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R Slater

Showing results (411-420 of 505) with videos related to

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Brain : a Journal of Neurology|July 28, 2006
Pre- and post-synaptic abnormalities associated with impaired neuromuscular transmission in a group of patients with 'limb-girdle myasthenia'C R Slater, P R W Fawcett, T J Walls, et al.
American Journal of Human Genetics|October 28, 2005
High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPsHoward R Slater, Dione K Bailey, Hua Ren, et al.
American Journal of Human Genetics|March 15, 2006
Analysis of SNP content of 82 common copy-number polymorphisms from the Database of Genomic VariationsHoward R Slater, Dione K Bailey, Hua Ren, et al.
Leukemia|February 24, 2001
Long-term follow-up of Dutch Childhood Leukemia Study Group (DCLSG) protocols for children with acute lymphoblastic leukemia, 1984-1991W A Kamps, A J Veerman, E R van Wering, et al.
The New England Journal of Medicine|January 25, 1996
Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastomaH Caron, P van Sluis, J de Kraker, et al.
Cytogenetic and Genome Research|November 20, 2002
Identification of a haplosufficient 3.6-Mb region in human chromosome 11q14.3-->q21L Li, P Moore, C Ngo, et al.
Circulation|February 1, 1994
Induction of myocardial insulin-like growth factor-I gene expression in left ventricular hypertrophyT J Donohue, L D Dworkin, M N Lango, et al.
Cancer Research|July 14, 1998
Human chromosome 21 determines growth factor dependence in human/mouse B-cell hybridomasS B Ebeling, H M Bos, R Slater, et al.
Nucleic Acids Research|October 20, 1998
Determination of spontaneous loss of heterozygosity mutations in Aprt heterozygous miceP P Van Sloun, S W Wijnhoven, H J Kool, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 13, 1998
Carcinogen-induced loss of heterozygosity at the Aprt locus in somatic cells of the mouseS W Wijnhoven, P P Van Sloun, H J Kool, et al.
Pageof 51

Showing results (411-420 of 505) with videos related to

Sort By:
Pageof 51
Brain : a Journal of Neurology|July 28, 2006
Pre- and post-synaptic abnormalities associated with impaired neuromuscular transmission in a group of patients with 'limb-girdle myasthenia'C R Slater, P R W Fawcett, T J Walls, et al.
American Journal of Human Genetics|October 28, 2005
High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPsHoward R Slater, Dione K Bailey, Hua Ren, et al.
American Journal of Human Genetics|March 15, 2006
Analysis of SNP content of 82 common copy-number polymorphisms from the Database of Genomic VariationsHoward R Slater, Dione K Bailey, Hua Ren, et al.
Leukemia|February 24, 2001
Long-term follow-up of Dutch Childhood Leukemia Study Group (DCLSG) protocols for children with acute lymphoblastic leukemia, 1984-1991W A Kamps, A J Veerman, E R van Wering, et al.
The New England Journal of Medicine|January 25, 1996
Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastomaH Caron, P van Sluis, J de Kraker, et al.
Cytogenetic and Genome Research|November 20, 2002
Identification of a haplosufficient 3.6-Mb region in human chromosome 11q14.3-->q21L Li, P Moore, C Ngo, et al.
Circulation|February 1, 1994
Induction of myocardial insulin-like growth factor-I gene expression in left ventricular hypertrophyT J Donohue, L D Dworkin, M N Lango, et al.
Cancer Research|July 14, 1998
Human chromosome 21 determines growth factor dependence in human/mouse B-cell hybridomasS B Ebeling, H M Bos, R Slater, et al.
Nucleic Acids Research|October 20, 1998
Determination of spontaneous loss of heterozygosity mutations in Aprt heterozygous miceP P Van Sloun, S W Wijnhoven, H J Kool, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 13, 1998
Carcinogen-induced loss of heterozygosity at the Aprt locus in somatic cells of the mouseS W Wijnhoven, P P Van Sloun, H J Kool, et al.
Pageof 51