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Open AccessTRIM32 biallelic defects cause limb-girdle muscular dystrophy R8: identification of two novel mutations and investigation of genotype–phenotype correlation
Limb-girdle muscular dystrophy R8 (LGMD R8) is a rare autosomal recessive muscle disease caused by TRIM32 gene biallelic defects. The genotype–phenotype correlation of this disease has been reported poorly. He...
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Erratum to: Experimental Study on Key Parameters of Bidirectional Cumulative Tensile Blasting with Coal-Containing Composite Roof
This erratum is published to notify a correction in first author’s name.
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Open AccessProgrammable graphene nanobubbles with three-fold symmetric pseudo-magnetic fields
Graphene nanobubbles (GNBs) have attracted much attention due to the ability to generate large pseudo-magnetic fields unattainable by ordinary laboratory magnets. However, GNBs are always randomly produced by ...
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Article
Open AccessOverstep** the upper refractive index limit to form ultra-narrow photonic nanojets
In general, photonic nanojets (PNJs) occur only when the refractive index (Ri) difference between the microparticle and background media is less than 2. The minimum full width at half-maximum (FWHM) of the PNJ is...
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Open AccessPolymorphisms of the IL27 gene in a Chinese Han population complicated with pre-eclampsia
IL-27 could inhibit the development of Th17 cells, and the Th17/regulatory T-cell imbalance may reverse maternal tolerance in pre-eclampsia (PE). The aim of this study was to investigate the association betwee...
