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CLCN7
The Mineralocorticoid Receptor Leads to Increased Expression of EGFR
Difference in Allelic Expression of the CLCN1 Gene and the Possible Influence on the Myotonia Congenita Phenotype
Identification of Key Genes and Pathways Involved in Response To
Ion Channels 3 1
CENTOGENE's Curated Gene List of Pathogenic and Likely Pathogenic
Chloride Channelopathies Rosa Planells-Cases, Thomas J
CENTOGENE's Severe and Early Onset Disorder Gene List
NIH Public Access Author Manuscript FEBS Lett
1 1 2 3 Cell Type-Specific Transcriptomics of Hypothalamic
Characterization of Renal Chloride Channel (CLCN5) Mutations in Dent’S Disease
Mutations of CLCN5 in Japanese Children with Idiopathic Low Molecular Weight Proteinuria, Hypercalciuria and Nephrocalcinosis
Genetic Analysis of CLCN7 in an Old Female Patient with Type II Autosomal Dominant Osteopetrosis
Identification and Characterization of a Novel CLCN7 Variant Associated
The Channelopathies: Novel Insights Into Molecular and Genetic Mechanisms of Human Disease
Clc-7 Deficiency Impairs Tooth Development and Eruption
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
CENTOGENE's Prenatal Gene List
Extra-Skeletal Manifestations in Mice Affected by Clcn7-Dependent
Top View
Supplementary Figure S1. Generation of Floxed Nphs2 Exon 2 Allele and Confirmation
The Molecular Basis for Dent's Disease: an X-Linked
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Chloride Channel Diseases Resulting from Impaired Transepithelial Transport Or Vesicular Function
Duran Et Al., 2010. Chloride Channels: Often Enigmatic
Ion Channels in the P14 Rat Brain
Potential Role of Increased Oxygenation in Altering Perinatal Adrenal Steroidogenesis
CLCN7 Gene Chloride Voltage-Gated Channel 7
Exploring the Role of Stromal Osmoregulation in Cancer and Disease Using Executable Modelling
Transport Activity and Presence of Clc-7/Ostm1 Complex Account for Different Cellular Functions
Ion Channel Expression in Human Melanoma Samples: in Silico Identification and Experimental Validation of Molecular Targets
Loss of the Clc-7 Chloride Channel Leads to Osteopetrosis in Mice and Man
Novel CLCN7 Mutations Cause Autosomal Dominant Osteopetrosis Type II and Intermediate Autosomal Recessive Osteopetrosis
S-Palmitoylation As a Functional Regulator of Proteins Associated
Supplementary Material
Abundance of Regulatory T Cell (Treg) As a Predictive Biomarker for Neoadjuvant Chemotherapy in Triple-Negative Breast Cancer
Ion Channelopathies in Endocrinology
Investigating the Role of BEST1 Protein in Best Vitelliform Macular