「RUNX1 rearrangement in mature B-cell acute lymphoblastic leukemia with non-L3 morphology」の関連論文
-
Biclonal Diffuse Large B-cell Lymphoma Commonly Characterized by Partial Trisomy 18q Involving MALT1 and BCL2
-
Cryptic insertion of CBFB into MYH11 leading to a type D fusion in acute myeloid leukemia with normal karyotype
-
Down syndrome-related transient abnormal myelopoiesis is attributed to a specific erythro-megakaryocytic subpopulation with GATA1 mutation
-
A RUNX-targeted gene switch-off approach modulates the BIRC5/PIF1-p21 pathway and reduces glioblastoma growth in mice
-
Two effects of GATA2 enhancer repositioning by 3q chromosomal rearrangements.
-
Establishment and Application of Anti-CD20 Monoclonal Antibodies using the Cell-based Immunization and Screening Method for the Detection of B Cells
-
Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings
-
Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings
-
Incontinentia pigmenti in a female infant with somatic mosaicism due to the IKBKG variant
-
Spontaneous regression of hidroacanthoma simplex after skin biopsy
-
Paraneoplastic Pemphigus Mimicking Toxic Epidermal Necrolysis Associated with Follicular Lymphoma: Possible Pathological Role of CD8 T Cells.
-
Single-cell transcriptomics of human cholesteatoma identifies an activin A-producing osteoclastogenic fibroblast subset inducing bone destruction
-
Pitfalls in establishing mouse model of female infertility by immunization with human centromere protein
-
Smooth muscle protein 22α‐Cre recombination in resting cardiac fibroblasts and hematopoietic precursors
-
CD4/CD8 double-negative T-cell lymphoma successfully treated with a combination of bexarotene and total skin electron beam therapy
-
Non-Genetic Cell-Surface Modification with a Self-Assembling Molecular Glue
-
Identification of novel genes associated with dysregulation of B cells in patients with primary Sjögren's syndrome (本文)
-
Identification of a novel causative mutation in KRT1 in diffuse palmoplantar keratoderma, facilitated by whole-exome sequencing
-
Pluripotent stem cell model of Shwachman-Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors
-
Osteogenic cocktail induces calcifications in human breast cancer cell line via placental alkaline phosphatase expression.
-
Partial Epithelial-Mesenchymal Transition Was Observed Under p63 Expression in Acquired Middle Ear Cholesteatoma and Congenital Cholesteatoma.
-
Autism-associated mutation in Hevin/Sparcl1 induces endoplasmic reticulum stress through structural instability
-
Construction of a single-cell atlas of non-hematopoietic cells in human lymph nodes and lymphoma for dissecting stromal remodeling
-
Identification of T cell receptors targeting a neoantigen derived from recurrently mutated FGFR3
-
Bioengineering and Cell-derived Strategies for Salivary Gland Regeneration
-
Re-generation of cytotoxic γδT cells with distinctive signatures from human γδT-derived iPSCs
-
Clinical and serological features of dermatomyositis and systemic lupus erythematosus patients with autoantibodies to ADAR1
-
Prognostic stratification for IDH-wild-type lower-grade astrocytoma by Sanger sequencing and copy-number alteration analysis with MLPA
-
Functional analysis of P53 negative regulators in Bombyx mori
-
Identification of novel mutations and reassignment of archival xeroderma pigmentosum group C cell strains from Japanese patients
-
精巣高発現タンパク質の精子形成における機能と応用
-
A mutation in DOK7 in congenital myasthenic syndrome forms aggresome in cultured cells, and reduces DOK7 expression and MuSK phosphorylation in patient-derived iPS cells
-
Analysis of disease model iPSCs derived from patients with a novel Fanconi anemia-like IBMFS ADH5/ALDH2 deficiency
-
HER2 G776S mutation promotes oncogenic potential in colorectal cancer cells when accompanied by loss of APC function
-
A novel cancer immunotherapy using tumor-infiltrating B cells in the APC (min/+) mouse model
-
ILF2 enhances the DNA cytosine deaminase activity of tumor mutator APOBEC3B in multiple myeloma cells
-
Group 1 innate lymphoid cells are involved in the progression of experimental anti-glomerular basement membrane glomerulonephritis and are regulated by peroxisome proliferator-activated receptor α
-
An experience in prenatal diagnosis via QF-PCR of a female child with a 9.9 Mb pure deletion at 18p11.32–11.22
-
St8sia1-deficiency in mice alters tumor environments of gliomas, leading to reduced disease severity
-
Increased CaV1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly
-
T2-FLAIR mismatch sign in dysembryoplastic neuroepithelial tumor
-
T2-FLAIR mismatch sign in dysembryoplastic neuroepithelial tumor
-
A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease
-
Long-Read Sequence Confirmed a Large Deletion Including MYH6 and MYH7 in an Infant of Atrial Septal Defect and Atrial Arrhythmias.
-
BRCA1 haploinsufficiency promotes chromosomal amplification under Fenton reaction-based carcinogenesis through ferroptosis-resistance
-
Dermal fibroblast-like cells reprogrammed directly from adipocytes in mouse (本文)
-
A simple method to distinguish residual elotuzumab from monoclonal paraprotein in immunofixation assays for multiple myeloma patients
-
Systematic analysis on the seeding activity of familial mutant forms of α-synuclein
-
Circulatory C-type natriuretic peptide reduces mucopolysaccharidosis-associated craniofacial hypoplasia in vivo
-
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