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P Zimmer

Showing results (111-120 of 167) with videos related to

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Molecular Medicine (Cambridge, Mass.)|August 17, 1999
Efficient mitochondrial import of newly synthesized ornithine transcarbamylase (OTC) and correction of secondary metabolic alterations in spf(ash) mice following gene therapy of OTC deficiencyK P Zimmer, M Bendiks, M Mori, et al.
International Reviews of Immunology|January 1, 1997
B cell development in miceJ F Kearney, W J Won, C Benedict, et al.
Fortschritte Der Neurologie-Psychiatrie|September 2, 2015
[Chemotherapy-induced Peripheral Neuropathy]I Bobylev, T Elter, C Schneider, et al.
European Journal of Immunology|August 1, 1991
Isolation of normal human follicular dendritic cells and CD4-independent in vitro infection by human immunodeficiency virus (HIV-1)I Stahmer, J P Zimmer, M Ernst, et al.
Joint Commission Journal on Quality and Patient Safety|February 19, 2008
Patient safety rounds in a pediatric tertiary care centerMichael L Rinke, Karen P Zimmer, Christoph U Lehmann, et al.
Human Gene Therapy|June 12, 2001
Differences in the human and mouse amino-terminal leader peptides of ornithine transcarbamylase affect mitochondrial import and efficacy of adenoviral vectorsX Ye, K P Zimmer, R Brown, et al.
Neuroscience Letters|January 14, 2018
The effects of exercise intensity and post-exercise recovery time on cortical activation as revealed by EEG alpha peak frequencyB Gutmann, P Zimmer, T Hülsdünker, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|May 16, 2006
Screening of blood donors for tissue transglutaminase antibodies in the Ryazan area (Russia)M Stroikova, N Augul, J Gureev, et al.
The Journal of Pathology|August 10, 1999
Intracellular transport of acid beta-glucosidase and lysosome-associated membrane proteins is affected in Gaucher's disease (G202R mutation)K P Zimmer, P le Coutre, H M Aerts, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
A novel point mutation at codon 269 of the ornithine transcarbamylase (OTC) gene causing neonatal onset of OTC deficiencyK P Zimmer, T Matsuura, J P Colombo, et al.
Pageof 17

Showing results (111-120 of 167) with videos related to

Sort By:
Pageof 17
Molecular Medicine (Cambridge, Mass.)|August 17, 1999
Efficient mitochondrial import of newly synthesized ornithine transcarbamylase (OTC) and correction of secondary metabolic alterations in spf(ash) mice following gene therapy of OTC deficiencyK P Zimmer, M Bendiks, M Mori, et al.
International Reviews of Immunology|January 1, 1997
B cell development in miceJ F Kearney, W J Won, C Benedict, et al.
Fortschritte Der Neurologie-Psychiatrie|September 2, 2015
[Chemotherapy-induced Peripheral Neuropathy]I Bobylev, T Elter, C Schneider, et al.
European Journal of Immunology|August 1, 1991
Isolation of normal human follicular dendritic cells and CD4-independent in vitro infection by human immunodeficiency virus (HIV-1)I Stahmer, J P Zimmer, M Ernst, et al.
Joint Commission Journal on Quality and Patient Safety|February 19, 2008
Patient safety rounds in a pediatric tertiary care centerMichael L Rinke, Karen P Zimmer, Christoph U Lehmann, et al.
Human Gene Therapy|June 12, 2001
Differences in the human and mouse amino-terminal leader peptides of ornithine transcarbamylase affect mitochondrial import and efficacy of adenoviral vectorsX Ye, K P Zimmer, R Brown, et al.
Neuroscience Letters|January 14, 2018
The effects of exercise intensity and post-exercise recovery time on cortical activation as revealed by EEG alpha peak frequencyB Gutmann, P Zimmer, T Hülsdünker, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|May 16, 2006
Screening of blood donors for tissue transglutaminase antibodies in the Ryazan area (Russia)M Stroikova, N Augul, J Gureev, et al.
The Journal of Pathology|August 10, 1999
Intracellular transport of acid beta-glucosidase and lysosome-associated membrane proteins is affected in Gaucher's disease (G202R mutation)K P Zimmer, P le Coutre, H M Aerts, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
A novel point mutation at codon 269 of the ornithine transcarbamylase (OTC) gene causing neonatal onset of OTC deficiencyK P Zimmer, T Matsuura, J P Colombo, et al.
Pageof 17