Latest papers

Two Australian families with inclusion-body myopathy, Paget's disease of bone and frontotemporal dementia: novel clinical and genetic findings.

The Swedish new variant of Chlamydia trachomatis: genome sequence, morphology, cell tropism and phenotypic characterization.

Ultrastructural aspects of enterocyte defects in infancy and childhood.

Characterization of anthocyanic vacuolar inclusions in Vitis vinifera L. cell suspension cultures.

Interferon-alpha 2b quantification in inclusion bodies using reversed phase-ultra performance liquid chromatography (RP-UPLC).

The high pH and pH-shift refolding technology.

FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion.

Transglutaminase-catalyzed crosslinking in neurological disease: from experimental evidence to therapeutic inhibition.

Development of an artificial chaperone system based on cyclodextrin.

Urea-gradient protein refolding in size exclusion chromatography.

Step-wise refolding of recombinant proteins.

Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder.

Thermal-assisted refolding: dilution folding initiated at high temperature.

Purification and refolding of Escherichia coli-expressed recombinant human interleukin-2.

Non-denaturing solubilization of inclusion bodies.

Fetal akinesia deformation sequence and neuroaxonal dystrophy without PLA2G6 mutation.

Diagnostic pitfalls in parathyroid gland cytology.

The Tobacco etch virus P3 protein forms mobile inclusions via the early secretory pathway and traffics along actin microfilaments

Ground-glass-like hepatocellular inclusions in the course of adult-onset Still's disease.

On track with P-bodies.