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The American Journal of Cardiology
|
March 20, 2016
Assessment of Device-Related Thrombus and Associated Clinical Outcomes With the WATCHMAN Left Atrial Appendage Closure Device for Embolic Protection in Patients With Atrial Fibrillation (from the PROTECT-AF Trial)
Michael L Main, Dali Fan, Vivek Y Reddy, et al.
Journal of Proteome Research
|
January 20, 2012
Association of medication with the human plasma N-glycome
Radka Saldova, Jennifer E Huffman, Barbara Adamczyk, et al.
Human Mutation
|
October 2, 2004
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome
Alan F Wright, Adam C Reddick, Sharon B Schwartz, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
March 7, 2015
Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study
Michelle Luciano, Victoria Svinti, Archie Campbell, et al.
AIDS Research and Treatment
|
December 31, 2014
Adapting and Implementing a Community Program to Improve Retention in Care among Patients with HIV in Southern Haiti: "Group of 6"
John A Naslund, Jodie Dionne-Odom, Cléonas Junior Destiné, et al.
The Lancet. Infectious Diseases
|
August 16, 2025
Safety and immunogenicity of novel live attenuated type 1 and type 3 oral poliomyelitis vaccines in healthy adults in the USA: a first-in-human, observer-masked, multicentre, phase 1 randomised controlled trial
Laina D Mercer, Arlene C Seña, E Ross Colgate, et al.
Molecular Genetics & Genomic Medicine
|
September 26, 2017
Protein structure and phenotypic analysis of pathogenic and population missense variants in <i>STXBP1</i>
Mohnish Suri, Jochem M G Evers, Roman A Laskowski, et al.
American Journal of Human Genetics
|
October 18, 2022
Reduced penetrance of MODY-associated HNF1A/HNF4A variants but not GCK variants in clinically unselected cohorts
Uyenlinh L Mirshahi, Kevin Colclough, Caroline F Wright, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 12, 2018
Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders
Caroline F Wright, Jeremy F McRae, Stephen Clayton, et al.
The New England Journal of Medicine
|
July 20, 2007
Complement C3 variant and the risk of age-related macular degeneration
John R W Yates, Tiina Sepp, Baljinder K Matharu, et al.
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Showing results (1131-1140 of 1,353) with videos related to
Sort By:
Page
of 136
The American Journal of Cardiology
|
March 20, 2016
Assessment of Device-Related Thrombus and Associated Clinical Outcomes With the WATCHMAN Left Atrial Appendage Closure Device for Embolic Protection in Patients With Atrial Fibrillation (from the PROTECT-AF Trial)
Michael L Main, Dali Fan, Vivek Y Reddy, et al.
Journal of Proteome Research
|
January 20, 2012
Association of medication with the human plasma N-glycome
Radka Saldova, Jennifer E Huffman, Barbara Adamczyk, et al.
Human Mutation
|
October 2, 2004
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome
Alan F Wright, Adam C Reddick, Sharon B Schwartz, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
March 7, 2015
Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study
Michelle Luciano, Victoria Svinti, Archie Campbell, et al.
AIDS Research and Treatment
|
December 31, 2014
Adapting and Implementing a Community Program to Improve Retention in Care among Patients with HIV in Southern Haiti: "Group of 6"
John A Naslund, Jodie Dionne-Odom, Cléonas Junior Destiné, et al.
The Lancet. Infectious Diseases
|
August 16, 2025
Safety and immunogenicity of novel live attenuated type 1 and type 3 oral poliomyelitis vaccines in healthy adults in the USA: a first-in-human, observer-masked, multicentre, phase 1 randomised controlled trial
Laina D Mercer, Arlene C Seña, E Ross Colgate, et al.
Molecular Genetics & Genomic Medicine
|
September 26, 2017
Protein structure and phenotypic analysis of pathogenic and population missense variants in <i>STXBP1</i>
Mohnish Suri, Jochem M G Evers, Roman A Laskowski, et al.
American Journal of Human Genetics
|
October 18, 2022
Reduced penetrance of MODY-associated HNF1A/HNF4A variants but not GCK variants in clinically unselected cohorts
Uyenlinh L Mirshahi, Kevin Colclough, Caroline F Wright, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 12, 2018
Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders
Caroline F Wright, Jeremy F McRae, Stephen Clayton, et al.
The New England Journal of Medicine
|
July 20, 2007
Complement C3 variant and the risk of age-related macular degeneration
John R W Yates, Tiina Sepp, Baljinder K Matharu, et al.
Page
of 136