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M Andersen

Showing results (1241-1250 of 1,297) with videos related to

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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 23, 2024
Longitudinal Glioma Monitoring via Cerebrospinal Fluid Cell-Free DNACecile Riviere-Cazaux, Xiaoxi Dong, Wei Mo, et al.
The New Phytologist|February 28, 2024
Toward a coordinated understanding of hydro-biogeochemical root functions in tropical forests for application in vegetation modelsDaniela F Cusack, Bradley Christoffersen, Chris M Smith-Martin, et al.
Nature Genetics|July 9, 2003
VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic deathDiether Lambrechts, Erik Storkebaum, Masafumi Morimoto, et al.
Science (New York, N.Y.)|March 9, 2023
Droplet-based forward genetic screening of astrocyte-microglia cross-talkMichael A Wheeler, Iain C Clark, Hong-Gyun Lee, et al.
Annals of Clinical and Translational Neurology|May 22, 2024
Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALSHeather Marriott, Thomas P Spargo, Ahmad Al Khleifat, et al.
JAMA Internal Medicine|July 19, 2021
Association of Cycling With All-Cause and Cardiovascular Disease Mortality Among Persons With Diabetes: The European Prospective Investigation Into Cancer and Nutrition (EPIC) StudyMathias Ried-Larsen, Martin Gillies Rasmussen, Kim Blond, et al.
American Journal of Human Genetics|September 3, 2016
Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal PolyneuropathiesMichaela Auer-Grumbach, Stefan Toegel, Maria Schabhüttl, et al.
Blood|June 2, 2021
A factor VIIIa-mimetic bispecific antibody, Mim8, ameliorates bleeding upon severe vascular challenge in hemophilia A miceHenrik Østergaard, Jacob Lund, Per J Greisen, et al.
Plos One|April 18, 2012
Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALSFrank P Diekstra, Christiaan G J Saris, Wouter van Rheenen, et al.
Human Mutation|July 18, 2017
The role of de novo mutations in the development of amyotrophic lateral sclerosisPerry T C van Doormaal, Nicola Ticozzi, Jochen H Weishaupt, et al.
Pageof 130

Showing results (1241-1250 of 1,297) with videos related to

Sort By:
Pageof 130
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 23, 2024
Longitudinal Glioma Monitoring via Cerebrospinal Fluid Cell-Free DNACecile Riviere-Cazaux, Xiaoxi Dong, Wei Mo, et al.
The New Phytologist|February 28, 2024
Toward a coordinated understanding of hydro-biogeochemical root functions in tropical forests for application in vegetation modelsDaniela F Cusack, Bradley Christoffersen, Chris M Smith-Martin, et al.
Nature Genetics|July 9, 2003
VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic deathDiether Lambrechts, Erik Storkebaum, Masafumi Morimoto, et al.
Science (New York, N.Y.)|March 9, 2023
Droplet-based forward genetic screening of astrocyte-microglia cross-talkMichael A Wheeler, Iain C Clark, Hong-Gyun Lee, et al.
Annals of Clinical and Translational Neurology|May 22, 2024
Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALSHeather Marriott, Thomas P Spargo, Ahmad Al Khleifat, et al.
JAMA Internal Medicine|July 19, 2021
Association of Cycling With All-Cause and Cardiovascular Disease Mortality Among Persons With Diabetes: The European Prospective Investigation Into Cancer and Nutrition (EPIC) StudyMathias Ried-Larsen, Martin Gillies Rasmussen, Kim Blond, et al.
American Journal of Human Genetics|September 3, 2016
Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal PolyneuropathiesMichaela Auer-Grumbach, Stefan Toegel, Maria Schabhüttl, et al.
Blood|June 2, 2021
A factor VIIIa-mimetic bispecific antibody, Mim8, ameliorates bleeding upon severe vascular challenge in hemophilia A miceHenrik Østergaard, Jacob Lund, Per J Greisen, et al.
Plos One|April 18, 2012
Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALSFrank P Diekstra, Christiaan G J Saris, Wouter van Rheenen, et al.
Human Mutation|July 18, 2017
The role of de novo mutations in the development of amyotrophic lateral sclerosisPerry T C van Doormaal, Nicola Ticozzi, Jochen H Weishaupt, et al.
Pageof 130