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F Baas

Showing results (171-180 of 245) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2006
Late onset axonal Charcot-Marie-Tooth phenotype caused by a novel myelin protein zero mutationH M E Bienfait, C G Faber, F Baas, et al.
Neurology|March 15, 2006
Phenotype-genotype correlation in Dutch patients with myoclonus-dystoniaM C F Gerrits, E M J Foncke, R de Haan, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 15, 1996
Peripheral neuropathy in mice transgenic for a human MDR3 P-glycoprotein mini-geneJ J Smit, F Baas, J E Hoogendijk, et al.
American Journal of Human Genetics|March 24, 2015
Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspringMirjam S de Pagter, Markus J van Roosmalen, Annette F Baas, et al.
Science (New York, N.Y.)|February 22, 2001
The human transcriptome map: clustering of highly expressed genes in chromosomal domainsH Caron, B van Schaik, M van der Mee, et al.
Neurology|January 21, 2009
A case of ALS-FTD in a large FALS pedigree with a K17I ANG mutationM A van Es, F P Diekstra, J H Veldink, et al.
Journal of Neurology|August 11, 2014
Mutation frequency of PRKAR1B and the major familial dementia genes in a Dutch early onset dementia cohortP E Cohn-Hokke, T H Wong, P Rizzu, et al.
Molecular Neurobiology|May 2, 2022
Treatment with IFB-088 Improves Neuropathy in CMT1A and CMT1B MiceYunhong Bai, Caroline Treins, Vera G Volpi, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 9, 1999
MRP3, an organic anion transporter able to transport anti-cancer drugsM Kool, M van der Linden, M de Haas, et al.
Circulation. Cardiovascular Genetics|May 11, 2013
Impact of inherited genetic variants associated with lipid profile, hypertension, and coronary artery disease on the risk of intracranial and abdominal aortic aneurysmsFemke N G van 't Hof, Ynte M Ruigrok, Annette F Baas, et al.
Pageof 25

Showing results (171-180 of 245) with videos related to

Sort By:
Pageof 25
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2006
Late onset axonal Charcot-Marie-Tooth phenotype caused by a novel myelin protein zero mutationH M E Bienfait, C G Faber, F Baas, et al.
Neurology|March 15, 2006
Phenotype-genotype correlation in Dutch patients with myoclonus-dystoniaM C F Gerrits, E M J Foncke, R de Haan, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 15, 1996
Peripheral neuropathy in mice transgenic for a human MDR3 P-glycoprotein mini-geneJ J Smit, F Baas, J E Hoogendijk, et al.
American Journal of Human Genetics|March 24, 2015
Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspringMirjam S de Pagter, Markus J van Roosmalen, Annette F Baas, et al.
Science (New York, N.Y.)|February 22, 2001
The human transcriptome map: clustering of highly expressed genes in chromosomal domainsH Caron, B van Schaik, M van der Mee, et al.
Neurology|January 21, 2009
A case of ALS-FTD in a large FALS pedigree with a K17I ANG mutationM A van Es, F P Diekstra, J H Veldink, et al.
Journal of Neurology|August 11, 2014
Mutation frequency of PRKAR1B and the major familial dementia genes in a Dutch early onset dementia cohortP E Cohn-Hokke, T H Wong, P Rizzu, et al.
Molecular Neurobiology|May 2, 2022
Treatment with IFB-088 Improves Neuropathy in CMT1A and CMT1B MiceYunhong Bai, Caroline Treins, Vera G Volpi, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 9, 1999
MRP3, an organic anion transporter able to transport anti-cancer drugsM Kool, M van der Linden, M de Haas, et al.
Circulation. Cardiovascular Genetics|May 11, 2013
Impact of inherited genetic variants associated with lipid profile, hypertension, and coronary artery disease on the risk of intracranial and abdominal aortic aneurysmsFemke N G van 't Hof, Ynte M Ruigrok, Annette F Baas, et al.
Pageof 25