C19orf12 CRISPR Knockout and Activation Products (h) | SCBT - Santa Cruz Biotechnology
What is C19orf12 Gene SPG43 NGS Genetic DNA Test ?
C19orf12 siRNA (h), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
Nazo, the Drosophila homolog of the NBIA-mutated protein – c19orf12, is required for triglyceride homeostasis | bioRxiv
Frontiers | The Downregulation of c19orf12 Negatively Affects Neuronal and Musculature Development in Zebrafish Embryos
Frontiers | Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+
![PDF] Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+ | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/dd2ecb2012d86f9d3853c6aef367791e936d0787/5-Figure1-1.png "PDF] Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+ | Semantic Scholar")
PDF] Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+ | Semantic Scholar
Brain iron and metabolic abnormalities in C19orf12 mutation carriers: A 7.0 tesla MRI study in mitochondrial membrane protein-associated neurodegeneration. - Munich Cluster for Systems Neurology - LMU Munich
C19orf12 antibody (27382-1-AP) | Proteintech
C19orf12 Gene - GeneCards | CS012 Protein | CS012 Antibody
Review: Insights into molecular mechanisms of disease in neurodegeneration with brain iron accumulation: unifying theories - Arber - 2016 - Neuropathology and Applied Neurobiology - Wiley Online Library
C19orf12 Gene - GeneCards | CS012 Protein | CS012 Antibody
Dominant mitochondrial membrane protein-associated neurodegeneration (MPAN) variants cluster within a specific C19orf12 isoform - ScienceDirect
![PDF] Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+ | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/dd2ecb2012d86f9d3853c6aef367791e936d0787/11-Figure9-1.png "PDF] Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+ | Semantic Scholar")
PDF] Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+ | Semantic Scholar
![PDF] Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/8f4b65f35621e9f879833a58183ba96b06f5ec7f/4-Figure2-1.png "PDF] Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation. | Semantic Scholar")
PDF] Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation. | Semantic Scholar
e Schematic representation of proteins cellular localization and... | Download Scientific Diagram
Frontiers | Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+
Redistribution of C19orf12 during oxidative stress. (Ai | Open-i
C19orf12 Gene - GeneCards | CS012 Protein | CS012 Antibody
Alignment of the fly C19orf12 orthologs (CG3740, CG11671) with human... | Download Scientific Diagram
LC3 puncta formation in C19orf12 D18G/L132Q fibroblasts after 24 h of... | Download Scientific Diagram
Recombinant Human C19ORF12 protein (ABIN2718593)
C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation - ScienceDirect
C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation - ScienceDirect
Frontiers | Case Report: Identification of a De novo C19orf12 Variant in a Patient With Mitochondrial Membrane Protein–Associated Neurodegeneration
Neurodegeneration of diPLA2-VIA −/− flies is rescued by MPAN-associated... | Download Scientific Diagram
