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Science (New York, N.Y.)
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November 11, 2021
Computed structures of core eukaryotic protein complexes
Ian R Humphreys, Jimin Pei, Minkyung Baek, et al.
Multiple Sclerosis and Related Disorders
|
February 26, 2022
Measuring productivity loss in early relapsing-remitting multiple sclerosis
Susana Sainz de la Maza, Jorge Maurino, Mónica Borges, et al.
Multiple Sclerosis and Related Disorders
|
August 27, 2022
Delayed cognitive processing and treatment status quo bias in early-stage multiple sclerosis
Gustavo Saposnik, Sanketh Andhavarapu, Susana Sainz de la Maza, et al.
Genome Medicine
|
May 12, 2026
Unprocessed U1 snRNAs as a biomarker of INTS11- and BRAT1-related neurodevelopmental disorders
Beatrice Valtorta, Zuzana Polackova, Reza Maroofian, et al.
Nature Communications
|
July 1, 2026
De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activity
Aleš Hnízda, Beatriz Martinez-Delgado, Diana Sanchez-Ponce, et al.
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Search research articles
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Showing results (91-100 of 95) with videos related to
Sort By:
Page
of 10
You have reached the last page of results.
This site can display upto 95 results.
Science (New York, N.Y.)
|
November 11, 2021
Computed structures of core eukaryotic protein complexes
Ian R Humphreys, Jimin Pei, Minkyung Baek, et al.
Multiple Sclerosis and Related Disorders
|
February 26, 2022
Measuring productivity loss in early relapsing-remitting multiple sclerosis
Susana Sainz de la Maza, Jorge Maurino, Mónica Borges, et al.
Multiple Sclerosis and Related Disorders
|
August 27, 2022
Delayed cognitive processing and treatment status quo bias in early-stage multiple sclerosis
Gustavo Saposnik, Sanketh Andhavarapu, Susana Sainz de la Maza, et al.
Genome Medicine
|
May 12, 2026
Unprocessed U1 snRNAs as a biomarker of INTS11- and BRAT1-related neurodevelopmental disorders
Beatrice Valtorta, Zuzana Polackova, Reza Maroofian, et al.
Nature Communications
|
July 1, 2026
De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activity
Aleš Hnízda, Beatriz Martinez-Delgado, Diana Sanchez-Ponce, et al.
Page
of 10