「Integrated Genomic Analysis Identifies UBTF Tandem Duplications as a Recurrent Lesion in Pediatric Acute Myeloid Leukemia」の関連論文
-
FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients
-
Comparative Plastid Genomics of Green-Colored Dinoflagellates Unveils Parallel Genome Compaction and RNA Editing
-
Disrupted Cav1.2 Selectivity Causes Overlapping Long QT and Brugada Syndrome Phenotypes in CACNA1C-E1115K iPS Cell Model
-
Tuft cell-like carcinomas: novel cancer subsets present in multiple organs sharing a unique gene expression signature
-
Network-guided analysis of hippocampal proteome identifies novel proteins that colocalize with Aβ in a mice model of early-stage Alzheimer’s disease
-
FE65 in breast cancer: its clinicopathological and biological significance
-
SOX6 is a Novel Immunohistochemical Marker for Differential Diagnosis of Epithelioid Mesothelioma From Lung Adenocarcinoma
-
SOX6 is a Novel Immunohistochemical Marker for Differential Diagnosis of Epithelioid Mesothelioma From Lung Adenocarcinoma
-
Clinical and genetic investigation of 136 Japanese patients with congenital hypothyroidism
-
CRISPR/Cas9-mediated genome-edited mice reveal 10 testis-enriched genes are dispensable for male fecundity
-
Real-world application of next-generation sequencing-based test for surgically resectable colorectal cancer in clinical practice (本文)
-
EVI1 and GATA2 misexpression induced by inv(3)(q21q26) contribute to megakaryocyte-lineage skewing and leukemogenesis.
-
Pharmacogenomic study of anti-tuberculosis drugs-induced liver injury in Thais
-
Epigenomic dysregulation in AFP-producing gastric cancer
-
Re-generation of cytotoxic γδT cells with distinctive signatures from human γδT-derived iPSCs
-
A genome-wide association study identifying single nucleotide polymorphisms in the PPFIBP2 gene was predictive for interstitial lung disease in rheumatoid arthritis patients
-
TEAD1 trapping by the Q353R–Lamin A/C causes dilated cardiomyopathy
-
Chemosensitivity of Patient-Derived Cancer Stem Cells Identifies Colorectal Cancer Patients with Potential Benefit from FGFR Inhibitor Therapy
-
Analyses of genetic and retinal lesions in Ccdc85c knockout rats: a rat model of genetic hydrocephalus
-
Molecular analysis of drug resistance associating gene mutations in Mycobacterium tuberculosis clinical isolates in Nepal [an abstract of entire text]
-
Thiopurine Use During Pregnancy Has Deleterious Effects on Offspring in Nudt15 R138C Knock-In Mice.
-
Homozygous variant p.Ser427Pro in PNPLA1 is a preventive factor from atopic dermatitis
-
All reported non-canonical splice site variants in GLA cause aberrant splicing
-
CD4/CD8 double-negative T-cell lymphoma successfully treated with a combination of bexarotene and total skin electron beam therapy
-
Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease
-
Trp53 Mutation in Keratin 5 (Krt5)-Expressing Basal Cells Facilitates the Development of Basal Squamous-Like Invasive Bladder Cancer in the Chemical Carcinogenesis of Mouse Bladder
-
A proteome signature of umbilical cord serum associated with congenital diaphragmatic hernia
-
Genomic analysis of multiple myeloma using targeted capture sequencing in the Japanese cohort
-
Post-induction MRD by FCM and GATA1-PCR are significant prognostic factors for myeloid leukemia of Down syndrome.
-
Single-cell transcriptomics of human cholesteatoma identifies an activin A-producing osteoclastogenic fibroblast subset inducing bone destruction
-
Genome-wide Survival Analysis for Macular Neovascularization Development in Central Serous Chorioretinopathy Revealed Shared Genetic Susceptibility with Polypoidal Choroidal Vasculopathy
-
Bioinformatics and Functional Analyses Implicate Potential Roles for EOGT and L-fringe in Pancreatic Cancers
-
Prickle2 and Igsf9b coordinately regulate the cytoarchitecture of the axon initial segment
-
外科的に切除された膵癌におけるST2発現の臨床病理学的及び予後との関連性の検討
-
Inventory and Evolution of Mitochondrion-localized Family A DNA Polymerases in Euglenozoa
-
Utility of plasma circulating tumor DNA and tumor DNA profiles in head and neck squamous cell carcinoma
-
Reverse Genetic Studies on Mitochondrial tRNA-related Disorders
-
A pipeline for complete characterization of complex germline rearrangements from long DNA reads
-
Inherent genomic properties underlie the epigenomic heterogeneity of human induced pluripotent stem cells
-
Combination of RERG and ZNF671 methylation rates in circulating cell-free DNA: A novel biomarker for screening of nasopharyngeal carcinoma
-
Orthogonal Protein-Responsive mRNA Switches for Mammalian Synthetic Biology
-
Constitutive activation of mTORC1 signaling induced by biallelic loss-of-function mutations in SZT2 underlies a discernible neurodevelopmental disease
-
Branchpoints as potential targets of exon-skipping therapies for genetic disorders
-
Diagnostic value of PET/CT with ¹¹C-methionine (MET) and ¹⁸F-fluorothymidine (FLT) in newly diagnosed glioma based on the 2016 WHO classification
-
Smooth muscle protein 22α‐Cre recombination in resting cardiac fibroblasts and hematopoietic precursors
-
Role of Tet2-deficient immune cells in lung cancer - a model of clonal hematopoiesis-derived immune cells in solid cancers
-
UBAP1 mutations cause juvenile-onset hereditary spastic paraplegias (SPG80) and impair UBAP1 targeting to endosomes
-
Inhibition of microRNA-33b specifically ameliorates abdominal aortic aneurysm formation via suppression of inflammatory pathways
-
Transcription of MERVL retrotransposons is required for preimplantation embryo development (本文)
-
Association of two variable number of tandem repeats in the monoamine oxidase A gene promoter with suicide completion: The present study and meta-analysis