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NUBPL
High-Throughput, Pooled Sequencing Identifies Mutations in NUBPL And
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
The Green Alga Chlamydomonas Reinhardtii: a New Model System To
A Novel Familial Case of Diffuse Leukodystrophy Related to NDUFV1 Compound Heterozygous Mutations
Human Mitochondrial Pathologies of the Respiratory Chain and ATP Synthase: Contributions from Studies of Saccharomyces Cerevisiae
Respiratory Chain Complex I Deficiency Caused by Mitochondrial DNA
1 NUBPL Mitochondrial Disease: New Patients and Review of the Genetic
STAT3 Targets Suggest Mechanisms of Aggressive Tumorigenesis in Diffuse Large B Cell Lymphoma
Discovery Proteomics in Aging Human Skeletal Muscle Finds Change In
Analysis of Human Mutations in the Supernumerary Subunits of Complex I
Mitochondrial DNA (Mtdna) Test Requisition
UNIVERSITY of CALIFORNIA, IRVINE Assessing the Impact Of
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
EGL Test Description
Genepanel Mitochondrial Diseases Genepanel Paediatric Cardiomyopathy AARS2 AARS2 ABAT ABCC6 ACAD9 ABCC9 ACO2 ACAD8 AFG3L2 ACAD9
Pathogenic Mutations in NUBPL Affect Complex I Activity and Cold Tolerance in the Yeast Model Yarrowia Lipolytica Andrew E
Mitochondrial Complex I Deficiency
Pathogenic Mutations in NUBPL Affect Complex I Activity and Cold Tolerance in the Yeast Model Yarrowia Lipolytica Andrew E
Top View
Insights Into the Pathogenic Character of a Common NUBPL Branch-Site Mutation Associated with Mitochondrial Disease and Complex I Deficiency Using a Yeast Model
Diagnosis and Management of Mitochondrial Disease: a Consensus Statement from the Mitochondrial Medicine Society
Comprehensive Diagnosis for Mitochondrial Disorders
Severe Multisystem Pathology, Metabolic Acidosis, Mitochondrial Dysfunction, and Early Death Associated with an X-Linked AIFM1 Variant
Responsive Nuclear Proteins in Collecting Duct Cells
NDUFA10 Mutations Cause Complex I Deficiency in a Patient with Leigh Disease
Molecular Basis of Leigh Syndrome: a Current Look Manuela Schubert Baldo* and Laura Vilarinho
Organ-Level Protein Networks As a Reference for the Host Effects of the Microbiome
STAT Autism and Intellectual Disability Panel
1 NUBPL Mitochondrial Disease: New Patients and Review of the Genetic
Whole Exome Sequencing Identifies Novel Candidate Mutations in a Chinese Family with Left Ventricular Noncompaction
Mitochondrial Medicine 2018: Nashville
Identification and Characterization of New Variants in FOXRED1 Gene
Blueprint Genetics NUBPL Single Gene Test
Supplementary Table 1. a Full List of Cancer Genes
1 Pathogenic Mutations in NUBPL Affect Complex I Activity and Cold