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E S Lander

Showing results (81-90 of 179) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|September 27, 1994
Genome-wide search for loss of heterozygosity in transgenic mouse tumors reveals candidate tumor suppressor genes on chromosomes 9 and 16W F Dietrich, E H Radany, J S Smith, et al.
Nature|October 20, 1988
Resolution of quantitative traits into Mendelian factors by using a complete linkage map of restriction fragment length polymorphismsA H Paterson, E S Lander, J D Hewitt, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2000
Expression analysis with oligonucleotide microarrays reveals that MYC regulates genes involved in growth, cell cycle, signaling, and adhesionH A Coller, C Grandori, P Tamayo, et al.
Genetics|December 1, 1988
Genetic analysis of the fungus, Bremia lactucae, using restriction fragment length polymorphismsS H Hulbert, T W Ilott, E J Legg, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 1999
Interpreting patterns of gene expression with self-organizing maps: methods and application to hematopoietic differentiationP Tamayo, D Slonim, J Mesirov, et al.
Science (New York, N.Y.)|June 20, 1997
A magnetic attraction to high-throughput genomicsT L Hawkins, K J McKernan, L B Jacotot, et al.
The Journal of Biological Chemistry|April 12, 2001
Growth factor-specific signaling pathway stimulation and gene expression mediated by ErbB receptorsC Sweeney, D Fambrough, C Huard, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 21, 1995
Mapping the mouse genome: current status and future prospectsW F Dietrich, N G Copeland, D J Gilbert, et al.
Genetics|June 1, 1992
A genetic map of the mouse suitable for typing intraspecific crossesW Dietrich, H Katz, S E Lincoln, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
Identification of the Finnish founder mutation for diastrophic dysplasia (DTD)J Hästbacka, A Kerrebrock, K Mokkala, et al.
Pageof 18

Showing results (81-90 of 179) with videos related to

Sort By:
Pageof 18
Proceedings of the National Academy of Sciences of the United States of America|September 27, 1994
Genome-wide search for loss of heterozygosity in transgenic mouse tumors reveals candidate tumor suppressor genes on chromosomes 9 and 16W F Dietrich, E H Radany, J S Smith, et al.
Nature|October 20, 1988
Resolution of quantitative traits into Mendelian factors by using a complete linkage map of restriction fragment length polymorphismsA H Paterson, E S Lander, J D Hewitt, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2000
Expression analysis with oligonucleotide microarrays reveals that MYC regulates genes involved in growth, cell cycle, signaling, and adhesionH A Coller, C Grandori, P Tamayo, et al.
Genetics|December 1, 1988
Genetic analysis of the fungus, Bremia lactucae, using restriction fragment length polymorphismsS H Hulbert, T W Ilott, E J Legg, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 1999
Interpreting patterns of gene expression with self-organizing maps: methods and application to hematopoietic differentiationP Tamayo, D Slonim, J Mesirov, et al.
Science (New York, N.Y.)|June 20, 1997
A magnetic attraction to high-throughput genomicsT L Hawkins, K J McKernan, L B Jacotot, et al.
The Journal of Biological Chemistry|April 12, 2001
Growth factor-specific signaling pathway stimulation and gene expression mediated by ErbB receptorsC Sweeney, D Fambrough, C Huard, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 21, 1995
Mapping the mouse genome: current status and future prospectsW F Dietrich, N G Copeland, D J Gilbert, et al.
Genetics|June 1, 1992
A genetic map of the mouse suitable for typing intraspecific crossesW Dietrich, H Katz, S E Lincoln, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
Identification of the Finnish founder mutation for diastrophic dysplasia (DTD)J Hästbacka, A Kerrebrock, K Mokkala, et al.
Pageof 18