(Q45907440)

http://europepmc.org/abstract/PMC/5698716

17 December 2017

5 references

3 October 2019

20 October 2019

18 December 2019

14 November 2020

8 December 2020

Molecular genetics of syndromic and non-syndromic forms of parathyroid carcinoma. (English)

1 reference

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17 December 2017

4 references

3 October 2019

20 October 2019

18 December 2019

14 November 2020

4 references

3 October 2019

20 October 2019

18 December 2019

14 November 2020

4 references

3 October 2019

20 October 2019

18 December 2019

14 November 2020

primary hyperparathyroidism

4 references

3 October 2019

20 October 2019

18 December 2019

14 November 2020

1 reference

3 October 2019

1 reference

3 April 2019

2 references

8 December 2020

2 references

14 November 2020

tumor suppressor proteins

1 reference

1 reference

20 October 2019

1 reference

18 December 2019

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28881068%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

author name string

Mark Stevenson

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28881068%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

Rajesh V Thakker

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28881068%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

language of work or name

1 reference

7 September 2017

1 reference

http://europepmc.org/abstract/PMC/5698716

17 December 2017

1 December 2017

8 references

13 March 2019

24 March 2019

3 April 2019

3 October 2019

20 October 2019

18 December 2019

14 November 2020

8 December 2020

9 references

13 March 2019

24 March 2019

3 April 2019

3 October 2019

20 October 2019

18 December 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28881068%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

14 November 2020

8 December 2020

38

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28881068%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

page(s)

1621-1648

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28881068%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28881068%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution

12 June 2020

copyright license

8 references

13 March 2019

24 March 2019

3 April 2019

3 October 2019

20 October 2019

18 December 2019

14 November 2020

8 December 2020

0 references

on focus list of Wikimedia project

ScienceSource

0 references

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24 May 2018

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24 May 2018

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24 May 2018

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24 May 2018

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24 May 2018

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24 May 2018

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24 May 2018

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24 May 2018

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24 May 2018

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24 May 2018

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24 May 2018

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24 May 2018

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Differential expression of microRNAs in human parathyroid carcinomas compared with normal parathyroid tissue

24 May 2018

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24 May 2018

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Activating and resistance mutations of EGFR in non-small-cell lung cancer: role in clinical response to EGFR tyrosine kinase inhibitors

24 May 2018

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Targeted overexpression of EZH2 in the mammary gland disrupts ductal morphogenesis and causes epithelial hyperplasia

24 May 2018

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Parathyroid carcinoma in multiple endocrine neoplasia type 1 with a classic germline mutation

24 May 2018

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24 May 2018

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Primary hyperparathyroidism and jaw tumor syndrome: a novel mutation of the HRPT2 gene

24 May 2018

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Human chorionic gonadotropin measurements in parathyroid carcinoma

24 May 2018

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Parafibromin, a component of the human PAF complex, regulates growth factors and is required for embryonic development and survival in adult mice

24 May 2018

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Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene

24 May 2018

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Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: lessons from recent developments in the IARC TP53 database

24 May 2018

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Activated beta-catenin in the novel human parathyroid tumor cell line sHPT-1.

24 May 2018

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Parafibromin inhibits cancer cell growth and causes G1 phase arrest

24 May 2018

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Parafibromin/Hyrax activates Wnt/Wg target gene transcription by direct association with beta-catenin/Armadillo

24 May 2018

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Familial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3-14

24 May 2018

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Dental findings in a family with hyperparathyroidism-jaw tumor syndrome and a novel HRPT2 gene mutation

24 May 2018

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The Polycomb group protein EZH2 directly controls DNA methylation

24 May 2018

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Utilisation of a cryptic non-canonical donor splice site of the gene encoding PARAFIBROMIN is associated with familial isolated primary hyperparathyroidism

24 May 2018

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The HRPT2 tumor suppressor gene product parafibromin associates with human PAF1 and RNA polymerase II

24 May 2018

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A systematic review of the diagnosis and treatment of primary hyperparathyroidism from 1995 to 2003.

24 May 2018

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A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing

24 May 2018

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The parafibromin tumor suppressor protein is part of a human Paf1 complex

24 May 2018

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A Novel IVS2-1G>A mutation causes aberrant splicing of the HRPT2 gene in a family with hyperparathyroidism-jaw tumor syndrome

24 May 2018

1 reference

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Parafibromin, product of the hyperparathyroidism-jaw tumor syndrome gene HRPT2, regulates cyclin D1/PRAD1 expression

24 May 2018

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Loss of parafibromin immunoreactivity is a distinguishing feature of parathyroid carcinoma

24 May 2018

1 reference

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Dependence receptors: between life and death.

24 May 2018

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Diseases associated with the extracellular calcium-sensing receptor

24 May 2018

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EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy

24 May 2018

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Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP)

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome.

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Somatic and Germ-Line Mutations of theHRPT2Gene in Sporadic Parathyroid Carcinoma

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Mutational and gross deletion study of the MEN1 gene and correlation with clinical features in Spanish patients

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Mutations of the BRAF gene in human cancer

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Inhibition of KIT tyrosine kinase activity: a novel molecular approach to the treatment of KIT-positive malignancies

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Familial isolated hyperparathyroidism: clinical and genetic characteristics of 36 kindreds

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

MEN-2A syndrome and pulmonary metastasis

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Familial isolated primary hyperparathyroidism--a multiple endocrine neoplasia type 1 variant?

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Hyperparathyroid and hypoparathyroid disorders

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Identification of MEN1 gene mutations in families with MEN 1 and related disorders

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Regulation of chromatin structure by site-specific histone H3 methyltransferases

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Familial hyperparathyroidism

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

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

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Two hundred eighty-six cases of parathyroid carcinoma treated in the U.S. between 1985-1995: a National Cancer Data Base Report. The American College of Surgeons Commission on Cancer and the American Cancer Society

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Identification of five novel germline mutations of the MEN1 gene in Japanese multiple endocrine neoplasia type 1 (MEN1) families

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Characterization of mutations in patients with multiple endocrine neoplasia type 1.

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

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

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

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

24 May 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

24 May 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

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

1 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

The molecular genetics of the multiple endocrine neoplasia syndromes

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Parathyroid carcinoma: a review of 62 patients

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Mutation and cancer: statistical study of retinoblastoma

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Parathyroid carcinoma: a collective review

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Parathyroid carcinoma.A study of 70 cases

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Natural history of parathyroid carcinoma. Diagnosis, treatment, and results

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Parathyroid carcinoma: clinical and pathologic features in 43 patients.

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Germline mutations of the MEN1 gene in Japanese kindred with multiple endocrine neoplasia type 1.

24 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

A radical revision of human genetics.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Hyperparathyroidism-jaw Tumor Syndrome: An Overlooked Cause of Severe Hypercalcemia.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

A Novel Mutation in a Patient with Hyperparathyroidism-Jaw Tumour Syndrome.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

EZH2 and ZFX oncogenes in malignant behaviour of parathyroid neoplasms.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

R248Q mutation--Beyond p53-DNA binding.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Whole-exome sequencing studies of parathyroid carcinomas reveal novel PRUNE2 mutations, distinctive mutational spectra related to APOBEC-catalyzed DNA mutagenesis and mutational enrichment in kinases associated with cell migration and invasion.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Identification of a germline mutation in the HRPT2 gene in a Chinese family with parathyroid carcinomas

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Familial isolated primary hyperparathyroidism/hyperparathyroidism-jaw tumour syndrome caused by germline gross deletion or point mutations of CDC73 gene in Chinese.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Missense mutation in the MEN1 gene discovered through whole exome sequencing co-segregates with familial hyperparathyroidism.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Intrathyroidal parathyroid carcinoma mimicking a thyroid nodule in a MEN type 1 patient

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Complete genomic landscape of a recurring sporadic parathyroid carcinoma.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

The microRNA cluster C19MC is deregulated in parathyroid tumours.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Hypermethylated in cancer 1 (HIC1), a tumor suppressor gene epigenetically deregulated in hyperparathyroid tumors by histone H3 lysine modification.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Detection of the first gross CDC73 germline deletion in an HPT-JT syndrome family.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

MafB interacts with Gcm2 and regulates parathyroid hormone expression and parathyroid development.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

The surgical strategy and the molecular analysis of patients with parathyroid cancer.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Parafibromin and APC as screening markers for malignant potential in atypical parathyroid adenomas.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

The effect of disease-associated HRPT2 mutations on splicing

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Parathyroid carcinoma with anaplastic feature: association of a p53 gene mutation with anaplastic transformation.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Familial hyperparathyroidism: surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutations.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Trends in the incidence and treatment of parathyroid cancer in the United States.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

A case of hyperparathyroidism-jaw tumour syndrome found in the treatment of an ossifying fibroma in the maxillary bone.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Parafibromin is a nuclear protein with a functional monopartite nuclear localization signal.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Diagnosis of parathyroid tumors in familial isolated hyperparathyroidism with HRPT2 mutation: implications for cancer surveillance.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Human malignant melanoma: detection of BRAF- and c-kit-activating mutations by high-resolution amplicon melting analysis

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Role of the RB1 family in stabilizing histone methylation at constitutive heterochromatin

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Novel intronic mutation of MEN1 gene causing familial isolated primary hyperparathyroidism

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Intragenic allelic loss and promoter hypermethylation of the RIZ1 tumor suppressor gene in parathyroid tumors and pheochromocytomas.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Trial to Predict Malignancy of Affected Parathyroid Glands in Primary Hyperparathyroidism

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

High prevalence of BRAF mutations in thyroid cancer: genetic evidence for constitutive activation of the RET/PTC-RAS-BRAF signaling pathway in papillary thyroid carcinoma

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Germline mutation profile of MEN1 in multiple endocrine neoplasia type 1: search for correlation between phenotype and the functional domains of the MEN1 protein.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Isolated familial hyperparathyroidism with a novel mutation of the MEN1 gene.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Multiple endocrine neoplasia type 1 (MEN1) gene mutations in a subset of patients with sporadic and familial primary hyperparathyroidism target the coding sequence but spare the promoter region.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

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

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

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

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Parathyroid carcinoma: 50-year experience at The Cleveland Clinic Foundation.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

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

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Prevalence of pheochromocytoma and hyperparathyroidism in multiple endocrine neoplasia type 2A: results of long-term follow-up.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

PRAD1 (cyclin D1): a parathyroid neoplasia gene on 11q13

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

CDC73 mutations and parafibromin immunohistochemistry in parathyroid tumors: clinical correlations in a single-centre patient cohort

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Downregulation of CASR expression and global loss of parafibromin staining are strong negative determinants of prognosis in parathyroid carcinoma

1 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

1 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5698716

Nephrolithiasis and bone involvement in primary hyperparathyroidism

1 December 2018

1 reference

12 December 2020

Alterations in the retinoblastoma pathway of cell cycle control in parathyroid tumors

1 reference

12 December 2020

Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases

1 reference

12 December 2020

Molecular characterization of parathyroid tumors from two patients with hereditary colorectal cancer syndromes

1 reference

12 December 2020

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

1 reference

12 December 2020

Nuclear Accumulation of B-Catenin in Human Endocrine Tumors: Association with Ki-67 (MIB-1) Proliferative Activity

1 reference

12 December 2020

Clinical Testing for Mutations in theMEN1Gene in Sweden: A Report on 200 Unrelated Cases

1 reference

12 December 2020

HRPT2 gene alterations in ossifying fibroma of the jaws

1 reference

12 December 2020

Mutational analyses of RB and BRCA2 as candidate tumour suppressor genes in parathyroid carcinoma

1 reference

12 December 2020

Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism-jaw tumour syndrome

1 reference

12 December 2020

10 Swiss kindreds with multiple endocrine neoplasia type 1: assessment of screening methods

1 reference

12 December 2020

Frequent Large GermlineHRPT2Deletions in a French National Cohort of Patients With Primary Hyperparathyroidism

1 reference

12 December 2020

Loss of parafibromin expression in a subset of parathyroid adenomas

1 reference

12 December 2020

Loss of the retinoblastoma tumor-suppressor gene in parathyroid carcinoma

1 reference

12 December 2020

Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene

1 reference

12 December 2020

Hereditary hyperparathyroidism associated with recurrent pancreatitis

1 reference

12 December 2020

Copy number variation in CCND1 gene is implicated in the pathogenesis of sporadic parathyroid carcinoma

1 reference

12 December 2020

Germline mutation of the multiple endocrine neoplasia type 1 (MEN1) gene in a family with primary hyperparathyroidism

1 reference

12 December 2020

Metastatic parathyroid carcinoma in the MEN2A syndrome

1 reference

12 December 2020

Carcinoma of two parathyroid glands caused by a novel MEN1 gene mutation - a rare feature of the MEN 1 syndrome

1 reference

12 December 2020

Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism

1 reference

12 December 2020

Absence of p53 point mutations in parathyroid adenoma and carcinoma

1 reference

12 December 2020

Identification of MEN1 and HRPT2 somatic mutations in paraffin-embedded (sporadic) parathyroid carcinomas

1 reference

12 December 2020

Parafibromin expression, single-gland involvement, and limited parathyroidectomy in familial isolated hyperparathyroidism

1 reference

12 December 2020

Surveillance for early detection of aggressive parathyroid disease: carcinoma and atypical adenoma in familial isolated hyperparathyroidism associated with a germline HRPT2 mutation

1 reference

12 December 2020

Genetic background influences embryonic lethality and the occurrence of neural tube defects in Men1 null mice: relevance to genetic modifiers

1 reference

12 December 2020

Parathyroid carcinoma: a 22-year experience

1 reference

12 December 2020

Incidence and prognosis of parathyroid gland carcinoma: a population-based study in The Netherlands estimating the preoperative diagnosis

1 reference

12 December 2020

Hyperparathyroidism-jaw tumor syndrome

1 reference

12 December 2020

Should parafibromin staining replace HRTP2 gene analysis as an additional tool for histologic diagnosis of parathyroid carcinoma?

1 reference

12 December 2020

HRPT2- (CDC73) RELATED HEREDITARY HYPERPARATHYROIDISM: A CASE SERIES FROM WESTERN INDIA

1 reference

12 December 2020

Hyperparathyroidism-jaw tumor syndrome: a report of three large kindred

1 reference

12 December 2020

Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13

1 reference

12 December 2020

Identification of De Novo Germline Mutations in the HRPT2 Gene in Two Apparently Sporadic Cases with Challenging Parathyroid Tumor Diagnoses

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

A newly recognized germline mutation of MEN1 gene identified in a patient with parathyroid adenoma and carcinoma

1 reference

12 December 2020

Letter 2: Intraoperative diagnosis and treatment of parathyroid cancer and atypical parathyroid adenoma (Br J Surg 2007; 94: 566-570)

1 reference

12 December 2020

Parathyroid carcinoma in a patient with non-secretory pituitary tumor: a variant of multiple endocrine neoplasia type-I?

1 reference

12 December 2020

Involvement of the MEN1 gene locus in familial isolated hyperparathyroidism

1 reference

12 December 2020

A novel CDC73 gene mutation in an Italian family with hyperparathyroidism-jaw tumour (HPT-JT) syndrome

1 reference

12 December 2020

Identification of the first germline HRPT2 whole-gene deletion in a patient with primary hyperparathyroidism

1 reference

12 December 2020

[Hyperparathyroidism-jaw tumor syndrome. A hereditary form of primary hyperparathyroidism with parathyroid carcinoma]

1 reference

12 December 2020

Genetic analyses in familial isolated hyperparathyroidism: implication for clinical assessment and surgical management

1 reference

12 December 2020

Parathyroid carcinoma in multiple endocrine neoplasia type 1 (MEN1) syndrome: two case reports of an unrecognised entity

1 reference

12 December 2020

Genetic analysis of the MEN1 gene and HPRT2 locus in two Italian kindreds with familial isolated hyperparathyroidism

1 reference

12 December 2020

Clinical studies of multiple endocrine neoplasia type 1 (MEN1)

1 reference

12 December 2020

Loss of nuclear expression of parafibromin distinguishes parathyroid carcinomas and hyperparathyroidism-jaw tumor (HPT-JT) syndrome-related adenomas from sporadic parathyroid adenomas and hyperplasias

1 reference

12 December 2020

p53 abnormalities in human parathyroid carcinoma

1 reference

12 December 2020

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

1 reference

12 December 2020

Differential expression of the calcium sensing receptor and combined loss of chromosomes 1q and 11q in parathyroid carcinoma

1 reference

12 December 2020

Re: Familial hyperparathyroidism: surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutations

1 reference

12 December 2020

Novel nonsense CDC73 mutations in Chinese patients with parathyroid tumors

1 reference

12 December 2020

Familial isolated primary hyperparathyroidism due to HRPT2 mutation

1 reference

12 December 2020

Hyperparathyroidism-jaw tumor syndrome: a case report

1 reference

12 December 2020

Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome

1 reference

12 December 2020

Parafibromin immunoreactivity: its use as an additional diagnostic marker for parathyroid tumor classification

1 reference

12 December 2020

Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors

1 reference

12 December 2020

Overexpression and genetic abnormality of p53 in parathyroid adenomas

1 reference

12 December 2020

Hyperparathyroidism-jaw tumor syndrome: a case report

1 reference

12 December 2020

Concurrent parathyroid adenomas and carcinoma in the setting of multiple endocrine neoplasia type 1: presentation as hypercalcemic crisis

1 reference

12 December 2020

Multiple endocrine neoplasia--syndromes of the twentieth century

1 reference

12 December 2020

Novel V184E MEN1 germline mutation in a Japanese kindred with familial hyperparathyroidism

1 reference

12 December 2020

HRPT2 mutational analysis of typical sporadic parathyroid adenomas

1 reference

12 December 2020

Loss of heterozygosity of selected tumor suppressor genes in parathyroid carcinoma

1 reference

12 December 2020

A novel mutation of the MEN1 gene in a Japanese kindred with familial isolated primary hyperparathyroidism

1 reference

12 December 2020

Accuracy of combined protein gene product 9.5 and parafibromin markers for immunohistochemical diagnosis of parathyroid carcinoma

1 reference

12 December 2020

Beta-catenin activation is not involved in sporadic parathyroid carcinomas and adenomas

1 reference

12 December 2020

A novel splice site mutation of the MEN1 gene identified in a patient with primary hyperparathyroidism

1 reference

12 December 2020

1 reference

12 December 2020

Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism

1 reference

12 December 2020

[An uncommon cause of hypercalcemia: synchronous carcinoma of two parathyroids in the context of hyperparathyroidism-jaw tumor syndrome]

1 reference

12 December 2020

Two hundred eighty-six cases of parathyroid carcinoma treated in the U.S. between 1985-1995

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FHUMU.23337

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1002/HUMU.23337

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28881068%20AND%20SRC:MED&resulttype=core&format=json

release_hjid4jpl5fh47f6lxezhjywvyi

12 June 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/hjid4jpl5fh47f6lxezhjywvyi

24 November 2022

mapped directly with Wikidata item

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28881068%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

1 reference