Martina Sarchi

Pavia, Italy

Last Updated: 09/26/2026

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Found 15 publications

Loss of function of the chromatin remodeling gene INO80D leads to neurogenic features of schizophrenia.

Loss of function of the chromatin remodeling gene INO80D leads to neurogenic features of schizophrenia.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: March 05, 2026

Inflammatory signatures in the spectrum of myeloid diseases.

Inflammatory signatures in the spectrum of myeloid diseases.

Journal: HemaSphere

Published: January 19, 2026

Evolutionary trajectories of myelodysplastic syndromes/neoplasms.

Evolutionary trajectories of myelodysplastic syndromes/neoplasms.

Journal: Seminars in cancer biology

Published: November 12, 2025

A vertically integrated system for tracking and assessing cell-cycle-aware phenotypes under confinement.

A vertically integrated system for tracking and assessing cell-cycle-aware phenotypes under confinement.

Journal: APL bioengineering

Published: October 10, 2025

CALIPERS: Cell cycle-aware live imaging for phenotyping experiments and regeneration studies.

CALIPERS: Cell cycle-aware live imaging for phenotyping experiments and regeneration studies.

Journal: Nature communications

Published: July 19, 2025

A precision medicine approach to the myelodysplastic syndrome with isolated deletion 5q, 50 years after its discovery.

A precision medicine approach to the myelodysplastic syndrome with isolated deletion 5q, 50 years after its discovery.

Journal: Blood

Published: April 09, 2025

Distinct routes of clonal progression in SF3B1-mutant myelodysplastic syndromes.

Distinct routes of clonal progression in SF3B1-mutant myelodysplastic syndromes.

Journal: Blood advances

Published: October 21, 2024

Understanding Human Oncogene Function and Cooperativity in Myeloid Malignancy Using iPSCs.

Understanding Human Oncogene Function and Cooperativity in Myeloid Malignancy Using iPSCs.

Journal: Experimental hematology

Published: July 11, 2024

Mis-splicing of Mitotic Regulators Sensitizes SF3B1-Mutated Human HSCs to CHK1 Inhibition.

Mis-splicing of Mitotic Regulators Sensitizes SF3B1-Mutated Human HSCs to CHK1 Inhibition.

Journal: Blood cancer discovery

Published: November 05, 2023

R-Loop Accumulation in Spliceosome Mutant Leukemias Confers Sensitivity to PARP1 Inhibition by Triggering Transcription-Replication Conflicts.

R-Loop Accumulation in Spliceosome Mutant Leukemias Confers Sensitivity to PARP1 Inhibition by Triggering Transcription-Replication Conflicts.

Journal: Cancer research

Published: October 16, 2023

GPATCH8 modulates mutant SF3B1 mis-splicing and pathogenicity in hematologic malignancies.

GPATCH8 modulates mutant SF3B1 mis-splicing and pathogenicity in hematologic malignancies.

Journal: Molecular cell

Published: September 26, 2023

Prevalence and clinical expression of germ line predisposition to myeloid neoplasms in adults with marrow hypocellularity.

Prevalence and clinical expression of germ line predisposition to myeloid neoplasms in adults with marrow hypocellularity.

Journal: Blood

Published: December 05, 2022

Showing 1-12 of 15

Last Updated: 09/26/2026