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Showing results (91-100 of 95) with videos related to

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Science (New York, N.Y.)|November 11, 2021
Computed structures of core eukaryotic protein complexesIan R Humphreys, Jimin Pei, Minkyung Baek, et al.
Multiple Sclerosis and Related Disorders|February 26, 2022
Measuring productivity loss in early relapsing-remitting multiple sclerosisSusana 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 sclerosisGustavo 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 disordersBeatrice 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 activityAleš Hnízda, Beatriz Martinez-Delgado, Diana Sanchez-Ponce, et al.
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Showing results (91-100 of 95) with videos related to

Sort By:
Pageof 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 complexesIan R Humphreys, Jimin Pei, Minkyung Baek, et al.
Multiple Sclerosis and Related Disorders|February 26, 2022
Measuring productivity loss in early relapsing-remitting multiple sclerosisSusana 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 sclerosisGustavo 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 disordersBeatrice 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 activityAleš Hnízda, Beatriz Martinez-Delgado, Diana Sanchez-Ponce, et al.
Pageof 10