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The Journal of Chemical Physics
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January 22, 2021
Spectroscopic and theoretical studies of UN and UN<sup></sup>
S R Battey, D H Bross, K A Peterson, et al.
Human Mutation
|
August 29, 2001
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship
N Gregersen, B S Andresen, M J Corydon, et al.
Molecular Genetics and Metabolism
|
February 4, 2014
Proteomic investigation of cultivated fibroblasts from patients with mitochondrial short-chain acyl-CoA dehydrogenase deficiency
Anders V Edhager, Vibeke Stenbroen, Nadia Sukusu Nielsen, et al.
Acta Cytologica
|
July 1, 1988
Malignant ascites of serous papillary ovarian adenocarcinoma. An immunocytochemical study of the tumor cells
J Guzman, M Hilgarth, K J Bross, et al.
Biology Open
|
August 2, 2015
Structure and signaling at hydroid polyp-stolon junctions, revisited
Katherine L Harmata, Emily L Somova, Austin P Parrin, et al.
Blut
|
February 19, 1979
The use of lymphocyte phosphoglucomutase as a genetic marker in bone marrow transplant recipients
G M Schmidt, K G Blume, K J Bross, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 21, 2023
Methanediol from cloud-processed formaldehyde is only a minor source of atmospheric formic acid
Thanh Lam Nguyen, Jozef Peeters, Jean-François Müller, et al.
Journal of Agricultural and Food Chemistry
|
May 1, 2010
NMR-based metabonomic investigation of heat stress in myotubes reveals a time-dependent change in the metabolites
Ida K Straadt, Jette F Young, Peter Bross, et al.
The Biological Bulletin
|
November 1, 2012
Within-colony migration of symbionts during bleaching of octocorals
Austin P Parrin, Katherine L Harmata, Sarah E Netherton, et al.
Human Mutation
|
July 19, 2002
Assessing the relative importance of the biophysical properties of amino acid substitutions associated with human genetic disease
Bent N Terp, David N Cooper, Inge T Christensen, et al.
Page
of 78
Search research articles
Search
Showing results (391-400 of 779) with videos related to
Sort By:
Page
of 78
The Journal of Chemical Physics
|
January 22, 2021
Spectroscopic and theoretical studies of UN and UN<sup></sup>
S R Battey, D H Bross, K A Peterson, et al.
Human Mutation
|
August 29, 2001
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship
N Gregersen, B S Andresen, M J Corydon, et al.
Molecular Genetics and Metabolism
|
February 4, 2014
Proteomic investigation of cultivated fibroblasts from patients with mitochondrial short-chain acyl-CoA dehydrogenase deficiency
Anders V Edhager, Vibeke Stenbroen, Nadia Sukusu Nielsen, et al.
Acta Cytologica
|
July 1, 1988
Malignant ascites of serous papillary ovarian adenocarcinoma. An immunocytochemical study of the tumor cells
J Guzman, M Hilgarth, K J Bross, et al.
Biology Open
|
August 2, 2015
Structure and signaling at hydroid polyp-stolon junctions, revisited
Katherine L Harmata, Emily L Somova, Austin P Parrin, et al.
Blut
|
February 19, 1979
The use of lymphocyte phosphoglucomutase as a genetic marker in bone marrow transplant recipients
G M Schmidt, K G Blume, K J Bross, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 21, 2023
Methanediol from cloud-processed formaldehyde is only a minor source of atmospheric formic acid
Thanh Lam Nguyen, Jozef Peeters, Jean-François Müller, et al.
Journal of Agricultural and Food Chemistry
|
May 1, 2010
NMR-based metabonomic investigation of heat stress in myotubes reveals a time-dependent change in the metabolites
Ida K Straadt, Jette F Young, Peter Bross, et al.
The Biological Bulletin
|
November 1, 2012
Within-colony migration of symbionts during bleaching of octocorals
Austin P Parrin, Katherine L Harmata, Sarah E Netherton, et al.
Human Mutation
|
July 19, 2002
Assessing the relative importance of the biophysical properties of amino acid substitutions associated with human genetic disease
Bent N Terp, David N Cooper, Inge T Christensen, et al.
Page
of 78