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ADCK3
The Landscape of Human Mutually Exclusive Splicing
Downloaded from the App Store and Nucleobase, Nucleotide and Nucleic Acid Metabolism 7 Google Play
ADCK3 Protein Recombinant Human Protein Expressed in Sf9 Cells
Human Mitochondrial Pathologies of the Respiratory Chain and ATP Synthase: Contributions from Studies of Saccharomyces Cerevisiae
Autosomal-Recessive Cerebellar Ataxia Caused by a Novel ADCK3
Functional Characterization of Human Adck3 and Adck4, Mitochondrial Atypical Kinases
Supplementary Information Contents
COQ8A Gene Coenzyme Q8A
Disorders of Human Coenzyme Q10 Metabolism: an Overview
ARTICLE ADCK3, an Ancestral Kinase, Is Mutated in a Form Of
ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS
Mitochondrial Function and Lifespan of Mice with Controlled Ubiquinone Biosynthesis
Cell-Type–Specific Eqtl of Primary Melanocytes Facilitates Identification of Melanoma Susceptibility Genes
Exploring the Mitochondrial Function in Muscle and Molecular Dysregulation in Cerebellum in a Mouse Model for ARCA2, a Recessive
1 Supplementary Information ADCK2 Haploinsufficiency Reduces
Srp55 Regulates a Splicing Network That Controls Human Pancreatic Beta Cell Function and Survival
Establishment and Characterization of New Tumor Xenografts and Cancer Cell Lines from EBV-Positive Nasopharyngeal Carcinoma
(ADCK3) Mutant Cells Display Signs of Oxidative Stress, Defects in Mitochondrial Homeostasis and Lysosomal Accumulation
Top View
GAK-1: a Chemical Probe for Cyclin G Associated Kinase (GAK)
Systems Genetics of the Lateral Septal Nucleus in Mouse: Heritability, Genetic Control, and Covariation with Behavioral and Morphological Traits
Genomics of Ovarian Cancer Progression Reveals Diverse Metastatic Trajectories Including Intraepithelial Metastasis to the Fallopian Tube
Integrative Pathway Dissection of Molecular Mechanisms of Moxldl-Induced Vascular Smooth Muscle Phenotype Transformation
ADCK3 (N323) Polyclonal Antibody
The Glomerular Filtration Barrier: a Structural Target for Novel Kidney Therapies
Specific Transcriptomic Signatures and Dual Regulation of Steroidogenesis Between Fetal and Adult Mouse Leydig Cells
Molecular Regulation of High Muscle Mass in Developing Blonde D'aquitaine Cattle Fetuses
ADCK4 Deficiency Destabilizes the Coenzyme Q Complex, Which Is Rescued by 2,4-Dihydroxybenzoic Acid Treatment”
(Coq10) Deficiency
Supplementary File 1
Phenotypic Variability in ARCA2 and Identification of a Core Ataxic Phenotype with Slow Progression
Mitochondrial COQ9 Is a Lipid-Binding Protein That Associates with COQ7 to Enable Coenzyme Q Biosynthesis
1 KLF2 and KLF4 Control Endothelial Identity and Vascular Integrity
Page 1 Exploring the Understudied Human Kinome for Research And
ADCK4 Mutations Promote Steroid-Resistant Nephrotic Syndrome Through Coq10 Biosynthesis Disruption
ADCK3 Rabbit Pab
Primary Coenzyme Q Deficiency Due to Novel ADCK3 Variants, Studies