Accès ouvert
2025
article
OpenAlex
Sixuan Pan, Kanish Mirchia, Emily Payne, Siyuan John Liu et autres
Tumor suppressor NF1 is recurrently mutated in glioblastoma, leading to aberrant activation of Ras/rapidly accelerated fibrosarcoma (RAF)/MEK signaling. However, how tumor heterogeneity shapes the molecular landscape and efficacy of targeted therapies remains unclear. Here, we combined bulk and single-cell genomics of human …
us
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Accès ouvert
2025
article
OpenAlex
Preeti Yadav, Javier Gómez Ortega, Prerna Dabral, Whitney Tamaki et autres
Idiopathic pulmonary fibrosis (IPF) is a disease of progressive lung remodeling and collagen deposition that leads to respiratory failure. Myeloid cells are abundant in IPF lung and in murine lung fibrosis, but their functional effects are incompletely understood. Using mouse and human …
us, cn, in, jp
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Accès ouvert
2024
conference-abstract
OpenAlex
Kanish Mirchia, Sixuan Pan, Emily Payne, Rachel M. Agoglia et autres
Abstract The advent of single cell techniques has advanced our understanding of glioblastoma (GBM) evolution and cell lineage relationships. However, study of mutational co-occurrence and clonal phylogeny has been hampered by limitations in single cell genotyping. Here, we perform semi-automated, rapid single …
us
(code pays fourni par la source)
Accès ouvert
2024
conference-abstract
OpenAlex
Kanish Mirchia, Sixuan Pan, Emily Payne, John Liu et autres
Abstract The tumor suppressor NF1 is frequently mutated in IDH-wildtype glioblastoma. However, the molecular subgroups and clinically relevant biomarkers within somatic NF1 mutant, IDH-wildtype glioblastomas remain incompletely understood. Here, we combine methylation arrays and targeted DNA sequencing to identify epigenetic subgroups and …
Accès ouvert
2024
preprint
OpenAlex
Sixuan Pan, Kai‐Chun Chang, Inés Fernández-Maestre, Stéphane Van Haver et autres
Abstract Single-cell transcriptomics is valuable for uncovering individual cell properties, particularly in highly heterogeneous systems. However, this technique often results in the analysis of many well- characterized cells, increasing costs and diluting rare cell populations. To address this, we developed PURE-seq (PIP-seq …
us
(code pays fourni par la source)
Accès ouvert
2024
preprint
OpenAlex
Adam R. Abate, Sixuan Pan, Kai‐Chun Chang, Inés Fernández-Maestre et autres
us
(code pays fourni par la source)
2024
preprint
OpenAlex
Sixuan Pan, Kanish Mirchia, Emily Payne, Siyuan John Liu et autres
NF1 is recurrently mutated in glioblastoma yet the molecular landscape and efficacy of targeted therapies remain unclear. Here, we combine bulk and single cell genomics of human somatic NF1 mutant, IDH-wildtype glioblastomas with functional genomic analysis of cell lines and mouse intracranial …
us
(code pays fourni par la source)
Accès ouvert
2023
article
OpenAlex
Lu-Jun Liang, Mingyu He, Sixuan Pan, Shiguo Zhou et autres