Associated Papers
Establishment and genomic profiling of cholangiocarcinoma cells with functional characterization.
Jaidee R et al.
Scientific Reports, 2025
40074934 (PubMed )
Supplement: 41598_2025_93192_MOESM2_ESM.pdf
Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles.
Bassani S et al.
Genome Medicine, 2024
In utero tumor development and identification of CTNNB1 mutation in a newborn case of ossifying renal tumor of infancy.
Kasai S et al.
Pediatric Blood & Cancer, 2024
38217079 (PubMed )
Supplement: supplement_1.xlsx › SNVs
Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles.
Bassani S et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
Analysis of rare driving events in pediatric acute myeloid leukemia.
Noort S et al.
Haematologica, 2023
35899387 (PubMed )
Supplement: 2021_280250_NOORT_SUPPL.pdf
Deep whole genome sequencing identifies recurrent genomic alterations in commonly used breast cancer cell lines and patient-derived xenograft models.
Deng N et al.
Breast Cancer Research : Bcr, 2022
36153537 (PubMed )
Supplement: 13058_2022_1540_MOESM2_ESM.xlsx › SuppTableS2
Retinoblastoma from human stem cell-derived retinal organoids.
Norrie JL et al.
Nature Communications, 2021
34315877 (PubMed )
Supplement: 41467_2021_24781_MOESM7_ESM.xlsx › WGS_retinoblastoma
Identification of Genetic Predisposition in Noncirrhotic Portal Hypertension Patients With Multiple Renal Cysts by Integrated Analysis of Whole-Genome and Single-Cell RNA Sequencing.
Wu Y et al.
Frontiers in Genetics, 2021
34868264 (PubMed )
Supplement: Table2.XLSX › Sheet1
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