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Neil V Morgan

Showing results (1-10 of 88) with videos related to

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Frontiers in Cardiovascular Medicine|July 6, 2019
Inherited Thrombocytopenia: Update on Genes and Genetic Variants Which may be Associated With BleedingIbrahim Almazni, Rachel Stapley, Neil V Morgan
Platelets|October 25, 2022
Inherited ADAMTS13 mutations associated with Thrombotic Thrombocytopenic Purpura: a short review and updateZoe Markham-Lee, Neil V Morgan, Jonas Emsley
Platelets|March 31, 2016
Inherited thrombocytopenia: novel insights into megakaryocyte maturation, proplatelet formation and platelet lifespanBen Johnson, Sarah J Fletcher, Neil V Morgan
Platelets|June 28, 2016
Inherited platelet disorders: Insight from platelet genomics using next-generation sequencingAnnabel Maclachlan, Steve P Watson, Neil V Morgan
Blood Advances|March 21, 2025
Venous thrombosis unchained: Pandora's box of noninflammatory mechanismsSophie R M Smith, Neil V Morgan, Alexander Brill
Human Mutation|September 16, 2020
A comprehensive bioinformatic analysis of 126 patients with an inherited platelet disorder to identify both sequence and copy number genetic variantsIbrahim Almazni, Rachel J Stapley, Abdullah O Khan, et al.
Human Reproduction Update|June 1, 2019
Potential genetic causes of miscarriage in euploid pregnancies: a systematic reviewEmily Colley, Susan Hamilton, Paul Smith, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|April 18, 2013
Variable presentation of primary immune deficiency: two cases with CD3 gamma deficiency presenting with only autoimmunityHuseyin Tokgoz, Umran Caliskan, Sevgi Keles, et al.
Scientific Reports|August 18, 2017
CRISPR-Cas9 Mediated Labelling Allows for Single Molecule Imaging and ResolutionAbdullah O Khan, Victoria A Simms, Jeremy A Pike, et al.
British Journal of Haematology|February 1, 2014
What is the role of genetic testing in the investigation of patients with suspected platelet function disorders?Martina E Daly, Vincenzo C Leo, Gillian C Lowe, et al.
Pageof 9

Showing results (1-10 of 88) with videos related to

Sort By:
Pageof 9
Frontiers in Cardiovascular Medicine|July 6, 2019
Inherited Thrombocytopenia: Update on Genes and Genetic Variants Which may be Associated With BleedingIbrahim Almazni, Rachel Stapley, Neil V Morgan
Platelets|October 25, 2022
Inherited ADAMTS13 mutations associated with Thrombotic Thrombocytopenic Purpura: a short review and updateZoe Markham-Lee, Neil V Morgan, Jonas Emsley
Platelets|March 31, 2016
Inherited thrombocytopenia: novel insights into megakaryocyte maturation, proplatelet formation and platelet lifespanBen Johnson, Sarah J Fletcher, Neil V Morgan
Platelets|June 28, 2016
Inherited platelet disorders: Insight from platelet genomics using next-generation sequencingAnnabel Maclachlan, Steve P Watson, Neil V Morgan
Blood Advances|March 21, 2025
Venous thrombosis unchained: Pandora's box of noninflammatory mechanismsSophie R M Smith, Neil V Morgan, Alexander Brill
Human Mutation|September 16, 2020
A comprehensive bioinformatic analysis of 126 patients with an inherited platelet disorder to identify both sequence and copy number genetic variantsIbrahim Almazni, Rachel J Stapley, Abdullah O Khan, et al.
Human Reproduction Update|June 1, 2019
Potential genetic causes of miscarriage in euploid pregnancies: a systematic reviewEmily Colley, Susan Hamilton, Paul Smith, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|April 18, 2013
Variable presentation of primary immune deficiency: two cases with CD3 gamma deficiency presenting with only autoimmunityHuseyin Tokgoz, Umran Caliskan, Sevgi Keles, et al.
Scientific Reports|August 18, 2017
CRISPR-Cas9 Mediated Labelling Allows for Single Molecule Imaging and ResolutionAbdullah O Khan, Victoria A Simms, Jeremy A Pike, et al.
British Journal of Haematology|February 1, 2014
What is the role of genetic testing in the investigation of patients with suspected platelet function disorders?Martina E Daly, Vincenzo C Leo, Gillian C Lowe, et al.
Pageof 9