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H Dahl

Showing results (191-200 of 233) with videos related to

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The Journal of the Acoustical Society of America|December 3, 2008
Mid-frequency acoustic propagation in shallow water on the New Jersey shelf. II. Intensity fluctuationDajun Tang, Frank S Henyey, Zhongkang Wang, et al.
Neuropediatrics|January 22, 2003
A case of diffuse leptomeningeal oligodendrogliomatosis associated with HHV-6 variant AT Stödberg, Y Deniz, N Esteitie, et al.
Applied and Environmental Microbiology|February 2, 2010
Functional genomic study of exogenous n-butanol stress in Escherichia coliBecky J Rutherford, Robert H Dahl, Richard E Price, et al.
Human Molecular Genetics|June 13, 1998
Reduced collagen VI causes Bethlem myopathy: a heterozygous COL6A1 nonsense mutation results in mRNA decay and functional haploinsufficiencyS R Lamandé, J F Bateman, W Hutchison, et al.
Mbio|November 6, 2014
Improving microbial biogasoline production in Escherichia coli using tolerance engineeringJee Loon Foo, Heather M Jensen, Robert H Dahl, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|October 29, 2019
Transcerebral exchange kinetics of large neutral amino acids during acute inspiratory hypoxia in humansRasmus H Dahl, Ronan M G Berg, Sarah Taudorf, et al.
Molecular Cancer Therapeutics|May 17, 2008
Comparison of antitumor effects of multitargeted tyrosine kinase inhibitors in acute myelogenous leukemiaShuiying Hu, Hongmei Niu, Patton Minkin, et al.
Journal of Medical Genetics|December 24, 1998
Segregation of mutations in arylsulphatase E and correlation with the clinical presentation of chondrodysplasia punctataL J Sheffield, A H Osborn, W M Hutchison, et al.
The Journal of Antimicrobial Chemotherapy|June 28, 2008
The AmpC phenotype in Norwegian clinical isolates of Escherichia coli is associated with an acquired ISEcp1-like ampC element or hyperproduction of the endogenous AmpCBjørg Haldorsen, Bettina Aasnaes, Kristin H Dahl, et al.
Journal of Inherited Metabolic Disease|December 22, 1999
Mitochondrial DNA mutations at nucleotide 8993 show a lack of tissue- or age-related variationS L White, S Shanske, J J McGill, et al.
Pageof 24

Showing results (191-200 of 233) with videos related to

Sort By:
Pageof 24
The Journal of the Acoustical Society of America|December 3, 2008
Mid-frequency acoustic propagation in shallow water on the New Jersey shelf. II. Intensity fluctuationDajun Tang, Frank S Henyey, Zhongkang Wang, et al.
Neuropediatrics|January 22, 2003
A case of diffuse leptomeningeal oligodendrogliomatosis associated with HHV-6 variant AT Stödberg, Y Deniz, N Esteitie, et al.
Applied and Environmental Microbiology|February 2, 2010
Functional genomic study of exogenous n-butanol stress in Escherichia coliBecky J Rutherford, Robert H Dahl, Richard E Price, et al.
Human Molecular Genetics|June 13, 1998
Reduced collagen VI causes Bethlem myopathy: a heterozygous COL6A1 nonsense mutation results in mRNA decay and functional haploinsufficiencyS R Lamandé, J F Bateman, W Hutchison, et al.
Mbio|November 6, 2014
Improving microbial biogasoline production in Escherichia coli using tolerance engineeringJee Loon Foo, Heather M Jensen, Robert H Dahl, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|October 29, 2019
Transcerebral exchange kinetics of large neutral amino acids during acute inspiratory hypoxia in humansRasmus H Dahl, Ronan M G Berg, Sarah Taudorf, et al.
Molecular Cancer Therapeutics|May 17, 2008
Comparison of antitumor effects of multitargeted tyrosine kinase inhibitors in acute myelogenous leukemiaShuiying Hu, Hongmei Niu, Patton Minkin, et al.
Journal of Medical Genetics|December 24, 1998
Segregation of mutations in arylsulphatase E and correlation with the clinical presentation of chondrodysplasia punctataL J Sheffield, A H Osborn, W M Hutchison, et al.
The Journal of Antimicrobial Chemotherapy|June 28, 2008
The AmpC phenotype in Norwegian clinical isolates of Escherichia coli is associated with an acquired ISEcp1-like ampC element or hyperproduction of the endogenous AmpCBjørg Haldorsen, Bettina Aasnaes, Kristin H Dahl, et al.
Journal of Inherited Metabolic Disease|December 22, 1999
Mitochondrial DNA mutations at nucleotide 8993 show a lack of tissue- or age-related variationS L White, S Shanske, J J McGill, et al.
Pageof 24