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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 diseases
Adam J de Smith, Anya Tsalenko, Nick Sampas, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 11, 2006
Genetic variation in putative regulatory loci controlling gene expression in breast cancer
Vessela N Kristensen, Hege Edvardsen, Anya Tsalenko, et al.
Physiological Genomics
|
March 20, 2003
Identification of endothelial cell genes by combined database mining and microarray analysis
Michael Ho, Eugene Yang, George Matcuk, et al.
Nature Biotechnology
|
June 30, 2015
Chemically modified guide RNAs enhance CRISPR-Cas genome editing in human primary cells
Ayal Hendel, Rasmus O Bak, Joseph T Clark, et al.
Circulation
|
December 6, 2006
Network analysis of human in-stent restenosis
Euan A Ashley, Rossella Ferrara, Jennifer Y King, et al.
Nature Methods
|
May 5, 2010
Characterization of missing human genome sequences and copy-number polymorphic insertions
Jeffrey M Kidd, Nick Sampas, Francesca Antonacci, et al.
American Journal of Human Genetics
|
February 29, 2008
The fine-scale and complex architecture of human copy-number variation
George H Perry, Amir Ben-Dor, Anya Tsalenko, et al.
Circulation
|
September 10, 2003
Novel role for the potent endogenous inotrope apelin in human cardiac dysfunction
Mary M Chen, Euan A Ashley, David X F Deng, et al.
Physiological Genomics
|
June 9, 2005
Pathway analysis of coronary atherosclerosis
Jennifer Y King, Rossella Ferrara, Raymond Tabibiazar, et al.
Nature Communications
|
April 28, 2023
PeakDecoder enables machine learning-based metabolite annotation and accurate profiling in multidimensional mass spectrometry measurements
Aivett Bilbao, Nathalie Munoz, Joonhoon Kim, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 30) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 30 results.
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 diseases
Adam J de Smith, Anya Tsalenko, Nick Sampas, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 11, 2006
Genetic variation in putative regulatory loci controlling gene expression in breast cancer
Vessela N Kristensen, Hege Edvardsen, Anya Tsalenko, et al.
Physiological Genomics
|
March 20, 2003
Identification of endothelial cell genes by combined database mining and microarray analysis
Michael Ho, Eugene Yang, George Matcuk, et al.
Nature Biotechnology
|
June 30, 2015
Chemically modified guide RNAs enhance CRISPR-Cas genome editing in human primary cells
Ayal Hendel, Rasmus O Bak, Joseph T Clark, et al.
Circulation
|
December 6, 2006
Network analysis of human in-stent restenosis
Euan A Ashley, Rossella Ferrara, Jennifer Y King, et al.
Nature Methods
|
May 5, 2010
Characterization of missing human genome sequences and copy-number polymorphic insertions
Jeffrey M Kidd, Nick Sampas, Francesca Antonacci, et al.
American Journal of Human Genetics
|
February 29, 2008
The fine-scale and complex architecture of human copy-number variation
George H Perry, Amir Ben-Dor, Anya Tsalenko, et al.
Circulation
|
September 10, 2003
Novel role for the potent endogenous inotrope apelin in human cardiac dysfunction
Mary M Chen, Euan A Ashley, David X F Deng, et al.
Physiological Genomics
|
June 9, 2005
Pathway analysis of coronary atherosclerosis
Jennifer Y King, Rossella Ferrara, Raymond Tabibiazar, et al.
Nature Communications
|
April 28, 2023
PeakDecoder enables machine learning-based metabolite annotation and accurate profiling in multidimensional mass spectrometry measurements
Aivett Bilbao, Nathalie Munoz, Joonhoon Kim, et al.
Page
of 3