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

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

scientific article published on 01 November 2004

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2004 (fr) наукова стаття, опублікована в листопаді 2004 (uk) im November 2004 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 01 November 2004 (en) artículu científicu espublizáu en payares de 2004 (ast)
publication date	wds:Q80974820-41B54EBC-E96B-4EE4-B0D1-48DF11605215
publication date	2004-11-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q80974820-506AAF15-1FA5-4BEF-A9BA-A3B83A6DD280 wds:Q80974820-63372BA9-5CB3-4C80-B7FA-DD6964E5BD36 wds:Q80974820-71B97B31-D985-45CD-A95C-14AF0B964CA0 wds:Q80974820-7B729572-142B-4E37-8FFE-993A6B975429 wds:Q80974820-91A58633-282B-440E-BCA2-B6E89474161F wds:Q80974820-9B1E4EF4-EA48-4E76-BD25-4E2D1CECDDC0 wds:Q80974820-BDF80B52-2903-41DC-AE2E-6237D1CAA50F wds:Q80974820-CE62FBD6-0686-4EDD-B389-9F4604A9BCCF wds:Q80974820-D8D11728-68EF-49C2-8AF0-99A27ED7DC57 wds:Q80974820-DCB962F2-1F43-4632-9080-6C2CD684A337 wds:Q80974820-DECF8C77-A90F-4C0C-AA16-3AE5998F7A5E wds:Q80974820-FA0F158E-B3E5-49FF-B0BA-35A6ED6685D0
author name string	Aldo Pinchera Paolo Miccoli Paolo Viacava Claudio Marcocci Elena Pardi Filomena Cetani Luisella Cianferotti Elisabetta Gazzerro Elena Ambrogini Piero Berti Simona Borsari Giada Dipollina
rdfs:label	Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors (en) Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors (nl)
skos:prefLabel	Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors (en) Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors (nl)
name	Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors (en) Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors (nl)
author	wds:Q80974820-7113E04A-4446-4D7E-A5D7-0B5AAF72BD24
author	Giacomo Colussi
title	wds:Q80974820-76FCAB0E-02D9-4C07-9D51-094289BDA948
title	Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors (en)
page(s)	wds:Q80974820-1CB86C5A-9425-429F-BB4E-CD5A83682201
page(s)	5583-5591
instance of	wds:Q80974820-49D168B4-5C70-49B9-8E77-EE932B796619
instance of	scholarly article
main subject	wds:Q80974820-2A38D329-A1F0-42E2-A25F-A69418CE143A
main subject	primary hyperparathyroidism
PubMed ID	wds:Q80974820-105E3843-5FC4-4A2F-A891-6767FC0B7CD9
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/15531515
PubMed ID	15531515
published in	wds:Q80974820-1C6658A9-505B-4FEF-BD05-6FFDD5E50363
published in	The Journal of Clinical Endocrinology and Metabolism
issue	wds:Q80974820-F570105F-671C-49BD-840C-4C05A45017E2
volume	wds:Q80974820-713817F2-7EC2-4DCD-83A5-ED2C6364509E
issue	11
volume	89
DOI	wds:Q80974820-01BA8CF2-8E14-4A71-AB18-D128E0639CC5
DOI	http://dx.doi.org/10.1210/JC.2004-0294
DOI	10.1210/JC.2004-0294
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q80974820
is cites work of	The parafibromin tumor suppressor protein inhibits cell proliferation by repression of the c-myc proto-oncogene Molecular alterations in sporadic primary hyperparathyroidism Parafibromin as a diagnostic instrument for parathyroid carcinoma-lone ranger or part of the posse? Downregulation of CASR expression and global loss of parafibromin staining are strong negative determinants of prognosis in parathyroid carcinoma Parathyroid cancer Parathyroid carcinoma Parathyroid carcinoma Oncogenic microRNA-155 down-regulates tumor suppressor CDC73 and promotes oral squamous cell carcinoma cell proliferation: implications for cancer therapeutics Sex and age modify biochemical and skeletal manifestations of chronic hyperparathyroidism by altering target organ responses to Ca2+ and parathyroid hormone in mice Genetic and epigenetic changes in sporadic endocrine tumors: parathyroid tumors Clinical and molecular genetics of parathyroid neoplasms Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors. Hereditary hyperparathyroidism--a consensus report of the European Society of Endocrine Surgeons (ESES). Novel HRPT2/CDC73 gene mutations and loss of expression of parafibromin in Chinese patients with clinically sporadic parathyroid carcinomas Defective nucleolar localization and dominant interfering properties of a parafibromin L95P missense mutant causing the hyperparathyroidism-jaw tumor syndrome CDC73 mutations and parafibromin immunohistochemistry in parathyroid tumors: clinical correlations in a single-centre patient cohort Identification of De Novo Germline Mutations in the HRPT2 Gene in Two Apparently Sporadic Cases with Challenging Parathyroid Tumor Diagnoses Sporadic human renal tumors display frequent allelic imbalances and novel mutations of the HRPT2 gene Novel nonsense CDC73 mutations in Chinese patients with parathyroid tumors Bilaterality weighs more than unilateral multifocality in predicting prognosis in papillary thyroid cancer Transcriptional repression of tumor suppressor CDC73, encoding an RNA polymerase II interactor, by Wilms tumor 1 protein (WT1) promotes cell proliferation: implication for cancer therapeutics CDC73 mutational status and loss of parafibromin in the outcome of parathyroid cancer. Understanding the genetic basis of parathyroid carcinoma Hyperparathyroidism 2 gene (HRPT2, CDC73) and parafibromin studies in two patients with primary hyperparathyroidism and uncertain pathological assessment Parafibromin and APC as screening markers for malignant potential in atypical parathyroid adenomas. [Indication and performance of endocrine surgery. The significance of molecular genetic examination] Metastatic calcifications and severe hypercalcemia in a patient with parathyroid carcinoma Hyperparathyroidism-jaw tumor syndrome: a report of three large kindred Diagnosis and management of parathyroid cancer. Missense mutation in the MEN1 gene discovered through whole exome sequencing co-segregates with familial hyperparathyroidism. Fine-needle aspiration cytology of parathyroid carcinoma mimic hürthle cell thyroid neoplasm CDC73 intragenic deletion in familial primary hyperparathyroidism associated with parathyroid carcinoma Hyperparathyroidism-jaw tumor syndrome: Results of operative management An adolescent case of familial hyperparathyroidism with a germline frameshift mutation of the CDC73 gene Genetic basis of familial isolated hyperparathyroidism: a case series and a narrative review of the literature Molecular genetics of syndromic and non-syndromic forms of parathyroid carcinoma. The surgical strategy and the molecular analysis of patients with parathyroid cancer. Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 180 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software