A role for heterochromatin protein 1γ at human telomeres.
about
The genetics of dyskeratosis congenitaFinding the end: recruitment of telomerase to telomeresShort telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancyMechanisms of functional promiscuity by HP1 proteinsStructure of active dimeric human telomerase.Persistent telomere cohesion triggers a prolonged anaphase.TRF1 ensures the centromeric function of Aurora-B and proper chromosome segregation.Functional interplay between SA1 and TRF1 in telomeric DNA binding and DNA-DNA pairingHoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1.Unraveling the pathogenesis of Hoyeraal-Hreidarsson syndrome, a complex telomere biology disorderDifferential contribution of HP1 proteins to DNA end resection and homology-directed repair.HP1γ expression is elevated in prostate cancer and is superior to Gleason score as a predictor of biochemical recurrence after radical prostatectomy.Loss of nucleolar histone chaperone NPM1 triggers rearrangement of heterochromatin and synergizes with a deficiency in DNA methyltransferase DNMT3A to drive ribosomal DNA transcription.Telomere-regulating genes and the telomere interactome in familial cancers.Cell cycle regulated phosphorylation of the telomere-associated protein TIN2Osteoarthritis and telomere shortening.The relationship between DNA methylation and telomere length in dyskeratosis congenita.The Shelterin TIN2 Subunit Mediates Recruitment of Telomerase to Telomeres.Telomeric G-quadruplexes are a substrate and site of localization for human telomeraseSwi1Timeless Prevents Repeat Instability at Fission Yeast Telomeres.Independent Mechanisms Target SMCHD1 to Trimethylated Histone H3 Lysine 9-Modified Chromatin and the Inactive X Chromosome.Nucleosome compaction facilitates HP1γ binding to methylated H3K9.A role for Separase in telomere protection.Control of telomerase action at human telomeresChromatin structure in telomere dynamicsOne identity or more for telomeres?TINF2 Gene Mutation in a Patient with Pulmonary Fibrosis.The shelterin complex and hematopoiesis.Guarding chromosomes from oxidative DNA damage to the very endSA1 binds directly to DNA through its unique AT-hook to promote sister chromatid cohesion at telomeresThe molecular genetics of the telomere biology disorders.Interplay between Epigenetics and Genetics in Cancer.A TIN2 dyskeratosis congenita mutation causes telomerase-independent telomere shortening in mice.Fundamental mechanisms of telomerase action in yeasts and mammals: understanding telomeres and telomerase in cancer cells.A role for sister telomere cohesion in telomere elongation by telomerase.Posttranslational control of telomere maintenance and the telomere damage response.Updates on the biology and management of dyskeratosis congenita and related telomere biology disorders.TRF2-tethered TIN2 can mediate telomere protection by TPP1/POT1.Cockayne Syndrome group B protein interacts with TRF2 and regulates telomere length and stabilityTIN2 stability is regulated by the E3 ligase Siah2.
P2860
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P2860
A role for heterochromatin protein 1γ at human telomeres.
description
2011 nî lūn-bûn
@nan
2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
A role for heterochromatin protein 1γ at human telomeres.
@ast
A role for heterochromatin protein 1γ at human telomeres.
@en
type
label
A role for heterochromatin protein 1γ at human telomeres.
@ast
A role for heterochromatin protein 1γ at human telomeres.
@en
prefLabel
A role for heterochromatin protein 1γ at human telomeres.
@ast
A role for heterochromatin protein 1γ at human telomeres.
@en
P2093
P2860
P50
P356
P1433
P1476
A role for heterochromatin protein 1γ at human telomeres.
@en
P2093
Alison A Bertuch
Benjamin R Houghtaling
Ghadir Sasa
Monica Bhanot
P2860
P304
P356
10.1101/GAD.17325211
P577
2011-08-24T00:00:00Z