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Amnionless
Fig. S1
Exome Sequencing Reveals Cubilin Mutation As a Single-Gene Cause of Proteinuria
Detailed Investigations of Proximal Tubular Function in Imerslund-Grasbeck Syndrome
Detailed Investigations of Proximal Tubular Function in Imerslund-Gräsbeck Syndrome
Gene Expression Analysis Defines the Proximal Tubule As the Compartment for Endocytic Receptor-Mediated Uptake in the Xenopus Pronephric Kidney
Genetic Heterogeneity of Megaloblastic Anaemia Type 1 in Tunisian Patients
M1BP Cooperates with CP190 to Activate Transcription at TAD Borders and Promote Chromatin Insulator Activity
The Benefits of Tubular Proteinuria: an Evolutionary Perspective
A Novel CLCN5 Mutation Associated With&Nbsp;Focal Segmental Glomerulosclerosis And&Nbsp;Podocyte Injury
Mutations in NUP160 Are Implicated in Steroid-Resistant Nephrotic Syndrome
Final Publishable Summary
Mutations in NUP160 Are Implicated in Steroid-Resistant Nephrotic Syndrome
CUBN Gene Cubilin
Deficits in Receptor-Mediated Endocytosis and Recycling in Cells from Mice with Gpr107 Locus Disruption
Lack of Megalin Expression in Adult Human Terminal Ileum Suggests Megalinindependent Cubilinamnionless Activity During Vitamin B
CUBN Is a Gene Locus for Albuminuria
Novel Compound Heterozygous Mutations in AMN Cause Imerslund-Gräsbeck Syndrome in Two Half-Sisters: a Case Report
AMN Gene Amnion Associated Transmembrane Protein
Top View
Lisa Gianesello , Giovanna Priante , Monica Ceol , Claudia M. Radu , Moin A. Saleem , Liliana Terrin , Franca Anglani , Dorella
The 13Th Annual International Mammalian Genome Society Conference: a Meeting Report
Evaluation of Genetic Variants for Type 2 Diabetes Associated Kidney Disease in African Americans
ABSTRACT GIACOMINI, JONATHAN JOSEPH. Tri-Trophic Interactions Between Plants, Their Mutualist Pollinators and Natural Enemies Of
Transcriptional Profiling of a Mouse Model of Infectious Colitis: the Role of Host Factors
Mutations in NUP160 Are Implicated in Steroid-Resistant Nephrotic Syndrome
The Role of Megalin (LRP-2/Gp330) During Development ⁎ Carolyn E
Leader of the Pack: Gene Mapping in Dogs and Other Model Organisms
Proximal Tubules Have the Capacity to Regulate Uptake of Albumin
Genetic Analyses in Dent Disease and Characterization of CLCN5 Mutations in Kidney Biopsies
Orphanet Journal of Rare Diseases Biomed Central
Hereditary Juvenile Cobalamin Deficiency Caused by Mutations in the Intrinsic Factor Gene
Human C-Terminal CUBN Variants Associate with Chronic Proteinuria and Normal Renal Function
A Nutrigenetic Approach to Examine the Relationship Between Vitamin B12 Status and Metabolic Traits in Multiple Ethnic Groups
Inherited Selective Cobalamin Malabsorption in Komondor Dogs Associated with a CUBN Splice Site Variant John C
Agonists and Antagonists of TGF-Β Family Ligands
Albumin Uptake in Human Podocytes: a Possible Role for the Cubilin
Amnionless-Mediated Glycosylation Is Crucial for Cell Surface Targeting Of
Modeling Monogenic Human Nephrotic Syndrome in the Drosophila Garland Cell Nephrocyte
Renal Handling of Albumin—From Early Findings to Current Concepts