Results 151 to 160 of about 58,892 (378)

TINF2 Gene Mutation in a Patient with Pulmonary Fibrosis

open access: yesCase Reports in Pulmonology, 2016
Pulmonary fibrosis is a frequent manifestation of telomere syndromes. Telomere gene mutations are found in up to 25% and 3% of patients with familial disease and sporadic disease, respectively. The telomere gene TINF2 encodes an eponymous protein that is
T. W. Hoffman   +6 more
doaj   +1 more source

EFTUD2 Regulates Cortical Morphogenesis via Modulation of Caspase‐3 and Aifm1 Splicing Pathways

open access: yesAdvanced Science, EarlyView.
EFTUD2, a spliceosomal GTPase linked to MFDM, regulates cortical development through apoptotic control. Conditional Eftud2 knockout in murine neural stem cells induces microcephaly and cortical disorganization, while pathogenic variants drive neuronal loss.
Liping Chen   +12 more
wiley   +1 more source

Correction of Data and Syndrome Errors by Stabilizer Codes [PDF]

open access: yesarXiv, 2016
Performing active quantum error correction to protect fragile quantum states highly depends on the correctness of error information--error syndromes. To obtain reliable error syndromes using imperfect physical circuits, we propose the idea of quantum data-syndrome (DS) codes that are capable of correcting both data qubits and syndrome bits errors.
arxiv  

The Immune Microenvironment: New Therapeutic Implications in Organ Fibrosis

open access: yesAdvanced Science, EarlyView.
This review summarizes recent advances in understanding the immune microenvironment's role in fibrosis, focusing on phenotypic/functional alterations of immune cells and their dynamic interactions with other cellular constituents within tissues. The authors further explore therapeutic opportunities and challenges in targeting immune microenvironment ...
Xiangqi Chen   +6 more
wiley   +1 more source

Chronic Exertional Compartment Syndrome in a High School Soccer Player

open access: yesCase Reports in Orthopedics, 2015
Chronic exertional compartment syndrome (CECS) is a relatively rare condition that affects young adult athletes and often causes them to present to the emergency department.
James J. Bresnahan, William L. Hennrikus
doaj   +1 more source

A High-Performance List Decoding Algorithm for Surface Codes with Erroneous Syndrome [PDF]

open access: yesarXiv
Quantum error-correcting codes (QECCs) are necessary for fault-tolerant quantum computation. Surface codes are a class of topological QECCs that have attracted significant attention due to their exceptional error-correcting capabilities and easy implementation.
arxiv  

Learning from the Syndrome [PDF]

open access: yesarXiv, 2018
In this paper, we introduce the syndrome loss, an alternative loss function for neural error-correcting decoders based on a relaxation of the syndrome. The syndrome loss penalizes the decoder for producing outputs that do not correspond to valid codewords.
arxiv  

Flexible intramedullary nailing in the treatment of diaphyseal fractures of the femur in preschool children [PDF]

open access: yes, 2008
Femur fractures in preschool children are mostly treated in a conservative way, by means of spica cast immobilisation or skin traction. In school age children the use of flexible intramedullary nails (FIN) is widely used and promoted.
De Ridder, Koen, MORTIER, DIETER
core   +1 more source

Mesenteric thrombosis: An unusual complication of severe acute pancreatitis—Report of two cases

open access: yesAdvances in Digestive Medicine, EarlyView.
Abstract The incidence of acute pancreatitis is 34 per 100 000 people in the general population and is on the rise. Approximately 15% to 20% of all patients experience severe pancreatitis, with a mortality rate nearing 20%. This condition is often linked to vascular complications, although mesenteric thrombosis is a rare presentation.
Asya Zubillaga‐Mares   +5 more
wiley   +1 more source

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