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SERAC1
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Chemical Modulation of Mitochondria–Endoplasmic Reticulum Contact Sites
Identification of the Rs797045105 in the SERAC1 Gene by Whole-Exome Sequencing in a Patient Suspicious of MEGDEL Syndrome
Identification of Genetic Modifiers in Hereditary Spastic Paraplegias Due to SPAST/SPG4 Mutations Livia Parodi
Downregulation of Carnitine Acyl-Carnitine Translocase by Mirnas
Non Commercial Use Only
SERAC1 Gene Serine Active Site Containing 1
Mutations and Protein Interaction Landscape Reveal Key Cellular Events Perturbed in Upper Motor Neurons with HSP and PLS
Downloaded from Ensembl
Functional Interpretation of ATAD3A Variants in Neuro-Mitochondrial Phenotypes
Hereditary Spastic Paraplegia Precision Panel Overview
Progressive Deafness–Dystonia Due to SERAC1 Mutations: a Study of 67 Cases
Supplementary Tables Supplementary Table S1. a List of 3,039 Genes
ZNF384-Related Fusion Genes Define a Subgroup of Childhood B-Cell
MEGDEL Syndrome: Expanding the Phenotype and New Mutations
Dissecting the Role of B2 Sine Rna Processing in Activation of Stress Response Genes in Mouse Brain Amyloid and Aging Pathology
Biallelic P4HTM Variants Associated with HIDEA Syndrome and Mitochondrial Respiratory Chain Complex I Deficiency ✉ Eleanor Hay 1, Louise C
Supplement 1: Genetic Sequencing and Filtering Strategy of Whole Exome Sequencing Data Based on the Initial Differential Diagnos
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SUPPLEMENTAL METHODS Flow Cytometry Analysis Phycoerythrin
(SERAC1) Mutations in a Patient with a Mitochondrial Encephalopathy
A Novel Mutation in the SERAC1 Gene Correlates with the Severe Manifestation of the MEGDEL Phenotype, As Revealed by Whole‑Exome Sequencing
Primate Specific Retrotransposons, Svas, in the Evolution of Networks That Alter Brain Function
1 KLF2 and KLF4 Control Endothelial Identity and Vascular Integrity
MEGDEL Syndrome
Leigh Syndrome: One Disorder, More Than 75 Monogenic Causes
Molecular Basis of Leigh Syndrome: a Current Look Manuela Schubert Baldo* and Laura Vilarinho
Gene Expression Analyses Identify Narp Contribution in the Development of L-DOPA-Induced Dyskinesia
Genomic Prediction for Growth Using a Low-Density SNP Panel in Dromedary Camels
Identification of Long-Lived Synaptic Proteins by Proteomic Analysis Of
Inbred Mouse Strains Expression in Primary Immunocytes Across
Mutations in Serac1 Or Synj2 Cause Proximal T Haplotype-Mediated Male Mouse Sterility but Not Transmission Ratio Distortion
News and Reports:Identification of the Rs797045105 in the SERAC1 Gene
SERAC1 Deficiency Causes Complicated
Dystonia Due to SERAC1 Mutations: a Study of 67 Cases
Correlated Gene Modules Uncovered by Single-Cell Transcriptomics with High Detectability and Accuracy Authors: Alec R
Barth Syndrome Et Al