CDC73 mutations and parafibromin immunohistochemistry in parathyroid tumors: clinical correlations in a single-centre patient cohort (Q57748219)

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article by Vito Guarnieri et al published 18 September 2012 in Cellular Oncology

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English	CDC73 mutations and parafibromin immunohistochemistry in parathyroid tumors: clinical correlations in a single-centre patient cohort	article by Vito Guarnieri et al published 18 September 2012 in Cellular Oncology

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scholarly article

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

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immunohistochemistry

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Nazzarena Malavolta

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Nazzarena Malavolta

18

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Vito Guarnieri

1

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Lucia Anna Muscarella

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Lucia Anna Muscarella

3

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Sabrina Corbetta

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Sabrina Corbetta

13

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Evaristo Maiello

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Evaristo Maiello

7

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Elisabetta Romagnoli

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Elisabetta Romagnoli

12

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Iacopo Chiodini

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Iacopo Chiodini

9

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Massimo Carella

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Massimo Carella

19

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16

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Anna Spada

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author name string

Claudia Battista

2

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Michele Bisceglia

4

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Danilo de Martino

5

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Filomena Baorda

6

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Leonardo D’Agruma

8

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Celeste Clemente

10

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Salvatore Minisola

11

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Raffaella Viti

14

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Cristina Eller-Vainicher

15

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Michela Iacobellis

17

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Lucie Canaff

20

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Geoffrey N. Hendy

21

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David E. C. Cole

22

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Alfredo Scillitani

23

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publication date

18 September 2012

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Cellular Oncology

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35

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411-422

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6

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https://scigraph.springernature.com/pub.10.1007/s13402-012-0100-x

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Hyperparathyroid and hypoparathyroid disorders

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https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

Clinical and molecular genetics of parathyroid neoplasms

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https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

Parathyroid cancer

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https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

Parathyroid carcinoma.A study of 70 cases

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https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

Challenging lesions in the differential diagnosis of endocrine tumors: parathyroid carcinoma

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https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

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

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https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

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

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https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

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

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https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours

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https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

Loss of parafibromin immunoreactivity is a distinguishing feature of parathyroid carcinoma

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https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

Defining a molecular phenotype for benign and malignant parathyroid tumors

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https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

Calcium-sensing receptor (CASR) mutations in hypercalcemic states: studies from a single endocrine clinic over three years

1 reference

https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

Cancer. Haploinsufficient gene selection in cancer.

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https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

Absence of nucleolar parafibromin immunoreactivity in subsets of parathyroid malignant tumours.

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https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

Rapid mutation screening for HRPT2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidism

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https://api.crossref.org/works/10.1007%2FS13402-012-0100-X

21 January 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22987117

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of parafibromin expression in a subset of parathyroid adenomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/22987117

12 December 2020

based on heuristic

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

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https://pubmed.ncbi.nlm.nih.gov/22987117

12 December 2020

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Parathyroid carcinoma

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https://pubmed.ncbi.nlm.nih.gov/22987117

12 December 2020

based on heuristic

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22987117

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22987117

12 December 2020

based on heuristic

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Clinical course of metastatic parathyroid cancer

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https://pubmed.ncbi.nlm.nih.gov/22987117

12 December 2020

based on heuristic

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22987117

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HRPT2 mutational analysis of typical sporadic parathyroid adenomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/22987117

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelotype of posterior uveal melanoma: implications for a bifurcated tumor progression pathway

1 reference

https://pubmed.ncbi.nlm.nih.gov/22987117

12 December 2020

based on heuristic

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22987117

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22987117

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22987117

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22987117

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of loss of heterozygosity/allelic imbalance scoring in tumor DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/22987117

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22987117

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S13402-012-0100-X

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