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Martin Lammens

Showing results (81-90 of 91) with videos related to

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Nature Communications|November 17, 2021
Organ-specific genome diversity of replication-competent SARS-CoV-2Jolien Van Cleemput, Willem van Snippenberg, Laurens Lambrechts, et al.
Blood|August 24, 2017
Dendritic cell vaccination as postremission treatment to prevent or delay relapse in acute myeloid leukemiaSébastien Anguille, Ann L Van de Velde, Evelien L Smits, et al.
Journal of Hematology & Oncology|January 24, 2025
WT1-mRNA dendritic cell vaccination of patients with glioblastoma multiforme, malignant pleural mesothelioma, metastatic breast cancer, and other solid tumors: type 1 T-lymphocyte responses are associated with clinical outcomeZwi N Berneman, Maxime De Laere, Paul Germonpré, et al.
Nature Communications|March 29, 2019
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusionsMontse Olivé, Martin Engvall, Gianina Ravenscroft, et al.
Nature Genetics|June 12, 2012
Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafnessSaskia B Wortmann, Frédéric M Vaz, Thatjana Gardeitchik, et al.
The New England Journal of Medicine|February 7, 2014
Multiple phenotypes in phosphoglucomutase 1 deficiencyLaura C Tegtmeyer, Stephan Rust, Monique van Scherpenzeel, et al.
Cardiovascular Research|August 23, 2022
The pulmonary vasculature in lethal COVID-19 and idiopathic pulmonary fibrosis at single-cell resolutionLaura P M H de Rooij, Lisa M Becker, Laure-Anne Teuwen, et al.
Journal of the American College of Cardiology|April 4, 2015
Mutations in a TGF-β ligand, TGFB3, cause syndromic aortic aneurysms and dissectionsAida M Bertoli-Avella, Elisabeth Gillis, Hiroko Morisaki, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|March 27, 2022
COVID-19-Associated cardiac pathology at the postmortem evaluation: a collaborative systematic reviewRaghed Almamlouk, Tarek Kashour, Sawsan Obeidat, et al.
American Journal of Human Genetics|June 11, 2013
Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathyGianina Ravenscroft, Satoko Miyatake, Vilma-Lotta Lehtokari, et al.
Pageof 10

Showing results (81-90 of 91) with videos related to

Sort By:
Pageof 10
Nature Communications|November 17, 2021
Organ-specific genome diversity of replication-competent SARS-CoV-2Jolien Van Cleemput, Willem van Snippenberg, Laurens Lambrechts, et al.
Blood|August 24, 2017
Dendritic cell vaccination as postremission treatment to prevent or delay relapse in acute myeloid leukemiaSébastien Anguille, Ann L Van de Velde, Evelien L Smits, et al.
Journal of Hematology & Oncology|January 24, 2025
WT1-mRNA dendritic cell vaccination of patients with glioblastoma multiforme, malignant pleural mesothelioma, metastatic breast cancer, and other solid tumors: type 1 T-lymphocyte responses are associated with clinical outcomeZwi N Berneman, Maxime De Laere, Paul Germonpré, et al.
Nature Communications|March 29, 2019
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusionsMontse Olivé, Martin Engvall, Gianina Ravenscroft, et al.
Nature Genetics|June 12, 2012
Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafnessSaskia B Wortmann, Frédéric M Vaz, Thatjana Gardeitchik, et al.
The New England Journal of Medicine|February 7, 2014
Multiple phenotypes in phosphoglucomutase 1 deficiencyLaura C Tegtmeyer, Stephan Rust, Monique van Scherpenzeel, et al.
Cardiovascular Research|August 23, 2022
The pulmonary vasculature in lethal COVID-19 and idiopathic pulmonary fibrosis at single-cell resolutionLaura P M H de Rooij, Lisa M Becker, Laure-Anne Teuwen, et al.
Journal of the American College of Cardiology|April 4, 2015
Mutations in a TGF-β ligand, TGFB3, cause syndromic aortic aneurysms and dissectionsAida M Bertoli-Avella, Elisabeth Gillis, Hiroko Morisaki, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|March 27, 2022
COVID-19-Associated cardiac pathology at the postmortem evaluation: a collaborative systematic reviewRaghed Almamlouk, Tarek Kashour, Sawsan Obeidat, et al.
American Journal of Human Genetics|June 11, 2013
Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathyGianina Ravenscroft, Satoko Miyatake, Vilma-Lotta Lehtokari, et al.
Pageof 10