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Neil V Morgan

Showing results (61-70 of 88) with videos related to

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Blood|October 9, 2013
Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defectsJacqueline Stockley, Neil V Morgan, Danai Bem, et al.
Blood|January 11, 2014
Characterization of multiple platelet activation pathways in patients with bleeding as a high-throughput screening option: use of 96-well Optimul assayMarie Lordkipanidzé, Gillian C Lowe, Nicholas S Kirkby, et al.
American Journal of Human Genetics|July 11, 2006
Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndromeNeil V Morgan, Louise A Brueton, Phillip Cox, et al.
American Journal of Human Genetics|March 9, 2010
Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome)Esther Meyer, Christopher Ricketts, Neil V Morgan, et al.
American Journal of Human Genetics|July 12, 2011
Inactivation of IL11 signaling causes craniosynostosis, delayed tooth eruption, and supernumerary teethPekka Nieminen, Neil V Morgan, Aimée L Fenwick, et al.
Gastroenterology|February 24, 2010
Mutations in TTC37 cause trichohepatoenteric syndrome (phenotypic diarrhea of infancy)Jane Louise Hartley, Nicholas C Zachos, Ban Dawood, et al.
Journal of Clinical Immunology|January 24, 2016
Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 DeficiencyTarana Singh Dang, Joseph D P Willet, Helen R Griffin, et al.
The Journal of Clinical Investigation|August 12, 2025
Platelet-specific SLFN14 deletion causes macrothrombocytopenia and platelet dysfunction through dysregulated megakaryocyte and platelet gene expressionRachel J Stapley, Xenia Sawkulycz, Gabriel Hm Da Mota Araujo, et al.
Blood Vessels, Thrombosis & Hemostasis|August 6, 2025
Human and mouse platelet transcriptomes and proteomes for phenotyping 3474 genes with hemostatic and platelet traitsJingnan Huang, Federico Marini, Fiorella A Solari, et al.
Haematologica|February 26, 2026
Scott syndrome with novel compound heterozygous pathogenic variants in <i>ANO6</i> and reduced thrombin generationAmna Ahmed, Samantha J Montague, Hrushikesh Vyas, et al.
Pageof 9

Showing results (61-70 of 88) with videos related to

Sort By:
Pageof 9
Blood|October 9, 2013
Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defectsJacqueline Stockley, Neil V Morgan, Danai Bem, et al.
Blood|January 11, 2014
Characterization of multiple platelet activation pathways in patients with bleeding as a high-throughput screening option: use of 96-well Optimul assayMarie Lordkipanidzé, Gillian C Lowe, Nicholas S Kirkby, et al.
American Journal of Human Genetics|July 11, 2006
Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndromeNeil V Morgan, Louise A Brueton, Phillip Cox, et al.
American Journal of Human Genetics|March 9, 2010
Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome)Esther Meyer, Christopher Ricketts, Neil V Morgan, et al.
American Journal of Human Genetics|July 12, 2011
Inactivation of IL11 signaling causes craniosynostosis, delayed tooth eruption, and supernumerary teethPekka Nieminen, Neil V Morgan, Aimée L Fenwick, et al.
Gastroenterology|February 24, 2010
Mutations in TTC37 cause trichohepatoenteric syndrome (phenotypic diarrhea of infancy)Jane Louise Hartley, Nicholas C Zachos, Ban Dawood, et al.
Journal of Clinical Immunology|January 24, 2016
Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 DeficiencyTarana Singh Dang, Joseph D P Willet, Helen R Griffin, et al.
The Journal of Clinical Investigation|August 12, 2025
Platelet-specific SLFN14 deletion causes macrothrombocytopenia and platelet dysfunction through dysregulated megakaryocyte and platelet gene expressionRachel J Stapley, Xenia Sawkulycz, Gabriel Hm Da Mota Araujo, et al.
Blood Vessels, Thrombosis & Hemostasis|August 6, 2025
Human and mouse platelet transcriptomes and proteomes for phenotyping 3474 genes with hemostatic and platelet traitsJingnan Huang, Federico Marini, Fiorella A Solari, et al.
Haematologica|February 26, 2026
Scott syndrome with novel compound heterozygous pathogenic variants in <i>ANO6</i> and reduced thrombin generationAmna Ahmed, Samantha J Montague, Hrushikesh Vyas, et al.
Pageof 9