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Retricted access

Research article

First published 2021-6

Brain and Placental Pathology in Fetal COL4A1 Related Disease

Patrick Shannon, Courtney Hum, Tony Parks [...]

Pediatric and Developmental Pathology

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Research article

First published 2022-10

Next-generation sequencing in a large pedigree segregating visceral artery aneurysms suggests potential role of COL4A1/COL4A2 in disease etiology

Iikki Donner, Lauri J Sipilä, Roosa-Maria Plaketti [...]

Vascular

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Research article

First published 2022-7

Prenatal Diagnosis of COL4A1 Mutations in Eight Cases: Further Delineation of the Neurohistopathological Phenotype

Francesca Gubana, Christo Christov, Thibault Coste [...]

Pediatric and Developmental Pathology

Open access

Research article

First published 2020

Overexpression of DDR1 Promotes Migration,Invasion,Though EMT-Related Molecule Expression and COL4A1/DDR1/MMP-2 Signaling Axis

Xin Xie, Hongchao He, Ning Zhang [...]

Technology in Cancer Research & Treatment

Open access

Research article

First published 2026-1

Temporal Transcriptomics Leads From Discovery to in Vivo Validation: COL4A3/COL4A6/ COL4A5 and ITGA8 as Novel Arthrofibrosis Biomarkers in Post-traumatic Joint Contracture

Yijia Wang, Hong Zeng, Zilin Li [...]

Dose-Response

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Research article

First published 2012-10

MiR-21 is Enriched in the RNA-Induced Silencing Complex and Targets COL4A1 in Human Granulosa Cell Lines

Yuri Mase, Osamu Ishibashi, Tomoko Ishikawa [...]

Reproductive Sciences

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Research article

First published 2023-09

Genotypic Analysis of COL4A1 Gene in Diabetic Nephropathy and Type 2 Diabetes Mellitus Patients: A Comparative Genetic Study

Neha Shukla, Shivani Kumari, Poornima Verma [...]

DNA and Cell Biology

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Research article

First published 2020-07

Downregulation of Collagen COL4A6 Is Associated with Prostate Cancer Progression and Metastasis

Jian-Bin Ma, Ji-Yu Bai, Hai-Bao Zhang [...]

Genetic Testing and Molecular Biomarkers

Open access

Case report

First published 2012

Alport Syndrome: De Novo Mutation in the COL4A5 Gene Converting Glycine 1205 to Valine

Pilar Antón-Martín, Cristina Aparicio López, Soraya Ramiro-León [...]

Clinical Medicine Insights: Pediatrics

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Research article

First published 2013-03

A Novel COL4A3 Mutation Causes Autosomal-Recessive Alport Syndrome in a Large Turkish Family

Asli Subasioglu Uzak, Bulent Tokgoz, Munis Dundar [...]

Genetic Testing and Molecular Biomarkers

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