Results 181 to 190 of about 4,920 (197)
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A Unique Case of COL4A3/4 and ACTN4 Mutations Combined

Journal of the American Society of Nephrology, 2020
Estibhaliz L. Perez Leal   +2 more
openaire   +1 more source

Heterozygous COL4A3/COL4A4 mutations: the hidden part of the iceberg?

Nephrology Dialysis Transplantation, 2022
Antonio Mastrangelo   +2 more
exaly  

Excess laminin α5 in Col4a3 null GBM

Matrix Biology, 2006
D ABRAHAMSON   +4 more
openaire   +1 more source

Dual Molecular Diagnosis: COL4A3 and PKD1

Journal of the American Society of Nephrology
Sydney Elizabeth Hartsell   +4 more
openaire   +1 more source

New Insights into Renal Failure in a Cohort of 317 Patients with Autosomal Dominant Forms of Alport Syndrome: Report of Two Novel Heterozygous Mutations in COL4A3

Journal of Clinical Medicine, 2022
Jose M Garcia-Aznar   +2 more
exaly  

Cochlea hypoxia in COL4a3 mice involves cytokine upregulation

Matrix Biology, 2008
Lara Dunn   +3 more
openaire   +1 more source

A Male Senior with Alport Syndrome in Digenic Inheritance of COL4A3 and 4A4

Journal of the American Society of Nephrology, 2021
openaire   +1 more source

Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidney disease from focal segmental glomerulosclerosis.

Nephrology Dialysis Transplantation, 2009
Constantinos Deltas   +2 more
exaly  

COL4A3 mutations cause focal segmental glomerulosclerosis

Journal of Molecular Cell Biology, 2015
Zhibin Ye, Landian HU, Weiming Wang
exaly  

High COL4A3 expression correlates with poor prognosis after cisplatin plus gemcitabine chemotherapy in non-small cell lung cancer

Tumor Biology, 2012
exaly  
alport syndrome
medicine
col4a4
col4a5
hematuria
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