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W Annaert

Showing results (21-30 of 29) with videos related to

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Langmuir : the ACS Journal of Surfaces and Colloids|March 14, 2009
Chemical and biological characterization of thiol SAMs for neuronal cell attachmentK Jans, B Van Meerbergen, G Reekmans, et al.
The Journal of Biological Chemistry|November 10, 2000
Processing of beta-secretase by furin and other members of the proprotein convertase familyJ W Creemers, D Ines Dominguez, E Plets, et al.
Human Molecular Genetics|August 7, 2001
Pathogenic APP mutations near the gamma-secretase cleavage site differentially affect Abeta secretion and APP C-terminal fragment stabilityC De Jonghe, C Esselens, S Kumar-Singh, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 24, 2009
Peptide-functionalized microfabricated structures for improved on-chip neuronal adhesionB Van Meerbergen, K Jans, J Loo, et al.
The Journal of Biological Chemistry|August 30, 2001
Elevation of beta-amyloid peptide 2-42 in sporadic and familial Alzheimer's disease and its generation in PS1 knockout cellsJ Wiltfang, H Esselmann, P Cupers, et al.
Nature|April 17, 1999
A presenilin-1-dependent gamma-secretase-like protease mediates release of Notch intracellular domainB De Strooper, W Annaert, P Cupers, et al.
Molecular Medicine (Cambridge, Mass.)|September 29, 1999
Developmental expression of wild-type and mutant presenilin-1 in hippocampal neurons from transgenic mice: evidence for novel species-specific properties of human presenilin-1L Lévesque, W Annaert, K Craessaerts, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 16, 1999
Presenilin 2 deficiency causes a mild pulmonary phenotype and no changes in amyloid precursor protein processing but enhances the embryonic lethal phenotype of presenilin 1 deficiencyA Herreman, D Hartmann, W Annaert, et al.
Molecular Neurodegeneration|July 16, 2026
Atypical chemokine receptor 3 regulates synaptic removal in disease astrocytesV Giusti, J Park, E Giusto, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Langmuir : the ACS Journal of Surfaces and Colloids|March 14, 2009
Chemical and biological characterization of thiol SAMs for neuronal cell attachmentK Jans, B Van Meerbergen, G Reekmans, et al.
The Journal of Biological Chemistry|November 10, 2000
Processing of beta-secretase by furin and other members of the proprotein convertase familyJ W Creemers, D Ines Dominguez, E Plets, et al.
Human Molecular Genetics|August 7, 2001
Pathogenic APP mutations near the gamma-secretase cleavage site differentially affect Abeta secretion and APP C-terminal fragment stabilityC De Jonghe, C Esselens, S Kumar-Singh, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 24, 2009
Peptide-functionalized microfabricated structures for improved on-chip neuronal adhesionB Van Meerbergen, K Jans, J Loo, et al.
The Journal of Biological Chemistry|August 30, 2001
Elevation of beta-amyloid peptide 2-42 in sporadic and familial Alzheimer's disease and its generation in PS1 knockout cellsJ Wiltfang, H Esselmann, P Cupers, et al.
Nature|April 17, 1999
A presenilin-1-dependent gamma-secretase-like protease mediates release of Notch intracellular domainB De Strooper, W Annaert, P Cupers, et al.
Molecular Medicine (Cambridge, Mass.)|September 29, 1999
Developmental expression of wild-type and mutant presenilin-1 in hippocampal neurons from transgenic mice: evidence for novel species-specific properties of human presenilin-1L Lévesque, W Annaert, K Craessaerts, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 16, 1999
Presenilin 2 deficiency causes a mild pulmonary phenotype and no changes in amyloid precursor protein processing but enhances the embryonic lethal phenotype of presenilin 1 deficiencyA Herreman, D Hartmann, W Annaert, et al.
Molecular Neurodegeneration|July 16, 2026
Atypical chemokine receptor 3 regulates synaptic removal in disease astrocytesV Giusti, J Park, E Giusto, et al.
Pageof 3