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Peter Tsang

Showing results (31-40 of 41) with videos related to

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American Journal of Human Genetics|March 15, 2011
Population-genetic properties of differentiated human copy-number polymorphismsCatarina D Campbell, Nick Sampas, Anya Tsalenko, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|August 13, 2014
Predicting walking function of patients one month poststroke using modified Rivermead mobility index on admissionSze-Tim Shum, Joseph Kam-Wah Chiu, Claudia Pui-Ling Tsang, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2004
Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNAMichael T Barrett, Alicia Scheffer, Amir Ben-Dor, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 7, 2013
R-loop formation at Snord116 mediates topotecan inhibition of Ube3a-antisense and allele-specific chromatin decondensationWeston T Powell, Rochelle L Coulson, Michael L Gonzales, et al.
Human Molecular Genetics|August 2, 2007
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseasesAdam J de Smith, Anya Tsalenko, Nick Sampas, et al.
Cell Stem Cell|July 10, 2012
Derivation conditions impact X-inactivation status in female human induced pluripotent stem cellsKiichiro Tomoda, Kazutoshi Takahashi, Karen Leung, et al.
Leukemia Research|March 2, 2020
Comparison of real-world treatment patterns in chronic lymphocytic leukemia management before and after availability of ibrutinib in the province of British Columbia, CanadaSteven J Huang, Alina S Gerrie, Sean Young, et al.
Leukemia Research|March 1, 2021
Impact of age and treatment institution type on outcomes of patients treated for chronic lymphocytic leukemia in British Columbia, CanadaSteven J Huang, Alina S Gerrie, Sean Young, et al.
American Journal of Human Genetics|February 29, 2008
The fine-scale and complex architecture of human copy-number variationGeorge H Perry, Amir Ben-Dor, Anya Tsalenko, et al.
Nature Methods|May 5, 2010
Characterization of missing human genome sequences and copy-number polymorphic insertionsJeffrey M Kidd, Nick Sampas, Francesca Antonacci, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
American Journal of Human Genetics|March 15, 2011
Population-genetic properties of differentiated human copy-number polymorphismsCatarina D Campbell, Nick Sampas, Anya Tsalenko, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|August 13, 2014
Predicting walking function of patients one month poststroke using modified Rivermead mobility index on admissionSze-Tim Shum, Joseph Kam-Wah Chiu, Claudia Pui-Ling Tsang, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2004
Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNAMichael T Barrett, Alicia Scheffer, Amir Ben-Dor, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 7, 2013
R-loop formation at Snord116 mediates topotecan inhibition of Ube3a-antisense and allele-specific chromatin decondensationWeston T Powell, Rochelle L Coulson, Michael L Gonzales, et al.
Human Molecular Genetics|August 2, 2007
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseasesAdam J de Smith, Anya Tsalenko, Nick Sampas, et al.
Cell Stem Cell|July 10, 2012
Derivation conditions impact X-inactivation status in female human induced pluripotent stem cellsKiichiro Tomoda, Kazutoshi Takahashi, Karen Leung, et al.
Leukemia Research|March 2, 2020
Comparison of real-world treatment patterns in chronic lymphocytic leukemia management before and after availability of ibrutinib in the province of British Columbia, CanadaSteven J Huang, Alina S Gerrie, Sean Young, et al.
Leukemia Research|March 1, 2021
Impact of age and treatment institution type on outcomes of patients treated for chronic lymphocytic leukemia in British Columbia, CanadaSteven J Huang, Alina S Gerrie, Sean Young, et al.
American Journal of Human Genetics|February 29, 2008
The fine-scale and complex architecture of human copy-number variationGeorge H Perry, Amir Ben-Dor, Anya Tsalenko, et al.
Nature Methods|May 5, 2010
Characterization of missing human genome sequences and copy-number polymorphic insertionsJeffrey M Kidd, Nick Sampas, Francesca Antonacci, et al.
Pageof 5