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F Baas

Showing results (91-100 of 245) with videos related to

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Neurobiology of Disease|January 12, 2011
Innate and adaptive immunity in amyotrophic lateral sclerosis: evidence of complement activationM Sta, R M R Sylva-Steenland, M Casula, et al.
BMJ Open|July 11, 2019
A tailored approach towards informing relatives at risk of inherited cardiac conditions: study protocol for a randomised controlled trialLieke M van den Heuvel, Yvonne M Hoedemaekers, Annette F Baas, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
An integrated map of chromosome 18 CAG trinucleotide repeat lociA J Grierson, M van Groenigen, N P Groot, et al.
The EMBO Journal|June 14, 2003
Activation of the tumour suppressor kinase LKB1 by the STE20-like pseudokinase STRADA F Baas, J Boudeau, G P Sapkota, et al.
Journal of Cardiovascular Translational Research|March 2, 2011
Genomic DNA pooling strategy for next-generation sequencing-based rare variant discovery in abdominal aortic aneurysm regions of interest-challenges and limitationsMagdalena Harakalova, Isaäc J Nijman, Jelena Medic, et al.
Human Genetics|January 1, 1985
The human thyroglobulin gene: a polymorphic marker localized distal to C-MYC on chromosome 8 band q24F Baas, H Bikker, A Geurts van Kessel, et al.
Journal of Vascular Surgery|October 23, 2013
Statin therapy is associated with improved survival after endovascular and open aneurysm repairJorg L de Bruin, Annette F Baas, Martijn W Heymans, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 1996
Microsatellite instability in childhood rhabdomyosarcoma is locus specific and correlates with fractional allelic lossM Visser, J Bras, C Sijmons, et al.
Current Topics in Microbiology and Immunology|January 1, 1988
Burkitt's lymphoma variant translocations: distribution of chromosomal breakpoints and perturbated regulation of a mutated c-myc geneB Henglein, M Lipp, P Hartl, et al.
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Hereditary motor and sensory neuropathy (HMSN) IA, developmental delay and autism related disorder in a boy with duplication (17)(p11.2p12)U Moog, J J Engelen, B W Weber, et al.
Pageof 25

Showing results (91-100 of 245) with videos related to

Sort By:
Pageof 25
Neurobiology of Disease|January 12, 2011
Innate and adaptive immunity in amyotrophic lateral sclerosis: evidence of complement activationM Sta, R M R Sylva-Steenland, M Casula, et al.
BMJ Open|July 11, 2019
A tailored approach towards informing relatives at risk of inherited cardiac conditions: study protocol for a randomised controlled trialLieke M van den Heuvel, Yvonne M Hoedemaekers, Annette F Baas, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
An integrated map of chromosome 18 CAG trinucleotide repeat lociA J Grierson, M van Groenigen, N P Groot, et al.
The EMBO Journal|June 14, 2003
Activation of the tumour suppressor kinase LKB1 by the STE20-like pseudokinase STRADA F Baas, J Boudeau, G P Sapkota, et al.
Journal of Cardiovascular Translational Research|March 2, 2011
Genomic DNA pooling strategy for next-generation sequencing-based rare variant discovery in abdominal aortic aneurysm regions of interest-challenges and limitationsMagdalena Harakalova, Isaäc J Nijman, Jelena Medic, et al.
Human Genetics|January 1, 1985
The human thyroglobulin gene: a polymorphic marker localized distal to C-MYC on chromosome 8 band q24F Baas, H Bikker, A Geurts van Kessel, et al.
Journal of Vascular Surgery|October 23, 2013
Statin therapy is associated with improved survival after endovascular and open aneurysm repairJorg L de Bruin, Annette F Baas, Martijn W Heymans, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 1996
Microsatellite instability in childhood rhabdomyosarcoma is locus specific and correlates with fractional allelic lossM Visser, J Bras, C Sijmons, et al.
Current Topics in Microbiology and Immunology|January 1, 1988
Burkitt's lymphoma variant translocations: distribution of chromosomal breakpoints and perturbated regulation of a mutated c-myc geneB Henglein, M Lipp, P Hartl, et al.
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Hereditary motor and sensory neuropathy (HMSN) IA, developmental delay and autism related disorder in a boy with duplication (17)(p11.2p12)U Moog, J J Engelen, B W Weber, et al.
Pageof 25