Pages that link to "Q48595784"
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The following pages link to Dynamin 2 mutations in Charcot-Marie-Tooth neuropathy highlight the importance of clathrin-mediated endocytosis in myelination (Q48595784):
Displaying 25 items.
- Crystal structure of the dynamin tetramer (Q27701888) (← links)
- Dynamin-2 mutations linked to Centronuclear Myopathy impair actin-dependent trafficking in muscle cells. (Q33870756) (← links)
- A kinase inhibitor screen reveals protein kinase C-dependent endocytic recycling of ErbB2 in breast cancer cells. (Q34430965) (← links)
- Myelin is dependent on the Charcot-Marie-Tooth Type 4H disease culprit protein FRABIN/FGD4 in Schwann cells (Q36474685) (← links)
- Molecular genetics of charcot-marie-tooth disease: from genes to genomes (Q36493294) (← links)
- Polarization and myelination in myelinating glia (Q36530065) (← links)
- Dynamin 2 homozygous mutation in humans with a lethal congenital syndrome. (Q36856483) (← links)
- Structural insights into the centronuclear myopathy-associated functions of BIN1 and dynamin 2. (Q37289753) (← links)
- Role of dynamin 2 in the disassembly of focal adhesions. (Q38100953) (← links)
- Dynamin-2 function and dysfunction along the secretory pathway. (Q38143006) (← links)
- Dynamin-2 in nervous system disorders. (Q38150395) (← links)
- Charcot-Marie-Tooth disease and pathways to molecular based therapies (Q38201741) (← links)
- Dynamin-2 mutations associated with centronuclear myopathy are hypermorphic and lead to T-tubule fragmentation (Q38850564) (← links)
- Focal adhesion kinases in adhesion structures and disease (Q42257455) (← links)
- Whole-exome sequencing in patients with inherited neuropathies: outcome and challenges (Q44303948) (← links)
- Phenotype variability and histopathological findings in patients with a novel DNM2 mutation (Q47877413) (← links)
- Loss of Dynamin 2 GTPase function results in microcytic anaemia (Q48201763) (← links)
- Schwann cell-specific deletion of the endosomal PI 3-kinase Vps34 leads to delayed radial sorting of axons, arrested myelination, and abnormal ErbB2-ErbB3 tyrosine kinase signaling. (Q48272328) (← links)
- A novel SPEG mutation causes non-compaction cardiomyopathy and neuropathy in a floppy infant with centronuclear myopathy (Q58696811) (← links)
- Dynamin 2 (DNM2) as Cause of, and Modifier for, Human Neuromuscular Disease (Q60054869) (← links)
- Schwann cells, but not Oligodendrocytes, Depend Strictly on Dynamin 2 Function (Q61447705) (← links)
- A Network-Based Bioinformatics Approach to Identify Molecular Biomarkers for Type 2 Diabetes that Are Linked to the Progression of Neurological Diseases (Q89634074) (← links)
- Mice carrying an analogous heterozygous Dynamin 2 K562E mutation that causes neuropathy in humans develop predominant characteristics of a primary myopathy (Q90026394) (← links)
- Correlative SICM-FCM reveals changes in morphology and kinetics of endocytic pits induced by disease-associated mutations in dynamin (Q90271579) (← links)
- Disruption of genes associated with Charcot-Marie-Tooth type 2 lead to common behavioural, cellular and molecular defects in Caenorhabditis elegans (Q91955757) (← links)