Loss of RB1 induces non-proliferative retinoma: increasing genomic instability correlates with progression to retinoblastoma. - Wikidata - awgldk - TriplyDB

Loss of RB1 induces non-proliferative retinoma: increasing genomic instability correlates with progression to retinoblastoma.

Loss of RB1 induces non-proliferative retinoma: increasing genomic instability correlates with progression to retinoblastoma.

http://www.wikidata.org/entity/Q50335530

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Loss of pRB causes centromere dysfunction and chromosomal instability Genetic perspective of retinoblastoma: From present to future Twists in views on RB functions in cellular signaling, metabolism and stem cells Understanding pRb: toward the necessary development of targeted treatments for retinoblastoma Adult onset retinoblastoma Ocular expression and distribution of products of the POAG-associated chromosome 9p21 gene region Genetic variations strongly influence phenotypic outcome in the mouse retina.Cdh11 acts as a tumor suppressor in a murine retinoblastoma model by facilitating tumor cell death.Overexpression of pyruvate dehydrogenase kinase 1 in retinoblastoma: A potential therapeutic opportunity for targeting vitreous seeds and hypoxic regions.Mutation spectrum of RB1 mutations in retinoblastoma cases from Singapore with implications for genetic management and counselling Genetic and Epigenetic Discoveries in Human Retinoblastoma Analysis of retinoblastoma age incidence data using a fully stochastic cancer model.Expression levels of autophagy related proteins and their prognostic significance in retinocytoma and retinoblastoma.Regulation of p14ARF expression by miR-24: a potential mechanism compromising the p53 response during retinoblastoma development.Analysis of MDM2 and MDM4 single nucleotide polymorphisms, mRNA splicing and protein expression in retinoblastoma.Retinoblastoma. Fifty years of progress. The LXXI Edward Jackson Memorial Lecture.The motor protein KIF14 inhibits tumor growth and cancer metastasis in lung adenocarcinoma Tumorspheres but not adherent cells derived from retinoblastoma tumors are of malignant origin.STAT3 inhibition suppresses proliferation of retinoblastoma through down-regulation of positive feedback loop of STAT3/miR-17-92 clusters.p16(INK4a) expression in retinoblastoma: a marker of differentiation grade.Transcriptional and epigenetic regulation of KIF14 overexpression in ovarian cancer.Direct involvement of retinoblastoma family proteins in DNA repair by non-homologous end-joining.Cancer genetics education in a low- to middle-income country: evaluation of an interactive workshop for clinicians in Kenya.Retinoblastoma genetics in India: From research to implementation.Retinoblastoma: Recent trends A mini review based on published literature.A Parent-of-Origin Effect Impacts the Phenotype in Low Penetrance Retinoblastoma Families Segregating the c.1981C>T/p.Arg661Trp Mutation of RB1 Loss of photoreceptorness and gain of genomic alterations in retinoblastoma reveal tumor progression.A Meta-Analysis of Retinoblastoma Copy Numbers Refines the List of Possible Driver Genes Involved in Tumor Progression.Intra-Arterial Chemotherapy as Primary Therapy for Retinoblastoma in Infants Less than 3 Months of Age: A Series of 10 Case-Studies.Next generation sequencing in sporadic retinoblastoma patients reveals somatic mosaicism Characterization and pharmacologic targeting of EZH2, a fetal retinal protein and epigenetic regulator, in human retinoblastoma.Role of B lymphoma Mo-MLV insertion region 1 in the oncogenic behavior of retinoblastomas.Somatic genomic alterations in retinoblastoma beyond RB1 are rare and limited to copy number changes.Expression of p14ARF, MDM2, and MDM4 in human retinoblastoma.The functional loss of the retinoblastoma tumour suppressor is a common event in basal-like and luminal B breast carcinomas Overexpression of the cellular DEK protein promotes epithelial transformation in vitro and in vivo Cross-species genomic and epigenomic landscape of retinoblastoma.Germline mutations in retinoma patients: relevance to low-penetrance and low-expressivity molecular basis.Insights from mouse models into human retinoblastoma Molecular karyotype of sporadic unilateral retinoblastoma tumors.

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Loss of RB1 induces non-proliferative retinoma: increasing genomic instability correlates with progression to retinoblastoma.

http://www.wikidata.org/entity/Q50335530

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2008年学术文章

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2008年学术文章

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2008年學術文章

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2008年學術文章

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name

Loss of RB1 induces non-prolif ...... progression to retinoblastoma.

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Loss of RB1 induces non-prolif ...... progression to retinoblastoma.

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type

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Loss of RB1 induces non-prolif ...... progression to retinoblastoma.

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Loss of RB1 induces non-prolif ...... progression to retinoblastoma.

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Loss of RB1 induces non-prolif ...... progression to retinoblastoma.

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Loss of RB1 induces non-prolif ...... progression to retinoblastoma.

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Human Molecular Genetics

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Loss of RB1 induces non-prolif ...... progression to retinoblastoma.

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Beata Piovesan

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Marija Orlic

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Nadia L Prigoda

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Paula Marrano

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Ralph C Eagle

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William Halliday

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P2860

Sensitive and efficient detection of RB1 gene mutations enhances care for families with retinoblastoma

Mutation and cancer: statistical study of retinoblastoma

A genetic model for colorectal tumorigenesis

Mutations of the human P gene associated with Type II oculocutaneous albinism (OCA2). Mutations in brief no. 205. Online

KIF14 is a candidate oncogene in the 1q minimal region of genomic gain in multiple cancers

Profiling genomic copy number changes in retinoblastoma beyond loss of RB1

KIF14 mRNA expression is a predictor of grade and outcome in breast cancer

KIF14 messenger RNA expression is independently prognostic for outcome in lung cancer

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype

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10.1093/HMG/DDN024

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10

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17

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Timothy W. Corson

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Brenda L. Gallie

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18211953

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