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Showing results (181-190 of 250) with videos related to

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Annals of Gastroenterology|January 30, 2026
MUC1 as a biomarker in primary sclerosing cholangitis and cholangiocarcinomaJana G Hashash, Pamela Beatty, Irene K Yan, et al.
Journal of Clinical Gastroenterology|September 5, 2023
Efficacy and Safety of Vedolizumab and Tumor Necrosis Factor Inhibitors in the Treatment of Steroid-refractory Microscopic Colitis: A Systematic Review and Meta-analysisNabil El Hage Chehade, Sara Ghoneim, Sagar Shah, et al.
Physiological Genomics|March 3, 2005
Phylogeny of Na+/Ca2+ exchanger (NCX) genes from genomic data identifies new gene duplications and a new family member in fish speciesChristian R Marshall, Joanne A Fox, Stefanie L Butland, et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases|December 27, 2016
Usutu virus, Belgium, 2016M Garigliany, A Linden, G Gilliau, et al.
The Journal of Clinical Investigation|October 1, 1991
Interleukin-5 and the posttreatment eosinophilia in patients with onchocerciasisA P Limaye, J S Abrams, J E Silver, et al.
Journal of Nanoscience and Nanotechnology|December 4, 2010
Quantum dot conjugates for targeted silencing of bcr/abl gene by RNA interference in human myelogenous leukemia K562 cellsYu Zhao, Lujing Zhao, Lijia Zhou, et al.
Seizure|May 25, 2002
So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutationV des Portes, L Abaoub, A Joannard, et al.
Molecular and Cellular Neurosciences|October 10, 2001
Doublecortin interacts with mu subunits of clathrin adaptor complexes in the developing nervous systemG Friocourt, P Chafey, P Billuart, et al.
Human Molecular Genetics|April 18, 1998
Spermine deficiency in Gy mice caused by deletion of the spermine synthase geneB Lorenz, F Francis, K Gempel, et al.
Oncogene|December 1, 1994
BMX, a novel nonreceptor tyrosine kinase gene of the BTK/ITK/TEC/TXK family located in chromosome Xp22.2L Tamagnone, I Lahtinen, T Mustonen, et al.
Pageof 25

Showing results (181-190 of 250) with videos related to

Sort By:
Pageof 25
Annals of Gastroenterology|January 30, 2026
MUC1 as a biomarker in primary sclerosing cholangitis and cholangiocarcinomaJana G Hashash, Pamela Beatty, Irene K Yan, et al.
Journal of Clinical Gastroenterology|September 5, 2023
Efficacy and Safety of Vedolizumab and Tumor Necrosis Factor Inhibitors in the Treatment of Steroid-refractory Microscopic Colitis: A Systematic Review and Meta-analysisNabil El Hage Chehade, Sara Ghoneim, Sagar Shah, et al.
Physiological Genomics|March 3, 2005
Phylogeny of Na+/Ca2+ exchanger (NCX) genes from genomic data identifies new gene duplications and a new family member in fish speciesChristian R Marshall, Joanne A Fox, Stefanie L Butland, et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases|December 27, 2016
Usutu virus, Belgium, 2016M Garigliany, A Linden, G Gilliau, et al.
The Journal of Clinical Investigation|October 1, 1991
Interleukin-5 and the posttreatment eosinophilia in patients with onchocerciasisA P Limaye, J S Abrams, J E Silver, et al.
Journal of Nanoscience and Nanotechnology|December 4, 2010
Quantum dot conjugates for targeted silencing of bcr/abl gene by RNA interference in human myelogenous leukemia K562 cellsYu Zhao, Lujing Zhao, Lijia Zhou, et al.
Seizure|May 25, 2002
So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutationV des Portes, L Abaoub, A Joannard, et al.
Molecular and Cellular Neurosciences|October 10, 2001
Doublecortin interacts with mu subunits of clathrin adaptor complexes in the developing nervous systemG Friocourt, P Chafey, P Billuart, et al.
Human Molecular Genetics|April 18, 1998
Spermine deficiency in Gy mice caused by deletion of the spermine synthase geneB Lorenz, F Francis, K Gempel, et al.
Oncogene|December 1, 1994
BMX, a novel nonreceptor tyrosine kinase gene of the BTK/ITK/TEC/TXK family located in chromosome Xp22.2L Tamagnone, I Lahtinen, T Mustonen, et al.
Pageof 25