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Showing results (1381-1390 of 1,398) with videos related to
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Genome Research
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December 8, 2006
Genome characteristics of facultatively symbiotic Frankia sp. strains reflect host range and host plant biogeography
Philippe Normand, Pascal Lapierre, Louis S Tisa, et al.
Neurosurgical Focus
|
March 31, 2021
Biographies of international women leaders in neurosurgery
Stephanie M Casillo, Anisha Venkatesh, Nallammai Muthiah, et al.
JAMA
|
October 3, 2019
Effect of Selepressin vs Placebo on Ventilator- and Vasopressor-Free Days in Patients With Septic Shock: The SEPSIS-ACT Randomized Clinical Trial
Pierre-Francois Laterre, Scott M Berry, Allan Blemings, et al.
Science (New York, N.Y.)
|
May 26, 2018
Phylogenomics reveals multiple losses of nitrogen-fixing root nodule symbiosis
Maximilian Griesmann, Yue Chang, Xin Liu, et al.
Journal of Medicinal Chemistry
|
March 22, 2017
Sulfonamides as Selective Na<sub>V</sub>1.7 Inhibitors: Optimizing Potency, Pharmacokinetics, and Metabolic Properties to Obtain Atropisomeric Quinolinone (AM-0466) that Affords Robust in Vivo Activity
Russell F Graceffa, Alessandro A Boezio, Jessica Able, et al.
Acta Crystallographica. Section D, Biological Crystallography
|
September 27, 2006
SPINE bioinformatics and data-management aspects of high-throughput structural biology
S Albeck, P Alzari, C Andreini, et al.
JAMA Network Open
|
May 25, 2023
Effect of P2Y12 Inhibitors on Organ Support-Free Survival in Critically Ill Patients Hospitalized for COVID-19: A Randomized Clinical Trial
Jeffrey S Berger, Matthew D Neal, Lucy Z Kornblith, et al.
Pediatric Neurology
|
November 19, 2025
Longitudinal Characterization of Males With X-Linked Creatine Transporter Deficiency: Final Results of a Multiyear Observational Study
Judith S Miller, Cristan Farmer, Susan Blair, et al.
American Journal of Medical Genetics. Part A
|
July 29, 2022
Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data
Amy Hardcastle, Aliska M Berry, Ian M Campbell, et al.
Human Mutation
|
April 26, 2019
Mutation update for the SATB2 gene
Yuri A Zarate, Katherine A Bosanko, Aisling R Caffrey, et al.
Page
of 140
Search research articles
Search
Showing results (1381-1390 of 1,398) with videos related to
Sort By:
Page
of 140
Genome Research
|
December 8, 2006
Genome characteristics of facultatively symbiotic Frankia sp. strains reflect host range and host plant biogeography
Philippe Normand, Pascal Lapierre, Louis S Tisa, et al.
Neurosurgical Focus
|
March 31, 2021
Biographies of international women leaders in neurosurgery
Stephanie M Casillo, Anisha Venkatesh, Nallammai Muthiah, et al.
JAMA
|
October 3, 2019
Effect of Selepressin vs Placebo on Ventilator- and Vasopressor-Free Days in Patients With Septic Shock: The SEPSIS-ACT Randomized Clinical Trial
Pierre-Francois Laterre, Scott M Berry, Allan Blemings, et al.
Science (New York, N.Y.)
|
May 26, 2018
Phylogenomics reveals multiple losses of nitrogen-fixing root nodule symbiosis
Maximilian Griesmann, Yue Chang, Xin Liu, et al.
Journal of Medicinal Chemistry
|
March 22, 2017
Sulfonamides as Selective Na<sub>V</sub>1.7 Inhibitors: Optimizing Potency, Pharmacokinetics, and Metabolic Properties to Obtain Atropisomeric Quinolinone (AM-0466) that Affords Robust in Vivo Activity
Russell F Graceffa, Alessandro A Boezio, Jessica Able, et al.
Acta Crystallographica. Section D, Biological Crystallography
|
September 27, 2006
SPINE bioinformatics and data-management aspects of high-throughput structural biology
S Albeck, P Alzari, C Andreini, et al.
JAMA Network Open
|
May 25, 2023
Effect of P2Y12 Inhibitors on Organ Support-Free Survival in Critically Ill Patients Hospitalized for COVID-19: A Randomized Clinical Trial
Jeffrey S Berger, Matthew D Neal, Lucy Z Kornblith, et al.
Pediatric Neurology
|
November 19, 2025
Longitudinal Characterization of Males With X-Linked Creatine Transporter Deficiency: Final Results of a Multiyear Observational Study
Judith S Miller, Cristan Farmer, Susan Blair, et al.
American Journal of Medical Genetics. Part A
|
July 29, 2022
Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data
Amy Hardcastle, Aliska M Berry, Ian M Campbell, et al.
Human Mutation
|
April 26, 2019
Mutation update for the SATB2 gene
Yuri A Zarate, Katherine A Bosanko, Aisling R Caffrey, et al.
Page
of 140