Associated Papers
Integrative scATAC-seq and mtDNA mutation analysis reveals disease-driven regulatory aberrations in AML.
Tian C et al.
Science Bulletin, 2025
Genotype-Phenotype Correlations in Denys-Drash Syndrome in Children.
Glénisson M et al.
Kidney International Reports, 2025
40303223 (PubMed )
Supplement: mmc1.pdf
The RTK-RAS signaling pathway is enriched in patients with rare acute myeloid leukemia harboring t(16;21)(p11;q22)/FUS::ERG.
Lai A et al.
Blood Science (baltimore, Md.), 2024
38742238 (PubMed )
Supplement: bs9-6-e00188-s001.pdf
High-Throughput Splicing Assays Identify Known and Novel WT1 Exon 9 Variants in Nephrotic Syndrome.
Smith C et al.
Kidney International Reports, 2023
37850022 (PubMed )
Supplement: mmc1.pdf
Genotype-Phenotype Correlation in WT1 Exon 8 to 9 Missense Variants.
Nagano C et al.
Kidney International Reports, 2021
34386660 (PubMed )
Supplement: mmc1.pdf
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