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The Journal of Allergy and Clinical Immunology
|
February 14, 2013
Common variable immunodeficiency as the initial presentation of dyskeratosis congenita
Eric J Allenspach, Cristian Bellodi, David Jeong, et al.
The Journal of Clinical Investigation
|
April 14, 2007
Fanconi anemia pathway-deficient tumor cells are hypersensitive to inhibition of ataxia telangiectasia mutated
Richard D Kennedy, Clark C Chen, Patricia Stuckert, et al.
Science Translational Medicine
|
May 13, 2016
Delayed globin synthesis leads to excess heme and the macrocytic anemia of Diamond Blackfan anemia and del(5q) myelodysplastic syndrome
Zhantao Yang, Siobán B Keel, Akiko Shimamura, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 2, 2018
Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene <i>BRCA1</i>
Aaron Seo, Orna Steinberg-Shemer, Sule Unal, et al.
Cell Stem Cell
|
April 23, 2013
Pluripotent stem cell models of Shwachman-Diamond syndrome reveal a common mechanism for pancreatic and hematopoietic dysfunction
Asmin Tulpule, James M Kelley, M William Lensch, et al.
The Journal of Clinical Investigation
|
March 8, 2008
Mitotic spindle destabilization and genomic instability in Shwachman-Diamond syndrome
Karyn M Austin, Mohan L Gupta, Scott A Coats, et al.
The Journal of Pediatrics
|
January 7, 2014
Variable clinical presentation of Shwachman-Diamond syndrome: update from the North American Shwachman-Diamond Syndrome Registry
Kasiani C Myers, Audrey Anna Bolyard, Barbara Otto, et al.
Blood
|
June 24, 2026
Direct and indirect regulation of fetal globin transcript by RNA-binding protein IGF2BP1
Steven Coyne, GueHo Hwang, Ting Wu, et al.
HGG Advances
|
January 20, 2022
Low frequency of treatable pediatric disease alleles in gnomAD: An opportunity for future genomic screening of newborns
Nina B Gold, Steven M Harrison, Jared H Rowe, et al.
Leukemia
|
October 21, 2022
Classification of rare pediatric myeloid neoplasia-Quo vadis?
Charlotte M Niemeyer, Martina Rudelius, Akiko Shimamura, et al.
Page
of 16
Search research articles
Search
Showing results (61-70 of 158) with videos related to
Sort By:
Page
of 16
The Journal of Allergy and Clinical Immunology
|
February 14, 2013
Common variable immunodeficiency as the initial presentation of dyskeratosis congenita
Eric J Allenspach, Cristian Bellodi, David Jeong, et al.
The Journal of Clinical Investigation
|
April 14, 2007
Fanconi anemia pathway-deficient tumor cells are hypersensitive to inhibition of ataxia telangiectasia mutated
Richard D Kennedy, Clark C Chen, Patricia Stuckert, et al.
Science Translational Medicine
|
May 13, 2016
Delayed globin synthesis leads to excess heme and the macrocytic anemia of Diamond Blackfan anemia and del(5q) myelodysplastic syndrome
Zhantao Yang, Siobán B Keel, Akiko Shimamura, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 2, 2018
Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene <i>BRCA1</i>
Aaron Seo, Orna Steinberg-Shemer, Sule Unal, et al.
Cell Stem Cell
|
April 23, 2013
Pluripotent stem cell models of Shwachman-Diamond syndrome reveal a common mechanism for pancreatic and hematopoietic dysfunction
Asmin Tulpule, James M Kelley, M William Lensch, et al.
The Journal of Clinical Investigation
|
March 8, 2008
Mitotic spindle destabilization and genomic instability in Shwachman-Diamond syndrome
Karyn M Austin, Mohan L Gupta, Scott A Coats, et al.
The Journal of Pediatrics
|
January 7, 2014
Variable clinical presentation of Shwachman-Diamond syndrome: update from the North American Shwachman-Diamond Syndrome Registry
Kasiani C Myers, Audrey Anna Bolyard, Barbara Otto, et al.
Blood
|
June 24, 2026
Direct and indirect regulation of fetal globin transcript by RNA-binding protein IGF2BP1
Steven Coyne, GueHo Hwang, Ting Wu, et al.
HGG Advances
|
January 20, 2022
Low frequency of treatable pediatric disease alleles in gnomAD: An opportunity for future genomic screening of newborns
Nina B Gold, Steven M Harrison, Jared H Rowe, et al.
Leukemia
|
October 21, 2022
Classification of rare pediatric myeloid neoplasia-Quo vadis?
Charlotte M Niemeyer, Martina Rudelius, Akiko Shimamura, et al.
Page
of 16