Search results (178)
« Back to PublicationsOff-the-shelf dual CAR-iNKT cell immunotherapy eradicates medullary and leptomeningeal high-risk KMT2A-rearranged leukemia.
Journal article
Ren H. et al, (2026), Blood, 147, 180 - 196
Enhancer heterogeneity in acute lymphoblastic leukemia drives differential gene expression in patients.
Journal article
Smith AL. et al, (2025), Blood, 146, 2073 - 2087
Clinical significance of preleukemic somatic GATA1 mutations in children with Down syndrome.
Journal article
Elliott N. et al, (2025), Blood, 146, 1561 - 1574
Genome-wide association study of somatic GATA1s mutations in newborns with Down syndrome.
Journal article
Li Y. et al, (2025), Blood Adv, 9, 4235 - 4243
Genome-wide association studies of Down syndrome associated congenital heart defects.
Preprint
Feldman ER. et al, (2024)
Introduction to a review series on globin disorders.
Journal article
Coates TD. and Roberts I., (2024), Blood, 144, 797 - 798
Harnessing Single-Cell Technologies in the Search for New Therapies for Diamond-Blackfan Anemia Syndrome.
Journal article
Iskander D. et al, (2024), Exp Hematol, 135
Backtracking to the future: unraveling the origins of childhood leukemia.
Journal article
de Smith AJ. et al, (2024), Leukemia, 38, 416 - 419
The Fetal Specific Gene LIN288 Is Essential for Human Fetal B-Lymphopoiesis and Initiation of KMT2A-AFF1+ Infant Acute Lymphoblastic Leukemia
Journal article
Ling RE. et al, (2024), BLOOD, 144, 199 - 200
Yolk sac cell atlas reveals multiorgan functions during human early development.
Journal article
Goh I. et al, (2023), Science, 381
LIN28B: an important onco-fetal gene in infant acute lymphoblastic leukaemia
Journal article
Ling R. et al, (2023), HemaSphere, 7
Epigenome-wide association study of acute lymphoblastic leukemia in children with Down syndrome.
Journal article
Li S. et al, (2022), Blood Adv, 6, 4132 - 4136
CD34+CD19-CD22+ B-cell progenitors may underlie phenotypic escape in patients treated with CD19-directed therapies.
Journal article
Bueno C. et al, (2022), Blood, 140, 38 - 44
Accelerated epigenetic aging in newborns with Down syndrome.
Journal article
Xu K. et al, (2022), Aging Cell, 21