Associated Papers
Single-cell profiling reveals reprogrammed hierarchy and disrupted immune-stromal ecosystem in TP53-mutated AML.
Qiu G et al.
Experimental Hematology & Oncology, 2026
41634865 (PubMed )
Supplement: 40164_2026_751_MOESM3_ESM.xlsx › Sheet1
The impact of RUNX2 gene variants on cleidocranial dysplasia phenotype: a systematic review.
Thaweesapphithak S et al.
Journal of Translational Medicine, 2024
39627759 (PubMed )
Supplement: 12967_2024_5904_MOESM1_ESM.xlsx › Supplement_table_1.
Reassessing the association: Evaluation of a polyalanine deletion variant of RUNX2 in non-syndromic sagittal and metopic craniosynostosis.
Walton IS et al.
Journal of Anatomy, 2024
38760592 (PubMed )
Supplement: JOA-245-874-s001.zip › joa14052-sup-0001-Supinfo › joa14052-sup-0002-Supinfo.xlsx › Sheet1
Novel PTCH1 mutation in Gorlin-Goltz syndrome potentially altered interactions with lipid bilayer.
Gao Q et al.
Oral Diseases, 2021
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