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tion with other posttranscriptional regulations such as nonsense and microRNA-mediated decay. A signal transduction network model for alternative splicing in jasmonate signaling pathway was generated, contributing to our understanding for this important, prevalent, but relatively unexplored regulatory mechanism in plants.

Nutrient-level intakes from home-prepared complementary foods are rarely estimated among infants and young children in low-income settings. The major constraints are related to lack of standard recipes and ingredients and portion sizes.

This article describes the feasibility, applicability, and validity of a post hoc qualitative methodology to estimate nutrient intakes in children using 24-h dietary recall.

Semistructured, interviewer-administered caregiver 24-h diet recalls were conducted to assess food intake among children participating in a randomized trial of complementary food supplementation at ages 6, 9, 12, 15, 18, and 24 mo in rural Bangladesh. At the end of the diet data collection, focus group discussions with mothers (

=6) and cooking activities (

=5) were conducted to obtain standard recipes (and ingredients) and portion sizes for reported foods given at different ages. Nutrient intakes were calculated for children in the control group (

=1438), and convergent validity of the data was td contexts. This trial was registered at clinicaltrials.gov as NCT01562379.

We demonstrated the use of a validated, qualitative methodology for estimating nutrient intakes in young children from complementary foods in undernourished contexts. check details This trial was registered at clinicaltrials.gov as NCT01562379.The complexes of TrR3 (Tr = B and Al; R = H, F, Cl, and Br) with three N-bases (NH3, CH2NH, and HCN) and three O-bases (CH3OH, H2CO, and CO) are utilized to explore the hybridization effect of N and O atoms on the strength, properties, and nature of the triel bond. The sp-hybridized O and N atoms form the weakest triel bond, followed by the sp2-hybridized O atom or the sp3-hybridized N atom, and the sp3-hybridized O atom or the sp2-hybridized N atom engages in the strongest triel bond. The hybridization effect is also related to the substituent of TrR3. Most complexes are dominated by electrostatic, with increasing polarization contribution from sp to sp2 to sp3. Although the CO oxygen engages in a weaker triel bond, its carbon atom is a better electron donor and the interaction energy even amounts to -37 kcal/mol in the BH3 complex.A coumarin-appended calixarene derivative ( CouC4A ) and a hybrid material generated by covalently linking this onto a silica surface ( CouC4A@SiO 2 ) were synthesized and were characterized by various analytical, spectroscopy, and microscopy methods. Both these materials are capable of sensing Fe3+ with greater sensitivity and selectivity. The sensitivity is enhanced by 30,000 fold on going from a simple solution phase to the silica surface with the limit of Fe3+ detection being 1.75 ± 0.4 pM when CouC4A@SiO 2 is used, and the sensing is partially reversible with phosphates, while it is completely reversible with adenosine 5′-triphosphate (ATP). While the calix precursor, CouC4A , has a limitation to work in water, anchoring this onto SiO2 endowed it with the benefit of its use in water as well as in buffer and thereby extends its application toward Fe3+ sensing even in the biorelevant medium such as fetal bovine serum and human serum. The hybrid material is biocompatible and shows ∼90% cell viability in the case of MDA-MB231 and 3T3 cell lines. CouC4A@SiO 2 functions as a reversible sensor for Fe3+ with the use of ATP in vitro as well as in biological cells. Thus, the inorganic-organic hybrid material, such as, CouC4A@SiO 2 , is an indispensable material for sensitive and selective detection of Fe3+ in a picomolar range in solution and in nanomolar to micromolar range in biorelevant fluids and biological cells, respectively.Stabilization for tetrylone complexes, which carry ylidone(0) ligands [(CO)5W-X (YCp*)2] (X = Ge, Sn, Pb; Y = B-Tl), has become an active theoretical research because of their promising application. Structure, bonding, and quantum properties of the transition-metal donor-acceptor complexes were theoretically investigated at the level of theory BP86 with several types of basis sets including SVP, TZVPP, and TZ2P+. The optimized structures reveal that all ligands X (YCp*)2 are strongly bonded in tilted modes to the metal fragment W(CO)5, and Cp* rings are mainly η5-bonded to atom X. DFT-based bonding analysis results in an implication that the stability of W-X bond strength primarily stems from the donation (CO)5W ← X(YCp*)2 formed by both σ- and π-bondings and the electrostatic interaction ΔEelstat. The W-X bond possesses a considerable polarizability toward atom X, and analysis on its hybridization is either sp2-characteristic or mainly p-characteristic. EDA-NOCV-based results further imply that the ligands XY perform as significant σ-donors but minor π-donors. The visual simulations of NOCV pairs and the deformation densities assemble a comprehensive summary on different components of the chemical bond via σ- and π-types in the complexes. This work contributes to the literature as an in-depth overview on predicted molecular structures and quantum parameters of the complexes [(CO)5W-X(YCp*)2] (X = Ge, Sn, Pb; Y = B-Tl), conducive to either further theoretical reference or extending experimental research.Crystallized powder of dihydroxide zirconium oxalate Zr(OH)2(C2O4) (ZrOx) was obtained by precipitation and the structure determined from powder X-ray data. The three-dimensional (3D) framework observed in (ZrOx) results from the interconnection of zirconium hydroxide chains 1∞[Zr(OH)2]2+ and zirconium oxalate chains 1∞[Zr(C2O4)2+]. Single crystals of (H11O5)2[Zr2(C2O4)5(H2O)4] (H2Zr2O5) were obtained by evaporation. The structure contains dimeric anions [Zr2(C2O4)5(H2O)4]2- connected through hydrogen bonds to hydroxonium ions (H11O5)+ to create a 3D supramolecular framework. The addition of ammonium or alkali nitrate led to the formation of single crystals of Na2[Zr(C2O4)3]·2H2O (Na2ZrOx3), M(H7O3)[Zr(C2O4)3]·H2O, M = K (KHZrOx3), M = NH4 (NH4HZrOx3), M(H5O2)0.5(H9O4)0.5[Zr(C2O4)3], M = Rb (RbHZrOx3), and M = Cs (CsHZrOx3). For the five compounds, the structure contains ribbons 1∞[ZrOx32-] formed by entities Zr(C2O4)4 sharing two oxalates. In (Na2ZrOx3), the shared oxalates are in cis positions and the chain 1∞[Zr-Ox] is stepped with a Zr-Zr-Zr angle of 98.