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PCBD1
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Oral Presentations
Massive Parallel Sequencing As a New Diagnostic Approach For
Blueprint Genetics Hyperphenylalaninemia Panel
Citrullinemia Type I Is Associated with a Novel
Human Induced Pluripotent Stem Cell–Derived Podocytes Mature Into Vascularized Glomeruli Upon Experimental Transplantation
Pcbd1 Antibody - C-Terminal Region Rabbit Polyclonal Antibody Catalog # AI10366
Inherited Disorders of Neurotransmitters: Classification and Practical Approaches for Diagnosis and Treatment
Pet-1 Controls Tetrahydrobiopterin Pathway and Slc22a3 Transporter Genes in Serotonin Neurons Steven C Wyler, Lauren J Donovan, Mia Yeager, and Evan Deneris ACS Chem
CENTOGENE's Severe and Early Onset Disorder Gene List
Inheritest 500 PLUS
Continuously Active Transcriptional Programs Are Required to Build Expansive Serotonergic Axon Architectures
Liver (Version 1).Xlsb
POSITIVE RESULT Pathogenic Variant Identified
Phenylketonuria Diagnosis by Massive Parallel Sequencing and Genotype-Phenotype Association in Brazilian Patients
Simple Screening Method for Autoantigen Proteins Using the N-Terminal Biotinylated Protein Library Produced by Wheat Cell-Free Synthesis
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Proteome Characteristics of Liver Tissue from Patients with Parenteral
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WO 2018/167621 Al 20 September 2018 (20.09.2018) W !P O PCT
Effects of Magnesium Deficiency on Mechanisms of Insulin Resistance in Type 2 Diabetes
Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder Technical Brief Number 23
Proteomic Analysis Identifies Distinct Glomerular Extracellular Matrix In
Consensus Guideline for the Diagnosis and Treatment of Tetrahydrobiopterin
The Study of the Full Spectrum of Variants Leading to Hyperphenylalaninemia Have Revealed 10 New Variants in the PAH Gene
Effect of Redox-Cycling Agents on Nitric Oxide Synthase Activity In
Targeted Genes and Methodology Details for Inborn Errors of Metabolism Custom Gene Panel
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
PCBD1 Gene Pterin-4 Alpha-Carbinolamine Dehydratase 1
Genomic Unity® Prenatal Analysis
Spectrum Analysis of Inborn Errors of Metabolism for Expanded Newborn
Recessive Mutations in PCBD1 Cause a New Type of Early-Onset Diabetes
Tetrahydrobiopterin Deficiency
WO 2017/051347 A2 30 March 2017 (30.03.2017) P O P C T
Blueprint Genetics Comprehensive Metabolism Panel
Integrated Omic Analysis of Lung Cancer Reveals Metabolism Proteome Signatures with Prognostic Impact
Genome-Wide Meta-Analysis Unravels Interactions Between Magnesium Homeostasis and Metabolic Phenotypes