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Blood
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May 5, 2007
Mutations in the SBDS gene in acquired aplastic anemia
Rodrigo T Calado, Solomon A Graf, Keisha L Wilkerson, et al.
European Journal of Haematology
|
July 5, 2024
Aberrant early hematopoietic progenitor formation marks the onset of hematopoietic defects in Shwachman-Diamond syndrome
Alejandra Lagos-Monzon, Stephanie Ng, Alice M Luca, et al.
British Journal of Haematology
|
June 3, 2008
Functional interaction between mutations in the granulocyte colony-stimulating factor receptor in severe congenital neutropenia
Alister C Ward, Judith Gits, Fidel Majeed, et al.
American Journal of Medical Genetics. Part A
|
July 16, 2008
An intronic mutation in DKC1 in an infant with Høyeraal-Hreidarsson syndrome
Toni Pearson, Fiona Curtis, Ayman Al-Eyadhy, et al.
Blood Advances
|
May 30, 2019
Primed PMNs in healthy mouse and human circulation are first responders during acute inflammation
Noah Fine, Oriyah Barzilay, Chunxiang Sun, et al.
Haematologica
|
August 20, 2016
Response to treatment with azacitidine in children with advanced myelodysplastic syndrome prior to hematopoietic stem cell transplantation
Nicolas Waespe, Machiel Van Den Akker, Robert J Klaassen, et al.
American Journal of Medical Genetics. Part A
|
May 29, 2012
Definition of a critical genetic interval related to kidney abnormalities in the Potocki-Lupski syndrome
Elaine Suk-Ying Goh, Irene C Perez, Cesar P Canales, et al.
Leukemia
|
June 1, 2022
Germline PTPN13 mutations in patients with bone marrow failure and acute lymphoblastic leukemia
Houtan Moshiri, David A Cabrera Riofrío, Yeon Jung Lim, et al.
Annals of the New York Academy of Sciences
|
December 24, 2011
Draft consensus guidelines for diagnosis and treatment of Shwachman-Diamond syndrome
Yigal Dror, Jean Donadieu, Jutta Koglmeier, et al.
Science (New York, N.Y.)
|
November 7, 2015
Distinct routes of lineage development reshape the human blood hierarchy across ontogeny
Faiyaz Notta, Sasan Zandi, Naoya Takayama, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 96) with videos related to
Sort By:
Page
of 10
Blood
|
May 5, 2007
Mutations in the SBDS gene in acquired aplastic anemia
Rodrigo T Calado, Solomon A Graf, Keisha L Wilkerson, et al.
European Journal of Haematology
|
July 5, 2024
Aberrant early hematopoietic progenitor formation marks the onset of hematopoietic defects in Shwachman-Diamond syndrome
Alejandra Lagos-Monzon, Stephanie Ng, Alice M Luca, et al.
British Journal of Haematology
|
June 3, 2008
Functional interaction between mutations in the granulocyte colony-stimulating factor receptor in severe congenital neutropenia
Alister C Ward, Judith Gits, Fidel Majeed, et al.
American Journal of Medical Genetics. Part A
|
July 16, 2008
An intronic mutation in DKC1 in an infant with Høyeraal-Hreidarsson syndrome
Toni Pearson, Fiona Curtis, Ayman Al-Eyadhy, et al.
Blood Advances
|
May 30, 2019
Primed PMNs in healthy mouse and human circulation are first responders during acute inflammation
Noah Fine, Oriyah Barzilay, Chunxiang Sun, et al.
Haematologica
|
August 20, 2016
Response to treatment with azacitidine in children with advanced myelodysplastic syndrome prior to hematopoietic stem cell transplantation
Nicolas Waespe, Machiel Van Den Akker, Robert J Klaassen, et al.
American Journal of Medical Genetics. Part A
|
May 29, 2012
Definition of a critical genetic interval related to kidney abnormalities in the Potocki-Lupski syndrome
Elaine Suk-Ying Goh, Irene C Perez, Cesar P Canales, et al.
Leukemia
|
June 1, 2022
Germline PTPN13 mutations in patients with bone marrow failure and acute lymphoblastic leukemia
Houtan Moshiri, David A Cabrera Riofrío, Yeon Jung Lim, et al.
Annals of the New York Academy of Sciences
|
December 24, 2011
Draft consensus guidelines for diagnosis and treatment of Shwachman-Diamond syndrome
Yigal Dror, Jean Donadieu, Jutta Koglmeier, et al.
Science (New York, N.Y.)
|
November 7, 2015
Distinct routes of lineage development reshape the human blood hierarchy across ontogeny
Faiyaz Notta, Sasan Zandi, Naoya Takayama, et al.
Page
of 10