Foraminifera of shallow and very shallow facies from the upper Eocene-lower Oligocene Kazandere Member, Soğucak Formation, Thrace Basin, northwest Turkey

The middle-late Eocene to early Oligocene sediments, mainly limestone of the Soğucak Formation with its shallow water marine foraminiferal species occur most widespread in the territory of the Thrace basin. So far, the very shallow water Priabonian sediments with here described foraminiferal species have not been reported from Tharece basin. The here established Kazandere memeber of the Soğurcak Formation located between Kıyıköy andKömürköy,(NW of Kırklarel) was studied with respect to the sedimentologic as (microscopic and macroscopic), environmental and descriptive paleontology of the bentic foraminifers. Furthermore, the Eocene-Oligocene boundary in the new member defined first by the here described very shallow-water Priabonian and known shallow-water early Oligocene foraminiferal species

Foraminifera of shallow and very shallow facies from the upper Eocene–lower Oligocene Kazandere Member, Soğucak Formation, Thrace Basin, northwest Turkey

The middle−upper Eocene to lower Oligocene Kazandere Limestone Member of the Soğucak Formation is widely represented in the Thrace Basin and rich in shallow-water marine foraminifera. Very shallow-water Priabonian facies described here include Borelis vonderschimitti, Borelis laxispira sp. nov., Chapmanina gassinensis, Chapmanina elongate sp. nov., Pfendericonusglobulus sp. nov., Orbitolites minimus,Coscinospira sp. Last occurrences of the aforementioned Priabonian species and first appearances of the shallow-water marine Rupelian species Nummulites fichteli, Nummulites vascus and Operculina complanata define the Eocene−Oligocene boundary in the new Kazandere Member at the northeast Thrace Basin

Common coeliacomesenteric trunk: a computed tomography radiological study

Background: There is an increasing trend for administration of invasive radiological interventions, laparoscopic surgery, and transplantation procedures in recent years, and determining the vascular variations prior to these procedures is crucially important. Coeliacomesenteric trunk (CMT) is among these variations. This study aimed to retrospectively evaluate this rare anomaly by computed tomography (CT). Materials and methods: A total of 1000 CT angiography images were analysed retrospectively, and the patients with mesenteric and coeliac arteries arising from the abdominal aorta with a single root were identified. The level that CMT arose, and its branching patterns were determined individually for all patients. Results: Ten patients (6 males and 4 females) with a mean age of 50.2 years (17–87 years) had CMT in CT images. Conclusions: The knowledge of variations in the CMT prior to vascular or laparoscopic interventions will contribute to early intervention in case of a complication, or to avoid from a potential damage

Changes in the superior longitudinal fasciculus and anterior thalamic radiation in the left brain are associated with developmental dyscalculia

Developmental dyscalculia is a neurodevelopmental disorder specific to arithmetic learning even with normal intelligence and age-appropriate education. Difficulties often persist from childhood through adulthood lowering the individual’s quality of life. However, the neural correlates of developmental dyscalculia are poorly understood. This study aimed to identify brain structural connectivity alterations in developmental dyscalculia. All participants were recruited from a large scale, non-referred population sample in a longitudinal design. We studied 10 children with developmental dyscalculia (11.3 ± 0.7 years) and 16 typically developing peers (11.2 ± 0.6 years) using diffusion-weighted magnetic resonance imaging. We assessed white matter microstructure with tract-based spatial statistics in regions-of-interest tracts that had previously been related to math ability in children. Then we used global probabilistic tractography for the first time to measure and compare tract length between developmental dyscalculia and typically developing groups. The high angular resolution diffusion-weighted magnetic resonance imaging and crossing-fiber probabilistic tractography allowed us to evaluate the length of the pathways compared to previous studies. The major findings of our study were reduced white matter coherence and shorter tract length of the left superior longitudinal/arcuate fasciculus and left anterior thalamic radiation in the developmental dyscalculia group. Furthermore, the lower white matter coherence and shorter pathways tended to be associated with the lower math performance. These results from the regional analyses indicate that learning, memory and language-related pathways in the left hemisphere might be related to developmental dyscalculia in children

Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations

Myosin Vb (MYO5B) is a motor protein that facilitates protein trafficking and recycling in polarized cells by RAB11- and RAB8-dependent mechanisms. Biallelic MYO5B mutations are identified in the majority of patients with microvillus inclusion disease (MVID). MVID is an intractable diarrhea of infantile onset with characteristic histopathologic findings that requires life-long parenteral nutrition or intestinal transplantation. A large number of such patients eventually develop cholestatic liver disease. Bi-allelic MYO5B mutations are also identified in a subset of patients with predominant early-onset cholestatic liver disease. We present here the compilation of 114 patients with disease-causing MYO5B genotypes, including 44 novel patients as well as 35 novel MYO5B mutations, and an analysis of MYO5B mutations with regard to functional consequences. Our data support the concept that (1) a complete lack of MYO5B protein or early MYO5B truncation causes predominant intestinal disease (MYO5B-MVID), (2) the expression of full-length mutant MYO5B proteins with residual function causes predominant cholestatic liver disease (MYO5B-PFIC), and (3) the expression of mutant MYO5B proteins without residual function causes both intestinal and hepatic disease (MYO5B-MIXED). Genotype-phenotype data are deposited in the existing open MYO5B database in order to improve disease diagnosis, prognosis, and genetic counseling.This research was funded by Jubiläumsfonds der Österreichischen Nationalbank, grant no.16678 (to A.R.J.), grant no. 18019 (to G.-F.V.) and Tiroler Wissenschaftsfonds, grant No. 0404/2386 (toG.-F.V.).info:eu-repo/semantics/publishedVersio

Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations.

Myosin Vb (MYO5B) is a motor protein that facilitates protein trafficking and recycling in polarized cells by RAB11- and RAB8-dependent mechanisms. Biallelic MYO5B mutations are identified in the majority of patients with microvillus inclusion disease (MVID). MVID is an intractable diarrhea of infantile onset with characteristic histopathologic findings that requires life-long parenteral nutrition or intestinal transplantation. A large number of such patients eventually develop cholestatic liver disease. Bi-allelic MYO5B mutations are also identified in a subset of patients with predominant early-onset cholestatic liver disease. We present here the compilation of 114 patients with disease-causing MYO5B genotypes, including 44 novel patients as well as 35 novel MYO5B mutations, and an analysis of MYO5B mutations with regard to functional consequences. Our data support the concept that (1) a complete lack of MYO5B protein or early MYO5B truncation causes predominant intestinal disease (MYO5B-MVID), (2) the expression of full-length mutant MYO5B proteins with residual function causes predominant cholestatic liver disease (MYO5B-PFIC), and (3) the expression of mutant MYO5B proteins without residual function causes both intestinal and hepatic disease (MYO5B-MIXED). Genotype-phenotype data are deposited in the existing open MYO5B database in order to improve disease diagnosis, prognosis, and genetic counseling

The effect of exposure time to clean room air on characteristic parameters of Au/Epilayer n-Si Schottky diodes

A study has been made on determination and comparison of current-voltage (I-V) and capacitance-voltage (C-V) characteristics parameters of Au/n-Si Schottky barrier diodes (SBDs) with and without thin native oxide layer fabricated on n-type Si grown by LPE (Liquid-phase Epitaxy) technique. The native oxide layer with different thicknesses on chemically cleaned on Si surface were obtained by exposing the surfaces to clean room air before evaporating metal. The native oxide thicknesses of samples D2, D3, D4 and D5 are in the form D2 < D3 < D4 \leq D5, depending on the exposing time. It has been seen that the values of barrier height Fb of samples D2(0.64 eV), D3(0.66 eV), D4(0.69 eV) and D5(0.69 eV) with the interfacial layer increased with increasing the exposure time and tended to that of the initial sample D1 (nonoxidezed sample, 0.74 eV), and thus also their I-V and C-V curves. The reverse current of sample D1 showed slight nonsaturating behavior. This ''soft'' behavior has been ascribed to the spatial inhomogeneity in the barrier heights at the MS interface. In particular, reverse bias curves of samples D2, D3, D4 and D5 have shown excellent saturation which may be attributed to the passivation of the semiconductor surface states by the native oxide layer which reduces the penetration of the wave functions of electron in the metal into the semiconductor. Especially, the I-V characteristics and experimental parameters of our devices are in agreement with recently reported results revealed by the pulsed surface photovoltage technique for the electronic properties of the HF-treated Si surface during initial oxidation in air

Evaluation of newborn mothers’ status of bonding to the baby, experiencing depression, and associated factors [Doğum Yapan Annelerin Bebeklerine Bağlanma ve Depresyon Yaşama Durumları ile Etkileyen Faktörlerin İncelenmesi]

Objective: The aim of this study is to evaluate newly delivered mothers’ status of bonding to their babies, their status of experiencing depression following delivery.and associated factors. Methods: The study was descriptive and sectional-type; and performed in a public hospital between February 1 and April 1 2015. Sample of the study was composed of 150 women who approved to participate in the study during this time interval. Participant information form. Mother to Infant Bonding Scale and Edinburgh Postnatal Depression Scale were used as data collection tools. Data were collected by face-to-face interview technique. Kruskal Wallis. Mann-Whitney U, student-t test and correlation analysis were used for statistical analysis of the data. Results: It was found that mean score of women from mother-to-infant bonding scale was 1.13±1.81.mean score from depression scale was 8.12±4.85 and 16.7% of the women were within the risk group for depression. A statistically significant difference was detected between mother to infant bonding status of women in the study and their status of willingness at last pregnancy (p0.05). There was a significant difference between women’s status of getting support from their spouses during the pregnancy and experiencing depression (p<0.05) (p=0.03). It was found that there was a positive and weak correlation between women’s status of experiencing depression and the level of mother-to-infant bonding; and the level of mother to infant bonding increased as the level of depression increased (p=0.09, r=0.21). Conclusion: Mother to infant bonding rates of the women in the study were found to be high; and it was determined that eager pregnancy strengthened the bond between the mother and the baby, support taken from the spouse during pregnancy affected the level of depression, and the level of mother-to-infant bonding increased as the level of depression increased. © 2019 Galenos Publishing House. All rights reserved