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COL4A5 Gene - GeneCards | CO4A5 Protein | CO4A5 Antibody
COL4A5 Gene - GeneCards | CO4A5 Protein | CO4A5 Antibody

IJMS | Free Full-Text | Kidney Injury by Variants in the COL4A5 Gene  Aggravated by Polymorphisms in Slit Diaphragm Genes Causes Focal Segmental  Glomerulosclerosis
IJMS | Free Full-Text | Kidney Injury by Variants in the COL4A5 Gene Aggravated by Polymorphisms in Slit Diaphragm Genes Causes Focal Segmental Glomerulosclerosis

COL4A5 Gene - GeneCards | CO4A5 Protein | CO4A5 Antibody
COL4A5 Gene - GeneCards | CO4A5 Protein | CO4A5 Antibody

COL4A5 Gene - GeneCards | CO4A5 Protein | CO4A5 Antibody
COL4A5 Gene - GeneCards | CO4A5 Protein | CO4A5 Antibody

Pathogenic Variants in the Genes Affected in Alport Syndrome (COL4A3–COL4A5)  and Their Association With Other Kidney Conditions: A Review - American  Journal of Kidney Diseases
Pathogenic Variants in the Genes Affected in Alport Syndrome (COL4A3–COL4A5) and Their Association With Other Kidney Conditions: A Review - American Journal of Kidney Diseases

Genotype–phenotype correlation in COL4A3 , COL4A4 and COL4A5 mutations....  | Download Scientific Diagram
Genotype–phenotype correlation in COL4A3 , COL4A4 and COL4A5 mutations.... | Download Scientific Diagram

Fusion of the COL4A5 Gene With NR2F2-AS1 in a Hemangioma Carrying a  t(X;15)(q22;q26) Chromosomal Translocation | Cancer Genomics & Proteomics
Fusion of the COL4A5 Gene With NR2F2-AS1 in a Hemangioma Carrying a t(X;15)(q22;q26) Chromosomal Translocation | Cancer Genomics & Proteomics

CJASN on X: "Digenic Alport syndrome refers to the inheritance of  pathogenic variants in COL4A5 plus COL4A3 or COL4A4 or in COL4A3 plus  COL4A4. This Review describes the expected clinical course of
CJASN on X: "Digenic Alport syndrome refers to the inheritance of pathogenic variants in COL4A5 plus COL4A3 or COL4A4 or in COL4A3 plus COL4A4. This Review describes the expected clinical course of

Genes | Free Full-Text | Novel Mutations in CLPP, LARS2, CDH23, and COL4A5  Identified in Familial Cases of Prelingual Hearing Loss
Genes | Free Full-Text | Novel Mutations in CLPP, LARS2, CDH23, and COL4A5 Identified in Familial Cases of Prelingual Hearing Loss

A) Location of single base mutations in exon 48 of the COL4A5 gene in... |  Download Scientific Diagram
A) Location of single base mutations in exon 48 of the COL4A5 gene in... | Download Scientific Diagram

The mutation features of the COL4A5 gene | Download Table
The mutation features of the COL4A5 gene | Download Table

Anti-COL4A5 antibody (ab231957) | Abcam
Anti-COL4A5 antibody (ab231957) | Abcam

Genes | Free Full-Text | Novel and Founder Pathogenic Variants in X-Linked  Alport Syndrome Families in Greece
Genes | Free Full-Text | Novel and Founder Pathogenic Variants in X-Linked Alport Syndrome Families in Greece

Collagen alpha-5 (IV) (Col4a5) antibody - BiCell Scientific®
Collagen alpha-5 (IV) (Col4a5) antibody - BiCell Scientific®

Genetic and molecular dynamics analysis of two variants of the COL4A5 gene  causing Alport syndrome | BMC Medical Genomics | Full Text
Genetic and molecular dynamics analysis of two variants of the COL4A5 gene causing Alport syndrome | BMC Medical Genomics | Full Text

Metformin ameliorates the severity of experimental Alport syndrome |  Scientific Reports
Metformin ameliorates the severity of experimental Alport syndrome | Scientific Reports

NanoLuc reporters identify COL4A5 nonsense mutations susceptible to  drug-induced stop codon readthrough - ScienceDirect
NanoLuc reporters identify COL4A5 nonsense mutations susceptible to drug-induced stop codon readthrough - ScienceDirect

Collagen alpha-5 (IV) (Col4a5) antibody - BiCell Scientific®
Collagen alpha-5 (IV) (Col4a5) antibody - BiCell Scientific®

Sequencing analysis of COL4A5 c.499delC (p.Pro167Gln f s * 36)... |  Download Scientific Diagram
Sequencing analysis of COL4A5 c.499delC (p.Pro167Gln f s * 36)... | Download Scientific Diagram

Aminoglycoside-induced premature termination codon readthrough of COL4A5  nonsense mutations that cause Alport syndrome | bioRxiv
Aminoglycoside-induced premature termination codon readthrough of COL4A5 nonsense mutations that cause Alport syndrome | bioRxiv

Development of an exon skipping therapy for X-linked Alport syndrome with  truncating variants in COL4A5 | Nature Communications
Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5 | Nature Communications

Distribution of small mutations in 30 out of 51 exons of the COL4A5-gene. |  Download Scientific Diagram
Distribution of small mutations in 30 out of 51 exons of the COL4A5-gene. | Download Scientific Diagram

Frontiers | Case report: Preimplantation genetic testing for X-linked  alport syndrome caused by variation in the COL4A5 gene
Frontiers | Case report: Preimplantation genetic testing for X-linked alport syndrome caused by variation in the COL4A5 gene

COL4a5 Antibody (ABIN7299170)
COL4a5 Antibody (ABIN7299170)

Frontiers | Molecular dynamics and minigene assay of new splicing variant  c.4298-20T>A of COL4A5 gene that cause Alport syndrome
Frontiers | Molecular dynamics and minigene assay of new splicing variant c.4298-20T>A of COL4A5 gene that cause Alport syndrome