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Methods in Molecular Biology (Clifton, N.J.)
|
February 22, 2008
Scaling of gene expression data allowing the comparison of different gene expression platforms
Fred van Ruissen, Gerben J Schaaf, Marcel Kool, et al.
Neuromuscular Disorders : NMD
|
September 11, 2007
Congenital hypomyelinating neuropathy, a long term follow-up study in an affected family
Liesbeth S Smit, Daniella Roofthooft, Fred van Ruissen, et al.
Journal of Neuroscience Research
|
June 21, 2006
Comparison of Schwann cell and sciatic nerve transcriptomes indicates that mouse is a valid model for the human peripheral nervous system
Anneloor L M A Ten Asbroek, Fred Van Ruissen, Jan M Ruijter, et al.
Journal of Neuroinflammation
|
April 9, 2016
Complement activation at the motor end-plates in amyotrophic lateral sclerosis
Nawal Bahia El Idrissi, Sanne Bosch, Valeria Ramaglia, et al.
Parkinsonism & Related Disorders
|
April 29, 2014
DRD1 rare variants associated with tardive-like dystonia: a pilot pathway sequencing study in dystonia
Justus L Groen, Katja Ritz, Tom T Warner, et al.
Journal of Neuroscience Methods
|
July 29, 2008
Myelination competent conditionally immortalized mouse Schwann cells
José T Saavedra, Ruud A Wolterman, Frank Baas, et al.
Plos One
|
February 1, 2012
Identification of novel candidate oncogenes in chromosome region 17p11.2-p12 in human osteosarcoma
Joeri Both, Thijs Wu, Johannes Bras, et al.
American Journal of Medical Genetics. Part A
|
November 19, 2016
A de novo missense mutation in the inositol 1,4,5-triphosphate receptor type 1 gene causing severe pontine and cerebellar hypoplasia: Expanding the phenotype of ITPR1-related spinocerebellar ataxia's
Tessa van Dijk, Peter Barth, Liesbeth Reneman, et al.
The Journal of Biological Chemistry
|
November 15, 2001
Kinked collagen VI tetramers and reduced microfibril formation as a result of Bethlem myopathy and introduced triple helical glycine mutations
Shireen R Lamandé, Matthias Mörgelin, Carly Selan, et al.
Human Molecular Genetics
|
December 10, 2003
Expression of complement components in the peripheral nervous system
Rosalein R de Jonge, Ivo N van Schaik, Jeroen P Vreijling, et al.
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of 24
Search research articles
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Showing results (21-30 of 231) with videos related to
Sort By:
Page
of 24
Methods in Molecular Biology (Clifton, N.J.)
|
February 22, 2008
Scaling of gene expression data allowing the comparison of different gene expression platforms
Fred van Ruissen, Gerben J Schaaf, Marcel Kool, et al.
Neuromuscular Disorders : NMD
|
September 11, 2007
Congenital hypomyelinating neuropathy, a long term follow-up study in an affected family
Liesbeth S Smit, Daniella Roofthooft, Fred van Ruissen, et al.
Journal of Neuroscience Research
|
June 21, 2006
Comparison of Schwann cell and sciatic nerve transcriptomes indicates that mouse is a valid model for the human peripheral nervous system
Anneloor L M A Ten Asbroek, Fred Van Ruissen, Jan M Ruijter, et al.
Journal of Neuroinflammation
|
April 9, 2016
Complement activation at the motor end-plates in amyotrophic lateral sclerosis
Nawal Bahia El Idrissi, Sanne Bosch, Valeria Ramaglia, et al.
Parkinsonism & Related Disorders
|
April 29, 2014
DRD1 rare variants associated with tardive-like dystonia: a pilot pathway sequencing study in dystonia
Justus L Groen, Katja Ritz, Tom T Warner, et al.
Journal of Neuroscience Methods
|
July 29, 2008
Myelination competent conditionally immortalized mouse Schwann cells
José T Saavedra, Ruud A Wolterman, Frank Baas, et al.
Plos One
|
February 1, 2012
Identification of novel candidate oncogenes in chromosome region 17p11.2-p12 in human osteosarcoma
Joeri Both, Thijs Wu, Johannes Bras, et al.
American Journal of Medical Genetics. Part A
|
November 19, 2016
A de novo missense mutation in the inositol 1,4,5-triphosphate receptor type 1 gene causing severe pontine and cerebellar hypoplasia: Expanding the phenotype of ITPR1-related spinocerebellar ataxia's
Tessa van Dijk, Peter Barth, Liesbeth Reneman, et al.
The Journal of Biological Chemistry
|
November 15, 2001
Kinked collagen VI tetramers and reduced microfibril formation as a result of Bethlem myopathy and introduced triple helical glycine mutations
Shireen R Lamandé, Matthias Mörgelin, Carly Selan, et al.
Human Molecular Genetics
|
December 10, 2003
Expression of complement components in the peripheral nervous system
Rosalein R de Jonge, Ivo N van Schaik, Jeroen P Vreijling, et al.
Page
of 24