Keywords: ADA2; Adenosine deaminase 2; ASH1L; Absent, Small, or Homeotic 1-like; BAF; BRG1 associated factor; BAH; Bromoadjacent homology; BAZ2A; Bromodomain adjacent to zinc finger domain protein 2A; BET; Bromodomain and Extra-Terminal domain; BRPF1; Bromodomain a
مقالات ISI (ترجمه نشده)
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Keywords: ALL; acute lymphoblastic leukemia; AML; acute myeloid leukemia; BWA; Burrows Wheeler Alignment tool; CGH; comparative genomic hybridization; CNV; copy number variations; DGV; database of genomic variants; EGA; European Genome-phenome Archive; FISH; fluore
Keywords: ASXL1; BAP1; CREBBP; DNMT3A; EP300; EZH2
Keywords: RTS, Rubinstein–Taybi syndrome; ID, intellectual disability; IUGR, intrauterin growth retardationArray-CGH; Intellectual disability; Facial dysmorphisms; CREBBP; Microduplication; Rubinstein–Taybi
MicroRNA-876-5p inhibits epithelial-mesenchymal transition and metastasis of hepatocellular carcinoma by targeting BCL6 corepressor like 1
Keywords: BCORL1; BCL6 corepressor like 1; HCC; hepatocellular carcinoma; EMT; epithelial-mesenchymal transition; miRNAs; microRNAs; TCGA; The Cancer Genome Atlas; GEO; Gene Expression Omnibus; 3â²-UTR; 3â²-untranslated region; CtBP; C-terminal Binding Protein; C
Structural dynamics and quantum mechanical aspects of shikonin derivatives as CREBBP bromodomain inhibitors
Keywords: CREBBP; Bromodomain; Molecular dynamics; Propionylshikonin; MM-PBSA; MM-GBSA; QM/MM;
Differential peripheral blood methylation by α-lipoic acid and EPA supplementation in overweight or obese women during a weight loss program
Keywords: ANOVA; analysis of variance; BMI; body mass index; CREBBP; CREB binding protein; DHA; docosahexaenoic acid; EPA; eicosapentaenoic acid; FDR; false discovery rate; FFA; free fatty acids; HAT; histone acyltransferases; FITM2; fat storage inducing transmembr
Maternally inherited autosomal dominant intellectual disability caused by 16p13.3 microduplication
Keywords: Chromosome 16p13.3 duplication syndrome; Maternal inheritance; Autosomal dominant; Intellectual disability; CREBBP
Clinical and mutational spectrum in Korean patients with Rubinstein–Taybi syndrome: The spectrum of brain MRI abnormalities
Keywords: Rubinstein–Taybi syndrome (RSTS); CREBBP; HAT domain; Brain MRI abnormalities; Genotype–phenotype
Histone hypoacetylation and increased histone deacetylases in peripheral blood mononuclear cells from patients with Graves' disease
Keywords: Graves' disease (GD); Histone modifications; Histone acetylation; Peripheral blood mononuclear cells (PBMCs); AS; ankylosing spondylitis; CD40; Cluster of Differentiation 40; CTLA4; CTLcytotoxic T lymphocyte-associated antigen-4; CREBBP; CREB binding prot
Duplication 16p13.3 and the CREBBP gene: Confirmation of the phenotype
Keywords: Microduplication; CREBBP; Rubinstein-Taybi syndrome; Genotype-phenotype correlation;
A submicroscopic deletion involving part of the CREBBP gene detected by array-CGH in a patient with Rubinstein-Taybi syndrome
Keywords: RSTS; Rubinstein-Taybi syndrome; OMIM; Online Mendelian inheritance in man; CREBBP; CREB binding protein; EP300; E1A binding protein p300; CGH; comparative genomic hybridization; PCR; polymerase chain reaction; Cy3-dUTP; deoxyuridine 5â²-triphosphate c
Possible influence of CREB1, CREBBP and CREM variants on diagnosis and treatment outcome in patients with schizophrenia
Keywords: Schizophrenia; CREB1; CREBBP; CREM;
Interstitial 16p13.3 microduplication: Case report and critical review of genotype–phenotype correlation
Keywords: CREBBP; 16p13.3 microduplication; SNP array analysis; Smallest region of overlapRTS, Rubinstein–Taybi syndrome; CREBBP, cAMP-response elements binding protein; ADCY9, adenylate cyclase 9; ASD, atrial septal defect; VSD, ventricular septal defect; SRO, sma
Case-control association study of 14 variants of CREB1, CREBBP and CREM on diagnosis and treatment outcome in major depressive disorder and bipolar disorder
Keywords: CREB1; CREBBP; CREM; Major depressive disorder; Bipolar disorder;
Computational prediction of the PolyQ and CAG repeat spinocerebellar ataxia network based on sequence identity to untranslated regions
Keywords: SCA; spinocerebellar ataxia; PolyQ; poly glutamine; LTP; long term potentiation; Nt; nucleotide; UTR; untranslated region; DAVID; Database for Annotation, Visualization and Integrated Discovery; CAG; cytosine-adenosine-guanosine; RefSeq; NCBI Referenc
Towards the elucidation of the regulatory network guiding the insulin producing cells' differentiation
Keywords: NGN3 (NEUROG3); neurogenin3; ESCs; Embryonic Stem Cells; TFBS; Transcription Factor Binding Sites; TFs; Transcription Factors; AP4 (TFAP4); Activating enhancer-binding Protein 4 (Transcription Factor AP-4); WISP1; WNT-Induced Secreted Protein 1; CTGF; Con
Genomic profiling of B-progenitor acute lymphoblastic leukemia
Keywords: ALL; acute lymphoblastic leukemia; genomic profiling; B-progenitor; IKZF1; BCR-ABL1-like; PAX5; JAK1/2; CRLF2; CREBBP
CREBBP Re-arrangements affect protein function and lead to aberrant neuronal differentiation
Keywords: CREBBP; Rubinstein–Taybi syndrome; Mental retardation; Neuronal differentiation; NT2TFs, transcription factors; CREBBP, c-AMP responsive element binding protein; RSTS, Rubinstein–Taybi syndrome; NT2, NTERA2-clone D1; ATRA, all-trans retinoic acid; CREB, c