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Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
January 4, 2008
Emergence of coagulase-negative staphylococci as a cause of native valve endocarditis
Vivian H Chu, Christopher W Woods, Jose M Miro, et al.
NPJ Digital Medicine
|
December 21, 2022
A survey on clinical natural language processing in the United Kingdom from 2007 to 2022
Honghan Wu, Minhong Wang, Jinge Wu, et al.
Nature Communications
|
August 17, 2022
GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements
Peter H Dixon, Adam P Levine, Inês Cebola, et al.
BMC Biology
|
November 2, 2017
Membrane dynamics and organelle biogenesis-lipid pipelines and vesicular carriers
Christopher J Stefan, William S Trimble, Sergio Grinstein, et al.
Elife
|
September 20, 2022
Diverse ancestry whole-genome sequencing association study identifies <i>TBX5</i> and <i>PTK7</i> as susceptibility genes for posterior urethral valves
Melanie M Y Chan, Omid Sadeghi-Alavijeh, Filipa M Lopes, et al.
JAMA
|
June 24, 2005
Staphylococcus aureus endocarditis: a consequence of medical progress
Vance G Fowler, Jose M Miro, Bruno Hoen, et al.
Plastic and Reconstructive Surgery
|
June 8, 2022
The First Successful Combined Full Face and Bilateral Hand Transplant
Elie P Ramly, Allyson R Alfonso, Zoe P Berman, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
May 8, 2020
Phase II Trial of IL-12 Plasmid Transfection and PD-1 Blockade in Immunologically Quiescent Melanoma
Alain P Algazi, Christopher G Twitty, Katy K Tsai, et al.
Journal of the American Society of Nephrology : JASN
|
January 11, 2020
Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy
Adam P Levine, Melanie M Y Chan, Omid Sadeghi-Alavijeh, et al.
Human Molecular Genetics
|
November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance
Steven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, et al.
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of 65
Search research articles
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Showing results (621-630 of 646) with videos related to
Sort By:
Page
of 65
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
January 4, 2008
Emergence of coagulase-negative staphylococci as a cause of native valve endocarditis
Vivian H Chu, Christopher W Woods, Jose M Miro, et al.
NPJ Digital Medicine
|
December 21, 2022
A survey on clinical natural language processing in the United Kingdom from 2007 to 2022
Honghan Wu, Minhong Wang, Jinge Wu, et al.
Nature Communications
|
August 17, 2022
GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements
Peter H Dixon, Adam P Levine, Inês Cebola, et al.
BMC Biology
|
November 2, 2017
Membrane dynamics and organelle biogenesis-lipid pipelines and vesicular carriers
Christopher J Stefan, William S Trimble, Sergio Grinstein, et al.
Elife
|
September 20, 2022
Diverse ancestry whole-genome sequencing association study identifies <i>TBX5</i> and <i>PTK7</i> as susceptibility genes for posterior urethral valves
Melanie M Y Chan, Omid Sadeghi-Alavijeh, Filipa M Lopes, et al.
JAMA
|
June 24, 2005
Staphylococcus aureus endocarditis: a consequence of medical progress
Vance G Fowler, Jose M Miro, Bruno Hoen, et al.
Plastic and Reconstructive Surgery
|
June 8, 2022
The First Successful Combined Full Face and Bilateral Hand Transplant
Elie P Ramly, Allyson R Alfonso, Zoe P Berman, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
May 8, 2020
Phase II Trial of IL-12 Plasmid Transfection and PD-1 Blockade in Immunologically Quiescent Melanoma
Alain P Algazi, Christopher G Twitty, Katy K Tsai, et al.
Journal of the American Society of Nephrology : JASN
|
January 11, 2020
Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy
Adam P Levine, Melanie M Y Chan, Omid Sadeghi-Alavijeh, et al.
Human Molecular Genetics
|
November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance
Steven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, et al.
Page
of 65