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Neil V Morgan

Showing results (11-20 of 88) with videos related to

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Platelets|May 19, 2022
Prevalence and natural history of variants in the <i>ANKRD26</i> gene: a short review and update of reported casesHrushikesh Vyas, Ahmad Alcheikh, Gillian Lowe, et al.
Research and Practice in Thrombosis and Haemostasis|April 9, 2026
Emicizumab prophylaxis in a preterm infant with severe hemophilia A: a case report on the feasibility of early useEman Hassan, Charles Percy, Amna Ahmed, et al.
The Journal of General Physiology|February 7, 2025
Structural and functional insights into α-actinin isoforms and their implications in cardiovascular diseaseMaya Noureddine, Halina Mikolajek, Neil V Morgan, et al.
RNA (New York, N.Y.)|April 22, 2018
Role of the novel endoribonuclease SLFN14 and its disease-causing mutations in ribosomal degradationSarah J Fletcher, Vera P Pisareva, Abdullah O Khan, et al.
Journal of Clinical Medicine|October 29, 2020
Cell-Free DNA in the Investigation of MiscarriageEmily Colley, Adam J Devall, Helen Williams, et al.
Platelets|March 8, 2017
Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet functionAnnabel Maclachlan, Gerry Dolan, Charlotte Grimley, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 16, 2026
Performing Large-Scale Genetic Analysis in the Bleeding Disorders CommunityAnna R Blankstein, Sterre P E Willems, Saskia E M Schols, et al.
The Turkish Journal of Pediatrics|June 2, 2009
Pantothenate kinase-associated neurodegeneration (PKAN): molecular confirmation of a Turkish patient with a rare frameshift mutation in the coding region of the PANK2 geneHakan Cangül, Ozlem Ozdemir, Tahsin Yakut, et al.
Platelets|February 22, 2021
A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorderIbrahim Almazni, Pavel Chudakou, Alison Dawson-Meadows, et al.
Journal of Thrombosis and Haemostasis : JTH|October 6, 2020
Novel gene variants in patients with platelet-based bleeding using combined exome sequencing and RNAseq murine expression dataAbdullah O Khan, Rachel J Stapley, Jeremy A Pike, et al.
Pageof 9

Showing results (11-20 of 88) with videos related to

Sort By:
Pageof 9
Platelets|May 19, 2022
Prevalence and natural history of variants in the <i>ANKRD26</i> gene: a short review and update of reported casesHrushikesh Vyas, Ahmad Alcheikh, Gillian Lowe, et al.
Research and Practice in Thrombosis and Haemostasis|April 9, 2026
Emicizumab prophylaxis in a preterm infant with severe hemophilia A: a case report on the feasibility of early useEman Hassan, Charles Percy, Amna Ahmed, et al.
The Journal of General Physiology|February 7, 2025
Structural and functional insights into α-actinin isoforms and their implications in cardiovascular diseaseMaya Noureddine, Halina Mikolajek, Neil V Morgan, et al.
RNA (New York, N.Y.)|April 22, 2018
Role of the novel endoribonuclease SLFN14 and its disease-causing mutations in ribosomal degradationSarah J Fletcher, Vera P Pisareva, Abdullah O Khan, et al.
Journal of Clinical Medicine|October 29, 2020
Cell-Free DNA in the Investigation of MiscarriageEmily Colley, Adam J Devall, Helen Williams, et al.
Platelets|March 8, 2017
Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet functionAnnabel Maclachlan, Gerry Dolan, Charlotte Grimley, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 16, 2026
Performing Large-Scale Genetic Analysis in the Bleeding Disorders CommunityAnna R Blankstein, Sterre P E Willems, Saskia E M Schols, et al.
The Turkish Journal of Pediatrics|June 2, 2009
Pantothenate kinase-associated neurodegeneration (PKAN): molecular confirmation of a Turkish patient with a rare frameshift mutation in the coding region of the PANK2 geneHakan Cangül, Ozlem Ozdemir, Tahsin Yakut, et al.
Platelets|February 22, 2021
A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorderIbrahim Almazni, Pavel Chudakou, Alison Dawson-Meadows, et al.
Journal of Thrombosis and Haemostasis : JTH|October 6, 2020
Novel gene variants in patients with platelet-based bleeding using combined exome sequencing and RNAseq murine expression dataAbdullah O Khan, Rachel J Stapley, Jeremy A Pike, et al.
Pageof 9