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Showing results (361-370 of 381) with videos related to

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Nature Genetics|November 1, 1996
Haemochromatosis and HLA-HA M Jouanolle, G Gandon, P Jézéquel, et al.
Molecular Syndromology|April 10, 2014
Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 DeletionsC Dubourg, F Bonnet-Brilhault, A Toutain, et al.
Scientific Reports|November 1, 2017
Klotho Inhibits Interleukin-8 Secretion from Cystic Fibrosis Airway EpitheliaStefanie Krick, Nathalie Baumlin, Sheyla Paredes Aller, et al.
Biochemical Genetics|January 11, 2017
Early Evaluation and Monitoring of Critical Patients with Acute Respiratory Distress Syndrome (ARDS) Using Specific Genetic PolymorphismsFlorin G Horhat, Fuat Gundogdu, Laurentiu V David, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 17, 2014
Large-scale topology and the default mode network in the mouse connectomeJames M Stafford, Benjamin R Jarrett, Oscar Miranda-Dominguez, et al.
Plos Computational Biology|November 21, 2012
Functional connectivity and tuning curves in populations of simultaneously recorded neuronsIan H Stevenson, Brian M London, Emily R Oby, et al.
Lancet (London, England)|October 7, 2000
Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosisV Scotet, M de Braekeleer, M Roussey, et al.
Ecotoxicology and Environmental Safety|January 20, 2021
Effects of diclofenac on sentinel species and aquatic communities in semi-natural conditionsS Joachim, R Beaudouin, G Daniele, et al.
Journal of Medical Genetics|January 20, 2004
The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loadingK J Livesey, V L C Wimhurst, K Carter, et al.
Molecular Syndromology|October 30, 2013
Array-CGH Analysis Suggests Genetic Heterogeneity in RhombencephalosynapsisF Démurger, L Pasquier, C Dubourg, et al.
Pageof 39

Showing results (361-370 of 381) with videos related to

Sort By:
Pageof 39
Nature Genetics|November 1, 1996
Haemochromatosis and HLA-HA M Jouanolle, G Gandon, P Jézéquel, et al.
Molecular Syndromology|April 10, 2014
Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 DeletionsC Dubourg, F Bonnet-Brilhault, A Toutain, et al.
Scientific Reports|November 1, 2017
Klotho Inhibits Interleukin-8 Secretion from Cystic Fibrosis Airway EpitheliaStefanie Krick, Nathalie Baumlin, Sheyla Paredes Aller, et al.
Biochemical Genetics|January 11, 2017
Early Evaluation and Monitoring of Critical Patients with Acute Respiratory Distress Syndrome (ARDS) Using Specific Genetic PolymorphismsFlorin G Horhat, Fuat Gundogdu, Laurentiu V David, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 17, 2014
Large-scale topology and the default mode network in the mouse connectomeJames M Stafford, Benjamin R Jarrett, Oscar Miranda-Dominguez, et al.
Plos Computational Biology|November 21, 2012
Functional connectivity and tuning curves in populations of simultaneously recorded neuronsIan H Stevenson, Brian M London, Emily R Oby, et al.
Lancet (London, England)|October 7, 2000
Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosisV Scotet, M de Braekeleer, M Roussey, et al.
Ecotoxicology and Environmental Safety|January 20, 2021
Effects of diclofenac on sentinel species and aquatic communities in semi-natural conditionsS Joachim, R Beaudouin, G Daniele, et al.
Journal of Medical Genetics|January 20, 2004
The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loadingK J Livesey, V L C Wimhurst, K Carter, et al.
Molecular Syndromology|October 30, 2013
Array-CGH Analysis Suggests Genetic Heterogeneity in RhombencephalosynapsisF Démurger, L Pasquier, C Dubourg, et al.
Pageof 39