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Nature Communications
|
September 27, 2024
Computer-aided drug design to generate a unique antibiotic family
Christopher J Barden, Fan Wu, J Pedro Fernandez-Murray, et al.
American Journal of Medical Quality : the Official Journal of the American College of Medical Quality
|
April 17, 2025
A Platform Designed to Empower Quality Improvement for Patients with Atrial Fibrillation
Thomas F Deering, Anne Marie Smith, John A Gillespie, et al.
The Journal of Physical Chemistry. A
|
June 1, 2023
Electronic Structure and Excited-State Dynamics of DNA-Templated Monomers and Aggregates of Asymmetric Polymethine Dyes
Katelyn M Duncan, Hannah M Byers, Madaline E Houdek, et al.
The Journal of Pediatrics
|
June 20, 2020
The Impact of Rapid Exome Sequencing on Medical Management of Critically Ill Children
Amanda S Freed, Sarah V Clowes Candadai, Megan C Sikes, et al.
Alternatives to Laboratory Animals : ATLA
|
October 8, 2009
An immunologic model for rapid vaccine assessment -- a clinical trial in a test tube
Russell G Higbee, Anthony M Byers, Vipra Dhir, et al.
JCI Insight
|
April 30, 2026
PD-1-targeted IL-15 mutein activates CD8+ and CD4+ T cells in infection and cancer
Isaraphorn Pratumchai, Marie Bernardo, Julien Tessier, et al.
Cancer Research Communications
|
September 25, 2024
A Precision Engineered Interleukin-2 for Bolstering CD8+ T- and NK-cell Activity without Eosinophilia and Vascular Leak Syndrome in Nonhuman Primates
Lina Ma, Nicole V Acuff, Ingrid B Joseph, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
September 29, 2012
Polymorphisms in the fetal progesterone receptor and a calcium-activated potassium channel isoform are associated with preterm birth in an Argentinian population
P C Mann, M E Cooper, K K Ryckman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 9, 2021
Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay
Uirá Souto Melo, Devon Bonner, Kevin C Kent Lloyd, et al.
Journal of Medical Genetics
|
July 5, 2022
Clinical, biochemical and genetic characteristics of MOGS-CDG: a rare congenital disorder of glycosylation
Shino Shimada, Bobby G Ng, Amy L White, et al.
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of 39
Search research articles
Search
Showing results (371-380 of 381) with videos related to
Sort By:
Page
of 39
Nature Communications
|
September 27, 2024
Computer-aided drug design to generate a unique antibiotic family
Christopher J Barden, Fan Wu, J Pedro Fernandez-Murray, et al.
American Journal of Medical Quality : the Official Journal of the American College of Medical Quality
|
April 17, 2025
A Platform Designed to Empower Quality Improvement for Patients with Atrial Fibrillation
Thomas F Deering, Anne Marie Smith, John A Gillespie, et al.
The Journal of Physical Chemistry. A
|
June 1, 2023
Electronic Structure and Excited-State Dynamics of DNA-Templated Monomers and Aggregates of Asymmetric Polymethine Dyes
Katelyn M Duncan, Hannah M Byers, Madaline E Houdek, et al.
The Journal of Pediatrics
|
June 20, 2020
The Impact of Rapid Exome Sequencing on Medical Management of Critically Ill Children
Amanda S Freed, Sarah V Clowes Candadai, Megan C Sikes, et al.
Alternatives to Laboratory Animals : ATLA
|
October 8, 2009
An immunologic model for rapid vaccine assessment -- a clinical trial in a test tube
Russell G Higbee, Anthony M Byers, Vipra Dhir, et al.
JCI Insight
|
April 30, 2026
PD-1-targeted IL-15 mutein activates CD8+ and CD4+ T cells in infection and cancer
Isaraphorn Pratumchai, Marie Bernardo, Julien Tessier, et al.
Cancer Research Communications
|
September 25, 2024
A Precision Engineered Interleukin-2 for Bolstering CD8+ T- and NK-cell Activity without Eosinophilia and Vascular Leak Syndrome in Nonhuman Primates
Lina Ma, Nicole V Acuff, Ingrid B Joseph, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
September 29, 2012
Polymorphisms in the fetal progesterone receptor and a calcium-activated potassium channel isoform are associated with preterm birth in an Argentinian population
P C Mann, M E Cooper, K K Ryckman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 9, 2021
Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay
Uirá Souto Melo, Devon Bonner, Kevin C Kent Lloyd, et al.
Journal of Medical Genetics
|
July 5, 2022
Clinical, biochemical and genetic characteristics of MOGS-CDG: a rare congenital disorder of glycosylation
Shino Shimada, Bobby G Ng, Amy L White, et al.
Page
of 39