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CLDN14
Genome Wide Association Study of Response to Interval and Continuous Exercise Training: the Predict‑HIIT Study Camilla J
Supplementary Table 1: Adhesion Genes Data Set
Supplementary Materials
A Common Variant in CLDN14 Is Associated with Primary Biliary
1 Integrative Omics Analyses Reveal Epigenetic Memory in Diabetic Renal
Application of Microarray-Based Comparative Genomic Hybridization in Prenatal and Postnatal Settings: Three Case Reports
Chromosome 21 Leading Edge Gene Set
6, -11 and -14 As Prognostic Markers in Human Breast Carcinoma
Genetic and Molecular Analysis of the CLDN14 Gene in Moroccan Family with Non‑Syndromic Hearing Loss
Detailed Clinical Features of Deafness Caused by a Claudin-14 Variant
Morphology, Behavior, and the Sonic Hedgehog Pathway in Mouse Models of Down Syndrome
Advanced Intercross Line Mapping of Eae5 Reveals Ncf-1 and CLDN4 As
“Down Syndrome: an Insight of the Disease” Ambreen Asim, Ashok Kumar, Srinivasan Muthuswamy, Shalu Jain and Sarita Agarwal*
Genetic Testing for Hereditary Hearing Loss
Supporting Information
SUPPLEMENTARY METHODS DNA Sequencing and Variant
Integrated Functional Genomic Analysis Enables Annotation of Kidney Genome-Wide Association Study Loci
Claudin 14 (CLDN14) (NM 001146078) Human Tagged ORF Clone Product Data
Top View
CLDN14 Monoclonal Antibody (M01), Clone 3D11
Integrated Bioinformatics Analysis Reveals Novel Key Biomarkers and Potential Candidate Small Molecule Drugs in Gestational Diabetes Mellitus
Phenotypic Variability of CLDN14 Mutations Causing DFNB29 Hearing Loss in the Pakistani Population
PDE1A Polymorphism Contributes to the Susceptibility
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses by a Synthetic TLR3 Ligand Mitigates
Parathyroid Hormone Controls Paracellular Ca2+ Transport in The
Tsnp-Based Identification of Allelic Loss of Gene Expression in a Patient with a Balanced Chromosomal Rearrangement ⁎ Gregory F
A Common Variant in CLDN14 Causes Precipitous, Prelingual Sensorineural Hearing Loss in Multiple Families Due to Founder Effect
In-Depth Bioinformatic Study of the CLDN16 Gene and Protein: Prediction of Subcellular Localization to Mitochondria
Claudin 6: Therapeutic Prospects for Tumours, and Mechanisms of Expression and Regulation (Review)
Clinical Utility of Genetic Testing in the Precision Diagnosis and Management of Pediatric
Multiplex Epithelium Dysfunction Due to CLDN10 Mutation: the HELIX Syndrome
Integrated Functional Genomic Analysis Enables Annotation of Kidney Genome-Wide Association Study Loci
Detailed Clinical Features of Deafness Caused by a Claudin-14 Variant
Primepcr™Assay Validation Report
Mutations in CLDN14 Are Associated with Different Hearing Thresholds
A Systems Proteomics View of the Endogenous Human Claudin Protein Family
Mouse Models of Human Claudin-Associated Disorders: Benefits and Limitations
Pressure and Distortion Regulate Human Mesenchymal Stem Cell Gene Expression
Improving Hearing Loss Gene Testing: a Systematic Review of Gene Evidence Toward More Efficient Next-Generation Sequencing–Based Diagnostic Testing and Interpretation
Case Report Application of Microarray-Based Comparative Genomic Hybridization in Prenatal and Postnatal Settings: Three Case Reports
Clinical Utility of Genetic Testing in the Precision Diagnosis and Management of Pediatric Patients with Kidney and Urinary Tract Diseases
Expression and Phylogeny of Claudins in Vertebrate Primordia
Epigenetic Regulation of Micrornas Controlling CLDN14 Expression As a Mechanism for Renal Calcium Handling
Genome-Wide Association Studies of Skeletal Phenotypes: What We Have Learned and Where We Are Headed
Claudins in Renal Physiology and Pathology
Genetics Home Reference; a Report to the Board of Scientific Counselors
Supplementary Materials: Small-Molecule Inhibition of Rho
File Download
The Expression Level of the CLDN14 Gene in Patients with Urolithiasis - a Preliminary Report
Targeted DNA Methylation Screen in the Mouse Mammary Genome Reveals a Parity-Induced Hypermethylation of Igf1r That Persists Long After Parturition Tiffany A
The Biology of Epithelial Cell Tight Junctions in the Kidney
PDF-Document
Nonsyndromic Deafness - Molecular Update
Claudin 14 (CLDN14) (NM 144492) Human Tagged ORF Clone Product Data
Integrative Analysis of Genetic Data Sets Reveals a Shared Innate Immune Component in Autism Spectrum Disorder and Its Co-Morbidities
Characterization of Rare Spindle and Root Cell Transcriptional Profiles in the Stria Vascularis of the Adult Mouse Cochlea
Table SⅠ. the Genes in Osgset. Human Symbol Name Gene ID
Multiplex Epithelium Dysfunction Due to CLDN10 Mutation: the HELIX Syndrome
Molecular Etiology of Hereditary Deafness Using Next Generation Sequencing in Northwest China
Epigenetic Regulation of Micrornas Controlling CLDN14 Expression As a Mechanism for Renal Calcium Handling