Nature of oxygen vacancy in accelerating redox kinetics of V/V in flow batteries.

The rational design of oxygen vacancy in metal oxide based catalysts is an effective strategy to enhance their intrinsic activity by influencing the microelectronic structure. However, the impact of oxygen vacancy on the reaction kinetics and the catalytic mechanism in vanadium redox flow batteries (VRFBs) remains under-explored. Herein, a novel approach is developed to regulate the concentration of oxygen vacancy in TiO nanoplates for high performance VRFBs.

Triglyceride-glucose index, renal function and cardiovascular disease: a national cohort study.

Background: The triglyceride-glucose (TyG) index is a predictor of cardiovascular diseases; however, to what extent the TyG index is associated with cardiovascular diseases through renal function is unclear. This study aimed to evaluate the complex association of the TyG index and renal function with cardiovascular diseases using a cohort design.

Methods: This study included participants from the China Health and Retirement Longitudinal Study (CHARLS) free of cardiovascular diseases at baseline.

The Role of Proton in High Power Density Vanadium Redox Flow Batteries.

To design high-performance vanadium redox flow batteries (VRFBs), the influence of proton on electrocatalysts cannot be neglected considering the abundance of proton in a highly acidic electrolyte. Herein, the impact of proton on metal oxide-based electrocatalysts in VRFBs is investigated, and a proton-incorporating strategy is introduced for high power density VRFBs, in addition to unraveling the catalytic mechanism. This study discloses that the metal oxide-based electrocatalyst (WO) undergoes surface reconstruction by forming HWO after incorporating proton.

Abnormal brain activities in multiple frequency bands in Parkinson's disease with apathy.

Background: Apathy is among the most prevalent and incapacitating non-motor symptoms of Parkinson's disease (PD). PD patients with apathy (PD-A) have been reported to have abnormal spontaneous brain activity mainly in 0.01-0.

Association Between Osseointegration of Lower Extremity Amputation and Mortality Among Adults.

Importance: Transcutaneous osseointegration post amputation (TOPA) creates a direct linkage between residual bone and an external prosthetic limb, providing superior mobility and quality of life compared with a socket prosthesis. The causes and potential risks of mortality after TOPA have not been investigated.

Objective: To investigate the association between TOPA and mortality and assess the potential risk factors.

Non-invasive physical therapy as salvage measure for ischemic skin flap: A literature review.

This review focuses on the available evidence regarding the molecular mechanisms and treatment potential of several non-surgical physical therapies for managing flap ischemia to propose a non-invasive, economical, and simple treatment to improve flap survival. A review of the literature was conducted on the topics of various non-invasive methods for the treatment of ischemic necrosis of the distal end of the flap between 1988 and 2019. A total of 52 published studies were reviewed on the applications of hyperbaric oxygen therapy, electrical stimulation therapy, heat stress pretreatment, phototherapy, and vibration therapy to manage skin flap necrosis.

Gold nanorods or nanospheres? Role of particle shape on tuning the shape memory effect of semicrystalline poly(ε-caprolactone) networks.

In this study, modified poly(ε-caprolactone) (PCL) tri-block copolymers were successfully synthesized through ring opening polymerization. The nanocomposite films containing either colloidal gold nanorods (AuNRs) or gold nanospheres (AuNSs) in the polymer matrix were fabricated without chemical modification to realize light-responsive shape memory behaviors. The localized surface plasmon resonance of AuNPs was utilized by irradiating the selective wavelength of light to create a photothermal effect.

Complete androgen insensitivity syndrome caused by c.1769-1G > C mutation and activation of a cryptic splice acceptor site in the androgen receptor gene.

Androgen insensitivity syndrome (AIS) is the most common cause of 46,XY disorders of sex development (46,XY DSD). This syndrome is an X-linked recessive genetic disease characterized by resistance to the actions of androgens in an individual with a male karyotype and it is caused by mutations in the androgen receptor (AR) gene. We evaluated two siblings with primary amenorrhea, normal secondary sex characteristics, absence of uterus and ovaries, intra-abdominal testis, and elevated testosterone levels.

Mutational analysis of the androgen receptor gene in two Chinese families with complete androgen insensitivity syndrome.

Androgens are essential for normal male sex differentiation and are responsible for the normal development of male secondary sexual characteristics at puberty. The physiological effects of androgens are mediated by the androgen receptor (AR). Mutations in the AR gene are the most common cause of androgen insensitivity syndrome.

Identification of a novel frameshift mutation of the gene in a family with multiple osteochondroma.

Multiple osteochondroma (MO), also known as multiple hereditary exostoses, is an autosomal dominant skeletal disorder with characteristic multiple cartilage-capped tumours (osteochondromas or exostoses) growing outward from the metaphyseal region of the long tubular bones. Mutations in exostosin glycosyltransferase 1 () or are the most commonly associated mutations with MO and are responsible for 70-95% of cases. In the present study, a genetic analysis was performed on a large family with MO using polymerase chain reaction and direct DNA sequencing of the entire coding regions of and .