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Human Mutation
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May 28, 2010
Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics
David N Cooper, Jian-Min Chen, Edward V Ball, et al.
Human Genetics
|
July 8, 1998
Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delay
M Upadhyaya, M Ruggieri, J Maynard, et al.
Proteins
|
October 5, 2017
Biological and functional relevance of CASP predictions
Tianyun Liu, Shirbi Ish-Shalom, Wen Torng, et al.
Aging Cell
|
June 15, 2007
Cellular senescence in human myoblasts is overcome by human telomerase reverse transcriptase and cyclin-dependent kinase 4: consequences in aging muscle and therapeutic strategies for muscular dystrophies
Chun-Hong Zhu, Vincent Mouly, Racquel N Cooper, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
May 22, 2021
The course and prognostic capability of motor difficulties in infants showing early signs of autism
Melissa K Licari, Kandice Varcin, Kristelle Hudry, et al.
Cancer Research
|
May 3, 2011
Considerations for the clinical application of chimeric antigen receptor T cells: observations from a recombinant DNA Advisory Committee Symposium held June 15, 2010
Hildegund C J Ertl, John Zaia, Steven A Rosenberg, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
June 7, 2017
Reproducibility of the plasma glucose response to moderate-intensity exercise in adolescents with Type 1 diabetes
M B Abraham, R J Davey, M N Cooper, et al.
Cancers
|
February 15, 2019
Nucleotide Weight Matrices Reveal Ubiquitous Mutational Footprints of AID/APOBEC Deaminases in Human Cancer Genomes
Igor B Rogozin, Abiel Roche-Lima, Artem G Lada, et al.
Molecular Biology and Evolution
|
January 6, 2026
A POMT2 missense substitution contributes to hypoxia adaptation in hibernating mammals
Jinjin Zhang, Xiuping Zhang, Ningyawen Liu, et al.
Journal of Leukocyte Biology
|
September 25, 2024
Limited proteolysis of neutrophil granule proteins by the bacterial protease RgpB depletes neutrophil antimicrobial capacity
Kelley N Cooper, Aleksandra Wielento, Savannah C Morris, et al.
Page
of 122
Search research articles
Search
Showing results (871-880 of 1,220) with videos related to
Sort By:
Page
of 122
Human Mutation
|
May 28, 2010
Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics
David N Cooper, Jian-Min Chen, Edward V Ball, et al.
Human Genetics
|
July 8, 1998
Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delay
M Upadhyaya, M Ruggieri, J Maynard, et al.
Proteins
|
October 5, 2017
Biological and functional relevance of CASP predictions
Tianyun Liu, Shirbi Ish-Shalom, Wen Torng, et al.
Aging Cell
|
June 15, 2007
Cellular senescence in human myoblasts is overcome by human telomerase reverse transcriptase and cyclin-dependent kinase 4: consequences in aging muscle and therapeutic strategies for muscular dystrophies
Chun-Hong Zhu, Vincent Mouly, Racquel N Cooper, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
May 22, 2021
The course and prognostic capability of motor difficulties in infants showing early signs of autism
Melissa K Licari, Kandice Varcin, Kristelle Hudry, et al.
Cancer Research
|
May 3, 2011
Considerations for the clinical application of chimeric antigen receptor T cells: observations from a recombinant DNA Advisory Committee Symposium held June 15, 2010
Hildegund C J Ertl, John Zaia, Steven A Rosenberg, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
June 7, 2017
Reproducibility of the plasma glucose response to moderate-intensity exercise in adolescents with Type 1 diabetes
M B Abraham, R J Davey, M N Cooper, et al.
Cancers
|
February 15, 2019
Nucleotide Weight Matrices Reveal Ubiquitous Mutational Footprints of AID/APOBEC Deaminases in Human Cancer Genomes
Igor B Rogozin, Abiel Roche-Lima, Artem G Lada, et al.
Molecular Biology and Evolution
|
January 6, 2026
A POMT2 missense substitution contributes to hypoxia adaptation in hibernating mammals
Jinjin Zhang, Xiuping Zhang, Ningyawen Liu, et al.
Journal of Leukocyte Biology
|
September 25, 2024
Limited proteolysis of neutrophil granule proteins by the bacterial protease RgpB depletes neutrophil antimicrobial capacity
Kelley N Cooper, Aleksandra Wielento, Savannah C Morris, et al.
Page
of 122