「Unexpected appearance of KMT2A::MLLT10 fusion transcript in acute myeloid leukemia with t(5;11)(q31;q23.3)」の関連論文
-
Identification of a multiresistant mosaic plasmid carrying a new segment of IS1216E-flanked optrA with integrated Tn551-ermB element in linezolid-resistant Enterococcus faecalis human isolate
-
FGF5 and EPAS1 gene polymorphisms are associated with high-altitude adaptation in Nepalese goat breeds
-
De Novo T790M Mutation in an L858R Epidermal Growth Factor Receptor Mutant-Associated Lung Adenocarcinoma
-
Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes
-
Orthogonal Protein-Responsive mRNA Switches for Mammalian Synthetic Biology
-
Long-Surviving Adult Siblings With Joubert Syndrome Harboring a Novel Compound Heterozygous CPLANE1 Variant
-
Genetic basis of female-limited polymorphism of the damselfly Ischnura senegalensis
-
T2-FLAIR mismatch sign in dysembryoplastic neuroepithelial tumor
-
T2-FLAIR mismatch sign in dysembryoplastic neuroepithelial tumor
-
Comparative Plastid Genomics of Green-Colored Dinoflagellates Unveils Parallel Genome Compaction and RNA Editing
-
The landscape of genetic aberrations in myxofibrosarcoma
-
Computational Analysis Reveals a Critical Point Mutation in the N-Terminal Region of the Signaling Lymphocytic Activation Molecule Responsible for the Cross-Species Infection with Canine Distemper Virus
-
Combination of target site mutation and associated CYPs confers high-level resistance to pyridaben in Tetranychus urticae
-
Inhibition of microRNA-33b specifically ameliorates abdominal aortic aneurysm formation via suppression of inflammatory pathways
-
ヒトヘルペスウイルス6Aテグメントタンパク質U14は、p65と相互作用してNF-κbシグナルを誘導する
-
Phosphorylation of the anaphase promoting complex activator FZR1/CDH1 is required for meiosis II entry in mouse male germ cell (本文)
-
Analysis of disease model iPSCs derived from patients with a novel Fanconi anemia-like IBMFS ADH5/ALDH2 deficiency
-
A pipeline for complete characterization of complex germline rearrangements from long DNA reads
-
Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis
-
Complete genome analyses of G12P[8] rotavirus strains from hospitalized children in Surabaya, Indonesia, 2017–2018
-
The relationship between DRD2 Taq1A polymorphism and white matter structure in healthy young adults.
-
A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease
-
TEAD1 trapping by the Q353R–Lamin A/C causes dilated cardiomyopathy
-
Disrupted Cav1.2 Selectivity Causes Overlapping Long QT and Brugada Syndrome Phenotypes in CACNA1C-E1115K iPS Cell Model
-
A novel variant fibrinogen, AαE11del, demonstrating the importance of AαE11 residue in thrombin binding
-
Systematic analysis on the seeding activity of familial mutant forms of α-synuclein
-
CEBPγ facilitates lamellipodia formation and cancer cell migration through CERS6 upregulation
-
Molecular genetic study of the FMR1 CGG repeat configurations in the Japanese population and patients with Fragile X-Associated Tremor/Ataxia Syndrome
-
Landscape of driver mutations and their clinical impacts in pediatric B-cell precursor acute lymphoblastic leukemia
-
Inhibition of cyclooxygenase-1 by nonsteroidal anti-inflammatory drugs demethylates MeR2 enhancer and promotes Mbnl1 transcription in myogenic cells
-
Next Generation Sequencing-Based Transcriptome Predicts Bevacizumab Efficacy in Combination with Temozolomide in Glioblastoma
-
Analyses of genetic and retinal lesions in Ccdc85c knockout rats: a rat model of genetic hydrocephalus
-
CRISPR/Cas9-based genome editing in mice uncovers 13 testis- or epididymis-enriched genes individually dispensable for male reproduction
-
Rab35–GEFs, DENND1A and folliculin differentially regulate podocalyxin trafficking in two- and three-dimensional epithelial cell cultures.
-
Severe neurodevelopmental disorder caused by an MEF2C nonsense mutation
-
MYCL promotes iPSC-like colony formation via MYC Box 0 and 2 domains
-
マウス精子形成過程におけるRSBN1の役割
-
The transcription factor ZFP64 facilitates climbing-fiber synapse elimination along signaling pathway mediated by P/Q-type voltage-dependent Ca2+ channel in the developing cerebellum
-
Studies on epidemiology, development of chemotherapy and genetic modification of piroplasmosis
-
Gene mapping of bruchid resistance in moth bean (Vigna aconitifolia)
-
Amplified EPOR/JAK2 Genes Define a Unique Subtype of Acute Erythroid Leukemia
-
Evaluation and selection of potent fluorescent immunosensors by combining fluorescent peptide and nanobodies displayed on yeast surface
-
St8sia1-deficiency in mice alters tumor environments of gliomas, leading to reduced disease severity
-
Genetic and Physiological Characterization of Tomato F-box Gene HAWAIIAN SKIRT Mutants
-
Comprehensive genomics in androgen receptor-dependent castration-resistant prostate cancer identifies an adaptation pathway mediated by opioid receptor kappa 1
-
G-quadruplex-forming nucleic acids interact with splicing factor 3B subunit 2 and suppress innate immune gene expression
-
Smooth muscle protein 22α‐Cre recombination in resting cardiac fibroblasts and hematopoietic precursors
-
Development, test and application of a new intra-taxon sampling method based on geographic information
-
A Single RET Mutation in Hirschsprung Disease Induces Intestinal Aganglionosis Via a Dominant-Negative Mechanism
-
The EZH2 inhibitor tazemetostat upregulates the expression of CCL17/TARC in B-cell lymphoma and enhances T-cell recruitment