Associated Papers
A heterozygous LAMA5 variant may contribute to slowly progressive, vinculin-enhanced familial FSGS and pulmonary defects.
Kaimori JY et al.
Jci Insight, 2022
An explainable model of host genetic interactions linked to COVID-19 severity.
Onoja A et al.
Communications Biology, 2022
36289370 (PubMed )
Supplement: 42003_2022_4073_MOESM4_ESM.xlsx › S1
A novel model of nephrotic syndrome results from a point mutation in Lama5 and is modified by genetic background.
Falcone S et al.
Kidney International, 2022
Case report: Genetic defects in laminin α5 cause infantile steroid-resistant nephrotic syndrome.
Sunwoo Y et al.
Frontiers in Pediatrics, 2022
Actionable perturbations of damage responses by TCL1/ATM and epigenetic lesions form the basis of T-PLL.
Schrader A et al.
Nature Communications, 2018
29449575 (PubMed )
Supplement: 41467_2017_2688_MOESM20_ESM.xlsx › d__Freq_TP093
Collagen (COL4A) mutations are the most frequent mutations underlying adult focal segmental glomerulosclerosis.
Gast C et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association, 2016
Integrative genomic and transcriptomic characterization of papillary carcinomas of the breast.
Piscuoglio S et al.
Molecular Oncology, 2014
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