December 2020

Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC.

1 reference

12 December 2020

Familial benign hypercalcemia (hypocalciuric hypercalcemia). Clinical and pathogenetic studies in 21 families

1 reference

12 December 2020

Tumor-specific decreased expression of calcium sensing receptor messenger ribonucleic acid in sporadic primary hyperparathyroidism

1 reference

12 December 2020

Mapping the Gene Causing Hereditary Primary Hyperparathyroidism in a Portuguese Kindred to Chromosome 1q22-q31

1 reference

12 December 2020

Insertion of an Alu sequence in the Ca(2+)-sensing receptor gene in familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

1 reference

12 December 2020

Allelic loss of the retinoblastoma tumor suppressor gene: a marker for aggressive parathyroid tumors?

1 reference

12 December 2020

Mutational analysis of the extracellular Ca(2+)-sensing receptor gene in human parathyroid tumors

1 reference

12 December 2020

Role of the RET proto-oncogene in sporadic hyperparathyroidism and in hyperparathyroidism of multiple endocrine neoplasia type 2.

1 reference

12 December 2020

Production of parathyroid hormone by a malignant nonparathyroid tumor in a hypercalcemic patient

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12 December 2020

Comparative genomic hybridization analysis of human parathyroid tumors

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12 December 2020

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

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12 December 2020

A novel cyclin encoded by a bcl1-linked candidate oncogene

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12 December 2020

The cyclins and cyclin-dependent kinase inhibitors in hormonal regulation of proliferation and differentiation

1 reference

12 December 2020

Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism

1 reference

12 December 2020

Absence of p53 point mutations in parathyroid adenoma and carcinoma

1 reference

12 December 2020

Monoclonality and abnormal parathyroid hormone genes in parathyroid adenomas

1 reference

12 December 2020

Identifiers

DOI

10.1023/A:1026518502081

1 reference

PubMed ID

11706744

Dimensions Publication ID

2 August 2017

0 references

1 reference

PubMed ID

11706744