Results 111 to 120 of about 14,329 (183)

Selective silencing of expanded CAG repeats: Chemically modified siRNA advances RNA-based therapies for polyglutamine diseases. [PDF]

Mol Ther Nucleic Acids
Scholten GJ, Hyde JT, Buijsen RAM.
europepmc   +1 more source

CAG-targeting artificial miRNA with reduced off-target risk for efficient lowering of pathogenic polyglutamine proteins. [PDF]

NAR Mol Med
Pewinska-Kolodziejczak M, Kotowska-Zimmer A, Przybyl L, Wronka D, Karlik A, Smuszkiewicz M, Balcerek J, Suszynska-Zajczyk J, Piaszyk-Borychowska A, Urbanek-Trzeciak M, Sablok G, Kozlowska E, Podkowinski J, Fiszer A, Kozlowski P, Handschuh L, Olejniczak M.   +16 more
europepmc   +1 more source

PCK2-Mediated PQBP1 Lactylation Promotes Asthmatic Inflammation through PRMT5 Inhibition. [PDF]

Research (Wash D C)
Bai Q, Ding N, Feng R, Shang F, Wang Z, Li L, Wang Z, Piao Y, Wang C, Song Y, Yan G.   +10 more
europepmc   +1 more source

Hereditary Ataxias: From Pathogenesis and Clinical Features to Neuroimaging, Fluid, and Digital Biomarkers-A Scoping Review. [PDF]

Int J Mol Sci
Bernardi E, López-Lombardía Ó, Olmedo-Saura G, Pagonabarraga J, Kulisevsky J, Pérez-Pérez J.   +5 more
europepmc   +1 more source

Dynamics of autophagy in response to high linear energy transfer radiation and cancer. [PDF]

Korean J Clin Oncol
Lal M.
europepmc   +1 more source

Correction: Dihedral angle measurements for structure determination by biomolecular solid-state NMR spectroscopy

Frontiers in Molecular Biosciences
Patrick C. A. van der Wel
doaj   +1 more source

Evolutionary perspective of the CAG/CAA interplay coding for pure polyglutamine stretches in proteins. [PDF]

NAR Genom Bioinform
Moreno-Rodríguez A, Pérez-Pulido AJ, Mier P.   +2 more
europepmc   +1 more source

Targeting UCHL3 attenuates pathological markers in neuronal models of Huntington's disease. [PDF]

Brain
Ishtayeh H, Battistoni E, Pochtar S, McHugh TLM, Tshilenge KT, Rossmiller B, Amer-Sarsour F, Berdichevsky Y, Muchtar N, Weil M, Ellerby LM, Ashkenazi A.   +11 more
europepmc   +1 more source

Unveiling a Rare Phenotypic Presentation of Mitofusin 2 Mutation as Cerebellar Ataxia. [PDF]

Ann Indian Acad Neurol
Robert P, Velayudhan SC, Aboobekar HA, Sudhakaran P.   +3 more
europepmc   +1 more source

Polyglutamine Disorders [PDF]

, 2018
openaire   +1 more source