C19orf12 protein (human) - STRING interaction network
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
C19orf12 Antibody (NBP1-94063): Novus Biologicals
Review: Insights into molecular mechanisms of disease in neurodegeneration with brain iron accumulation: unifying theories - Arber - 2016 - Neuropathology and Applied Neurobiology - Wiley Online Library
Nazo, the Drosophila homolog of the NBIA-mutated protein – c19orf12, is required for triglyceride homeostasis | bioRxiv
SPG43 and ALS-like syndrome in the same family due to compound heterozygous mutations of the C19orf12 gene: a case description and brief review | SpringerLink
C19orf12 CRISPR Knockout and Activation Products (h) | SCBT - Santa Cruz Biotechnology
Alignment of the fly C19orf12 orthologs (CG3740, CG11671) with human... | Download Scientific Diagram
![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
Frontiers | Case Report: Identification of a De novo C19orf12 Variant in a Patient With Mitochondrial Membrane Protein–Associated Neurodegeneration
C19orf12 Gene - GeneCards | CS012 Protein | CS012 Antibody
Recombinant Human C19ORF12 protein (ABIN2718593)
C19orf12 Gene - GeneCards | CS012 Protein | CS012 Antibody
Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation - ScienceDirect
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+
Pharmaceutics | Free Full-Text | Identification of Autophagy as a Functional Target Suitable for the Pharmacological Treatment of Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN) In Vitro
C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation - ScienceDirect
C19orf12 Polyclonal Antibody (27382-1-AP)
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
What is C19orf12 Gene SPG43 NGS Genetic DNA Test ?
