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SLC25A46
Targeted Genes and Methodology Details for Neuromuscular Genetic Panels
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Genetic Heterogeneity of Motor Neuropathies
Epistasis-Driven Identification of SLC25A51 As a Regulator of Human
Comparison of Human Solute Carriers
Frontiersin.Org 1 April 2015 | Volume 9 | Article 123 Saunders Et Al
Viewed in [41])
Diseases Caused by Mutations in Mitochondrial Carrier Genes SLC25: a Review
The SLC25 Carrier Family: Important Transport Proteins in Mitochondrial Physiology and Pathology
RNA-Seq Reveals Conservation of Function Among the Yolk Sacs Of
Aagab S00002 Aars S00003 Aars2 S00004 Aass S02483
Integrated Identification of Key Genes and Pathways in Alzheimer's Disease Via Comprehensive Bioinformatical Analyses
Pdf PMID: 23988125 28
A Yeast-Based Model for Hereditary Motor and Sensory Neuropathies: a Simple System for Complex, Heterogeneous Diseases
Wo 2008/156655 A9
Supplemental Figures 04 12 2017
STAT3 Targets Suggest Mechanisms of Aggressive Tumorigenesis in Diffuse Large B Cell Lymphoma
Novel Insights Into SLC25A46-Related Pathologies in a Genetic Mouse Model
Top View
Supplementary Data
Complement Activation in Peritoneal Dialysis–Induced Arteriolopathy
Mitokondriesykdommer V03
Influx Mechanisms in the Embryonic and Adult Rat Choroid Plexus: a Transcriptome Study
UCLA Electronic Theses and Dissertations
5779 Protein Identified, 4414 with 2 Or More Peptides, FDR 0.01
Altered Slc25 Family Gene Expression As Markers of Mitochondrial Dysfunction in Brain Regions Under Experimental Mixed Anxiety/Depression‑Like Disorder Vladimir N
T Lymphocytes Mrna, and Protein Expression in Activated
Supplemental Data
Shared Genetic Architecture Between Asthma and Allergic Diseases: a Genome-Wide Cross Trait Analysis of 112,000 Individuals from UK Biobank
Mitochondrial Oxodicarboxylate Carrier Deficiency Is Associated with Mitochondrial
Drosophila Melanogaster Mitochondrial Carriers: Similarities and Differences with the Human Carriers
The DJ1-Nrf2-STING Axis Mediates the Neuroprotective Effects of Withaferin a in Parkinson’S Disease
Bovine and Murine Models Highlight Novel Roles for SLC25A46 In
Figure S1. Amplification of PEDV M Gene and PCR Sequencing. (A) PCR Products of PEDV M Gene
Molecular Basis of Leigh Syndrome: a Current Look Manuela Schubert Baldo* and Laura Vilarinho
Pluripotency Characterization of Human Ipsc Lines from Three Healthy Donors
WO 2018/029586 Al 15 February 2018 (15.02.2018) W!P O PCT