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Profil bibliographique

Sixuan Pan

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

8Publications signalées
30Citations signalées
2Affiliations récentes

Les institutions déclarées

Les domaines associés

Glioma Diagnosis and TreatmentT-cell and B-cell ImmunologyCancer Genomics and DiagnosticsSingle-cell and spatial transcriptomicsMicroRNA in disease regulation

Les publications récentes

Accès ouvert 2025 article OpenAlex

Tumor heterogeneity underlies clinical outcome and MEK inhibitor response in somatic NF1-mutant glioblastoma

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 …

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5 citations JCI Insight
Accès ouvert 2025 article OpenAlex

Myeloid-mesenchymal crosstalk drives ARG1-dependent profibrotic metabolism via ornithine in lung fibrosis

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 …

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24 citations Journal of Clinical Investigation
Accès ouvert 2024 conference-abstract OpenAlex

PATH-54. HIGH-THROUGHPUT SINGLE NUCLEAR DNA SEQUENCING OF HUMAN SPORADICNF1 MUTANT IDH-WILDTYPE GLIOBLASTOMAS REVEALS PATTERNS OF TUMOR EVOLUTION AND RECURRENCE

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 …

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0 citations Neuro-Oncology
Accès ouvert 2024 conference-abstract OpenAlex

PATH-53. DNA MUTATION SEQUENCING AND METHYLATION ANALYSIS OF SOMATICNF1 MUTANT IDH-WILDTYPE GLIOBLASTOMA IDENTIFIES THREE EPIGENETIC GROUPS ANDCDKN2A/B LOSS AS A NEGATIVE PROGNOSTIC BIOMARKER

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 …

0 citations Neuro-Oncology
Accès ouvert 2024 preprint OpenAlex

PURE-seq identifies Egr1 as a Potential Master Regulator in Murine Aging by Sequencing Long-Term Hematopoietic Stem Cells

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 …

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1 citation bioRxiv (Cold Spring Harbor Laboratory)
2024 preprint OpenAlex

Multiplatform molecular profiling and functional genomic screens identify prognostic signatures and mechanisms underlying MEK inhibitor response in somatic NF1 mutant glioblastoma

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)

2 citations bioRxiv (Cold Spring Harbor Laboratory)

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