The Ital-FLAMES survey of the Sagittarius dwarf Spheroidal galaxy. I. Chemical abundances of bright RGB stars

We present iron and $\alpha$ element (Mg, Ca, Ti) abundances for a sample of 15 Red Giant Branch stars belonging to the main body of the Sagittarius dwarf Spheroidal galaxy. Abundances have been obtained from spectra collected using the high resolution spectrograph FLAMES-UVES mounted at the VLT. Stars of our sample have a mean metallicity of [Fe/H]=-0.41$\pm$0.20 with a metal poor tail extending to [Fe/H]=-1.52. The $\alpha$ element abundance ratios are slightly subsolar for metallicities higher than [Fe/H]\gtsima-1, suggesting a slow star formation rate. The [$\alpha$/Fe] of stars having [Fe/H]$<$-1 are compatible to what observed in Milky Way stars of comparable metallicity.Comment: 16 pages, 10 figures, 6 tables. Accepted for publication in A&A. Minor changes in the tex

Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland

<p>Abstract</p> <p>Background</p> <p>The 22q11.2 microdeletion syndrome (22q11.2 deletion syndrome -22q11.2DS) refers to congenital abnormalities, including primarily heart defects and facial dysmorphy, thymic hypoplasia, cleft palate and hypocalcaemia. Microdeletion within chromosomal region 22q11.2 constitutes the molecular basis of this syndrome. The 22q11.2 microdeletion syndrome occurs in 1/4000 births. The aim of this study was to determine the frequency of 22q11.2 microdeletion in 87 children suffering from a congenital heart defect (conotruncal or non-conotruncal) coexisting with at least one additional 22q11.2DS feature and to carry out 22q11.2 microdeletion testing of the deleted children's parents. We also attempted to identify the most frequent heart defects in both groups and phenotypic traits of patients with microdeletion to determine selection criteria for at risk patients.</p> <p>Methods</p> <p>The analysis of microdeletions was conducted using fluorescence <it>in situ </it>hybridization (FISH) on metaphase chromosomes and interphase nuclei isolated from venous peripheral blood cultures. A molecular probe (Tuple) specific to the <it>HIRA (TUPLE1, DGCR1</it>) region at 22q11 was used for the hybridisation.</p> <p>Results</p> <p>Microdeletions of 22q11.2 region were detected in 13 children with a congenital heart defect (14.94% of the examined group). Microdeletion of 22q11.2 occurred in 20% and 11.54% of the conotruncal and non-conotruncal groups respectively. Tetralogy of Fallot was the most frequent heart defect in the first group of children with 22q11.2 microdeletion, while ventricular septal defect and atrial septal defect/ventricular septal defect were most frequent in the second group. The microdeletion was also detected in one of the parents of the deleted child (6.25%) without congenital heart defect, but with slight dysmorphism. In the remaining children, 22q11.2 microdeletion originated <it>de novo</it>.</p> <p>Conclusions</p> <p>Patients with 22q11.2DS exhibit wide spectrum of phenotypic characteristics, ranging from discreet to quite strong. The deletion was inherited by one child. Our study suggests that screening for 22q11.2 microdeletion should be performed in children with conotruncal and non-conotruncal heart defects and with at least one typical feature of 22q11.2DS as well as in the deleted children's parents.</p

Probing the helical forms of Ca²⁺-guluronan junction zones in alginate gels by molecular dynamics 1: Duplexes

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Aqueous RAFT polymerization of N-acryloylmorpholine, synthesis of an ABA triblock glycopolymer and study of its self-association behavior

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