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Winberg

Showing results (551-560 of 615) with videos related to

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Nutrients|December 17, 2024
Sirtuin Proteins and Memory: A Promising Target in Alzheimer's Disease Therapy?Francesca Fernandez, Lyn R Griffiths, Heidi G Sutherland, et al.
American Journal of Clinical Pathology|June 1, 1981
Terminal deoxynucleotidyl transferase activity in neoplastic and nonneoplastic hematopoietic cellsR M Bearman, C D Winberg, W C Maslow, et al.
Cancer|July 15, 1987
Antigenically defined subgroups of lymphoblastic lymphoma. Relationship to clinical presentation and biologic behaviorK Sheibani, B N Nathwani, C D Winberg, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Chimerism resulting from parthenogenetic activation and dispermic fertilizationJohanna Winberg, Peter Gustavsson, Kristina Lagerstedt-Robinson, et al.
Comparative Biochemistry and Physiology. Part A, Molecular & Integrative Physiology|April 18, 2015
Increased reactivity and monoamine dysregulation following stress in triploid Atlantic salmon (Salmo salar)Thomas William Kenneth Fraser, Marco Antonio Vindas, Per Gunnar Fjelldal, et al.
Genomics|January 15, 1994
NotI linking clones as a tool for joining physical and genetic maps of the human genomeR L Allikmets, V I Kashuba, B Pettersson, et al.
Journal of Cellular Biochemistry|September 2, 2018
PNPLA3 variant M148 causes resistance to starvation-mediated lipid droplet autophagy in human hepatocytesFlorentina Negoita, Julia Blomdahl, Sebastian Wasserstrom, et al.
Plos One|August 4, 2018
The selectivity of galardin and an azasugar-based hydroxamate compound for human matrix metalloproteases and bacterial metalloproteasesIngebrigt Sylte, Rangita Dawadi, Nabin Malla, et al.
Mbio|January 23, 2020
Neurotrophic Factors Protect the Intestinal Barrier from Rotavirus Insult in MiceMarie Hagbom, Felipe Meira De Faria, Martin E Winberg, et al.
Human Molecular Genetics|July 1, 1997
Modulation of disease severity of dystrophic epidermolysis bullosa by a splice site mutation in combination with a missense mutation in the COL7A1 geneJ O Winberg, N Hammami-Hauasli, O Nilssen, et al.
Pageof 62

Showing results (551-560 of 615) with videos related to

Sort By:
Pageof 62
Nutrients|December 17, 2024
Sirtuin Proteins and Memory: A Promising Target in Alzheimer's Disease Therapy?Francesca Fernandez, Lyn R Griffiths, Heidi G Sutherland, et al.
American Journal of Clinical Pathology|June 1, 1981
Terminal deoxynucleotidyl transferase activity in neoplastic and nonneoplastic hematopoietic cellsR M Bearman, C D Winberg, W C Maslow, et al.
Cancer|July 15, 1987
Antigenically defined subgroups of lymphoblastic lymphoma. Relationship to clinical presentation and biologic behaviorK Sheibani, B N Nathwani, C D Winberg, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Chimerism resulting from parthenogenetic activation and dispermic fertilizationJohanna Winberg, Peter Gustavsson, Kristina Lagerstedt-Robinson, et al.
Comparative Biochemistry and Physiology. Part A, Molecular & Integrative Physiology|April 18, 2015
Increased reactivity and monoamine dysregulation following stress in triploid Atlantic salmon (Salmo salar)Thomas William Kenneth Fraser, Marco Antonio Vindas, Per Gunnar Fjelldal, et al.
Genomics|January 15, 1994
NotI linking clones as a tool for joining physical and genetic maps of the human genomeR L Allikmets, V I Kashuba, B Pettersson, et al.
Journal of Cellular Biochemistry|September 2, 2018
PNPLA3 variant M148 causes resistance to starvation-mediated lipid droplet autophagy in human hepatocytesFlorentina Negoita, Julia Blomdahl, Sebastian Wasserstrom, et al.
Plos One|August 4, 2018
The selectivity of galardin and an azasugar-based hydroxamate compound for human matrix metalloproteases and bacterial metalloproteasesIngebrigt Sylte, Rangita Dawadi, Nabin Malla, et al.
Mbio|January 23, 2020
Neurotrophic Factors Protect the Intestinal Barrier from Rotavirus Insult in MiceMarie Hagbom, Felipe Meira De Faria, Martin E Winberg, et al.
Human Molecular Genetics|July 1, 1997
Modulation of disease severity of dystrophic epidermolysis bullosa by a splice site mutation in combination with a missense mutation in the COL7A1 geneJ O Winberg, N Hammami-Hauasli, O Nilssen, et al.
Pageof 62