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Neil V Morgan

Showing results (81-90 of 88) with videos related to

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Human Molecular Genetics|March 6, 2016
Germline ESR2 mutation predisposes to medullary thyroid carcinoma and causes up-regulation of RET expressionJoel Smith, Martin L Read, Jon Hoffman, et al.
Cell|December 20, 2014
Dual proteolytic pathways govern glycolysis and immune competenceWei Lu, Yu Zhang, David O McDonald, et al.
Haematologica|August 2, 2016
Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defectsBen Johnson, Gillian C Lowe, Jane Futterer, et al.
Cardiovascular Research|August 12, 2024
PITX2 deficiency leads to atrial mitochondrial dysfunctionJasmeet S Reyat, Laura C Sommerfeld, Molly O'Reilly, et al.
Nature Genetics|February 8, 2005
Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndromeIrene A Aligianis, Colin A Johnson, Paul Gissen, et al.
Nature Genetics|January 18, 2006
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk ratUrsula M Smith, Mark Consugar, Louise J Tee, et al.
Research and Practice in Thrombosis and Haemostasis|April 3, 2025
Illustrated capsules from the Advanced Course in Platelet ResearchChristian Andrea Di Buduo, Vittorio Abbonante, Alessandro Malara, et al.
Blood Advances|July 5, 2023
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41Claire C Homan, Michael W Drazer, Kai Yu, et al.
Pageof 9

Showing results (81-90 of 88) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 88 results.
Human Molecular Genetics|March 6, 2016
Germline ESR2 mutation predisposes to medullary thyroid carcinoma and causes up-regulation of RET expressionJoel Smith, Martin L Read, Jon Hoffman, et al.
Cell|December 20, 2014
Dual proteolytic pathways govern glycolysis and immune competenceWei Lu, Yu Zhang, David O McDonald, et al.
Haematologica|August 2, 2016
Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defectsBen Johnson, Gillian C Lowe, Jane Futterer, et al.
Cardiovascular Research|August 12, 2024
PITX2 deficiency leads to atrial mitochondrial dysfunctionJasmeet S Reyat, Laura C Sommerfeld, Molly O'Reilly, et al.
Nature Genetics|February 8, 2005
Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndromeIrene A Aligianis, Colin A Johnson, Paul Gissen, et al.
Nature Genetics|January 18, 2006
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk ratUrsula M Smith, Mark Consugar, Louise J Tee, et al.
Research and Practice in Thrombosis and Haemostasis|April 3, 2025
Illustrated capsules from the Advanced Course in Platelet ResearchChristian Andrea Di Buduo, Vittorio Abbonante, Alessandro Malara, et al.
Blood Advances|July 5, 2023
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41Claire C Homan, Michael W Drazer, Kai Yu, et al.
Pageof 9