222 results on '"Rakovic, Aleksandar"'
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2. α‐Synuclein Pathology in PRKN‐Linked Parkinson's Disease: New Insights from a Blood‐Based Seed Amplification Assay
3. Induced pluripotent stem cells for modeling of X-linked dystonia-parkinsonism
4. Contributors
5. Dichloroacetate prevents restenosis in preclinical animal models of vessel injury
6. PINK1-dependent mitophagy is driven by the UPS and can occur independently of LC3 conversion
7. Author Reply to Peer Reviews of Multi-omics analysis identifies LBX1 and NHLH1 as central regulators of human midbrain dopaminergic neuron differentiation
8. Multi-omics analysis identifies LBX1 and NHLH1 as central regulators of human midbrain dopaminergic neuron differentiation
9. DJ-1 regulates mitochondrial gene expression during ischemia and reperfusion
10. Generation of four human-derived iPSC TorsinA-3xFLAG reporter lines from a DYT-TOR1A patient
11. USP14 inhibition corrects an in vivo model of impaired mitophagy
12. Mutant WDR45 Leads to Altered Ferritinophagy and Ferroptosis in β-Propeller Protein-Associated Neurodegeneration
13. Repeat‐Associated Non‐ AUG Translation of AGAGGG Repeats that Cause X ‐Linked Dystonia‐Parkinsonism
14. Parkin Deficiency Impairs Mitochondrial DNA Dynamics and Propagates Inflammation.
15. Patient-derived cells – an irreplaceable tool for research of reduced penetrance in movement disorders
16. REPUBLIKA SRBIJA I REPUBLIKA SRPSKA: OBOSTRANI IDENTITET DRŽAVNOSTI SRBIJE
17. Parkin Deficiency Impairs Mitochondrial DNA Dynamics and Propagates Inflammation
18. Electrophysiological Properties of Induced Pluripotent Stem Cell-Derived Midbrain Dopaminergic Neurons Correlate With Expression of Tyrosine Hydroxylase
19. H-ABC– and dystonia-causing TUBB4A mutations show distinct pathogenic effects
20. Transcriptional Alterations in X-Linked Dystonia–Parkinsonism Caused by the SVA Retrotransposon
21. Parkinson's Disease Phenotypes in Patient Neuronal Cultures and Brain Organoids Improved by 2‐Hydroxypropyl‐β‐Cyclodextrin Treatment
22. Chapter 10 - Induced pluripotent stem cells for modeling of X-linked dystonia-parkinsonism
23. Mutations in THAP1 ( DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study
24. Brain Regional Differences in Hexanucleotide Repeat Length in X-Linked Dystonia-Parkinsonism Using Nanopore Sequencing
25. Parkinson’s disease phenotypes in patient neuronal cultures and brain organoids improved by 2-Hydroxypropyl-b-Cyclodextrin treatment
26. Unraveling Cellular Phenotypes of Novel TorsinA/TOR1A Mutations
27. SVETOGORSKI MODEL: NEPRIMENjIV NA KOSOVU I METOHIJI
28. sGC Activity and Regulation of Blood Flow in a Zebrafish Model System
29. Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene
30. Truncating mutations in THAP1 define the nuclear localization signal
31. Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency? Response from the authors
32. Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency?
33. Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patients
34. Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinsonʼs disease
35. Mutations in RHOT1 disrupt ER-mitochondria contact sites interfering with calcium homeostasis and mitochondrial dynamics in Parkinson's disease.
36. ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome
37. Osteoclast imbalance in primary familial brain calcification: evidence for its role in brain calcification
38. Motor protein binding and mitochondrial transport are altered by pathogenic TUBB4A variants
39. Parkinson’s disease phenotypes in patient specific brain organoids are improved by HP-β-CD treatment
40. A hexanucleotide repeat modifies expressivity of X‐linked dystonia parkinsonism
41. Parkin Interacts with Apoptosis-Inducing Factor and Interferes with Its Translocation to the Nucleus in Neuronal Cells
42. Screening study of TUBB4A in isolated dystonia
43. Corrigendum: SLP-2 interacts with Parkin in mitochondria and prevents mitochondrial dysfunction in Parkin-deficient human iPSC-derived neurons and Drosophila
44. PINK1-dependent mitophagy is driven by the UPS and can occur independently of LC3 conversion
45. USP 14 inhibition corrects an in vivo model of impaired mitophagy
46. Motor protein binding and mitochondrial transport are altered by pathogenic TUBB4A variants
47. Iron overload is accompanied by mitochondrial and lysosomal dysfunction in WDR45 mutant cells
48. Genome editing in induced pluripotent stem cells rescues TAF1 levels in X‐linked dystonia‐parkinsonism
49. Mfn2 ubiquitination by PINK1/parkin gates the p97-dependent release of ER from mitochondria to drive mitophagy
50. Author response: Mfn2 ubiquitination by PINK1/parkin gates the p97-dependent release of ER from mitochondria to drive mitophagy
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