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UBIAD1
UBIAD1-Mediated Vitamin K2 Synthesis Is Required for Vascular Endothelial Cell Survival and Development Jeffrey M
A Chromosome Level Genome of Astyanax Mexicanus Surface Fish for Comparing Population
Centre for Arab Genomic Studies a Division of Sheikh Hamdan Award for Medical Sciences
Mouse Ubiad1 Conditional Knockout Project (CRISPR/Cas9)
Integrated Epigenomic Analysis Stratifies Chromatin Remodellers Into
Downloaded Per Proteome Cohort Via the Web- Site Links of Table 1, Also Providing Information on the Deposited Spectral Datasets
Sheet1 Page 1 Gene Symbol Gene Description Entrez Gene ID
The IC3D Classification of the Corneal Dystrophies
A Common Genetic Architecture Enables the Lossy Compression of Large CRISPR Libraries
A Mutation in the UBIAD1 Gene in a Han Chinese Family with Schnyder Corneal Dystrophy
Identification of the First De Novo UBIAD1 Gene Mutation Associated with Schnyder Corneal Dystrophy
Towards Integrated Oncogenic Marker Recognition Through Mutual
A Novel UBIAD1 Mutation Identified in a Chinese Family with Schnyder Crystalline Corneal Dystrophy
Mutations in the UBIAD1 Gene, Encoding a Potential
Fusion Transcripts in Normal Human Cortex Increase with Age and Show
(M) of SARS-Cov-2
Mutations in the UBIAD1 Gene, Encoding a Potential
1 Supplementary Material Figure S1. Volcano Plot of Differentially
Top View
Functional Study of SCCD Pathogenic Gene UBIAD1 (Review)
UBIAD1 Mutation Alters a Mitochondrial Prenyltransferase to Cause Schnyder Corneal Dystrophy
Enzymes in the Cholesterol Synthesis Pathway: Interactomics in the Cancer Context
Using Massively Parallel Sequencing to Determine the Genetic Basis of Leigh Syndrome, the Most Common Mitochondrial Disorder Affecting Children
Ocular Phenotype Associated with DYRK1A Variants
Quantitative Proteome Pro Ling of Respiratory
Primepcr™Assay Validation Report
Genetic Imbalance in Patients with Cervical Artery Dissection
In Vitro Amyloid Aggregate Forming Ability of TGFBI Mutants That Cause Corneal Dystrophies
A Database for High-Throughput CRISPR/Cas9 Screens Benedikt Rauscher1,†, Florian Heigwer1,†, Marco Breinig1, Jan Winter1 and Michael Boutros1,2,*
US 2010/0233700 A1 WEISS (43) Pub
Epigenome-Wide DNA Methylation Profiling in Progressive