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S Kenwrick

Showing results (1-10 of 57) with videos related to

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Ernst Schering Research Foundation Workshop|February 28, 2002
Incontinentia pigmenti: the first single gene disorder due to disrupted NF-kappa B functionS Kenwrick
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|October 22, 1998
Neural cell adhesion molecule L1: relating disease to functionS Kenwrick, P Doherty
Lancet (London, England)|January 21, 1995
Gene analysis of L1 neural cell adhesion molecule in prenatal diagnosis of hydrocephalusM Jouet, S Kenwrick
American Journal of Human Genetics|December 1, 1989
A contiguous, 3-Mb physical map of Xq28 extending from the colorblindness locus to DXS15S Kenwrick, J Gitschier
Journal of Medical Genetics|January 1, 1996
X linked hydrocephalus and MASA syndromeS Kenwrick, M Jouet, D Donnai
Nature Genetics|October 1, 1992
Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X-linked hydrocephalusA Rosenthal, M Jouet, S Kenwrick
Brain Research. Molecular Brain Research|June 1, 1995
Exon 2 of the gene for neural cell adhesion molecule L1 is alternatively spliced in B cellsM Jouet, A Rosenthal, S Kenwrick
Human Molecular Genetics|April 18, 2000
Neural cell recognition molecule L1: relating biological complexity to human disease mutationsS Kenwrick, A Watkins, E De Angelis
Current Opinion in Neurobiology|May 6, 1998
Neural cell recognition molecule L1: from cell biology to human hereditary brain malformationsT Brümmendorf, S Kenwrick, F G Rathjen
Journal of Medical Genetics|March 1, 1996
Discordant segregation of Xq28 markers and a mutation in the L1 gene in a family with X linked hydrocephalusM Jouet, L Strain, D Bonthron, et al.
Pageof 6

Showing results (1-10 of 57) with videos related to

Sort By:
Pageof 6
Ernst Schering Research Foundation Workshop|February 28, 2002
Incontinentia pigmenti: the first single gene disorder due to disrupted NF-kappa B functionS Kenwrick
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|October 22, 1998
Neural cell adhesion molecule L1: relating disease to functionS Kenwrick, P Doherty
Lancet (London, England)|January 21, 1995
Gene analysis of L1 neural cell adhesion molecule in prenatal diagnosis of hydrocephalusM Jouet, S Kenwrick
American Journal of Human Genetics|December 1, 1989
A contiguous, 3-Mb physical map of Xq28 extending from the colorblindness locus to DXS15S Kenwrick, J Gitschier
Journal of Medical Genetics|January 1, 1996
X linked hydrocephalus and MASA syndromeS Kenwrick, M Jouet, D Donnai
Nature Genetics|October 1, 1992
Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X-linked hydrocephalusA Rosenthal, M Jouet, S Kenwrick
Brain Research. Molecular Brain Research|June 1, 1995
Exon 2 of the gene for neural cell adhesion molecule L1 is alternatively spliced in B cellsM Jouet, A Rosenthal, S Kenwrick
Human Molecular Genetics|April 18, 2000
Neural cell recognition molecule L1: relating biological complexity to human disease mutationsS Kenwrick, A Watkins, E De Angelis
Current Opinion in Neurobiology|May 6, 1998
Neural cell recognition molecule L1: from cell biology to human hereditary brain malformationsT Brümmendorf, S Kenwrick, F G Rathjen
Journal of Medical Genetics|March 1, 1996
Discordant segregation of Xq28 markers and a mutation in the L1 gene in a family with X linked hydrocephalusM Jouet, L Strain, D Bonthron, et al.
Pageof 6