Results 101 to 110 of about 1,071 (153)

CLN6’s luminal tail-mediated functional interference between CLN6 mutants as a novel pathomechanism for the neuronal ceroid lipofuscinoses

open access: yesCLN6’s luminal tail-mediated functional interference between CLN6 mutants as a novel pathomechanism for the neuronal ceroid lipofuscinoses
CLN6 (Ceroid Lipofuscinosis, Neuronal, 6) is a 311-amino acid protein spanning the endoplasmic reticulum membrane. Mutations in CLN6 are linked to CLN6 disease, a hereditary neurodegenerative disorder categorized into the neuronal ceroid lipofuscinoses.
openaire  

Genetic Heterogeneity Underlying Phenotypes with Early-Onset Cerebellar Atrophy. [PDF]

open access: yesInt J Mol Sci, 2023
Martínez-Rubio D   +14 more
europepmc   +1 more source

Corrigendum to A CLN6-CLN8 complex recruits lysosomal enzymes at the ER for Golgi transfer. [PDF]

open access: yesJ Clin Invest
Bajaj L   +15 more
europepmc   +1 more source

Structural adaptability and hydrogen bonding in a dissymmetric pyrimidine thioether ligand. [PDF]

open access: yesActa Crystallogr C Struct Chem
Anoliefo K   +4 more
europepmc   +1 more source

Neuropsychiatric manifestations of Kufs disease. [PDF]

open access: yesIndian J Psychiatry
Vijayan S, Selvaraj A.
europepmc   +1 more source

Neuronal ceroid lipofuscinosis: underlying mechanisms and emerging therapeutic targets. [PDF]

open access: yesNat Rev Neurol
Ziółkowska EA   +5 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy