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Keratin 12
Cellular and Molecular Signatures in the Disease Tissue of Early
140503 IPF Signatures Supplement Withfigs Thorax
A Novel Keratin 12 Mutation in a German Kindred with Meesmann's
Keratin 12-Deficient Mice Have Fragile Corneal Epithelia
Transcriptional Correlates of Proximal-Distal Identify and Regeneration Timing in Axolotl Limbs S
S Epithelial Corneal Dystrophy Phenotype Due to A
Genomics of Inherited Bone Marrow Failure and Myelodysplasia Michael
UCLA Electronic Theses and Dissertations
Mass Spectrometry Analysis Reveals Dynamic Changes of Protein
Mapping Transmembrane Binding Partners for E-Cadherin Ectodomains
Table S1 Changes in the Expression Levels of Genes Induced by Sevoflurane
Filaments and Phenotypes
Supplementary File 1
The Proteins of Keratoconus: a Literature Review Exploring Their Contribution to the Pathophysiology of the Disease
The Novel Desmin Mutant P.A120D Impairs Filament Formation, Prevents Intercalated Disk Localization and Causes Sudden Cardiac Death
B. Bougas Et Al. 13 SI TABLE S3 List of Differentially Expressed Genes Between Laval
Mrna Expression in Human Leiomyoma and Eker Rats As Measured by Microarray Analysis
Downloaded from the Mouse Lysosome Gene Database, Mlgdb
Top View
Withaferin-A Can Be Used to Modulate the Keratin Network of Intermediate Filaments in Human Epidermal Keratinocytes
Keratins in Health and Cancer: More Than Mere Epithelial Cell Markers
Impact of MLL5 Expression on Decitabine Efficacy and DNA Methylation in Acute Myeloid Leukemia
Keratins and Skin Disorders
A Novel Mutation of the Keratin 12 Gene Responsible for a Severe Phenotype of Meesmann’S Corneal Dystrophy Lori S
SKU# Product Description TP300009 Recombinant Protein of Human
Gene Transfer Tech Note 2552 the Gene Gun: Current Applications in Cutaneous Gene Therapy
Asrani Et Al 1
Supporting Information for Proteomics DOI 10.1002/Pmic.200600011
(12) United States Patent (10) Patent No.: US 8,889,361 B2 Chen (45) Date of Patent: Nov
Keratin 12 Missense Mutation Induces the Unfolded Protein Response and Apoptosis in Meesmann Epithelial Corneal Dystrophy
A Novel Mutation in KRT12 Associated with Meesmann's Epithelial Corneal
Characterisation of EST03G12 and Elucidation of Its Role in Amoebic Gill Disease (AGD) Severity
Molecular Genetics and Genotype-Phenotype Correlation Of
Supplemental Table 2: UC Vs. NL Gene List Gene Name Symbol
First Line of Title
Effect of Korean Red Ginseng Treatment on the Gene Expression Profile of Diabetic Rat Retina
Supplementary Table 1. a Full List of Cancer Genes