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Cytometry. Part B, Clinical Cytometry
|
June 3, 2017
Standardized high-sensitivity flow cytometry testing for paroxysmal nocturnal hemoglobinuria in children with acquired bone marrow failure disorders: A single center US study
Rachel E Donohue, Andrea N Marcogliese, Ghadir S Sasa, et al.
International Journal of Radiation Oncology, Biology, Physics
|
May 20, 2008
Changes mimicking new leptomeningeal disease after intensity-modulated radiotherapy for medulloblastoma
Jodi A Muscal, Jeremy Y Jones, Arnold C Paulino, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
June 30, 2016
Shorter Remission Telomere Length Predicts Delayed Neutrophil Recovery After Acute Myeloid Leukemia Therapy: A Report From the Children's Oncology Group
Robert B Gerbing, Todd A Alonzo, Lillian Sung, et al.
Leukemia & Lymphoma
|
June 14, 2012
Proposal for the clinical detection and management of patients and their family members with familial myelodysplastic syndrome/acute leukemia predisposition syndromes
Jane E Churpek, Rachelle Lorenz, Siya Nedumgottil, et al.
Plos Genetics
|
September 19, 2009
Segregating YKU80 and TLC1 alleles underlying natural variation in telomere properties in wild yeast
Gianni Liti, Svasti Haricharan, Francisco A Cubillos, et al.
Molecular and Cellular Biology
|
March 28, 2018
The C-Terminal Extension Unique to the Long Isoform of the Shelterin Component TIN2 Enhances Its Interaction with TRF2 in a Phosphorylation- and Dyskeratosis Congenita Cluster-Dependent Fashion
Nya D Nelson, Lois M Dodson, Laura Escudero, et al.
Human Mutation
|
August 27, 2019
From incomplete penetrance with normal telomere length to severe disease and telomere shortening in a family with monoallelic and biallelic PARN pathogenic variants
Lois M Dodson, Alessandro Baldan, Mikael Nissbeck, et al.
American Journal of Medical Genetics. Part A
|
September 10, 2020
Hematologic presentation and the role of untargeted metabolomics analysis in monitoring treatment for riboflavin transporter deficiency
Nishitha R Pillai, Hitha Amin, Charul Gijavanekar, et al.
Genetics
|
March 4, 2018
Ku DNA End-Binding Activity Promotes Repair Fidelity and Influences End-Processing During Nonhomologous End-Joining in <i>Saccharomyces cerevisiae</i>
Charlene H Emerson, Christopher R Lopez, Albert Ribes-Zamora, et al.
Blood Advances
|
January 4, 2018
Somatic mutations in children with <i>GATA2</i>-associated myelodysplastic syndrome who lack other features of GATA2 deficiency
Kevin E Fisher, Amy P Hsu, Christopher L Williams, et al.
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Search research articles
Search
Showing results (41-50 of 77) with videos related to
Sort By:
Page
of 8
Cytometry. Part B, Clinical Cytometry
|
June 3, 2017
Standardized high-sensitivity flow cytometry testing for paroxysmal nocturnal hemoglobinuria in children with acquired bone marrow failure disorders: A single center US study
Rachel E Donohue, Andrea N Marcogliese, Ghadir S Sasa, et al.
International Journal of Radiation Oncology, Biology, Physics
|
May 20, 2008
Changes mimicking new leptomeningeal disease after intensity-modulated radiotherapy for medulloblastoma
Jodi A Muscal, Jeremy Y Jones, Arnold C Paulino, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
June 30, 2016
Shorter Remission Telomere Length Predicts Delayed Neutrophil Recovery After Acute Myeloid Leukemia Therapy: A Report From the Children's Oncology Group
Robert B Gerbing, Todd A Alonzo, Lillian Sung, et al.
Leukemia & Lymphoma
|
June 14, 2012
Proposal for the clinical detection and management of patients and their family members with familial myelodysplastic syndrome/acute leukemia predisposition syndromes
Jane E Churpek, Rachelle Lorenz, Siya Nedumgottil, et al.
Plos Genetics
|
September 19, 2009
Segregating YKU80 and TLC1 alleles underlying natural variation in telomere properties in wild yeast
Gianni Liti, Svasti Haricharan, Francisco A Cubillos, et al.
Molecular and Cellular Biology
|
March 28, 2018
The C-Terminal Extension Unique to the Long Isoform of the Shelterin Component TIN2 Enhances Its Interaction with TRF2 in a Phosphorylation- and Dyskeratosis Congenita Cluster-Dependent Fashion
Nya D Nelson, Lois M Dodson, Laura Escudero, et al.
Human Mutation
|
August 27, 2019
From incomplete penetrance with normal telomere length to severe disease and telomere shortening in a family with monoallelic and biallelic PARN pathogenic variants
Lois M Dodson, Alessandro Baldan, Mikael Nissbeck, et al.
American Journal of Medical Genetics. Part A
|
September 10, 2020
Hematologic presentation and the role of untargeted metabolomics analysis in monitoring treatment for riboflavin transporter deficiency
Nishitha R Pillai, Hitha Amin, Charul Gijavanekar, et al.
Genetics
|
March 4, 2018
Ku DNA End-Binding Activity Promotes Repair Fidelity and Influences End-Processing During Nonhomologous End-Joining in <i>Saccharomyces cerevisiae</i>
Charlene H Emerson, Christopher R Lopez, Albert Ribes-Zamora, et al.
Blood Advances
|
January 4, 2018
Somatic mutations in children with <i>GATA2</i>-associated myelodysplastic syndrome who lack other features of GATA2 deficiency
Kevin E Fisher, Amy P Hsu, Christopher L Williams, et al.
Page
of 8