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Cubilin
CLCN5 Gene Chloride Voltage-Gated Channel 5
Exome Sequencing Reveals Cubilin Mutation As a Single-Gene Cause of Proteinuria
Detailed Investigations of Proximal Tubular Function in Imerslund-Grasbeck Syndrome
The Path to an Orally Administered Protein Therapeutic for the Treatment of Diabetes Mellitus
Genetic Heterogeneity of Megaloblastic Anaemia Type 1 in Tunisian Patients
Inherited LRP2 Dysfunction in Human Disease and Animal Models
Structural and Functional Characterisation of the Cobalamin Transport Protein Haptocorrin
Structural Assembly of the Megadalton-Sized Receptor for Intestinal Vitamin B12 Uptake and Kidney Protein Reabsorption
CUBN Gene Cubilin
Not All Proteinuria Is Created Equal
A Study of Associations Between CUBN, HNF1A, and LIPC Gene
Deficits in Receptor-Mediated Endocytosis and Recycling in Cells from Mice with Gpr107 Locus Disruption
LRP2 Gene LDL Receptor Related Protein 2
Role of Neutrophil Gelatinase‑Associated Lipocalin in Renal Cell Carcinoma (Review)
Using Ontology Fingerprints to Evaluate Genome-Wide Association Study Results Lam C
6D3088491ebd90fb2e943c079fb
Cubilin (Y-20): Sc-20607
BMC Genomics Biomed Central
Top View
Association Analysis of the Cubilin (CUBN) and Megalin (LRP2) Genes with ESRD in African Americans
Recombinant Human Transcobalamin II Catalog Number: 7895-TC
An Update on Vitamin B12-Related Gene Polymorphisms and B12 Status S
Identification of Potential and Novel Target Genes in Pituitary Prolactinoma by Bioinformatics Analysis
The Role of Megalin (LRP-2/Gp330) During Development ⁎ Carolyn E
Insights Into 3D Structure of ADAMTS13: a Stepping Stone Towards Novel Therapeutic Treatment of Thrombotic Thrombocytopenic Purpura
Mtor Regulates Endocytosis and Nutrient Transport in Proximal Tubular Cells
Genetic Analyses in Dent Disease and Characterization of CLCN5 Mutations in Kidney Biopsies
Cubilin Expression Is Monoallelic and Epigenetically Augmented Via Ppars Aseem Et Al
Vitamin B12 Deficiency from the Perspective of a Practicing Hematologist
Structural Assembly of the Megadalton-Sized Receptor for Intestinal Vitamin B12 Uptake and Kidney Protein Reabsorption
Orphanet Journal of Rare Diseases Biomed Central
Amalgamation of Protein Sequence, Structure and Textual Information for Improving Protein-Protein Interaction Identification
Human C-Terminal CUBN Variants Associate with Chronic Proteinuria and Normal Renal Function
Renal Albumin Absorption in Physiology and Pathology H Birn1 and EI Christensen1
Crystal Structure of Human Intrinsic Factor: Cobalamin Complex at 2.6-ล
Loss of Cubilin, the Intrinsic Factor-Vitamin B12 Receptor, Impairs
Albumin Uptake in Human Podocytes: a Possible Role for the Cubilin
Amnionless-Mediated Glycosylation Is Crucial for Cell Surface Targeting Of
Renal Handling of Albumin—From Early Findings to Current Concepts
Vitamin B12 Deficiency Diagnosis and Markers