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Annals of Neurology
|
December 23, 2011
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
Michael A van Es, Helenius J Schelhaas, Paul W J van Vught, et al.
Nature Biotechnology
|
August 29, 2020
Evaluation of SARS-CoV-2 serology assays reveals a range of test performance
Jeffrey D Whitman, Joseph Hiatt, Cody T Mowery, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 9, 2020
Test performance evaluation of SARS-CoV-2 serological assays
Jeffrey D Whitman, Joseph Hiatt, Cody T Mowery, et al.
Science (New York, N.Y.)
|
October 16, 2020
Comparative host-coronavirus protein interaction networks reveal pan-viral disease mechanisms
David E Gordon, Joseph Hiatt, Mehdi Bouhaddou, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
Siwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Page
of 39
Search research articles
Search
Showing results (381-390 of 385) with videos related to
Sort By:
Page
of 39
You have reached the last page of results.
This site can display upto 385 results.
Annals of Neurology
|
December 23, 2011
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
Michael A van Es, Helenius J Schelhaas, Paul W J van Vught, et al.
Nature Biotechnology
|
August 29, 2020
Evaluation of SARS-CoV-2 serology assays reveals a range of test performance
Jeffrey D Whitman, Joseph Hiatt, Cody T Mowery, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 9, 2020
Test performance evaluation of SARS-CoV-2 serological assays
Jeffrey D Whitman, Joseph Hiatt, Cody T Mowery, et al.
Science (New York, N.Y.)
|
October 16, 2020
Comparative host-coronavirus protein interaction networks reveal pan-viral disease mechanisms
David E Gordon, Joseph Hiatt, Mehdi Bouhaddou, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
Siwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Page
of 39