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Biochemistry, ISSN 0006-2960, 11/2018, Volume 57, Issue 46, pp. 6538 - 6550
Dynein adaptor proteins such as Bicaudal D2 (BicD2) are integral components of the dynein transport machinery, as they recognize cargoes for cell... 
PROTEIN | SPINAL MUSCULAR-ATROPHY | HELA-CELLS | STRUCTURAL BASIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | MOLECULAR ARCHITECTURE | COILED-COIL | MOTOR ADAPTER | DYNEIN RECRUITMENT | APICAL NUCLEAR MIGRATION | DYNACTIN RECRUITS
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2017, Volume 114, Issue 9, pp. E1597 - E1606
Journal Article
Brain, ISSN 0006-8950, 2017, Volume 140, Issue 2, pp. 287 - 305
Hereditary spastic paraplegias are heterogeneous neurodegenerative disorders characterized by progressive spasticity of the lower limbs due to degeneration of... 
Parkinsonism | Lysosomes | Neuronal ceroid lipofuscinosis | Hereditary spastic paraplegia (HSP) | Kufor-Rakeb syndrome | parkinsonism | CLINICAL SPECTRUM | PARK9 | ALPHA-SYNUCLEIN | hereditary spastic paraplegia (HSP) | neuronal ceroid lipofuscinosis | NEUROSCIENCES | CLINICAL NEUROLOGY | ATPASE ATP13A2 | SPINAL MUSCULAR-ATROPHY | LYSOSOMAL DYSFUNCTION | lysosomes | AUTOSOMAL-DOMINANT | MOTOR ADAPTER | PARKINSONS-DISEASE | Spastic Paraplegia, Hereditary - genetics | Cells, Cultured - cytology | Humans | Middle Aged | Cercopithecus aethiops | Family Health | Male | Mitochondria - ultrastructure | Spastic Paraplegia, Hereditary - diagnostic imaging | Mental Disorders - genetics | Psychiatric Status Rating Scales | Lysosomes - metabolism | Proton-Translocating ATPases - genetics | Cells, Cultured - ultrastructure | Cognition Disorders - etiology | Adult | Mental Disorders - etiology | Lysosomes - drug effects | Genetic Predisposition to Disease - genetics | Gene Expression Regulation - genetics | Enzyme Inhibitors - pharmacology | Cognition Disorders - genetics | Mitochondria - metabolism | Mitochondria - drug effects | Mutation - genetics | Gene Expression Regulation - drug effects | Lysosomes - ultrastructure | Neuropsychological Tests | Leupeptins - pharmacology | Animals | Spastic Paraplegia, Hereditary - complications | 1040 | Original
Journal Article
Brain, ISSN 0006-8950, 02/2015, Volume 138, Issue 2, pp. 293 - 310
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 05/2014, Volume 85, Issue 5, pp. 590 - 592
  While all variants reported so far for the BICD2 coiled-coil domain 3 (Rab6-binding region) present with SMA as the main phenotype (p.Glu774Gly 2 ;... 
SURGERY | MOTOR ADAPTER | PSYCHIATRY | CLINICAL NEUROLOGY | Humans | Microtubule-Associated Proteins | Male | Mutation - genetics | Muscular Atrophy, Spinal - pathology | Carrier Proteins - genetics | Muscular Atrophy, Spinal - genetics | Phenotype | Pedigree | Adult | Female | Aged | Muscular Atrophy, Spinal - complications | Genotype & phenotype | Walking | Mutation | Patients | Rodents
Journal Article
Journal Article