TIN2 Protein Dyskeratosis Congenita Missense Mutants Are Defective in Association with Telomerase
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Title
TIN2 Protein Dyskeratosis Congenita Missense Mutants Are Defective in Association with Telomerase
Authors
Keywords
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Journal
JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 286, Issue 26, Pages 23022-23030
Publisher
American Society for Biochemistry & Molecular Biology (ASBMB)
Online
2011-05-03
DOI
10.1074/jbc.m111.225870
References
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Note: Only part of the references are listed.- Disruption of telomerase trafficking by TCAB1 mutation causes dyskeratosis congenita
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- TIN2-Tethered TPP1 Recruits Human Telomerase to Telomeres In Vivo
- (2010) E. Abreu et al. MOLECULAR AND CELLULAR BIOLOGY
- Dyskeratosis congenita, stem cells and telomeres
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- (2009) Kaori K. Takai et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- TRF2 functions as a protein hub and regulates telomere maintenance by recognizing specific peptide motifs
- (2009) Hyeung Kim et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- A Human Telomerase Holoenzyme Protein Required for Cajal Body Localization and Telomere Synthesis
- (2009) A. S. Venteicher et al. SCIENCE
- TINF2, a Component of the Shelterin Telomere Protection Complex, Is Mutated in Dyskeratosis Congenita
- (2008) Sharon A. Savage et al. AMERICAN JOURNAL OF HUMAN GENETICS
- How Shelterin Protects Mammalian Telomeres
- (2008) Wilhelm Palm et al. Annual Review of Genetics
- Telomere maintenance and human bone marrow failure
- (2008) R. T. Calado et al. BLOOD
- TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromes
- (2008) A. J. Walne et al. BLOOD
- Ataxia and pancytopenia caused by a mutation in TINF2
- (2008) Elena Tsangaris et al. HUMAN GENETICS
- Distinct Roles of TRF1 in the Regulation of Telomere Structure and Lengthening
- (2008) Keiji Okamoto et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Telomere dysfunction and cell survival: roles for distinct TIN2-containing complexes
- (2008) Sahn-ho Kim et al. JOURNAL OF CELL BIOLOGY
- Nanog and Oct4 associate with unique transcriptional repression complexes in embryonic stem cells
- (2008) Jiancong Liang et al. NATURE CELL BIOLOGY
- TINF2mutations in children with severe aplastic anemia
- (2008) Hong-Yan Du et al. PEDIATRIC BLOOD & CANCER
- Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita
- (2008) T. Vulliamy et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The role of telomere biology in bone marrow failure and other disorders
- (2007) Sharon A. Savage et al. MECHANISMS OF AGEING AND DEVELOPMENT
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