Functionomics of NCC Mutations in Gitelman Syndrome Using a Novel Mammalian Cell-Based Activity Assay

American Journal of Physiology - Renal Physiology - United States
doi 10.1152/ajprenal.00124.2016
Full Text
Abstract

Available in full text

Date
Authors
Publisher

American Physiological Society

Related search

Differential Diagnosis of Bartter Syndrome, Gitelman Syndrome, and Pseudo–Bartter/Gitelman Syndrome Based on Clinical Characteristics

Genetics in Medicine
MedicineGenetics
2015English

Gitelman Syndrome

Hypertension
Internal Medicine
2009English

Gitelman Syndrome

2020English

A Rare Cause of Rhabdomyolysis: Gitelman Syndrome

International Journal of Case Reports and Images
2015English

ELISA-based Assay of Immunoglobulin G Antibodies Against Mammalian Cell Entry 1A (Mce1A) Protein: A Novel Diagnostic Approach for Leprosy

Memorias do Instituto Oswaldo Cruz
MedicineMicrobiology
2017English

Exonic Mutations in the SLC12A3 Gene Cause Exon Skipping and Premature Termination in Gitelman Syndrome

Journal of the American Society of Nephrology : JASN
MedicineNephrology
2014English

Development of a Novel Cell-Based Assay to Monitor the Transactivation Activity of the HSV-1 Protein ICP0

Antiviral Research
VirologyPharmacology
2015English

Interface Specificity of Phospholipase Activity Using a Novel Surface Dilution Kinetic Assay

Biophysical Journal
Biophysics
2012English

A Novel Sensitive Cell-Based Immunoenzymatic Assay for Palytoxin Quantitation in Mussels

Toxins
MutagenesisToxicologyHealth
2018English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy