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M A Morris

Showing results (131-140 of 152) with videos related to

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Human Mutation|January 1, 1997
Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiencyJ Villard, W Reith, E Barras, et al.
Cytogenetics and Cell Genetics|July 7, 1999
Assignment of the human dynein heavy chain gene DNAH17L to human chromosome 17p12 by in situ hybridization and radiation hybrid mappingL Bartoloni, J Blouin, A J Sainsbury, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 5, 2000
Ly49I NK cell receptor transgene inhibition of rejection of H2b mouse bone marrow transplantsJ Liu, M A Morris, P Nguyen, et al.
Journal of the American Chemical Society|July 19, 2001
Synthesis and characterization of dimensionally ordered semiconductor nanowires within mesoporous silicaN R Coleman, N O'Sullivan, K M Ryan, et al.
Journal of Medical Genetics|January 1, 1997
Fortuitous detection of uniparental isodisomy of chromosome 6M C Bittencourt, M A Morris, J Chabod, et al.
Journal of Neuroendocrinology|March 27, 2001
The differential regulation of CART gene expression in a pituitary cell line and primary cell cultures of ovine pars tuberalis cellsP Barrett, M A Morris, K M Moar, et al.
Faraday Discussions|January 31, 2004
The synthesis of matrices of embedded semiconducting nanowiresKirk Ziegler, Kevin M Ryan, Rory Rice, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 1995
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11M Karayiorgou, M A Morris, B Morrow, et al.
Human Molecular Genetics|July 1, 1994
Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cellsJ P Rossiter, M Young, M L Kimberland, et al.
Neurology|April 1, 2009
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutationsK Vahedi, C Depienne, D Le Fort, et al.
Pageof 16

Showing results (131-140 of 152) with videos related to

Sort By:
Pageof 16
Human Mutation|January 1, 1997
Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiencyJ Villard, W Reith, E Barras, et al.
Cytogenetics and Cell Genetics|July 7, 1999
Assignment of the human dynein heavy chain gene DNAH17L to human chromosome 17p12 by in situ hybridization and radiation hybrid mappingL Bartoloni, J Blouin, A J Sainsbury, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 5, 2000
Ly49I NK cell receptor transgene inhibition of rejection of H2b mouse bone marrow transplantsJ Liu, M A Morris, P Nguyen, et al.
Journal of the American Chemical Society|July 19, 2001
Synthesis and characterization of dimensionally ordered semiconductor nanowires within mesoporous silicaN R Coleman, N O'Sullivan, K M Ryan, et al.
Journal of Medical Genetics|January 1, 1997
Fortuitous detection of uniparental isodisomy of chromosome 6M C Bittencourt, M A Morris, J Chabod, et al.
Journal of Neuroendocrinology|March 27, 2001
The differential regulation of CART gene expression in a pituitary cell line and primary cell cultures of ovine pars tuberalis cellsP Barrett, M A Morris, K M Moar, et al.
Faraday Discussions|January 31, 2004
The synthesis of matrices of embedded semiconducting nanowiresKirk Ziegler, Kevin M Ryan, Rory Rice, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 1995
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11M Karayiorgou, M A Morris, B Morrow, et al.
Human Molecular Genetics|July 1, 1994
Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cellsJ P Rossiter, M Young, M L Kimberland, et al.
Neurology|April 1, 2009
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutationsK Vahedi, C Depienne, D Le Fort, et al.
Pageof 16