Search research articles
Contact Us
Filters
Showing results (41-50 of 58) with videos related to
Page
of 6
Sort By:
Nature Communications
|
February 18, 2022
A late-stage assembly checkpoint of the human mitochondrial ribosome large subunit
Pedro Rebelo-Guiomar, Simone Pellegrino, Kyle C Dent, et al.
Hemasphere
|
July 11, 2020
Congenital and Acquired Chronic Neutropenias: Challenges, Perspectives and Implementation of the EuNet-INNOCHRON Action
Helen A Papadaki, Irene Mavroudi, Antonio Almeida, et al.
Hemasphere
|
April 3, 2023
The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST Action
Francesca Fioredda, Julia Skokowa, Hannah Tamary, et al.
The New England Journal of Medicine
|
February 3, 2007
JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis
Linda M Scott, Wei Tong, Ross L Levine, et al.
Nature Medicine
|
December 8, 2009
A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q- syndrome
Jillian L Barlow, Lesley F Drynan, Duncan R Hewett, et al.
Genes & Development
|
May 4, 2011
Uncoupling of GTP hydrolysis from eIF6 release on the ribosome causes Shwachman-Diamond syndrome
Andrew J Finch, Christine Hilcenko, Nicolas Basse, et al.
Hemasphere
|
April 17, 2025
European guidelines on treatment and supportive measures in chronic neutropenias: A consensus between the European Hematology Association and the EuNet-INNOCHRON COST Action based on a systematic evidence review
Francesca Fioredda, Michail Spanoudakis, Julia Skokowa, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
September 11, 2020
Novel RPL13 Variants and Variable Clinical Expressivity in a Human Ribosomopathy With Spondyloepimetaphyseal Dysplasia
Alice Costantini, Jessica J Alm, Francesca Tonelli, et al.
Blood
|
June 2, 2019
EFL1 mutations impair eIF6 release to cause Shwachman-Diamond syndrome
Shengjiang Tan, Laëtitia Kermasson, Angela Hoslin, et al.
Nature Communications
|
August 22, 2023
Convergent somatic evolution commences in utero in a germline ribosomopathy
Heather E Machado, Nina F Øbro, Nicholas Williams, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 58) with videos related to
Sort By:
Page
of 6
Nature Communications
|
February 18, 2022
A late-stage assembly checkpoint of the human mitochondrial ribosome large subunit
Pedro Rebelo-Guiomar, Simone Pellegrino, Kyle C Dent, et al.
Hemasphere
|
July 11, 2020
Congenital and Acquired Chronic Neutropenias: Challenges, Perspectives and Implementation of the EuNet-INNOCHRON Action
Helen A Papadaki, Irene Mavroudi, Antonio Almeida, et al.
Hemasphere
|
April 3, 2023
The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST Action
Francesca Fioredda, Julia Skokowa, Hannah Tamary, et al.
The New England Journal of Medicine
|
February 3, 2007
JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis
Linda M Scott, Wei Tong, Ross L Levine, et al.
Nature Medicine
|
December 8, 2009
A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q- syndrome
Jillian L Barlow, Lesley F Drynan, Duncan R Hewett, et al.
Genes & Development
|
May 4, 2011
Uncoupling of GTP hydrolysis from eIF6 release on the ribosome causes Shwachman-Diamond syndrome
Andrew J Finch, Christine Hilcenko, Nicolas Basse, et al.
Hemasphere
|
April 17, 2025
European guidelines on treatment and supportive measures in chronic neutropenias: A consensus between the European Hematology Association and the EuNet-INNOCHRON COST Action based on a systematic evidence review
Francesca Fioredda, Michail Spanoudakis, Julia Skokowa, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
September 11, 2020
Novel RPL13 Variants and Variable Clinical Expressivity in a Human Ribosomopathy With Spondyloepimetaphyseal Dysplasia
Alice Costantini, Jessica J Alm, Francesca Tonelli, et al.
Blood
|
June 2, 2019
EFL1 mutations impair eIF6 release to cause Shwachman-Diamond syndrome
Shengjiang Tan, Laëtitia Kermasson, Angela Hoslin, et al.
Nature Communications
|
August 22, 2023
Convergent somatic evolution commences in utero in a germline ribosomopathy
Heather E Machado, Nina F Øbro, Nicholas Williams, et al.
Page
of 6