DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» Cubam
Cubam
Detailed Investigations of Proximal Tubular Function in Imerslund-Grasbeck Syndrome
Full-Text
Detailed Investigations of Proximal Tubular Function in Imerslund-Gräsbeck Syndrome
AMN Directs Endocytosis of the Intrinsic Factor‐Vitamin B12
The Path to an Orally Administered Protein Therapeutic for the Treatment of Diabetes Mellitus
Genetic Heterogeneity of Megaloblastic Anaemia Type 1 in Tunisian Patients
Cubam Receptor-Mediated Endocytosis in Hindgut-Derived Pseudoplacenta of A
Structural and Functional Characterisation of the Cobalamin Transport Protein Haptocorrin
Novel Compound Heterozygous Mutations in AMN Cause Imerslund-Gräsbeck Syndrome in Two Half-Sisters: a Case Report Emma Montgomery1, John A
Human Amnionless Antibody
Cubam Receptor-Mediated Endocytosis in Hindgut-Derived Pseudoplacenta of a Viviparous Teleost Xenotoca Eiseni
Severe Megaloblastic Anemia: Vitamin Deficiency and Other Causes
Imerslund-Gräsbeck Syndrome in a 25-Month-Old Italian Girl Caused by a Homozygous Mutation In
Lack of Megalin Expression in Adult Human Terminal Ileum Suggests Megalinindependent Cubilinamnionless Activity During Vitamin B
Novel Compound Heterozygous Mutations in AMN Cause Imerslund-Gräsbeck Syndrome in Two Half-Sisters: a Case Report
Recombinant Human Amnionless Catalog Number: 1860-AM
Recombinant Human Transcobalamin II Catalog Number: 7895-TC
Vitamin B12 Deficiency Sally P
Top View
An Update on Vitamin B12-Related Gene Polymorphisms and B12 Status S
Dissertation
University of Veterinary Medicine Budapest, Hungary Department of Animal Breeding Canine Imerslund-Gräsbeck Syndrome
Cubam Receptor-Mediated Endocytosis in Hindgut-Derived Pseudoplacenta of a Viviparous Teleost Xenotoca Eiseni
Vitamin B12 Deficiency from the Perspective of a Practicing Hematologist
2.2.7.2 Cdna Library from Origene
Fig. 15.1. Physiologic Processes That Influence Plasma Or Serum Concentrations of TLI, PLI, Or TAP. • TLI: Most Trypsinogen Is
Structural Assembly of the Megadalton-Sized Receptor for Intestinal Vitamin B12 Uptake and Kidney Protein Reabsorption
Orphanet Journal of Rare Diseases Biomed Central
Hereditary Juvenile Cobalamin Deficiency Caused by Mutations in the Intrinsic Factor Gene
Kalitsal Megaloblastik Anemiler
A Cellular Model of Albumin Endocytosis Uncovers a Link Between Membrane and Nuclear Proteins Seiya Urae1,2, Yutaka Harita1,*, Tomohiro Udagawa3, Koji L
171Thesis.Pdf
Inherited Selective Cobalamin Malabsorption in Komondor Dogs Associated with a CUBN Splice Site Variant John C
Cobalamin Kevin S
Vitamin B12 Deficiency and Clinical Laboratory: Lessons Revisited and Clarified in Seven Questions
Albumin Uptake in Human Podocytes: a Possible Role for the Cubilin
Amnionless-Mediated Glycosylation Is Crucial for Cell Surface Targeting Of
Revisiting Vitamin B12 Deficiency: a Clinician's Guide for the 21St Century
Hypervitaminemia B12: a Biological Marker Yet to Be Known
Cubam Receptor-Mediated Endocytosis in Hindgut-Derived Pseudoplacenta
Renal Handling of Albumin—From Early Findings to Current Concepts
Imerslund-Gräsbeck Syndrome)