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Title
Dyskeratosis Congenita
Authors
Keywords
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Journal
Hematology-American Society of Hematology Education Program
Volume 2011, Issue 1, Pages 480-486
Publisher
American Society of Hematology
Online
2011-12-08
DOI
10.1182/asheducation-2011.1.480
References
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Related references
Note: Only part of the references are listed.- Disruption of telomerase trafficking by TCAB1 mutation causes dyskeratosis congenita
- (2011) F. Zhong et al. GENES & DEVELOPMENT
- Disease-specific hematopoietic cell transplantation: nonmyeloablative conditioning regimen for dyskeratosis congenita
- (2010) A C Dietz et al. BONE MARROW TRANSPLANTATION
- Dyskeratosis congenita
- (2010) Monica Bessler et al. FEBS LETTERS
- Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund–Thomson syndrome
- (2010) Amanda J. Walne et al. HUMAN MOLECULAR GENETICS
- Telomere elongation in induced pluripotent stem cells from dyskeratosis congenita patients
- (2010) Suneet Agarwal et al. NATURE
- Sex hormones, acting on the TERT gene, increase telomerase activity in human primary hematopoietic cells
- (2009) R. T. Calado et al. BLOOD
- Defining the pathogenic role of telomerase mutations in myelodysplastic syndrome and acute myeloid leukemia
- (2009) Michael Kirwan et al. HUMAN MUTATION
- A Spectrum of Severe Familial Liver Disorders Associate with Telomerase Mutations
- (2009) Rodrigo T. Calado et al. PLoS One
- Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia
- (2009) R. T. Calado et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- 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
- TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements
- (2008) H.-Y. Du et al. BLOOD
- Characterization of primitive hematopoietic cells from patients with dyskeratosis congenita
- (2008) F. D. Goldman 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
- ExogenousTERCalone can enhance proliferative potential, telomerase activity and telomere length in lymphocytes from dyskeratosis congenita patients
- (2008) Michael Kirwan et al. BRITISH JOURNAL OF HAEMATOLOGY
- 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
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