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Transfusion
|
April 24, 2018
Variable serologic and other phenotypes due to KLF1 mutations
Kevin Gillinder, Graham Magor, Andrew Perkins
Stem Cell Reviews and Reports
|
August 20, 2013
Neural crest stem cell-specific deletion of the Pygopus2 gene modulates hair follicle development
Alla Narytnyk, Kevin Gillinder, Bernard Verdon, et al.
Nature Communications
|
August 15, 2024
Mutations in linker-2 of KLF1 impair expression of membrane transporters and cytoskeletal proteins causing hemolysis
Stephen Huang, Casie Reed, Melissa Ilsley, et al.
Development (Cambridge, England)
|
February 2, 2017
Neomorphic effects of the neonatal anemia (Nan-Eklf) mutation contribute to deficits throughout development
Antanas Planutis, Li Xue, Cecelia D Trainor, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
November 16, 2006
Crim1KST264/KST264 mice display a disruption of the Crim1 gene resulting in perinatal lethality with defects in multiple organ systems
David J Pennisi, Lorine Wilkinson, Gabriel Kolle, et al.
Scientific Reports
|
August 22, 2018
EPO does not promote interaction between the erythropoietin and beta-common receptors
Karen S Cheung Tung Shing, Sophie E Broughton, Tracy L Nero, et al.
Scientific Reports
|
May 22, 2019
Author Correction: EPO does not promote interaction between the erythropoietin and beta-common receptors
Karen S Cheung Tung Shing, Sophie E Broughton, Tracy L Nero, et al.
Iscience
|
November 22, 2021
A model of impaired Langerhans cell maturation associated with HPV induced epithelial hyperplasia
Zewen K Tuong, Samuel W Lukowski, Quan H Nguyen, et al.
Blood
|
May 6, 2020
The EMT modulator SNAI1 contributes to AML pathogenesis via its interaction with LSD1
Catherine L Carmichael, Jueqiong Wang, Thao Nguyen, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Transfusion
|
April 24, 2018
Variable serologic and other phenotypes due to KLF1 mutations
Kevin Gillinder, Graham Magor, Andrew Perkins
Stem Cell Reviews and Reports
|
August 20, 2013
Neural crest stem cell-specific deletion of the Pygopus2 gene modulates hair follicle development
Alla Narytnyk, Kevin Gillinder, Bernard Verdon, et al.
Nature Communications
|
August 15, 2024
Mutations in linker-2 of KLF1 impair expression of membrane transporters and cytoskeletal proteins causing hemolysis
Stephen Huang, Casie Reed, Melissa Ilsley, et al.
Development (Cambridge, England)
|
February 2, 2017
Neomorphic effects of the neonatal anemia (Nan-Eklf) mutation contribute to deficits throughout development
Antanas Planutis, Li Xue, Cecelia D Trainor, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
November 16, 2006
Crim1KST264/KST264 mice display a disruption of the Crim1 gene resulting in perinatal lethality with defects in multiple organ systems
David J Pennisi, Lorine Wilkinson, Gabriel Kolle, et al.
Scientific Reports
|
August 22, 2018
EPO does not promote interaction between the erythropoietin and beta-common receptors
Karen S Cheung Tung Shing, Sophie E Broughton, Tracy L Nero, et al.
Scientific Reports
|
May 22, 2019
Author Correction: EPO does not promote interaction between the erythropoietin and beta-common receptors
Karen S Cheung Tung Shing, Sophie E Broughton, Tracy L Nero, et al.
Iscience
|
November 22, 2021
A model of impaired Langerhans cell maturation associated with HPV induced epithelial hyperplasia
Zewen K Tuong, Samuel W Lukowski, Quan H Nguyen, et al.
Blood
|
May 6, 2020
The EMT modulator SNAI1 contributes to AML pathogenesis via its interaction with LSD1
Catherine L Carmichael, Jueqiong Wang, Thao Nguyen, et al.
Page
of 1