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Rob Willemsen

Showing results (111-120 of 157) with videos related to

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Molecular & Cellular Proteomics : MCP|February 11, 2009
Exosomal secretion of cytoplasmic prostate cancer xenograft-derived proteinsFlip H Jansen, Jeroen Krijgsveld, Angelique van Rijswijk, et al.
Acta Neuropathologica Communications|December 13, 2016
Retraction Note to: A new inducible transgenic mouse model for C9orf72-associated GGGGCC repeat expansion supports a gain-of-function mechanism in C9orf72-associated ALS and FTDRenate K Hukema, Fréderike W Riemslagh, Shamiram Melhem, et al.
Human Molecular Genetics|August 15, 2018
Protein synthesis levels are increased in a subset of individuals with fragile X syndromeSébastien Jacquemont, Laura Pacini, Aia E Jønch, et al.
Human Molecular Genetics|March 29, 2018
Protein synthesis levels are increased in a subset of individuals with fragile X syndromeSébastien Jacquemont, Laura Pacini, Aia E Jønch, et al.
Cell Cycle (Georgetown, Tex.)|December 9, 2014
Induced expression of expanded CGG RNA causes mitochondrial dysfunction in vivoRenate K Hukema, Ronald A M Buijsen, Chris Raske, et al.
Annals of Neurology|March 14, 2002
A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's diseaseSonia M Rosso, Esther van Herpen, Wout Deelen, et al.
Stem Cell Reports|November 25, 2014
DAZL limits pluripotency, differentiation, and apoptosis in developing primordial germ cellsHsu-Hsin Chen, Maaike Welling, Donald B Bloch, et al.
Human Molecular Genetics|February 2, 2002
The severe G480C cystic fibrosis mutation, when replicated in the mouse, demonstrates mistrafficking, normal survival and organ-specific bioelectricsPaul Dickinson, Stephen N Smith, Sheila Webb, et al.
Hepatology (Baltimore, Md.)|August 27, 2003
Timing and sequence of differentiation of embryonic rat hepatocytes along the biliary epithelial lineageRobbert G E Notenboom, Marius A van den Bergh Weerman, Koert P Dingemans, et al.
Brain : a Journal of Neurology|March 16, 2007
TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutationsHarro Seelaar, H Jurgen Schelhaas, Asma Azmani, et al.
Pageof 16

Showing results (111-120 of 157) with videos related to

Sort By:
Pageof 16
Molecular & Cellular Proteomics : MCP|February 11, 2009
Exosomal secretion of cytoplasmic prostate cancer xenograft-derived proteinsFlip H Jansen, Jeroen Krijgsveld, Angelique van Rijswijk, et al.
Acta Neuropathologica Communications|December 13, 2016
Retraction Note to: A new inducible transgenic mouse model for C9orf72-associated GGGGCC repeat expansion supports a gain-of-function mechanism in C9orf72-associated ALS and FTDRenate K Hukema, Fréderike W Riemslagh, Shamiram Melhem, et al.
Human Molecular Genetics|August 15, 2018
Protein synthesis levels are increased in a subset of individuals with fragile X syndromeSébastien Jacquemont, Laura Pacini, Aia E Jønch, et al.
Human Molecular Genetics|March 29, 2018
Protein synthesis levels are increased in a subset of individuals with fragile X syndromeSébastien Jacquemont, Laura Pacini, Aia E Jønch, et al.
Cell Cycle (Georgetown, Tex.)|December 9, 2014
Induced expression of expanded CGG RNA causes mitochondrial dysfunction in vivoRenate K Hukema, Ronald A M Buijsen, Chris Raske, et al.
Annals of Neurology|March 14, 2002
A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's diseaseSonia M Rosso, Esther van Herpen, Wout Deelen, et al.
Stem Cell Reports|November 25, 2014
DAZL limits pluripotency, differentiation, and apoptosis in developing primordial germ cellsHsu-Hsin Chen, Maaike Welling, Donald B Bloch, et al.
Human Molecular Genetics|February 2, 2002
The severe G480C cystic fibrosis mutation, when replicated in the mouse, demonstrates mistrafficking, normal survival and organ-specific bioelectricsPaul Dickinson, Stephen N Smith, Sheila Webb, et al.
Hepatology (Baltimore, Md.)|August 27, 2003
Timing and sequence of differentiation of embryonic rat hepatocytes along the biliary epithelial lineageRobbert G E Notenboom, Marius A van den Bergh Weerman, Koert P Dingemans, et al.
Brain : a Journal of Neurology|March 16, 2007
TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutationsHarro Seelaar, H Jurgen Schelhaas, Asma Azmani, et al.
Pageof 16