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18 results with keyword: 'computational biology acute myeloid leukemia cebpa abnormalities'

Computational Biology in Acute Myeloid Leukemia with CEBPA Abnormalities

To compare different methods and to analyze the promoter array data, we made use of a dataset that was obtained from a ChIP of beta-estradiol induced C/EBPα in a

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2021
>Challenges faced by the travel and transportation industry

 Maximum Size: 1 month of revenue data  Compute Time: 3-10 min.. Compute Time

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2021
A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome

+: trisomy; ACAs: Acquired chromosomal abnormalities; AMKL: Acute megakaryoblastic leukemia; AML: Acute myeloid leukemia; del: deletion; der: derivative; DS: Down syndrome;

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2020
Bonamia ostreae in the Native Oyster Ostrea edulis

Comparison of light microscopic techniques for the diagnosis of the infection of the European flat oyster Ostrea edulis by the protozoan Bonamia ostreae.. Cochennec-Laureau

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2021
Mutational spectrum of acute myeloid leukemia patients with double

The aim of this study was to profile the spectrum of genetic mutations in acute myeloid leukemia (AML) patients co-occurring with CEBPA double mutation (CEBPA dm ).. Out of these,

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2020
Nanopore targeted sequencing for rapid gene mutations detection in acute myeloid leukemia

Keywords: nanopore targeted sequencing; acute myeloid leukemia; mutational analysis; FLT3 internal tandem duplications; biallelic CEBPA mutations1. Recurring molecular lesions

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2021
Investigation of CEBPA and CEBPA-AS Genes Expression in Acute Myeloid Leukemia

Furthermore, the prognosis of patients with AML has been associated with CEBPA mRNA expression levels in patients with an intermediate- risk karyotype.. Significant

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2020
Quantitative Assessment of WT1 Expression by Real Time Quantitative PCR in Pediatric Patients with Acute Myeloblastic Leukemia

Prognostic significance of, and gene and microRNA expression signatures associated with, CEBPA mutations in cytogenetically normal acute myeloid leukemia with high-risk

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2020
A 3-miRNA signature predicts prognosis of pediatric and adolescent cytogenetically normal acute myeloid leukemia

Prognostic significance of, and gene and microRNA expression signatures associated with, CEBPA mutations in cytogenetically normal acute myeloid leukemia with high- risk

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2020
Down syndrome associated childhood myeloid leukemia with yet unreported acquired chromosomal abnormalities and a new potential adverse marker: dup(1)(q25q44)

ACAs: Additional cytogenetic abnormalities; aMCB: Array-proven high-resolution multicolor banding; AMKL: Acute megakaryoblastic leukemia; AML: Acute myeloid leukemia; DAPI: 4 ′

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2020
Demand Response Opportunities and Enabling Technologies for Data Centers: Findings from Field Studies

The results from the implementation of manual DR strategies for both IT equipment (server, storage) and site infrastructure (cooling) identified that similar data centers

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2021
SETBP1 dysregulation in congenital disorders and myeloid neoplasms

childhood Acute Myeloid Leukemia; sAML, secondary Acute Myeloid Leukemia; AML, Acute Myeloid Leukemia; t-MN, therapy-related Myeloid Neoplasms; MPN, Myeloproliferative

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2020
Achieving Regulatory Success: Areas of focus for biotechnology companies. Michael J. Schlosser, PhD, DABT April 21, 2013

• Understanding regulatory guidances and their level of enforcement is critical for not being under or over compliant. • Incorporate available predictive tools

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Original Article Double CEBPA mutations are prognostically favorable in non-M3 acute myeloid leukemia patients with wild-type NPM1 and FLT3-ITD

Monoallelic CEBPA mutations in normal karyotype acute myeloid leukemia: indepen- dent favorable prognostic factor within NPM1 mutated patients. CEB- PA single mutation can be

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2020
The Philadelphia chromosome in leukemogenesis

Ph: Philadelphia chromosome; CML: chronic myeloid leukemia; ALL: acute lymphoblastic leukemia; AML: acute myeloid leukemia; MPAL: mixed‑pheno‑ type acute leukemia; TK: tyrosine

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Weth, Verena
  

(2015):


	Untersuchungen zur Rolle der Rezeptortyrosinkinasen FLT3, DDR1 und DDR2 in der akuten myeloischen Leukämie.


Dissertation, LMU München: Medizinische Fakultät

Port, M., et al., Prognostic significance of FLT3 internal tandem duplication, nucleophosmin 1, and CEBPA gene mutations for acute myeloid leukemia patients with normal karyotype and

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2020
Genetic Characterization and Risk Stratification of Acute Myeloid Leukemia

Acute myeloid leukemia with biallelic CEBPA gene mutations and normal karyotype represents a distinct genetic entity associated with a favorable clinical outcome. Bakshi SR,

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2020
Landscape of gene fusions in epithelial cancers: seq and ye shall find

ACC: Adenoid cystic carcinoma; ALL: Acute lymphoblastic leukemia; AML: Acute myeloid leukemia; APL: Acute promyelocytic leukemia, cholangio cholangiocarcinoma; CML: Chronic

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2020

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