DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» YME1L1
YME1L1
M-AAA and I-AAA Complexes Coordinate to Regulate OMA1, The
Mitochondrial Protein Quality Control Mechanisms
Aneuploidy: Using Genetic Instability to Preserve a Haploid Genome?
Thrombocytopenia-Associated Mutations in Ser/Thr Kinase MASTL Deregulate Actin Cytoskeletal Dynamics in Platelets
Oxygen Tension Modulates the Mitochondrial Genetic Bottleneck and Influences the Segregation of a Heteroplasmic Mtdna Variant in Vitro
Duodenal Mucosal Mitochondrial Gene Expression Is Associated with Delayed Gastric Emptying in Diabetic Gastroenteropathy
LONP1 Is Required for Maturation of a Subset of Mitochondrial Proteins and Its Loss Elicits
MMP-25 Metalloprotease Regulates Innate Immune Response Through NF- Κb Signaling Clara Soria-Valles, Ana Gutiérrez-Fernández, Fernando G
C6orf203 Controls OXPHOS Function Through Modulation of Mitochondrial Protein Biosynthesis
Blueprint Genetics Optic Atrophy Panel
Prioritizing and Characterizing Functionally Relevant Genes Across Human Tissues
Protein Degradation in Mitochondria: Implications for Oxidative Stress, Aging and Disease: a Novel Etiological Classi®Cation of Mitochondrial Proteolytic Disorders
Network-Based Analysis of Key Regulatory Genes Implicated in Type
Migration of Mitochondrial DNA in the Nuclear Genome of Colorectal Adenocarcinoma Vinodh Srinivasainagendra1, Michael W
Role of the AAA Protease Yme1 in Folding of Proteins in the Mitochondrial Intermembrane Space
Correction for Aras Et Al., Mitochondrial Nuclear Retrograde Regulator 1 (MNRR1) Rescues the Cellular Phenotype of MELAS by Indu
Global Networks of Functional Coupling in Eukaryotes from Comprehensive Data Integration
Mitochondrial Dynamics: Molecular Mechanisms, Related Primary Mitochondrial Disorders and Therapeutic Approaches
Top View
Duodenal Mucosal Mitochondrial Gene Expression Is Associated with Delayed Gastric Emptying in Diabetic Gastroenteropathy
Network Mining Approach to Cancer Biomarker Discovery
HIGD‑1B Inhibits Hypoxia‑Induced Mitochondrial Fragmentation by Regulating OPA1 Cleavage in Cardiomyocytes
AAA Proteases: Guardians of Mitochondrial Function and Homeostasis
Clinical Utility Gene Card For: Inherited Optic Neuropathies Including Next-Generation Sequencing-Based Approaches
Promoterless Transposon Mutagenesis Drives Solid Cancers Via Tumor Suppressor Inactivation
Metalloproteases of the Inner Mitochondrial Membrane Roman M
YME1L1 (N-18): Sc-139302
Global Networks of Functional Coupling in Eukaryotes from Comprehensive Data Integration
Mitochondrial Membrane Dynamics and Inherited Optic Neuropathies
(MNRR1) Rescues the Cellular Phenotype of MELAS by Indu
Dominant Mutations in MIEF1 Affect Mitochondrial Dynamics and Cause a Singular Late Onset Optic Neuropathy Majida Charif1,2†, Yvette C
Title Integration of Proteomics with Genomics and Transcriptomics
Mitochondrial ATP-Dependent Proteases—Biological Function and Potential Anti-Cancer Targets
OPA1 Processing in Cell Death and Disease – the Long and Short of It Thomas Macvicar and Thomas Langer*
(Mtupr) Induced by MPP+ in Human SH-SY5Y Neurob
Machine Learning Analysis Identifies Genes Differentiating Triple Negative
Homozygous YME1L1 Mutation Causes Mitochondriopathy with Optic Atrophy and 2 Mitochondrial Network Fragmentation