Results 31 to 40 of about 208,269 (282)

Error correction in the transmission and processing of information, provided in RNS, by method of syndrome decoding

open access: yesНаука. Инновации. Технологии, 2022
In article conducted the development of the method of syndrome decoding error correction codes in the RNS, based on the method of expanding the bases RNS. Presents the basics of excess RNS.
Nikolay Ivanovich Chervyakov   +1 more
doaj  

Association of treatment satisfaction and psychopathological sub-syndromes among involuntary patients with psychotic disorders [PDF]

open access: yes, 2011
Publisher's version: http://www.springerlink.com/content ...
A Luszczynska   +34 more
core   +1 more source

Syndrome Measurement Strategies for the [[7,1,3]] Code

open access: yes, 2015
Quantum error correction (QEC) entails the encoding of quantum information into a QEC code space, measuring error syndromes to properly locate and identify errors, and, if necessary, applying a proper recovery operation.
Weinstein, Yaakov S.
core   +1 more source

Changes in Body Composition in Children and Young People Undergoing Treatment for Acute Lymphoblastic Leukemia: A Systematic Review and Meta‐Analysis

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Ongoing evidence indicates increased risk of sarcopenic obesity among children and young people (CYP) with acute lymphoblastic leukemia (ALL), often beginning early in treatment, persisting into survivorship. This review evaluates current literature on body composition in CYP with ALL during and after treatment.
Lina A. Zahed   +5 more
wiley   +1 more source

Clinical Characteristics and Prognostic Risk Factors for Pediatric B‐Cell Lymphoblastic Lymphoma: A Multicenter Retrospective Cohort Study for China Net Childhood Lymphoma

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background B‐cell lymphoblastic lymphoma (B‐LBL) represents a rare variety of non‐Hodgkin lymphoma, with limited research on its biology, progression, and management. Methods A retrospective analysis was performed on the clinical characteristics of 256 patients aged ≤18 years who received treatment under the China Net Childhood Lymphoma (CNCL)‐
Zhijuan Liu   +20 more
wiley   +1 more source

A TWO-STAGE APPROACH FOR COMBINING GENE EXPRESSION AND MUTATION WITH CLINICAL DATA IMPROVES SURVIVAL PREDICTION IN MYELODYSPLASTIC SYNDROMES AND OVARIAN CANCER

open access: yesJournal of Bioinformatics and Genomics, 2016
Motivation: Many traditional clinical prognostic factors have been known for cancer for years, but usually provide poor survival prediction. Genomic information is more easily available now which offers opportunities to build more accurate prognostic ...
Yan Li   +7 more
doaj   +1 more source

Optimal correction of concatenated fault-tolerant quantum codes

open access: yes, 2011
We present a method of concatenated quantum error correction in which improved classical processing is used with existing quantum codes and fault-tolerant circuits to more reliably correct errors.
A. Kitaev   +18 more
core   +1 more source

The role of histone modifications in transcription regulation upon DNA damage

open access: yesFEBS Letters, EarlyView.
This review discusses the critical role of histone modifications in regulating gene expression during the DNA damage response (DDR). By modulating chromatin structure and recruiting repair factors, these post‐translational modifications fine‐tune transcriptional programmes to maintain genomic stability.
Angelina Job Kolady, Siyao Wang
wiley   +1 more source

Effect of ancilla's structure on quantum error correction using the 7-qubit Calderbank-Shor-Steane code

open access: yes, 2004
In this work we discuss the ability of different types of ancillas to control the decoherence of a qubit interacting with an environment. The error is introduced into the numerical simulation via a depolarizing isotropic channel.
A. L. Sanz   +5 more
core   +1 more source

Structural instability impairs function of the UDP‐xylose synthase 1 Ile181Asn variant associated with short‐stature genetic syndrome in humans

open access: yesFEBS Letters, EarlyView.
The Ile181Asn variant of human UDP‐xylose synthase (hUXS1), associated with a short‐stature genetic syndrome, has previously been reported as inactive. Our findings demonstrate that Ile181Asn‐hUXS1 retains catalytic activity similar to the wild‐type but exhibits reduced stability, a looser oligomeric state, and an increased tendency to precipitate ...
Tuo Li   +2 more
wiley   +1 more source

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