Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Maria M. Zwartkruis"'
Autor:
Astrid T. van der Geest, Channa E. Jakobs, Tijana Ljubikj, Christiaan F. M. Huffels, Marta Cañizares Luna, Renata Vieira de Sá, Youri Adolfs, Marina de Wit, Daan H. Rutten, Marthe Kaal, Maria M. Zwartkruis, Mireia Carcolé, Ewout J. N. Groen, Elly M. Hol, Onur Basak, Adrian M. Isaacs, Henk-Jan Westeneng, Leonard H. van den Berg, Jan H. Veldink, Domino K. Schlegel, R. Jeroen Pasterkamp
Publikováno v:
Acta Neuropathologica Communications, Vol 12, Iss 1, Pp 1-31 (2024)
Abstract A hexanucleotide repeat expansion (HRE) in C9ORF72 is the most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Human brain imaging and experimental studies indicate early changes in brain struct
Externí odkaz:
https://doaj.org/article/081ca424a8b945aa9f02a6c9589c4317
Autor:
Nefeli Kakava-Georgiadou, Maria M. Zwartkruis, Clara Bullich-Vilarrubias, Mieneke C. M. Luijendijk, Keith M. Garner, Geoffrey van der Plasse, Roger A. H. Adan
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 12 (2019)
Development of tools to manipulate activity of specific neurons is important for dissecting the function of neural circuits. Viral vectors and conditional transgenic animal lines that target recombinases to specific cells facilitate the successful ma
Externí odkaz:
https://doaj.org/article/eec5557d9899403bacbfd9f1f042c672
Autor:
Maria M Zwartkruis, Ewout JN Groen
Publikováno v:
EMBO Molecular Medicine, Vol 16, Iss 4, Pp 672-674 (2024)
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease caused by loss-of-function of SMN1. SMA is characterized by degeneration of motor neurons in the spinal cord, leading to progressive muscle weakness and atrophy. One of thr
Externí odkaz:
https://doaj.org/article/fbf3aa65ac1a407598986c7f5eeb5034