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TTC19
PARL Deficiency in Mouse Causes Complex III Defects, Coenzyme Q Depletion, and Leigh-Like Syndrome
UQCRFS1N Assembles Mitochondrial Respiratory Complex-III Into an Asymmetric 21-Subunit Dimer
Supplementary Information ADC Mar 2017
Clinical and Molecular Characterization of Three Patients
Introduction Results Patients and Methods
A Novel Mutation in TTC19 Associated with Isolated Complex III Deficiency
Transcriptomic and Proteomic Landscape of Mitochondrial
Thesis Reference
Mitochondrial Structure and Bioenergetics in Normal and Disease Conditions
Exome Sequencing Reveals a Novel TTC19 Mutation in an Autosomal
PARL Deficiency in Mouse Causes Complex III Defects, Coenzyme Q Depletion, and Leigh-Like Syndrome
Nuclear Gene Mutations As the Cause of Mitochondrial Complex III Deficiency
Leigh Syndrome
Organization of the Respiratory Supercomplexes in Cells with Defective Complex III: Structural Features and Metabolic Consequences
Mitochondrial DNA (Mtdna) Test Requisition
Mitochondrial Complex III Deficiency
TTC19 (NM 017775) Human Tagged ORF Clone Product Data
Mitochondrial DNA (Mtdna) Test Requisition
Top View
Complex III Mitochondrial Leukoencephalopathy Masquerading Acute Demyelinating Syndrome Due to a Novel Variant in CYC1
Mitochondria in Epithelial Ovarian Carcinoma Exhibit Abnormal Phenotypes and Blunted Associations with Biobehavioral Factors Snehal Bindra1, Marlon A
The Road to the Structure of the Mitochondrial Respiratory Chain Supercomplex
A Japanese Case of Cerebellar Ataxia, Spastic Paraparesis and Deep Sensory Impairment Associated with a Novel Homozygous TTC19 Mutation
Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
Comprehensive Diagnosis for Mitochondrial Disorders
Mitochondrial Complex III Deficiency Caused by TTC19 Defects: Report of a Novel Mutation and Review of Literature
Exploiting Pyocyanin to Treat Mitochondrial Disease Due to Respiratory Complex III Dysfunction
Molecular Basis of Leigh Syndrome: a Current Look Manuela Schubert Baldo* and Laura Vilarinho
Respiratory Supercomplexes: Structure, Function and Assembly REVIEW
Mutations in TTC19
Respiratory Chain Complex III Deficiency Due to Mutated BCS1L: A
The Road to the Structure of the Mitochondrial Respiratory Chain Supercomplex
Submission Disease Characterized by Disrupted Biology Study Proposedpdf That Parlexerts Pro-Apoptotic Effects Via 94 27 Energy Production
A Novel Mutation Inttc19 Associated with Isolated Complex III Deficiency