Met Receptor Inhibitor SU11274 Localizes in the Endoplasmic Reticulum

We discovered that SU11274, a class I c-Met inhibitor, fluoresces when excited by 488 nm laser light and showed rapid specific accumulation in distinct subcellular compartments. Given that SU11274 reduces cancer cell viability, we exploited these newly identified spectral properties to determine SU11274 intracellular distribution and accumulation in human pancreatic cancer cells. The aim of the studies reported here was to identify organelle(s) to which SU11274 is trafficked. We conclude that SU11274 rapidly and predominantly accumulates in the endoplasmic reticulum

Molecular analysis of intragenic recombination at the tryptophan synthetase locus in Neurospora crassa

Fifteen different classically generated and mapped mutations at the tryptophan synthetase locus in Neurospora crassa have been characterized to the level of the primary sequence of the gene. This sequence analysis has demonstrated that intragenic recombination is accurate to order mutations within one open reading frame. While classic genetic analysis correctly ordered the mutations, the position of mutations characterized by gene sequence analysis was more accurate. A leaky mutation was found to have a wild-type primary sequence. The presence of unique polymorphisms in the primary sequence of the trp-3 gene from strain 861 confirms that it has a unique history relative to the other strains studied. Most strains that were previously shown to be immunologically nonreactive with antibody preparations raised against tryptophan synthetase protein were shown to have nonsense mutations. This work defines 14 alleles of the N. crassa trp-3 gene.Citation: "Molecular analysis of intragenic recombination at the tryptophan synthetase locus in Neurospora crassa" (December 2013) A. Wiest D. Barchers M. Eaton R. Henderson R. Schnittker K. Mccluskey. Journal of Genetics, Indian Academy of Science. Volume 92 Issue 3. 523-528.Citation: Wiest, A., . . . & McCluskey, K. (2013). Molecular analysis of intragenic recombination at the tryptophan synthetase locus in Neurospora crassa. Journal of Genetics, 92(1), 523–528. https://doi.org/https://doi.org/10.1007/s12041-013-0305-

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The neuronal correlates of mirror illusion in children with spastic hemiparesis: a study with functional magnetic resonance imaging.

To investigate the neuronal activation pattern underlying the effects of mirror illusion in children/adolescents with normal motor development and in children/adolescents with hemiparesis and preserved contralateral corticospinal organisation. The type of cortical reorganisation was classified according to results of transcranial magnetic stimulation. Only subjects with congenital lesions and physiological contralateral cortical reorganisation were included. Functional magnetic resonance imaging was performed to investigate neuronal activation patterns with and without a mirror box. Each test consisted of a unimanual and a bimanual motor task. Seven children/adolescents with congenital hemiparesis (10-20 years old, three boys and four girls) and seven healthy subjects (8-17 years old, four boys and three girls) participated in this study. In the bimanual experiment, children with hemiparesis showed a significant effect of the mirror illusion (p<0.001 at voxel level, family-wise error corrected at cluster level) in the dorsolateral prefrontal cortex and anterior cingulate cortex of the affected and unaffected hemispheres, respectively. No significant effects of the mirror illusion were observed in unimanual experiments and in healthy participants. Mirror illusion in children/adolescents with hemiparesis leads to activation of brain areas involved in visual conflict detection and cognitive control to resolve this conflict. This effect is observed only in bimanual training. We consider that for mirror therapy in children and adolescents with hemiparesis a bimanual approach is more suitable than a unimanual approach

The Archaeology of First World War U-boat Losses in the English Channel and its Impact on the Historical Record

This paper examines how the archaeological record of 35 known U-boat wrecks sunk in WW1 in the English Channel compares with the assessment of U-boat destructions made by the Admiralty’s Antisubmarine Division (ASD) in 1919. Comparison of the two shows that only 48% of the 37 assessments was correct. This divergence between the extant archaeology and the 1919 assessment was partly caused by over optimism at ASD regarding reported attacks. However, it is also observed that ASD’s own processes were on occasion overridden by a need to overstate Allied successes, and should be seen in the broader context of a wider range of inefficiencies that confronted the Naval Staff during WW1. The same mistakes seem entirely absent from the WW2 records in the same geographical area. The research reveals that the radio silence observed by the Flanders Flotilla proved a challenge to combating its U-boats at sea, making the tracking of the U-boats and the rerouting of Allied ships practically impossible. This was a factor in the early adoption of “controlled sailings” in the Channel. It may have also been the driving factor behind the Navy’s pressure to attack the Flanders bases by land in 1917, a key component often overlooked by historians

Comparison of the solophenyl-red polarization method and the immunohistochemical analysis for collagen type III

In the present study, we have compared the staining pattern of the Solophenyl-Red 3 BL-method for the visualization of collagen type III with the immunohistochemical staining in serial sections from 7 skin wounds (wound age 3 days up to 4 weeks) to elucidate the specifity of the histochemical staining method. Large amounts of collagen type III were clearly detectable in the investigated wounds using the immunohistochemical technique. In the sections stained with Solophenyl-Red, however, only 3 out of 7 skin lesions showed a significant positive red staining at the wound margin or in the granulation tissue, while the adjacent normal connective tissue revealed a typical intensive staining. Using polarization microscopy no characteristic bright green fibrils, as reported for collagen type 111, could be seen in the wound areas without positive Solophenyl-Red staining. Since the localization of collagen type III detected by immunohistochemistry and the presumed distribution of this collagen type by the Solophenyl-Red method was not identical, the histochemical polarization method has to be regarded as non-specific for visualization of this collagen type