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Frank Baas

Showing results (41-50 of 231) with videos related to

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Plos One|January 1, 2015
Focal chromosomal copy number aberrations identify CMTM8 and GPR177 as new candidate driver genes in osteosarcomaJoeri Both, Oscar Krijgsman, Johannes Bras, et al.
Journal of Inherited Metabolic Disease|February 22, 2018
A SEPSECS mutation in a 23-year-old woman with microcephaly and progressive cerebellar ataxiaTessa van Dijk, Jan-Dirk Vermeij, Silvana van Koningsbruggen, et al.
BMC Medicine|November 14, 2009
Oral high dose ascorbic acid treatment for one year in young CMT1A patients: a randomised, double-blind, placebo-controlled phase II trialCamiel Verhamme, Rob J de Haan, Marinus Vermeulen, et al.
Psychiatry Research|September 14, 2007
Catechol-O-methyltransferase gene and obsessive-compulsive symptoms in patients with recent-onset schizophrenia: preliminary resultsJanneke Zinkstok, Lonneke van Nimwegen, Therese van Amelsvoort, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|July 27, 2007
Disrupted dopaminergic neurotransmission in 22q11 deletion syndromeErik Boot, Jan Booij, Janneke Zinkstok, et al.
BMC Genomics|June 16, 2005
Evaluation of the similarity of gene expression data estimated with SAGE and Affymetrix GeneChipsFred van Ruissen, Jan M Ruijter, Gerben J Schaaf, et al.
Genomics|May 31, 2002
Ribonuclease H1 maps to chromosome 2 and has at least three pseudogene loci in the human genomeAnneloor L M A ten Asbroek, Marjon van Groenigen, Marja E Jakobs, et al.
Neuroscience Letters|July 22, 2006
The COMT val158met polymorphism and brain morphometry in healthy young adultsJanneke Zinkstok, Nicole Schmitz, Therese van Amelsvoort, et al.
American Journal of Human Genetics|March 16, 2007
Germline mutation of INI1/SMARCB1 in familial schwannomatosisTheo J M Hulsebos, Astrid S Plomp, Ruud A Wolterman, et al.
Genomics Data|October 21, 2015
Next-generation sequencing of microRNAs in primary human polarized macrophagesViviana Cobos Jiménez, Antonius M Willemsen, Edward J Bradley, et al.
Pageof 24

Showing results (41-50 of 231) with videos related to

Sort By:
Pageof 24
Plos One|January 1, 2015
Focal chromosomal copy number aberrations identify CMTM8 and GPR177 as new candidate driver genes in osteosarcomaJoeri Both, Oscar Krijgsman, Johannes Bras, et al.
Journal of Inherited Metabolic Disease|February 22, 2018
A SEPSECS mutation in a 23-year-old woman with microcephaly and progressive cerebellar ataxiaTessa van Dijk, Jan-Dirk Vermeij, Silvana van Koningsbruggen, et al.
BMC Medicine|November 14, 2009
Oral high dose ascorbic acid treatment for one year in young CMT1A patients: a randomised, double-blind, placebo-controlled phase II trialCamiel Verhamme, Rob J de Haan, Marinus Vermeulen, et al.
Psychiatry Research|September 14, 2007
Catechol-O-methyltransferase gene and obsessive-compulsive symptoms in patients with recent-onset schizophrenia: preliminary resultsJanneke Zinkstok, Lonneke van Nimwegen, Therese van Amelsvoort, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|July 27, 2007
Disrupted dopaminergic neurotransmission in 22q11 deletion syndromeErik Boot, Jan Booij, Janneke Zinkstok, et al.
BMC Genomics|June 16, 2005
Evaluation of the similarity of gene expression data estimated with SAGE and Affymetrix GeneChipsFred van Ruissen, Jan M Ruijter, Gerben J Schaaf, et al.
Genomics|May 31, 2002
Ribonuclease H1 maps to chromosome 2 and has at least three pseudogene loci in the human genomeAnneloor L M A ten Asbroek, Marjon van Groenigen, Marja E Jakobs, et al.
Neuroscience Letters|July 22, 2006
The COMT val158met polymorphism and brain morphometry in healthy young adultsJanneke Zinkstok, Nicole Schmitz, Therese van Amelsvoort, et al.
American Journal of Human Genetics|March 16, 2007
Germline mutation of INI1/SMARCB1 in familial schwannomatosisTheo J M Hulsebos, Astrid S Plomp, Ruud A Wolterman, et al.
Genomics Data|October 21, 2015
Next-generation sequencing of microRNAs in primary human polarized macrophagesViviana Cobos Jiménez, Antonius M Willemsen, Edward J Bradley, et al.
Pageof 24