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M Goossens

Showing results (331-340 of 364) with videos related to

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Nature Genetics|June 3, 2000
Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiencyI Netchine, M L Sobrier, H Krude, et al.
The European Journal of Neuroscience|February 27, 2004
Simple spike and complex spike activity of floccular Purkinje cells during the optokinetic reflex in mice lacking cerebellar long-term depressionH H L M Goossens, F E Hoebeek, A M Van Alphen, et al.
Blood|December 1, 1990
The molecular genetic analysis of hemophilia A: a directed search strategy for the detection of point mutations in the human factor VIII geneJ K Pattinson, D S Millar, J H McVey, et al.
British Journal of Cancer|November 23, 2006
Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instabilityC M Kets, J H J M van Krieken, K M Hebeda, et al.
World Journal of Urology|September 30, 2020
Changes in serum PSA after endoscopic enucleation of the prostate are predictive for the future diagnosis of prostate cancerE Lambert, M Goossens, E Palagonia, et al.
Lancet (London, England)|September 26, 1987
DNA polymorphism of human porphobilinogen deaminase gene in acute intermittent porphyriaD H Llewellyn, G H Elder, N A Kalsheker, et al.
Surgical Endoscopy|May 8, 2007
Acquiring basic endoscopy skills by training on the GI Mentor IIS N Buzink, A D Koch, J Heemskerk, et al.
Human Mutation|September 12, 2000
NF1 gene analysis focused on CpG-rich exons in a cohort of 93 patients with neurofibromatosis type 1E Girodon-Boulandet, J Pantel, C Cazeneuve, et al.
Hernia : the Journal of Hernias and Abdominal Wall Surgery|April 22, 2017
The 'AbdoMAN': an artificial abdominal wall simulator for biomechanical studies on laparotomy closure techniquesL F Kroese, J J Harlaar, C Ordrenneau, et al.
FEBS Letters|November 21, 1998
Human Prop-1: cloning, mapping, genomic structure. Mutations in familial combined pituitary hormone deficiencyP Duquesnoy, A Roy, F Dastot, et al.
Pageof 37

Showing results (331-340 of 364) with videos related to

Sort By:
Pageof 37
Nature Genetics|June 3, 2000
Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiencyI Netchine, M L Sobrier, H Krude, et al.
The European Journal of Neuroscience|February 27, 2004
Simple spike and complex spike activity of floccular Purkinje cells during the optokinetic reflex in mice lacking cerebellar long-term depressionH H L M Goossens, F E Hoebeek, A M Van Alphen, et al.
Blood|December 1, 1990
The molecular genetic analysis of hemophilia A: a directed search strategy for the detection of point mutations in the human factor VIII geneJ K Pattinson, D S Millar, J H McVey, et al.
British Journal of Cancer|November 23, 2006
Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instabilityC M Kets, J H J M van Krieken, K M Hebeda, et al.
World Journal of Urology|September 30, 2020
Changes in serum PSA after endoscopic enucleation of the prostate are predictive for the future diagnosis of prostate cancerE Lambert, M Goossens, E Palagonia, et al.
Lancet (London, England)|September 26, 1987
DNA polymorphism of human porphobilinogen deaminase gene in acute intermittent porphyriaD H Llewellyn, G H Elder, N A Kalsheker, et al.
Surgical Endoscopy|May 8, 2007
Acquiring basic endoscopy skills by training on the GI Mentor IIS N Buzink, A D Koch, J Heemskerk, et al.
Human Mutation|September 12, 2000
NF1 gene analysis focused on CpG-rich exons in a cohort of 93 patients with neurofibromatosis type 1E Girodon-Boulandet, J Pantel, C Cazeneuve, et al.
Hernia : the Journal of Hernias and Abdominal Wall Surgery|April 22, 2017
The 'AbdoMAN': an artificial abdominal wall simulator for biomechanical studies on laparotomy closure techniquesL F Kroese, J J Harlaar, C Ordrenneau, et al.
FEBS Letters|November 21, 1998
Human Prop-1: cloning, mapping, genomic structure. Mutations in familial combined pituitary hormone deficiencyP Duquesnoy, A Roy, F Dastot, et al.
Pageof 37