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ATP6V1B1
ATP6V1B1 Gene Atpase H+ Transporting V1 Subunit B1
Inherited Renal Tubulopathies—Challenges and Controversies
Identification of Eight Exonic Variants in the SLC4A1, ATP6V1B1 And
Primary Distal Renal Tubular Acidosis: Novel Findings in Patients Studied by Next-Generation Sequencing
New Tests 2 Test Updates 4 CPT Code Updates 11 Deleted Tests 11 Diagnostics Update Volume XXI, No
Exploration of the Relationships Between Tumor Mutation Burden with Immune Infiltrates in Clear Cell Renal Cell Carcinoma
Renal Β-Intercalated Cells Maintain Body Fluid and Electrolyte Balance
Molecular Architecture Underlying Fluid Absorption by the Developing Inner
(V)-Atpase Interactome: Identification of Proteins Involved in Trafficking
Large-Scale Proteomics and Phosphoproteomics of Urinary Exosomes
Distal Renal Tubular Acidosis Developments in Its Diagnosis and Pathophysiology
SUPPLEMENTARY APPENDIX Exome Sequencing Reveals Heterogeneous Clonal Dynamics in Donor Cell Myeloid Neoplasms After Stem Cell Transplantation
The Digestive Tract As an Essential Organ for Water Acquisition in Marine Teleosts: Lessons from Euryhaline Eels Yoshio Takei
Screening and Function Discussion of a Hereditary Renal Tubular Acidosis
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Title Downregulated ATP6V1B1 Expression Acidifies the Intracellular
Kidney Vacuolar H -Atpase: Physiology and Regulation
Atp6v0a4 Knockout Mouse Is a Model of Distal Renal Tubular Acidosis with Hearing Loss, with Additional Extrarenal Phenotype
Top View
Genomic Profiling of Primary Histiocytic Sarcoma Reveals Two Molecular
Distinct Requirements for Energy Metabolism in Mouse Primordial Germ Cells and Their Reprogramming to Embryonic Germ Cells
New Findings on the Pathogenesis of Distal Renal Tubular Acidosis
Clinical Utility of Genetic Testing in the Precision Diagnosis and Management of Pediatric Patients with Kidney and Urinary Tract Diseases
24H-Gene Variation Effect of Combined Bevacizumab/Erlotinib in Advanced Non-Squamous Non-Small Cell Lung Cancer Using Exon Array
Negative Female
Multi-Level Proteomics Reveals Host-Perturbation Strategies Of
Investigating the Role of BEST1 Protein in Best Vitelliform Macular
FRONTIERS in NEPHROLOGY Inherited Distal Renal Tubular
Autosomal Recessive Cutis Laxa Syndrome Revisited
The Medaka Mutation Tintachina Sheds Light on the Evolution of V
List for Testing Done out of Québec LABORATOIRE CLINIQUES CUSM MUHC CLINICAL LABS
Large-Scale Proteomics and Phosphoproteomics of Urinary Exosomes
A Role for VAX2 in Correct Retinal Function Revealed by a Novel
Supplementary Table 4. Gene-Set Differential Expression Analysis of TKI Resistance Sample (R2) Versus Pre-TKI Sample (R1) Using Rnaseq Exon Expression Data
Novel ATP6V1B1 and ATP6V0A4 Mutations in Autosomal Recessive Distal Renal Tubular Acidosis with New Evidence for Hearing Loss
The V-Atpase A3 Subunit: Structure, Function and Therapeutic Potential of an Essential Biomolecule in Osteoclastic Bone Resorption
Seq2pathway Vignette
Renal Tubular Acidosis Manifesting As Severe Metabolic Bone Disease
Expression Pattern and Biological Significance of the Lncrna ST3GAL6-AS1 in Multiple Myeloma
The Lysosomal V-Atpase B1 Subunit in Proximal Tubule Is Linked to Nephropathic Cystinosis
Acidosis and Urinary Calcium Excretion: Insights from Genetic Disorders