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CLDN16
A Gene Expression Resource Generated by Genome-Wide Lacz
XIST-Induced Silencing of Flanking Genes Is Achieved by Additive Action of Repeat a Monomers in Human Somatic Cells
Supplementary Materials
Whole Exome Sequencing Identifies Causative Mutations in the Majority of Consanguineous Or Familial Cases with Childhood-Onset Increased Renal Echogenicity
The Role of Tight Junctions in Paracellular Ion Transport in the Renal Tubule: Lessons Learned from a Rare Inherited Tubular Disorder
Whole Exome Sequencing Identifies Causative Mutations in the Majority of Consanguineous Or Familial Cases with Childhood-Onset I
Single Cell Transcriptional and Chromatin Accessibility Profiling Redefine Cellular Heterogeneity in the Adult Human Kidney
Claudin 16 Antibody / CLDN16 (RQ5716)
Claudin-14 Gene Polymorphisms and Urine Calcium Excretion
VU Research Portal
Gnomad Lof Supplement
Blueprint Genetics Nephrolithiasis Panel
Clinical Utility Gene Card For: Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis With/Without Severe Ocular Involvement
Novel Variant in CLDN16: a Further Step in the Diagnosis of Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis—A Case Report
Mouse Models of Human Claudin-Associated Disorders: Benefits and Limitations
A Novel Claudin 16 Mutation Associated with Childhood Hypercalciuria Abolishes Binding to ZO-1 and Results in Lysosomal Mistargeting Dominik Mu¨Ller,1,* P
Identification of Important Cell Cycle Regulators And
Genetic'dissection'of'growth'and' Meat'quality'traits'in'pigs''
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Claudins in Renal Physiology and Pathology
Prevalence of Monogenic Causes in Pediatric Patients with Nephrolithiasis Or Nephrocalcinosis
Genome-Wide Identification of Copy Number Variation Using High-Density
Claudin-16 and Claudin-19 Interact and Form a Cation-Selective Tight Junction Complex
CLDN16 Genotype Predicts Renal Decline in Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis
Characterization of Two Novel Mutations in the Claudin-16 and Claudin-19 Genes That Cause Familial Hypomagnesemia with Hypercalciuria and T Nephrocalcinosis
A Deep-Learning Framework That Reveals Promoter Activity
Structural and Functional Analysis of Centromeric Chromatin
(A) Electrophoresis and Rine Values of Samples
Single Cell Transcriptional and Chromatin Accessibility Profiling Redefine Cellular Heterogeneity in the Adult Human Kidney
Transcriptome Profile of Human Fibroblasts in an Ex Vivo Culture
Recent Advances in Molecular Genetics of Hereditary Magnesium-Losing Disorders
Article Familial Hypomagnesemia with Hypercalciuria And
Exonic CLDN16 Mutations Associated with Familial Hypomagnesemia With
Tcdd Disrupts Gene Expression in the Developing Mouse Kidney
Identification of the First Large Deletion in the CLDN16 Gene in a Patient
Epigenetic Regulation in the Placenta and Its Role in Fetal Growth
Description of Strs in Trinucleotide-Repeat Diseases
Multiplex Epithelium Dysfunction Due to CLDN10 Mutation: the HELIX Syndrome