23 results on '"Gimber, Niclas"'
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2. ISG15 blocks cardiac glycolysis and ensures sufficient mitochondrial energy production during Coxsackievirus B3 infection
3. The ARFRP1-dependent Golgi scaffolding protein GOPC is required for insulin secretion from pancreatic β-cells
4. The cell adhesion protein CAR is a negative regulator of synaptic transmission
5. A Conserved Cysteine Residue in Coxsackievirus B3 Protein 3A with Implication for Elevated Virulence
6. The synaptic scaffold protein MPP2 interacts with GABAA receptors at the periphery of the postsynaptic density of glutamatergic synapses
7. A cytosolic disulfide bridge‐supported dimerization is crucial for stability and cellular distribution of Coxsackievirus B3 protein 3A
8. Lysosomal Pathology and Osteopetrosis upon Loss of H⁺-Driven Lysosomal Cl¯ Accumulation
9. The synaptic scaffold protein MPP2 interacts with GABAA receptors at the periphery of the postsynaptic density of glutamatergic synapses.
10. Uncoupling endosomal CLC chloride/proton exchange causes severe neurodegeneration
11. Interleukin‐12/23 deficiency differentially affects pathology in male and female Alzheimer's disease‐like mice
12. The Axonal Membrane Protein PRG2 Inhibits PTEN and Directs Growth to Branches
13. RIM-BP2 primes synaptic vesicles via recruitment of Munc13-1 at hippocampal mossy fiber synapses
14. Vasopressin Increases Urinary Acidification via V1a Receptors in Collecting Duct Intercalated Cells
15. A SEPT1-based scaffold is required for Golgi integrity and function
16. Beclin1‐driven autophagy modulates the inflammatory response of microglia via NLRP 3
17. Imaging post-exocytic dynamics of synaptic vesicle proteins
18. A SEPT1-based scaffold is required for Golgi integrity and function.
19. Vesicular Synaptobrevin/VAMP2 Levels Guarded by AP180 Control Efficient Neurotransmission
20. Diffusional spread and confinement of newly exocytosed synaptic vesicle proteins
21. Splice-Site Mutations Cause Rrp6-Mediated Nuclear Retention of the Unspliced RNAs and Transcriptional Down-Regulation of the Splicing-Defective Genes
22. Lysosomal Pathology and Osteopetrosis upon Loss of H + -Driven Lysosomal Cl – Accumulation
23. Lysosomal Pathology and Osteopetrosis upon Loss of H+-Driven Lysosomal Cl- Accumulation.
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