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Rob Willemsen

Showing results (101-110 of 157) with videos related to

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Human Molecular Genetics|May 7, 2004
Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivoEdwin J Mientjes, Rob Willemsen, Laura L Kirkpatrick, et al.
Disease Models & Mechanisms|October 25, 2021
Reduction of oxidative stress suppresses poly-GR-mediated toxicity in zebrafish embryosFréderike W Riemslagh, Rob F M Verhagen, Esmay C van der Toorn, et al.
Translational Vision Science & Technology|March 14, 2022
Zebrafish: An In Vivo Screening Model to Study Ocular PhenotypesWim H Quint, Kirke C D Tadema, Johan H C Crins, et al.
American Journal of Respiratory Cell and Molecular Biology|February 21, 2004
Proteomic analysis of exosomes isolated from human malignant pleural effusionsMartin P Bard, Joost P Hegmans, Annabrita Hemmes, et al.
Acta Neuropathologica Communications|December 5, 2014
FMRpolyG-positive inclusions in CNS and non-CNS organs of a fragile X premutation carrier with fragile X-associated tremor/ataxia syndromeRonald A M Buijsen, Chantal Sellier, Lies-Anne W F M Severijnen, et al.
EMBO Molecular Medicine|February 20, 2015
A novel fragile X syndrome mutation reveals a conserved role for the carboxy-terminus in FMRP localization and functionZeynep Okray, Celine E F de Esch, Hilde Van Esch, et al.
Journal of Neurodevelopmental Disorders|August 20, 2014
Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndromeRobert F Berman, Ronald Am Buijsen, Karen Usdin, et al.
Acta Neuropathologica Communications|December 20, 2014
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.
Plos One|June 29, 2018
IDH1-mutated transgenic zebrafish lines: An in-vivo model for drug screening and functional analysisYa Gao, Maurice de Wit, Eduard A Struys, et al.
Plos One|February 25, 2011
Loss of nuclear activity of the FBXO7 protein in patients with parkinsonian-pyramidal syndrome (PARK15)Tianna Zhao, Esther De Graaff, Guido J Breedveld, et al.
Pageof 16

Showing results (101-110 of 157) with videos related to

Sort By:
Pageof 16
Human Molecular Genetics|May 7, 2004
Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivoEdwin J Mientjes, Rob Willemsen, Laura L Kirkpatrick, et al.
Disease Models & Mechanisms|October 25, 2021
Reduction of oxidative stress suppresses poly-GR-mediated toxicity in zebrafish embryosFréderike W Riemslagh, Rob F M Verhagen, Esmay C van der Toorn, et al.
Translational Vision Science & Technology|March 14, 2022
Zebrafish: An In Vivo Screening Model to Study Ocular PhenotypesWim H Quint, Kirke C D Tadema, Johan H C Crins, et al.
American Journal of Respiratory Cell and Molecular Biology|February 21, 2004
Proteomic analysis of exosomes isolated from human malignant pleural effusionsMartin P Bard, Joost P Hegmans, Annabrita Hemmes, et al.
Acta Neuropathologica Communications|December 5, 2014
FMRpolyG-positive inclusions in CNS and non-CNS organs of a fragile X premutation carrier with fragile X-associated tremor/ataxia syndromeRonald A M Buijsen, Chantal Sellier, Lies-Anne W F M Severijnen, et al.
EMBO Molecular Medicine|February 20, 2015
A novel fragile X syndrome mutation reveals a conserved role for the carboxy-terminus in FMRP localization and functionZeynep Okray, Celine E F de Esch, Hilde Van Esch, et al.
Journal of Neurodevelopmental Disorders|August 20, 2014
Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndromeRobert F Berman, Ronald Am Buijsen, Karen Usdin, et al.
Acta Neuropathologica Communications|December 20, 2014
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.
Plos One|June 29, 2018
IDH1-mutated transgenic zebrafish lines: An in-vivo model for drug screening and functional analysisYa Gao, Maurice de Wit, Eduard A Struys, et al.
Plos One|February 25, 2011
Loss of nuclear activity of the FBXO7 protein in patients with parkinsonian-pyramidal syndrome (PARK15)Tianna Zhao, Esther De Graaff, Guido J Breedveld, et al.
Pageof 16