Pulsed high magnetic field measurement via a Rubidium vapor sensor

We present a new technique to measure pulsed magnetic fields based on the use of Rubidium in gas phase as a metrological standard. We have therefore developed an instrument based on laser inducing transitions at about 780~nm (D2 line) in a Rubidium gas contained in a mini-cell of 3~mm~x~3~mm cross section. To be able to insert such a cell in a standard high field pulsed magnet we have realized a fibred probe kept at a fixed temperature. Transition frequencies for both the $\pi$ (light polarization parallel to the magnetic field) and $\sigma$ (light polarization perpendicular to the magnetic field) configurations are measured by a commercial wavemeter. One innovation of our sensor is that in addition of monitoring the light transmitted by the Rb cell, which is usual, we also monitor the fluorescence emission of the gas sample from a very small volume with the advantage of reducing the impact of the field inhomogeneity on the field measurement. Our sensor has been tested up to about 58~T.Comment: Submitted to Review Scientific Instrument

Impact of surface electric properties of carbon-based thin films on platelets activation for nano-medical and nano-sensing applications

Electric surface properties of biomaterials, playing key role to various biointerfacial interactions, were related to hemocompatibility and biosensing phenomena. In this study, the examination of surface electric properties of amorphous hydrogenated carbon thin films (a-C:H) was carried out by means of electrostatic force microscope (EFM) and observation of differences in spatial charge distribution on the surface of the examined films during platelets adhesion was made. The thrombogenic potential of a-C:H thin films developed by magnetron sputtering with ~42% sp3 content and hydrogen partial pressure during deposition was evaluated, by in situ observation with atomic force microscope (AFM) of platelets’ activation and their subsequent adhesion. Platelet-rich plasma drawn from healthy donors was used and semi-contact mode of AFM was applied. Platelets behavior and their correlation with the electric surface properties of the examined a-C:H films by EFM was made for hemocompatibility enhancement and sensing platelets that are less electrical negatively charged and with higher tendency to aggregate and form thrombus. The results are discussed in view of the effect of different deposition conditions of hydrogenated carbon films on their structural and morphological characteristics, surface roughness and electrical properties attributing to different hemocompatibility and sensing aspects

Grandparents as Foster Parents: Psychological Distress, Commitment, and Sensitivity to their Grandchildren

Grandparents are increasingly solicited to become foster parents. This study aims to describe the psychological distress, parental sensitivity, and parental commitment of a group of Quebec foster grandparents. Forty-eight foster parents were assessed in this study, including 12 grandparents. Psychological distress was assessed using the Symptom Checklist–90–R (SCL–90–R®; Derogatis & Lazarus 1994), parental sensitivity using the short version of the Maternal Behavior Q-Sort (Tarabulsy et al., 2009; Pederson & Moran, 1995) and commitment using a semi-structured interview (This is My Baby; TIMB: Bates & Dozier, 1998). Results indicate no difference between foster parents and grandparents as a function of parental characteristics, sensitivity and commitment. However, results show an association between grandparent status and depressive symptoms even after controlling for family income and child externalization. Challenges faced by foster grandparents are discussed as well as their need of support from child welfare protection

A bacteria-specific 2[4Fe-4S] ferredoxin is essential in Pseudomonas aeruginosa

<p>Abstract</p> <p>Background</p> <p>Ferredoxins are small iron-sulfur proteins belonging to all domains of life. A sub-group binds two [4Fe-4S] clusters with unequal and extremely low values of the reduction potentials. These unusual properties are associated with two specific fragments of sequence. The functional importance of the very low potential ferredoxins is unknown.</p> <p>Results</p> <p>A bioinformatic screening of the sequence features defining very low potential 2[4Fe-4S] ferredoxins has revealed the almost exclusive presence of the corresponding <it>fdx </it>gene in the <it>Proteobacteria </it>phylum, without occurrence in <it>Archaea </it>and <it>Eukaryota</it>. The transcript was found to be monocistronic in <it>Pseudomonas aeruginosa</it>, and not part of an operon in most bacteria. Only <it>fdx </it>genes of bacteria which anaerobically degrade aromatic compounds belong to operons. As this pathway is not present in all bacteria having very low potential 2[4Fe-4S] ferredoxins, these proteins cannot exclusively be reductants of benzoyl CoA reductases. Expression of the ferredoxin gene did not change in response to varying growth conditions, including upon macrophage infection or aerobic growth with 4-hydroxy benzoate as carbon source. However, it increased along the growth curve in <it>Pseudomonas aeruginosa </it>and in <it>Escherichia coli</it>. The sequence immediately 5' upstream of the coding sequence contributed to the promotor activity. Deleting the <it>fdx </it>gene in <it>Pseudomonas aeruginosa </it>abolished growth, unless a plasmid copy of the gene was provided to the deleted strain.</p> <p>Conclusions</p> <p>The gene of the very low potential 2[4Fe-4S] ferredoxin displays characteristics of a housekeeping gene, and it belongs to the minority of genes that are essential in <it>Pseudomonas aeruginosa</it>. These data identify a new potential antimicrobial target in this and other pathogenic <it>Proteobacteria</it>.</p

Electronic structure of indium selenide probed by magnetoabsorption spectroscopy under high pressure

We report on an investigation of the peculiar electronic structure of the layered semiconductor InSe by magneto-optical experiments under high pressure up to 5 GPa. Magneto-absorption spectroscopy is performed under pulsed magnetic field up to 53 T using a specific setup. Excitonic magnetofingerprints and high-field oscillatory magnetoabsorption yield significant details on the band structure. In addition, the application of an external pressure unveils phenomena that confirm the specific k·p model proposed for this compound on the basis of earlier measurements

Distinct regions of RPB11 are required for heterodimerization with RPB3 in human and yeast RNA polymerase II

In Saccharomyces cerevisiae, RNA polymerase II assembly is probably initiated by the formation of the RPB3–RPB11 heterodimer. RPB3 is encoded by a single copy gene in the yeast, mouse and human genomes. The RPB11 gene is also unique in yeast and mouse, but in humans a gene family has been identified that potentially encodes several RPB11 proteins differing mainly in their C-terminal regions. We compared the abilities of both yeast and human proteins to heterodimerize. We show that the yeast RPB3/RPB11 heterodimer critically depends on the presence of the C-terminal region of RPB11. In contrast, the human heterodimer tolerates significant changes in RPB11 C-terminus, allowing two human RPB11 variants to heterodimerize with the same efficiency with RPB3. In keeping with this observation, the interactions between the conserved N-terminal ‘α-motifs’ is much more important for heterodimerization of the human subunits than for those in yeast. These data indicate that the heterodimerization interfaces have been modified during the course of evolution to allow a recent diversification of the human RPB11 subunits that remains compatible with heterodimerization with RPB3

A human RNA polymerase II subunit is encoded by a recently generated multigene family

BACKGROUND: The sequences encoding the yeast RNA polymerase II (RPB) subunits are single copy genes. RESULTS: While those characterized so far for the human (h) RPB are also unique, we show that hRPB subunit 11 (hRPB11) is encoded by a multigene family, mapping on chromosome 7 at loci p12, q11.23 and q22. We focused on two members of this family, hRPB11a and hRPB11b: the first encodes subunit hRPB11a, which represents the major RPB11 component of the mammalian RPB complex ; the second generates polypeptides hRPB11bα and hRPB11bβ through differential splicing of its transcript and shares homologies with components of the hPMS2L multigene family related to genes involved in mismatch-repair functions (MMR). Both hRPB11a and b genes are transcribed in all human tissues tested. Using an inter-species complementation assay, we show that only hRPB11bα is functional in yeast. In marked contrast, we found that the unique murine homolog of RPB11 gene maps on chromosome 5 (band G), and encodes a single polypeptide which is identical to subunit hRPB11a. CONCLUSIONS: The type hRPB11b gene appears to result from recent genomic recombination events in the evolution of primates, involving sequence elements related to the MMR apparatus

Presence of autism, hyperserotonemia, and severe expressive language impairment in Williams-Beuren syndrome.

International audienceBACKGROUND: Deletion of the Williams-Beuren syndrome (WBS) critical region (WBSCR), at 7q11.23, causes a developmental disorder commonly characterized by hypersociability and excessive talkativeness and often considered the opposite behavioral phenotype to autism. Duplication of the WBSCR leads to severe delay in expressive language. Gene-dosage effects on language development at 7q11.23 have been hypothesized. METHODS: Molecular characterization of the WBSCR was performed by fluorescence in situ hybridization and high-resolution single-nucleotide polymorphism array in two individuals with severe autism enrolled in a genetic study of autism who showed typical WBS facial dysmorphism on systematic clinical genetic examination. The serotonin transporter promoter polymorphism (5-HTTLPR, locus SLC6A4) was genotyped. Platelet serotonin levels and urinary 6-sulfatoxymelatonin excretion were measured. Behavioral and cognitive phenotypes were examined. RESULTS: The two patients had common WBSCR deletions between proximal and medial low copy repeat clusters, met diagnostic criteria for autism and displayed severe impairment in communication, including a total absence of expressive speech. Both patients carried the 5-HTTLPR ss genotype and exhibited platelet hyperserotonemia and low melatonin production. CONCLUSIONS: Our observations indicate that behaviors and neurochemical phenotypes typically associated with autism can occur in patients with common WBSCR deletions. The results raise intriguing questions about phenotypic heterogeneity in WBS and regarding genetic and/or environmental factors interacting with specific genes at 7q11.23 sensitive to dosage alterations that can influence the development of social communication skills. Thus, the influence of WBSCR genes on social communication expression might be dramatically modified by other genes, such as 5-HTTLPR, known to influence the severity of social communication impairments in autism, or by environmental factors, such as hyperserotonemia, given that hyperserotonemia is found in WBS associated with autism but not in WBS without autism. In this regard, WBS provides a potentially fruitful model with which to develop integrated genetic, cognitive, behavioral and neurochemical approaches to study genotype-phenotype correlations, possible gene-environment interactions and genetic background effects. The results underscore the importance of considering careful clinical and molecular genetic examination of individuals diagnosed with autism

Identification of priority areas for plant conservation in Madagascar using Red List criteria: rare and threatened Pandanaceae indicate sites in need of protection

A major problem in establishing effective protocols for conserving Madagascar's biodiversity is the lack of reliable information for the identification of priority sites in need of protection. Analyses of field data and information from herbarium collections for members of the plant family Pandanaceae (85 spp. of Pandanus; 6 spp. of Martellidendron) showed how risk of extinction assessments can inform conservation planning. Application of IUCN Red List categories and criteria showed that 91% of the species are threatened. Mapping occurrence revealed centres of richness and rarity as well as gaps in Madagascar's existing protected area network. Protection of 10 additional sites would be required to encompass the 19 species currently lacking representation in the reserve network, within which east coast littoral forests are particularly under represented and important. The effect of scale on assessments of risk of extinction was explored by applying different grid cell sizes to estimate area of occupancy. Using a grid cell size within the range suggested by IUCN overestimates threatened status if based solely upon specimen data. For poorly inventoried countries such as Madagascar measures of range size based on such data should be complemented with field observations to determine population size, sensitivity to disturbance, and specific threats to habitat and therefore potential population decline. The analysis of such data can make an important contribution to the conservation planning process by identifying threatened species and revealing the highest priority sites for their conservatio