「Oncogenic FGFR1 mutation and amplification in common cellular origin in a composite tumor with neuroblastoma and pheochromocytoma」の関連論文
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Patient-derived ovarian cancer organoids capture the genomic profiles of primary tumours applicable for drug sensitivity and resistance testing (本文)
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An autopsy case of primary gliosarcoma with multiple extracranial metastases: pathology after administration of bevacizumab and genetic profile
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The landscape of genetic aberrations in myxofibrosarcoma
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Evolutionary histories of breast cancer and related clones
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In silico study of RNA-seq and H3 Trimethylation ChIP-seq analysis in combination with laser-microdissection on human lung cancer cells
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Functional and genomic characterization of patient-derived xenograft model to study adaptation to mTORC1 inhibitor in clear cell renal cell carcinoma
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Immunohistochemical assessment of sex-determining region Y (SRY)-related high mobility group (HMG)-box 2 (Sox2) and Krüppel-like factor 4 (Klf4) in ameloblastomas
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Single-cell transcriptomics of human cholesteatoma identifies an activin A-producing osteoclastogenic fibroblast subset inducing bone destruction
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Amplified EPOR/JAK2 Genes Define a Unique Subtype of Acute Erythroid Leukemia
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Downregulation of lncRNA PVT1 inhibits proliferation and migration of mesothelioma cells by targeting FOXM1
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Downregulation of lncRNA PVT1 inhibits proliferation and migration of mesothelioma cells by targeting FOXM1
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A RUNX-targeted gene switch-off approach modulates the BIRC5/PIF1-p21 pathway and reduces glioblastoma growth in mice
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Genomic stability of mouse spermatogonial stem cells in vitro
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Comprehensive genomics in androgen receptor-dependent castration-resistant prostate cancer identifies an adaptation pathway mediated by opioid receptor kappa 1
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Sarcomatoid mesothelioma diagnosed in a patient with mesothelioma in situ: a case report on morphologic differences after 9-month interval with details analysis of cytology in early-stage mesothelioma
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Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis
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Comprehensive analysis of full-length transcripts reveals novel splicing abnormalities and oncogenic transcripts in liver cancer
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A case of Erdheim–Chester disease with the BRAF V600E mutation diagnosed via endoscopic sinus surgery
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Genomic analysis of multiple myeloma using targeted capture sequencing in the Japanese cohort
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Frequent PIK3CA mutations in eutopic endometrium of patients with ovarian clear cell carcinoma
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Complex roles of the actin-binding protein Girdin/GIV in DNA damage-induced apoptosis of cancer cells
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A novel cancer immunotherapy using tumor-infiltrating B cells in the APC (min/+) mouse model
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Clinical impact of detecting low-frequency variants in cell-free DNA on treatment of castration-resistant prostate cancer
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Real-world application of next-generation sequencing-based test for surgically resectable colorectal cancer in clinical practice (本文)
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Urinary MicroRNA-Based Diagnostic Model for Central Nervous System Tumors Using Nanowire Scaffolds
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Genetic and Physiological Characterization of Tomato F-box Gene HAWAIIAN SKIRT Mutants
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Development of an in vitro carcinogenesis model of human papillomavirus-induced cervical adenocarcinoma (本文)
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Next Generation Sequencing-Based Transcriptome Predicts Bevacizumab Efficacy in Combination with Temozolomide in Glioblastoma
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卵巣低異型度漿液性癌のin vitro発癌モデル
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Identification and characterization of slow‑cycling cells in Ewing sarcoma
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Gut contractile organoids: a novel model system to study the cellular synchronization in gastrointestinal motility
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A pipeline for complete characterization of complex germline rearrangements from long DNA reads
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Prognostic stratification for IDH-wild-type lower-grade astrocytoma by Sanger sequencing and copy-number alteration analysis with MLPA
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Cooperative participation of epigenomic and genomic alterations in the clinicopathological diversity of gastric adenocarcinomas : significance of cell adhesion and epithelial–mesenchymal transition-related signaling pathways (本文)
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Studies on the pathological mechanism of alopecia areata in C3H/HeJ mouse model
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Long-Read Sequence Confirmed a Large Deletion Including MYH6 and MYH7 in an Infant of Atrial Septal Defect and Atrial Arrhythmias.
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Pharmacogenomic study of anti-tuberculosis drugs-induced liver injury in Thais
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Chemosensitivity of Patient-Derived Cancer Stem Cells Identifies Colorectal Cancer Patients with Potential Benefit from FGFR Inhibitor Therapy
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Bioengineering and Cell-derived Strategies for Salivary Gland Regeneration
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Glucose transporter Glut1 controls diffuse invasion phenotype with perineuronal satellitosis in diffuse glioma microenvironment
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In silico analysis of inner ear development using public whole embryonic body single-cell RNA-sequencing data
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Studies on Cytotoxic Effects of Tumor Necrosis Factor-Related Apoptosis Inducing Ligand (TRAIL) to Canine Cell Lines Derived from Hemangiosarcoma and Mammary Epithelial Tumor
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Variation of body weight and seasonal reproduction in populations from different latitudes: genetic analyses using wild-derived medaka fish
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Dermal fibroblast-like cells reprogrammed directly from adipocytes in mouse (本文)
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Significance of PD-L1 expression in carbon-ion radiotherapy for uterine cervical adeno/adenosquamous carcinoma (本文)
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Constitutive activation of mTORC1 signaling induced by biallelic loss-of-function mutations in SZT2 underlies a discernible neurodevelopmental disease
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Elucidation of cause and natural feature of cheating rhizobia, and host defense mechanism against them
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Colorectal cancer-derived CAT1-positive extracellular vesicles alter nitric oxide metabolism in endothelial cells and promote angiogenesis
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A cerebrospinal fluid microRNA analysis: Progressive supranuclear palsy
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A proteome signature of umbilical cord serum associated with congenital diaphragmatic hernia