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

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

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

http://www.wikidata.org/entity/Q33209570

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Cherubism: best clinical practice Transcriptional activators enhance polyadenylation of mRNA precursors The parafibromin tumor suppressor protein inhibits cell proliferation by repression of the c-myc proto-oncogene The PAF complex synergizes with MLL fusion proteins at HOX loci to promote leukemogenesis Parathyroid cancer Genetic and epigenetic changes in sporadic endocrine tumors: parathyroid tumors Cdc73 Subunit of Paf1 Complex Contains C-terminal Ras-like Domain That Promotes Association of Paf1 Complex with Chromatin The Paf1 complex is required for efficient transcription elongation by RNA polymerase I The RNA polymerase-associated factor 1 complex (Paf1C) directly increases the elongation rate of RNA polymerase I and is required for efficient regulation of rRNA synthesis.Hyperparathyroidism jaw tumour syndrome: a pictoral review Genomic profiling reveals mutational landscape in parathyroid carcinomas The parafibromin tumor suppressor protein interacts with actin-binding proteins actinin-2 and actinin-3.The human RNA polymerase II-associated factor 1 (hPaf1): a new regulator of cell-cycle progression.The tumor suppressor, parafibromin, mediates histone H3 K9 methylation for cyclin D1 repression.Characterization of a new CDC73 missense mutation that impairs Parafibromin expression and nucleolar localization.Mice deleted for cell division cycle 73 gene develop parathyroid and uterine tumours: model for the hyperparathyroidism-jaw tumour syndrome Genome-wide and locus specific alterations in CDC73/HRPT2-mutated parathyroid tumors.Fibro-osseous lesions of the craniofacial skeleton: an update.Parathyroid cancer.Defective nucleolar localization and dominant interfering properties of a parafibromin L95P missense mutant causing the hyperparathyroidism-jaw tumor syndrome.Cytoplasmic polyadenylation element binding protein is a conserved target of tumor suppressor HRPT2/CDC73.Parathyroid carcinoma: current understanding and new insights into gene expression and intraoperative parathyroid hormone kinetics An adolescent case of familial hyperparathyroidism with a germline frameshift mutation of the CDC73 gene.Meta-analysis reveals conserved cell cycle transcriptional network across multiple human cell types.Downregulated parafibromin expression is a promising marker for pathogenesis, invasion, metastasis and prognosis of gastric carcinomas.The many roles of the conserved eukaryotic Paf1 complex in regulating transcription, histone modifications, and disease states.Bruton's tyrosine kinase revealed as a negative regulator of Wnt-beta-catenin signaling.IL-1β-specific recruitment of GCN5 histone acetyltransferase induces the release of PAF1 from chromatin for the de-repression of inflammatory response genes.Decreased expression of calcium-sensing receptor and parafibromin in secondary hyperparathyroidism with an abnormal whole PTH/intact PTH ratio.Non-functional parathyroid carcinoma: a review of the literature and report of a case requiring extensive surgery.CDC73 gene mutations in sporadic ossifying fibroma of the jaws.The Paf1 complex: platform or player in RNA polymerase II transcription?Diagnosis and management of parathyroid cancer.Molecular diagnosis of primary hyperparathyroidism in familial cancer syndromes.Genetic basis of familial isolated hyperparathyroidism: a case series and a narrative review of the literature.Molecular genetics and epigenetics of nonfamilial (sporadic) parathyroid tumours.Ctr9, a Key Component of the Paf1 Complex, Affects Proliferation and Terminal Differentiation in the Developing Drosophila Nervous System.The clinicopathological significances and biological functions of parafibromin expression in head and neck squamous cell carcinomas.Molecular diagnosis of parathyroid carcinoma: a reality in the near future.Parafibromin tumor suppressor enhances cell growth in the cells expressing SV40 large T antigen.

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P2860

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

http://www.wikidata.org/entity/Q33209570

description

2005 nî lūn-bûn

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2005 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2005 թվականի փետրվարին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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Parafibromin, product of the h ...... es cyclin D1/PRAD1 expression.

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Parafibromin, product of the h ...... es cyclin D1/PRAD1 expression.

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Parafibromin, product of the h ...... es cyclin D1/PRAD1 expression.

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Parafibromin, product of the h ...... es cyclin D1/PRAD1 expression.

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Parafibromin, product of the h ...... es cyclin D1/PRAD1 expression.

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Parafibromin, product of the h ...... es cyclin D1/PRAD1 expression.

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Parafibromin, product of the h ...... es cyclin D1/PRAD1 expression.

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Geoffrey E Woodard

http://www.w3.org/2001/XMLSchema#string

Jian-Hua Zhang

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Ling Lin

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Stephen J Marx

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Sunita K Agarwal

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William F Simonds

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P2860

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

HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours

Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma.

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

Parathyroid carcinoma in familial hyperparathyroidism

Fibrous dysplasia of the bone. Review of twenty-four cases.

Familial hyperparathyroidism associated with jaw fibroma: case report and literature review.

P2888

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1272-1276

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7

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24

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Sunita K Agarwal

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8148173

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15580289

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hyperparathyroidism

hyperparathyroidism-jaw tumor syndrome