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JCO Precision Oncology
|
September 27, 2021
Ovarian Failure Preceding Head and Neck Squamous Cell Carcinoma Identifies an Adult-Onset Cancer-Prone Syndrome Caused by <i>FANCM</i> Mutations
Paz J Vellanki, Emily A DeBoy, M Malek Bawadkji, et al.
Journal of Medical Genetics
|
March 19, 2011
Decreased dyskerin levels as a mechanism of telomere shortening in X-linked dyskeratosis congenita
Erin M Parry, Jonathan K Alder, Stella S Lee, et al.
Plos One
|
March 23, 2011
Short telomeres compromise β-cell signaling and survival
Nini Guo, Erin M Parry, Luo-Sheng Li, et al.
American Journal of Human Genetics
|
April 30, 2024
Telomere-lengthening germline variants predispose to a syndromic papillary thyroid cancer subtype
Emily A DeBoy, Anna M Nicosia, Sandya Liyanarachchi, et al.
Blood
|
February 21, 2020
Cancer spectrum and outcomes in the Mendelian short telomere syndromes
Kristen E Schratz, Lisa Haley, Sonye K Danoff, et al.
The Journal of Clinical Investigation
|
August 3, 2021
Somatic reversion impacts myelodysplastic syndromes and acute myeloid leukemia evolution in the short telomere disorders
Kristen E Schratz, Valeriya Gaysinskaya, Zoe L Cosner, et al.
Human Mutation
|
August 16, 2013
Telomere phenotypes in females with heterozygous mutations in the dyskeratosis congenita 1 (DKC1) gene
Jonathan K Alder, Erin M Parry, Srinivasan Yegnasubramanian, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 5, 2015
Telomere dysfunction causes alveolar stem cell failure
Jonathan K Alder, Christina E Barkauskas, Nathachit Limjunyawong, et al.
Journal of Clinical Immunology
|
April 12, 2016
Ligase-4 Deficiency Causes Distinctive Immune Abnormalities in Asymptomatic Individuals
Kerstin Felgentreff, Sachin N Baxi, Yu Nee Lee, et al.
Chest
|
March 26, 2022
The Role of Genetic Testing in Pulmonary Fibrosis: A Perspective From the Pulmonary Fibrosis Foundation Genetic Testing Work Group
Chad A Newton, Justin M Oldham, Carolyn Applegate, et al.
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of 8
Search research articles
Search
Showing results (41-50 of 75) with videos related to
Sort By:
Page
of 8
JCO Precision Oncology
|
September 27, 2021
Ovarian Failure Preceding Head and Neck Squamous Cell Carcinoma Identifies an Adult-Onset Cancer-Prone Syndrome Caused by <i>FANCM</i> Mutations
Paz J Vellanki, Emily A DeBoy, M Malek Bawadkji, et al.
Journal of Medical Genetics
|
March 19, 2011
Decreased dyskerin levels as a mechanism of telomere shortening in X-linked dyskeratosis congenita
Erin M Parry, Jonathan K Alder, Stella S Lee, et al.
Plos One
|
March 23, 2011
Short telomeres compromise β-cell signaling and survival
Nini Guo, Erin M Parry, Luo-Sheng Li, et al.
American Journal of Human Genetics
|
April 30, 2024
Telomere-lengthening germline variants predispose to a syndromic papillary thyroid cancer subtype
Emily A DeBoy, Anna M Nicosia, Sandya Liyanarachchi, et al.
Blood
|
February 21, 2020
Cancer spectrum and outcomes in the Mendelian short telomere syndromes
Kristen E Schratz, Lisa Haley, Sonye K Danoff, et al.
The Journal of Clinical Investigation
|
August 3, 2021
Somatic reversion impacts myelodysplastic syndromes and acute myeloid leukemia evolution in the short telomere disorders
Kristen E Schratz, Valeriya Gaysinskaya, Zoe L Cosner, et al.
Human Mutation
|
August 16, 2013
Telomere phenotypes in females with heterozygous mutations in the dyskeratosis congenita 1 (DKC1) gene
Jonathan K Alder, Erin M Parry, Srinivasan Yegnasubramanian, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 5, 2015
Telomere dysfunction causes alveolar stem cell failure
Jonathan K Alder, Christina E Barkauskas, Nathachit Limjunyawong, et al.
Journal of Clinical Immunology
|
April 12, 2016
Ligase-4 Deficiency Causes Distinctive Immune Abnormalities in Asymptomatic Individuals
Kerstin Felgentreff, Sachin N Baxi, Yu Nee Lee, et al.
Chest
|
March 26, 2022
The Role of Genetic Testing in Pulmonary Fibrosis: A Perspective From the Pulmonary Fibrosis Foundation Genetic Testing Work Group
Chad A Newton, Justin M Oldham, Carolyn Applegate, et al.
Page
of 8