DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» MOCS3
MOCS3
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
The Microbiota-Produced N-Formyl Peptide Fmlf Promotes Obesity-Induced Glucose
SALL1 Mutation Analysis in Townes-Brocks Syndrome: 11 Novel
Clinical and Biochemical Spectrum of Molybdenum Cofactor Deficiency
Diverse Mechanisms of Sulfur Decoration in Bacterial Trna and Their Cellular Functions
Transcriptomic Analysis of Early Stages of Intestinal Regeneration in Holothuria Glaberrima David J
Exome Sequencing and Array-Based Comparative Genomic Hybridisation Analysis of Preferential 6-Methylmercaptopurine Producers
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
Supplemental Figures 04 12 2017
Evidence for the Physiological Role of a Rhodanese-Like Protein for the Biosynthesis of the Molybdenum Cofactor in Humans
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses by a Synthetic TLR3 Ligand Mitigates
Supplementary Information For
MOL #82305 TITLE PAGE Title: Induced CYP3A4 Expression In
Activating the Ubiquitin Family : UBA6 Challenges the Field
Lessons Learned from the Initial Sequencing of the Pig Genome
MOCS3 Antibody (N-Term) Blocking Peptide Synthetic Peptide Catalog # Bp19278a
Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
Top View
Targeted Genes and Methodology Details for Inborn Errors of Metabolism Custom Gene Panel
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
Molybdenum Cofactor Deficiency Type B Knock-In Mouse Models Carrying Patient-Identical Mutations and Their Rescue by Singular AAV Injections
Molybdenum Cofactor Deficiency Jochen Reiss, Rita Hahnewald
Child Neurology: Molybdenum Cofactor Deficiency Madhu Nagappa, Parayil S
Requisition Form for Invitae Internal Use Only PTC Pinpoint™ CP Spectrum Sponsored Testing Program TRF910-1
Lessons Learned from the Initial Sequencing of the Pig Genome: Comparative Analysis of an 8 Mb Region of Pig Chromosome 17 Elizabeth A
Metabolic and Monogenic Causes of Seizures in Neonates and Young Infants
Molybdenum Cofactor Deficiency (Mocd): a Rare Genetic Disorder in Newborns
Anti-MOCS3 Antibody (ARG59958)
Investigations Into the Influence of Parathyroid Hormone on Gene Expression in the Colorectal Epithelium
Integrated Omic Analysis of Lung Cancer Reveals Metabolism Proteome Signatures with Prognostic Impact
Mocd Natural History
Gene Copy Number Change Events at Chromosome 20 and Their Association with Recurrence in Gastric Cancer Patients
Generated by SRI International Pathway Tools Version 25.0 on Mon
Responsive Nuclear Proteins in Collecting Duct Cells
Juul Et Al. – Supplementary Material Explanation of Data Presented In
Proteasome Inhibitors to Alleviate Aberrant IKBKAP Mrna Splicing and Low IKAP/Help1 Synthesis in Familial Dysautonomia Mylène Hervé, El Chérif Ibrahim