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B Neuhaus

Showing results (31-40 of 42) with videos related to

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Journal of the American Chemical Society|February 20, 2004
Solution NMR studies of the A beta(1-40) and A beta(1-42) peptides establish that the Met35 oxidation state affects the mechanism of amyloid formationLiming Hou, Haiyan Shao, Yongbo Zhang, et al.
Msphere|February 7, 2020
Influenza A Virus Field Surveillance at a Swine-Human InterfaceBenjamin L Rambo-Martin, Matthew W Keller, Malania M Wilson, et al.
HGG Advances|February 15, 2024
Clinical, immunohistochemical, and genetic characterization of splice-altering biallelic DES variants: Therapeutic implicationsJanelle Geist Hauserman, Chamindra G Laverty, Sandra Donkervoort, et al.
Acta Neuropathologica|February 1, 2019
ACTN2 mutations cause "Multiple structured Core Disease" (MsCD)Xavière Lornage, Norma B Romero, Claire A Grosgogeat, et al.
Neurology. Genetics|June 25, 2024
Phase 1 Open-Label Study of Omigapil in Patients With LAMA2- or COL6-Related DystrophyA Reghan Foley, Pomi Yun, Meganne E Leach, et al.
Annals of Clinical and Translational Neurology|February 9, 2025
Clinical characterization of Collagen XII-related disease caused by biallelic COL12A1 variantsRiley M McCarty, Dimah Saade, Pinki Munot, et al.
American Journal of Human Genetics|November 20, 2020
Pathogenic Variants in the Myosin Chaperone UNC-45B Cause Progressive Myopathy with Eccentric CoresSandra Donkervoort, Carl E Kutzner, Ying Hu, et al.
Science Translational Medicine|April 3, 2024
Pathogenic <i>TNNI1</i> variants disrupt sarcomere contractility resulting in hypo- and hypercontractile muscle diseaseSandra Donkervoort, Martijn van de Locht, Dario Ronchi, et al.
Nature Medicine|June 1, 2021
Childhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesisPayam Mohassel, Sandra Donkervoort, Museer A Lone, et al.
Brain : a Journal of Neurology|February 9, 2021
An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathyAlistair T Pagnamenta, Rauan Kaiyrzhanov, Yaqun Zou, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Journal of the American Chemical Society|February 20, 2004
Solution NMR studies of the A beta(1-40) and A beta(1-42) peptides establish that the Met35 oxidation state affects the mechanism of amyloid formationLiming Hou, Haiyan Shao, Yongbo Zhang, et al.
Msphere|February 7, 2020
Influenza A Virus Field Surveillance at a Swine-Human InterfaceBenjamin L Rambo-Martin, Matthew W Keller, Malania M Wilson, et al.
HGG Advances|February 15, 2024
Clinical, immunohistochemical, and genetic characterization of splice-altering biallelic DES variants: Therapeutic implicationsJanelle Geist Hauserman, Chamindra G Laverty, Sandra Donkervoort, et al.
Acta Neuropathologica|February 1, 2019
ACTN2 mutations cause "Multiple structured Core Disease" (MsCD)Xavière Lornage, Norma B Romero, Claire A Grosgogeat, et al.
Neurology. Genetics|June 25, 2024
Phase 1 Open-Label Study of Omigapil in Patients With LAMA2- or COL6-Related DystrophyA Reghan Foley, Pomi Yun, Meganne E Leach, et al.
Annals of Clinical and Translational Neurology|February 9, 2025
Clinical characterization of Collagen XII-related disease caused by biallelic COL12A1 variantsRiley M McCarty, Dimah Saade, Pinki Munot, et al.
American Journal of Human Genetics|November 20, 2020
Pathogenic Variants in the Myosin Chaperone UNC-45B Cause Progressive Myopathy with Eccentric CoresSandra Donkervoort, Carl E Kutzner, Ying Hu, et al.
Science Translational Medicine|April 3, 2024
Pathogenic <i>TNNI1</i> variants disrupt sarcomere contractility resulting in hypo- and hypercontractile muscle diseaseSandra Donkervoort, Martijn van de Locht, Dario Ronchi, et al.
Nature Medicine|June 1, 2021
Childhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesisPayam Mohassel, Sandra Donkervoort, Museer A Lone, et al.
Brain : a Journal of Neurology|February 9, 2021
An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathyAlistair T Pagnamenta, Rauan Kaiyrzhanov, Yaqun Zou, et al.
Pageof 5