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Scientific Reports
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October 4, 2019
Optimised insert design for improved single-molecule imaging and quantification through CRISPR-Cas9 mediated knock-in
Abdullah O Khan, Carl W White, Jeremy A Pike, et al.
Haematologica
|
January 13, 2022
Sorting nexin 24 is required for α-granule biogenesis and cargo delivery in megakaryocytes
Joanne Lacey, Simon J Webster, Paul R Heath, et al.
Journal of Clinical Immunology
|
September 25, 2015
Astute Clinician Report: A Novel 10 bp Frameshift Deletion in Exon 2 of ICOS Causes a Combined Immunodeficiency Associated with an Enteritis and Hepatitis
Nic Robertson, Karin R Engelhardt, Neil V Morgan, et al.
Blood Advances
|
January 26, 2021
Heterozygous mutation SLFN14 K208N in mice mediates species-specific differences in platelet and erythroid lineage commitment
Rachel J Stapley, Christopher W Smith, Elizabeth J Haining, et al.
Haematologica
|
December 17, 2020
Post-translational polymodification of β1-tubulin regulates motor protein localisation in platelet production and function
Abdullah O Khan, Alexandre Slater, Annabel Maclachlan, et al.
Cell
|
August 16, 2016
The Deubiquitinase OTULIN Is an Essential Negative Regulator of Inflammation and Autoimmunity
Rune Busk Damgaard, Jennifer A Walker, Paola Marco-Casanova, et al.
Blood
|
January 20, 2005
A common Fanconi anemia mutation in black populations of sub-Saharan Africa
Neil V Morgan, Fahmida Essop, Ilja Demuth, et al.
American Journal of Human Genetics
|
December 31, 2005
A germline mutation in BLOC1S3/reduced pigmentation causes a novel variant of Hermansky-Pudlak syndrome (HPS8)
Neil V Morgan, Shanaz Pasha, Colin A Johnson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 9, 2013
STAT2 deficiency and susceptibility to viral illness in humans
Sophie Hambleton, Stephen Goodbourn, Dan F Young, et al.
Thrombosis and Haemostasis
|
January 9, 2015
Diversity and impact of rare variants in genes encoding the platelet G protein-coupled receptors
Matthew L Jones, Jane E Norman, Neil V Morgan, et al.
Page
of 9
Search research articles
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Showing results (31-40 of 88) with videos related to
Sort By:
Page
of 9
Scientific Reports
|
October 4, 2019
Optimised insert design for improved single-molecule imaging and quantification through CRISPR-Cas9 mediated knock-in
Abdullah O Khan, Carl W White, Jeremy A Pike, et al.
Haematologica
|
January 13, 2022
Sorting nexin 24 is required for α-granule biogenesis and cargo delivery in megakaryocytes
Joanne Lacey, Simon J Webster, Paul R Heath, et al.
Journal of Clinical Immunology
|
September 25, 2015
Astute Clinician Report: A Novel 10 bp Frameshift Deletion in Exon 2 of ICOS Causes a Combined Immunodeficiency Associated with an Enteritis and Hepatitis
Nic Robertson, Karin R Engelhardt, Neil V Morgan, et al.
Blood Advances
|
January 26, 2021
Heterozygous mutation SLFN14 K208N in mice mediates species-specific differences in platelet and erythroid lineage commitment
Rachel J Stapley, Christopher W Smith, Elizabeth J Haining, et al.
Haematologica
|
December 17, 2020
Post-translational polymodification of β1-tubulin regulates motor protein localisation in platelet production and function
Abdullah O Khan, Alexandre Slater, Annabel Maclachlan, et al.
Cell
|
August 16, 2016
The Deubiquitinase OTULIN Is an Essential Negative Regulator of Inflammation and Autoimmunity
Rune Busk Damgaard, Jennifer A Walker, Paola Marco-Casanova, et al.
Blood
|
January 20, 2005
A common Fanconi anemia mutation in black populations of sub-Saharan Africa
Neil V Morgan, Fahmida Essop, Ilja Demuth, et al.
American Journal of Human Genetics
|
December 31, 2005
A germline mutation in BLOC1S3/reduced pigmentation causes a novel variant of Hermansky-Pudlak syndrome (HPS8)
Neil V Morgan, Shanaz Pasha, Colin A Johnson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 9, 2013
STAT2 deficiency and susceptibility to viral illness in humans
Sophie Hambleton, Stephen Goodbourn, Dan F Young, et al.
Thrombosis and Haemostasis
|
January 9, 2015
Diversity and impact of rare variants in genes encoding the platelet G protein-coupled receptors
Matthew L Jones, Jane E Norman, Neil V Morgan, et al.
Page
of 9