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J Ignatius

Showing results (71-80 of 91) with videos related to

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The Journal of Cell Biology|August 1, 1990
Molecular cloning of the rat integrin alpha 1-subunit: a receptor for laminin and collagenM J Ignatius, T H Large, M Houde, et al.
Human Mutation|June 20, 1998
Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease and related neuropathiesK Silander, P Meretoja, V Juvonen, et al.
Clinical Genetics|June 29, 2017
A homozygous I684T in GLE1 as a novel cause of arthrogryposis and motor neuron lossT Paakkola, K Vuopala, H Kokkonen, et al.
American Journal of Human Genetics|October 27, 1997
Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis: private and recurrent mutations in an isolated populationE Laiho, J Ignatius, H Mikkola, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1986
Expression of apolipoprotein E during nerve degeneration and regenerationM J Ignatius, P J Gebicke-Härter, J H Skene, et al.
Clinical Genetics|May 12, 2010
ERCC6 founder mutation identified in Finnish patients with COFS syndromeE Jaakkola, A Mustonen, P Olsen, et al.
IMJ. Illinois Medical Journal|January 1, 1983
Management of glioblastoma multiforme by irradiation and chemotherapyW M Shehata, R L Meyer, F K Jazy, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in ScandinaviaJ Jonasson, V Juvonen, P Sistonen, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1990
Neuronal receptors that regulate axon growthL F Reichardt, B Bossy, S Carbonetto, et al.
Genomics|February 1, 1992
Linkage analysis of spinal muscular atrophyR J Daniels, N H Thomas, R N MacKinnon, et al.
Pageof 10

Showing results (71-80 of 91) with videos related to

Sort By:
Pageof 10
The Journal of Cell Biology|August 1, 1990
Molecular cloning of the rat integrin alpha 1-subunit: a receptor for laminin and collagenM J Ignatius, T H Large, M Houde, et al.
Human Mutation|June 20, 1998
Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease and related neuropathiesK Silander, P Meretoja, V Juvonen, et al.
Clinical Genetics|June 29, 2017
A homozygous I684T in GLE1 as a novel cause of arthrogryposis and motor neuron lossT Paakkola, K Vuopala, H Kokkonen, et al.
American Journal of Human Genetics|October 27, 1997
Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis: private and recurrent mutations in an isolated populationE Laiho, J Ignatius, H Mikkola, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1986
Expression of apolipoprotein E during nerve degeneration and regenerationM J Ignatius, P J Gebicke-Härter, J H Skene, et al.
Clinical Genetics|May 12, 2010
ERCC6 founder mutation identified in Finnish patients with COFS syndromeE Jaakkola, A Mustonen, P Olsen, et al.
IMJ. Illinois Medical Journal|January 1, 1983
Management of glioblastoma multiforme by irradiation and chemotherapyW M Shehata, R L Meyer, F K Jazy, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in ScandinaviaJ Jonasson, V Juvonen, P Sistonen, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1990
Neuronal receptors that regulate axon growthL F Reichardt, B Bossy, S Carbonetto, et al.
Genomics|February 1, 1992
Linkage analysis of spinal muscular atrophyR J Daniels, N H Thomas, R N MacKinnon, et al.
Pageof 10