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Rob Willemsen

Showing results (61-70 of 157) with videos related to

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Cell Cycle (Georgetown, Tex.)|May 6, 2011
Defect of development of ocular vasculature in Glut1/SLC2A1 knockdown in vivoPing-Pin Zheng, Edwin Romme, Peter J van der Spek, et al.
Zebrafish|June 21, 2011
HeNe laser (633 nm)-coupled confocal microscope allows simulating magnetic resonance imaging/computed tomography scan of the brain and eye: a noninvasive optical approach applicable to small laboratory animalsPing-Pin Zheng, Edwin Romme, Peter J van der Spek, et al.
Human Molecular Genetics|February 8, 2013
The 3' UTR of FMR1 mRNA is a target of miR-101, miR-129-5p and miR-221: implications for the molecular pathology of FXTAS at the synapseSamantha Zongaro, Renate Hukema, Simona D'Antoni, et al.
Annals of Neurology|January 4, 2011
Glut1/SLC2A1 is crucial for the development of the blood-brain barrier in vivoPing-Pin Zheng, Edwin Romme, Peter J van der Spek, et al.
Behavioural Brain Research|May 7, 2005
Cognitive decline, neuromotor and behavioural disturbances in a mouse model for fragile-X-associated tremor/ataxia syndrome (FXTAS)Debby Van Dam, Vanessa Errijgers, R Frank Kooy, et al.
Neuropharmacology|December 26, 2016
Impaired GABAergic inhibition in the hippocampus of Fmr1 knockout miceVictor Sabanov, Sien Braat, Laura D'Andrea, et al.
Neurobiology of Disease|January 15, 2014
Blood expression profiles of fragile X premutation carriers identify candidate genes involved in neurodegenerative and infertility phenotypesElisabet Mateu-Huertas, Laia Rodriguez-Revenga, Maria Isabel Alvarez-Mora, et al.
Experimental Neurology|September 24, 2004
Transport kinetics of FMRP containing the I304N mutation of severe fragile X syndrome in neurites of living rat PC12 cellsMariëtte Schrier, Lies-Anne Severijnen, Surya Reis, et al.
Neurobiology of Disease|October 4, 2005
Expression profiling suggests underexpression of the GABA(A) receptor subunit delta in the fragile X knockout mouse modelIlse Gantois, Jo Vandesompele, Frank Speleman, et al.
Brain : a Journal of Neurology|November 22, 2014
Reply: PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion diseaseTsz Hang Wong, Annemieke J M H Verkerk, Annemieke J Rozemuller, et al.
Pageof 16

Showing results (61-70 of 157) with videos related to

Sort By:
Pageof 16
Cell Cycle (Georgetown, Tex.)|May 6, 2011
Defect of development of ocular vasculature in Glut1/SLC2A1 knockdown in vivoPing-Pin Zheng, Edwin Romme, Peter J van der Spek, et al.
Zebrafish|June 21, 2011
HeNe laser (633 nm)-coupled confocal microscope allows simulating magnetic resonance imaging/computed tomography scan of the brain and eye: a noninvasive optical approach applicable to small laboratory animalsPing-Pin Zheng, Edwin Romme, Peter J van der Spek, et al.
Human Molecular Genetics|February 8, 2013
The 3' UTR of FMR1 mRNA is a target of miR-101, miR-129-5p and miR-221: implications for the molecular pathology of FXTAS at the synapseSamantha Zongaro, Renate Hukema, Simona D'Antoni, et al.
Annals of Neurology|January 4, 2011
Glut1/SLC2A1 is crucial for the development of the blood-brain barrier in vivoPing-Pin Zheng, Edwin Romme, Peter J van der Spek, et al.
Behavioural Brain Research|May 7, 2005
Cognitive decline, neuromotor and behavioural disturbances in a mouse model for fragile-X-associated tremor/ataxia syndrome (FXTAS)Debby Van Dam, Vanessa Errijgers, R Frank Kooy, et al.
Neuropharmacology|December 26, 2016
Impaired GABAergic inhibition in the hippocampus of Fmr1 knockout miceVictor Sabanov, Sien Braat, Laura D'Andrea, et al.
Neurobiology of Disease|January 15, 2014
Blood expression profiles of fragile X premutation carriers identify candidate genes involved in neurodegenerative and infertility phenotypesElisabet Mateu-Huertas, Laia Rodriguez-Revenga, Maria Isabel Alvarez-Mora, et al.
Experimental Neurology|September 24, 2004
Transport kinetics of FMRP containing the I304N mutation of severe fragile X syndrome in neurites of living rat PC12 cellsMariëtte Schrier, Lies-Anne Severijnen, Surya Reis, et al.
Neurobiology of Disease|October 4, 2005
Expression profiling suggests underexpression of the GABA(A) receptor subunit delta in the fragile X knockout mouse modelIlse Gantois, Jo Vandesompele, Frank Speleman, et al.
Brain : a Journal of Neurology|November 22, 2014
Reply: PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion diseaseTsz Hang Wong, Annemieke J M H Verkerk, Annemieke J Rozemuller, et al.
Pageof 16