User profiles for Minoo Ashtiani
Minoo AshtianiBioinformatician, Princess Máxima Center for Pediatric Oncology Verified email at prinsesmaximacentrum.nl Cited by 317 |
[HTML][HTML] A systematic survey of centrality measures for protein-protein interaction networks
M Ashtiani, A Salehzadeh-Yazdi… - BMC systems …, 2018 - Springer
Background Numerous centrality measures have been introduced to identify “central” nodes
in large networks. The availability of a wide range of measures for ranking influential nodes …
in large networks. The availability of a wide range of measures for ranking influential nodes …
[HTML][HTML] Nanoparticle-mediated targeting of the fusion gene RUNX1/ETO in t(8;21)-positive acute myeloid leukaemia
A hallmark of acute myeloid leukaemias (AMLs) are chromosomal rearrangements that give
rise to novel leukaemia-specific fusion genes. Most of these fusion genes are both initiating …
rise to novel leukaemia-specific fusion genes. Most of these fusion genes are both initiating …
CINNA: an R/CRAN package to decipher Central Informative Nodes in Network Analysis
Motivation Centrality analysis involves a series of ambiguities in that there are numerous
well-known centrality measures with differing algorithms for establishing which nodes in a …
well-known centrality measures with differing algorithms for establishing which nodes in a …
Acute myeloid leukemias with UBTF tandem duplications are sensitive to menin inhibitors
…, B Arthur, T Westover, ME Thomas III, M Ashtiani… - Blood, 2024 - ashpublications.org
UBTF tandem duplications (UBTF-TDs) have recently emerged as a recurrent alteration in
pediatric and adult acute myeloid leukemia (AML). UBTF-TD leukemias are characterized by a …
pediatric and adult acute myeloid leukemia (AML). UBTF-TD leukemias are characterized by a …
Epigenetic regulator genes direct lineage switching in MLL/AF4 leukemia
The fusion gene MLL/AF4 defines a high-risk subtype of pro-B acute lymphoblastic leukemia.
Relapse can be associated with a lineage switch from acute lymphoblastic to acute …
Relapse can be associated with a lineage switch from acute lymphoblastic to acute …
[HTML][HTML] The MLL–Menin Interaction is a Therapeutic Vulnerability in NUP98-rearranged AML
…, S Troester, K Szoltysek, R Cameron, M Ashtiani… - …, 2023 - journals.lww.com
Chromosomal translocations involving the NUP98 locus are among the most prevalent
rearrangements in pediatric acute myeloid leukemia (AML). AML with NUP98 fusions is …
rearrangements in pediatric acute myeloid leukemia (AML). AML with NUP98 fusions is …
Valproic acid inhibits the protective effects of stromal cells against chemotherapy in breast cancer: Insights from proteomics and systems biology
Interaction between tumor and stromal cells is beginning to be decoded as a contributor to
chemotherapy resistance. Here, we aim to take a system‐level approach to explore a …
chemotherapy resistance. Here, we aim to take a system‐level approach to explore a …
[PDF][PDF] CINNA: An R package for deciphering Central Informative Nodes in Network Analysis
Nowadays, reconstructed networks originated from various contexts become more complex
and larger, which make them more difficult to figure out. Recognizing influential nodes helps …
and larger, which make them more difficult to figure out. Recognizing influential nodes helps …
Repurposing CD19-directed immunotherapies for pediatric t (8; 21) acute myeloid leukemia
…, JB Koedijk, NE Wijnen, T Meulendijks, M Ashtiani… - bioRxiv, 2024 - biorxiv.org
In contrast to patients with B cell precursor acute lymphoblastic leukemia (BCP-ALL),
patients with acute myeloid leukemia (AML) have not yet benefited from recent advances in …
patients with acute myeloid leukemia (AML) have not yet benefited from recent advances in …
RUNX1:: RUNX1T1 Impairs the Differentiation Potential of Primary AML Cells
PK Derevianko, LE Swart, M Ashtiani, S Kellaway… - Blood, 2023 - Elsevier
Acute myeloid leukemias (AMLs) are often driven by genomic translocations, of which t(8;21)
is the most frequent. The resulting gene fusion RUNX1::RUNX1T has been shown in cell …
is the most frequent. The resulting gene fusion RUNX1::RUNX1T has been shown in cell …