Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy - Test2 - elhamkhani - TriplyDB

Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy

Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy

http://www.wikidata.org/entity/Q26852788

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Cell biology of disease: Telomeropathies: an emerging spectrum disorder Genomic characterization of the inherited bone marrow failure syndromes.Dyskeratosis congenita caused by a novel TERT point mutation in siblings with pancytopenia and exudative retinopathy.Bone marrow morphology and disease progression in congenital thrombocytopenia: a detailed clinicopathologic and genetic study of eight cases.Transcriptional analysis of apoptotic cerebellar granule neurons following rescue by gastric inhibitory polypeptide Telomere biology and translational research.The diagnosis and treatment of dyskeratosis congenita: a review.Telomere maintenance mechanisms in cancer: clinical implications Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly.Potential relationship between inadequate response to DNA damage and development of myelodysplastic syndrome.Association between regulator of telomere elongation helicase 1 polymorphism and susceptibility to glioma.TeloPIN: a database of telomeric proteins interaction network in mammalian cells Telomere length variation: A potential new telomere biomarker for lung cancer risk.Poly(A)-specific ribonuclease deficiency impacts telomere biology and causes dyskeratosis congenita.mRNA deadenylation and telomere disease.Identification of Genes That Modulate Susceptibility to Formaldehyde and Imatinib by Functional Genomic Screening in Human Haploid KBM7 Cells.Clinical utility gene card for: Dyskeratosis congenita - update 2015.Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis Nature vs nurture: interplay between the genetic control of telomere length and environmental factors.Clinical outcomes of lung transplant recipients with telomerase mutations.Biology of telomeres: lessons from budding yeast.Telomerase promoter mutations in cancer: an emerging molecular biomarker?Understanding chronic neutropenia: life is short.Involvement of Atm and Trp53 in neural cell loss due to Terf2 inactivation during mouse brain development Comparison of different methods for telomere length measurement in whole blood and blood cell subsets: Recommendations for telomere length measurement in hematological diseases.Reverse Expression of Aging-Associated Molecules through Transfection of miRNAs to Aged Mice.Genome-wide studies of telomere biology in budding yeast Familial Myelodysplastic/Acute Leukemia Syndromes-Myeloid Neoplasms with Germline Predisposition Retinal findings and a novel TINF2 mutation in Revesz syndrome: Clinical and molecular correlations with pediatric retinal vasculopathies.Effects of TIN2 on telomeres and chromosomes in the human gastric epithelial cell line GES-1.

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Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy

http://www.wikidata.org/entity/Q26852788

description

2013 nî lūn-bûn

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2013 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

@zh-hk

2013年論文

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2013年論文

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2013年论文

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name

Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy

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Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy

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Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy

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type

label

Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy

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Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy

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Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy

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prefLabel

Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy

@ast

Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy

@en

Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy

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J.TRSL.2013.05.003

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Translational Research

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Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy

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P2093

Alison A. Bertuch

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

Maria M. Gramatges

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P2860

Shortened telomere length is associated with increased risk of cancer: a meta-analysis

Mammalian telomeres end in a large duplex loop

A telomerase component is defective in the human disease dyskeratosis congenita

Telomere shortening triggers senescence of human cells through a pathway involving ATM, p53, and p21(CIP1), but not p16(INK4a)

RPA-like mammalian Ctc1-Stn1-Ten1 complex binds to single-stranded DNA and protects telomeres independently of the Pot1 pathway

Conserved telomere maintenance component 1 interacts with STN1 and maintains chromosome ends in higher eukaryotes

hEST2, the putative human telomerase catalytic subunit gene, is up-regulated in tumor cells and during immortalization

Reconstitution of human telomerase with the template RNA component hTR and the catalytic protein subunit hTRT

TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromes

A human telomerase holoenzyme protein required for Cajal body localization and telomere synthesis

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10.1016/J.TRSL.2013.05.003

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6

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2013-12-01T00:00:00Z

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3834083

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