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Showing results (671-680 of 694) with videos related to

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JCI Insight|November 18, 2025
Genital herpes shedding episodes associate with altered spatial organization and activation of mucosal immune cellsFinn MacLean, Rachael M Zemek, Adino Tesfahun Tsegaye, et al.
Pediatric Research|April 28, 2006
Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiencyStefan Kölker, Sven F Garbade, Cheryl R Greenberg, et al.
Human Mutation|November 2, 2006
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycansJoan C Marini, Antonella Forlino, Wayne A Cabral, et al.
Basic & Clinical Pharmacology & Toxicology|June 14, 2023
Appetite stimulation with cannabis-based medicine and methods for assessment of glomerular filtration in older patients with medical illness: A study protocolR L Nielsen, O Bornaes, I K Storgaard, et al.
Journal of Inherited Metabolic Disease|January 19, 2026
Pregnancies in Women With Long-Chain Fatty Acid Oxidation Disorders: Results of a European and North American SurveySarah C Grünert, Mirjam Langeveld, Lisa Rudolph, et al.
Science (New York, N.Y.)|July 10, 2025
Origins and diversity of Greenland's <i>Qimmit</i> revealed with genomes of ancient and modern sled dogsT R Feuerborn, M Appelt, K Bougiouri, et al.
Human Genetics|December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndromeR S Møller, L R Jensen, S M Maas, et al.
Human Molecular Genetics|October 3, 2022
Pathogenic variants in GCSH encoding the moonlighting H-protein cause combined nonketotic hyperglycinemia and lipoate deficiencyLaura Arribas-Carreira, Cristina Dallabona, Michael A Swanson, et al.
Brain : a Journal of Neurology|December 17, 2013
Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5Peter R Baker, Marisa W Friederich, Michael A Swanson, et al.
ESMO Open|June 15, 2024
Assessment of the current and emerging criteria for the histopathological classification of lung neuroendocrine tumours in the lungNENomics projectÉ Mathian, Y Drouet, A Sexton-Oates, et al.
Pageof 70

Showing results (671-680 of 694) with videos related to

Sort By:
Pageof 70
JCI Insight|November 18, 2025
Genital herpes shedding episodes associate with altered spatial organization and activation of mucosal immune cellsFinn MacLean, Rachael M Zemek, Adino Tesfahun Tsegaye, et al.
Pediatric Research|April 28, 2006
Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiencyStefan Kölker, Sven F Garbade, Cheryl R Greenberg, et al.
Human Mutation|November 2, 2006
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycansJoan C Marini, Antonella Forlino, Wayne A Cabral, et al.
Basic & Clinical Pharmacology & Toxicology|June 14, 2023
Appetite stimulation with cannabis-based medicine and methods for assessment of glomerular filtration in older patients with medical illness: A study protocolR L Nielsen, O Bornaes, I K Storgaard, et al.
Journal of Inherited Metabolic Disease|January 19, 2026
Pregnancies in Women With Long-Chain Fatty Acid Oxidation Disorders: Results of a European and North American SurveySarah C Grünert, Mirjam Langeveld, Lisa Rudolph, et al.
Science (New York, N.Y.)|July 10, 2025
Origins and diversity of Greenland's <i>Qimmit</i> revealed with genomes of ancient and modern sled dogsT R Feuerborn, M Appelt, K Bougiouri, et al.
Human Genetics|December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndromeR S Møller, L R Jensen, S M Maas, et al.
Human Molecular Genetics|October 3, 2022
Pathogenic variants in GCSH encoding the moonlighting H-protein cause combined nonketotic hyperglycinemia and lipoate deficiencyLaura Arribas-Carreira, Cristina Dallabona, Michael A Swanson, et al.
Brain : a Journal of Neurology|December 17, 2013
Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5Peter R Baker, Marisa W Friederich, Michael A Swanson, et al.
ESMO Open|June 15, 2024
Assessment of the current and emerging criteria for the histopathological classification of lung neuroendocrine tumours in the lungNENomics projectÉ Mathian, Y Drouet, A Sexton-Oates, et al.
Pageof 70