M De Visser - JoVE Visualize

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Plasmid|March 10, 2022

Estimating plasmid conjugation rates: A new computational tool and a critical comparison of methodsJana S Huisman, Fabienne Benz, Sarah J N Duxbury, et al.

Human Molecular Genetics|December 1, 2001

Dystrophin muscle enhancer 1 is implicated in the activation of non-muscle isoforms in the skeletal muscle of patients with X-linked dilated cardiomyopathyC Bastianutto, J A Bestard, K Lahnakoski, et al.

European Journal of Neurology|March 28, 2013

Long-term follow-up study on patients with Miyoshi phenotype of distal muscular dystrophyW H J P Linssen, W G de Voogt, M Krahn, et al.

Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|August 26, 2017

Metabolic dysregulation accelerates injury-induced joint degeneration, driven by local inflammation; an in vivo rat studyHuub M de Visser, Simon C Mastbergen, Anne E Kozijn, et al.

Journal of Molecular Biology|May 26, 2015

Negative Epistasis and Evolvability in TEM-1 β-Lactamase--The Thin Line between an Enzyme's Conformational Freedom and DisorderEynat Dellus-Gur, Mikael Elias, Emilia Caselli, et al.

European Journal of Nuclear Medicine and Molecular Imaging|February 9, 2007

Novel 111In-labelled bombesin analogues for molecular imaging of prostate tumoursM de Visser, H F Bernard, J L Erion, et al.

Neuromuscular Disorders : NMD|November 1, 1995

A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysisC Wallgren-Pettersson, K Avela, S Marchand, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 2005

Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsyP J Lamont, B Udd, F L Mastaglia, et al.

Human Genetics|April 1, 1997

Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)E A Janssen, S Kemp, G W Hensels, et al.

European Neurology|March 20, 2009

Clinical identification of dysarthria types among neurologists, residents in neurology and speech therapistsM Van der Graaff, T Kuiper, A Zwinderman, et al.

Pageof 25

Showing results (151-160 of 246) with videos related to

Sort By:

Pageof 25

Plasmid|March 10, 2022

Estimating plasmid conjugation rates: A new computational tool and a critical comparison of methodsJana S Huisman, Fabienne Benz, Sarah J N Duxbury, et al.

Human Molecular Genetics|December 1, 2001

Dystrophin muscle enhancer 1 is implicated in the activation of non-muscle isoforms in the skeletal muscle of patients with X-linked dilated cardiomyopathyC Bastianutto, J A Bestard, K Lahnakoski, et al.

European Journal of Neurology|March 28, 2013

Long-term follow-up study on patients with Miyoshi phenotype of distal muscular dystrophyW H J P Linssen, W G de Voogt, M Krahn, et al.

Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|August 26, 2017

Metabolic dysregulation accelerates injury-induced joint degeneration, driven by local inflammation; an in vivo rat studyHuub M de Visser, Simon C Mastbergen, Anne E Kozijn, et al.

Journal of Molecular Biology|May 26, 2015

Negative Epistasis and Evolvability in TEM-1 β-Lactamase--The Thin Line between an Enzyme's Conformational Freedom and DisorderEynat Dellus-Gur, Mikael Elias, Emilia Caselli, et al.

European Journal of Nuclear Medicine and Molecular Imaging|February 9, 2007

Novel 111In-labelled bombesin analogues for molecular imaging of prostate tumoursM de Visser, H F Bernard, J L Erion, et al.

Neuromuscular Disorders : NMD|November 1, 1995

A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysisC Wallgren-Pettersson, K Avela, S Marchand, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|August 17, 2005

Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsyP J Lamont, B Udd, F L Mastaglia, et al.

Human Genetics|April 1, 1997

Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)E A Janssen, S Kemp, G W Hensels, et al.

European Neurology|March 20, 2009

Clinical identification of dysarthria types among neurologists, residents in neurology and speech therapistsM Van der Graaff, T Kuiper, A Zwinderman, et al.

Pageof 25