Results 31 to 40 of about 2,687 (150)

An Aerodynamic Optimization Approach for Wind Turbine Blades Using Proper Generalized Decomposition

open access: yesEnergies
A new approach for optimizing the blade profile of a horizontal axis wind turbine is proposed in this paper, based on the combination of the Blade Element Momentum (BEM) method and Proper Generalized Decomposition (PGD).
Nacer Eddine Boumezbeur, Arezki Smaili
doaj   +1 more source

Identification of circulating miRNAs differentially expressed in patients with Limb-girdle, Duchenne or facioscapulohumeral muscular dystrophies

open access: yesOrphanet Journal of Rare Diseases, 2022
Background Limb-girdle muscular dystrophy (LGMD) is a rare neuromuscular disease including a growing and heterogeneous number of subtypes with variable phenotype.
José Luis García-Giménez   +8 more
doaj   +1 more source

Bio‐inspired vision: From principle, material architectures to system‐level integration

open access: yesFlexMat, EarlyView.
This review introduces the development and mechanism of electronic and ionic bio‐inspired vision devices respectively. Then, it explores the impact of structure on bio‐inspired visual performance from the scale of intrinsic materials and device. Finally, it concludes that only by combining advanced software and technology can more complex vision ...
Zewan Lin   +4 more
wiley   +1 more source

Combined sequence and copy number analysis improves diagnosis of limb girdle and other myopathies

open access: yesAnnals of Clinical and Translational Neurology, 2023
Objective Clinical and genetic heterogeneities make diagnosis of limb‐girdle muscular dystrophy (LGMD) and other overlapping disorders of muscle weakness complicated and expensive.
Babi R. R. Nallamilli   +8 more
doaj   +1 more source

With Regard to the Expression Status of Sarcolemmal Aquaporin 4 in Human Muscular Dystrophies

open access: yesNeurology and Clinical Neuroscience, EarlyView.
ABSTRACT Human muscular dystrophies are inherited muscle‐wasting diseases caused by the various kinds of gene mutations. Among them, Duchenne muscular dystrophy (DMD) is a representative type. Before the discovery of the causative dystrophin gene of DMD, the fragile myofiber plasma membrane was thought to be the trigger of myofiber necrosis in DMD ...
Yoshihiro Wakayama, Takahiro Jimi
wiley   +1 more source

Genetic and phenotypic characteristics of 3 patients with limb-girdle muscular dystrophy: experience in a medical center in Mexico

open access: yesEgyptian Journal of Medical Human Genetics
Introduction Limb-girdle muscular dystrophy (LGMD) is a heterogeneous group of genetically inherited muscular disorders. Due to the inherent phenotypic variation among different LGMD forms, clinical diagnosis remains challenging.
Valentina Martínez-Montoya   +4 more
doaj   +1 more source

Proteomic Profiling of Myofiber Repair Annexins and Their Role in Duchenne Muscular Dystrophy

open access: yesPROTEOMICS, EarlyView.
ABSTRACT Myofiber regeneration and membrane repair play crucial roles in maintaining the continuous physiological functioning of the neuromuscular system. A swift and efficient repair mechanism enables the rapid restoration of sarcolemmal integrity following cellular impairment in damaged skeletal muscles.
Paul Dowling   +6 more
wiley   +1 more source

Limb-Girdle Muscular Dystrophies (LGMD): Clinical features, diagnosis and genetic variability through next generation sequencing

open access: yesGlobal Medical Genetics
Background: Limb-Girdle Muscular Dystrophy (LGMD) is a rare heterogeneous group of neuromuscular disorders distinguished by progressive weakness of limb-girdle muscles.
Priyanshu Mathur   +5 more
doaj   +1 more source

Diagnostic utility of inflammatory markers in formalin‐fixed and paraffin‐embedded muscle biopsies for idiopathic inflammatory myopathies

open access: yesHistopathology, EarlyView.
Formalin‐fixed, paraffin‐embedded (FFPE) muscle tissue supports robust immunohistochemical detection of MHC II, MxA, and p62 with performance comparable to frozen sections. This approach reliably identifies the pathological signatures of inclusion body myositis, dermatomyositis, immune‐mediated necrotizing myopathy, and overlap myositis, enhancing the ...
Chinnawut Suriyonplengsaeng   +1 more
wiley   +1 more source

An Engineering Approach to Improve Performance Predictions for Wind Turbine Applications: Comparison with Full Navier-Stokes Model and Experimental Measurements [PDF]

open access: yesJournal of Applied Fluid Mechanics
Accurate predictions of aerodynamic performance and near wake expansion around Horizontal Axis Wind Turbine (HAWT) rotors is pivotal for studying wind turbine wake interactions and optimizing wind farm layouts.
M. N. Hamlaoui   +3 more
doaj   +1 more source

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