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Human Genomics
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March 19, 2013
How to create innovation by building the translation bridge from basic research into medicinal drugs: an industrial perspective
Paul G Germann, Alexander Schuhmacher, Juan Harrison, et al.
Human Genomics
|
July 9, 2013
Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations
Lili Ding, Tilahun Abebe, Joseph Beyene, et al.
Human Genomics
|
December 19, 2012
Genotype-phenotype associations in neurofibromatosis type 1 (NF1): an increased risk of tumor complications in patients with NF1 splice-site mutations?
Adila Alkindy, Nadia Chuzhanova, Usha Kini, et al.
Human Genomics
|
December 19, 2012
Usability survey of biomedical question answering systems
Michael A Bauer, Daniel Berleant
Human Genomics
|
December 4, 2012
The human crystallin gene families
Graeme Wistow
Human Genomics
|
May 3, 2013
Vive la différence: naming structural variants in the human reference genome
Ruth L Seal, Mathew W Wright, Kristian A Gray, et al.
Human Genomics
|
June 7, 2013
New susceptibility locus for obesity and dyslipidaemia on chromosome 3q22.3
Maie Alshahid, Salma M Wakil, Mohammed Al-Najai, et al.
Human Genomics
|
December 30, 2009
Detecting genes contributing to longevity using twin data
Alexander Begun
Human Genomics
|
December 30, 2009
R and Bioconductor solutions for alternative splicing detection
Tzulip Phang
Human Genomics
|
January 12, 2019
Population and breast cancer patients' analysis reveals the diversity of genomic variation of the BRCA genes in the Mexican population
J C Fernández-Lopez, S Romero-Córdoba, R Rebollar-Vega, et al.
Page
of 111
Search research articles
Search
Showing results (871-880 of 1,110) with videos related to
Sort By:
Page
of 111
Human Genomics
|
March 19, 2013
How to create innovation by building the translation bridge from basic research into medicinal drugs: an industrial perspective
Paul G Germann, Alexander Schuhmacher, Juan Harrison, et al.
Human Genomics
|
July 9, 2013
Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations
Lili Ding, Tilahun Abebe, Joseph Beyene, et al.
Human Genomics
|
December 19, 2012
Genotype-phenotype associations in neurofibromatosis type 1 (NF1): an increased risk of tumor complications in patients with NF1 splice-site mutations?
Adila Alkindy, Nadia Chuzhanova, Usha Kini, et al.
Human Genomics
|
December 19, 2012
Usability survey of biomedical question answering systems
Michael A Bauer, Daniel Berleant
Human Genomics
|
December 4, 2012
The human crystallin gene families
Graeme Wistow
Human Genomics
|
May 3, 2013
Vive la différence: naming structural variants in the human reference genome
Ruth L Seal, Mathew W Wright, Kristian A Gray, et al.
Human Genomics
|
June 7, 2013
New susceptibility locus for obesity and dyslipidaemia on chromosome 3q22.3
Maie Alshahid, Salma M Wakil, Mohammed Al-Najai, et al.
Human Genomics
|
December 30, 2009
Detecting genes contributing to longevity using twin data
Alexander Begun
Human Genomics
|
December 30, 2009
R and Bioconductor solutions for alternative splicing detection
Tzulip Phang
Human Genomics
|
January 12, 2019
Population and breast cancer patients' analysis reveals the diversity of genomic variation of the BRCA genes in the Mexican population
J C Fernández-Lopez, S Romero-Córdoba, R Rebollar-Vega, et al.
Page
of 111