National interest of the Republic of Serbia for participation of Serbian Armed Forces in peacekeeping operations by Radojević Slobodan, Blagojević Srđan

“…Namely, the Serbian Armed Forces inherits the tradition of many years of participation in UN and EU peacekeeping operations. …”
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Colloidal Spin Ice Cellular Automata for Logic Design by Vasileios P. Karkanis, Nikolaos I. Dourvas, Andrew Adamatzky, Panagiotis Dimitrakis, Georgios Ch. Sirakoulis

“…An engineered system that exhibits a variety of interesting properties, such as collective dynamics that are not inherited in their building blocks, is the artificial spin ice (ASI) meta-materials. …”
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Effects of reproductive technologies and SPF status on some physiological and behavioral characteristics in rats with arterial hypertension (ISIAH strain) by D. S. Ragaeva, T. O. Abramova, I. N. Rozhkova, E. Yu. Brusentsev, E. V. Kalinichenko, T. N. Igonina, S. Ya. Amstislavsky

“…In the present study, a comparison of body weight, blood pressure (BP) and behavior in the «elevated plus maze» (EPM) test was made between three groups of ISIAH (inherited stress induced arterial hypertension) rats: a group of animals that were born and raised in a conventional animal facility and two groups from an SPF animal facility (one with animals born naturally and another with animals resulting from ART). …”
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Timing of dietary effects on the epigenome and their potential protective effects against toxins by Lynnea A. Nicholls, Kendall A. Zeile, London D. Scotto, Rebecca J. Ryznar

“…Numerous studies in humans and animals suggest that diet has the potential to modify the epigenome and these modifications can be inherited transgenerationally, but few studies investigate how diet can protect against negative effects of toxins. …”
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Breeding improvement of spring Indian dwarf wheat <i>Triticum sphaerococcum</i> Percival under the conditions of the Middle Volga region by Dam. F. Askhadullin, Dan. F. Askhadullin, N. Z. Vasilova, M. R. Tazutdinova, I. I. Khusainova, G. R. Gayfullina, E. S. Kirillova, N. S. lysenko

“…The main problem in the improvement of T. sphaerococcum is the pleiotropic effect of grain roundness and ear compactness caused by the S-D1 and C2 genes. These genes are inherited together with negative features peculiar to this species: small grain, and low ear productivity. …”
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Overexpression of the Synthetic Chimeric Native-T-phylloplanin-GFP Genes Optimized for Monocot and Dicot Plants Renders Enhanced Resistance to Blue Mold Disease in Tobacco (N. taba... by Dipak K. Sahoo, Sumita Raha, James T. Hall, Indu B. Maiti

“…The chimeric gene, expressed in transgenic tobacco, was stably inherited in successive plant generations as shown by molecular characterization, GFP quantification, and confocal fluorescent microscopy. …”
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The added role of Doppler ultrasound evaluation of sickle cell disease vasculopathy as a state of arterial stiffness and decreased nitric oxide bioavailability by Marwa Mohammed Mohammed Onsy, Sonia Ali El-Saiedi, Douaa Mohammed Mohammed Elsheshtawy, Marwa Abd-Elhady Abd-Elsamad

“…Abstract Background Sickle cell disease is an inherited hemoglobinopathy resulting in chronic hemolysis and painful vaso-occlusive crises. …”
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Reconfigurable Photonic Lattices Based on Atomic Coherence by Jiaqi Yuan, Shun Liang, Qingsong Yu, Changbiao Li, Yanpeng Zhang, Min Xiao, Zhaoyang Zhang

“…Recently, the concept of electromagnetically induced photonic lattice (EIPL) is proposed under the well‐known electromagnetically induced transparency (EIT) in coherently prepared multilevel alkali‐metal atomic systems, where the strong coupling beams producing EIT possess spatially periodic intensity profiles. The inherited instantaneous tunability of susceptibility from EIT‐modulated atomic coherence allows for the easy reconfigurability of EIPLs, which gives rise to exotic beam dynamics under such a readily controllable framework. …”
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The Prevalence of Using Traditional, Complementary, and Integrative Medicine by Patients with Epidermolysis Bullosa by Mohammad Mahdi Parvizi, Nasrin Saki, Ehsan Amiri-Ardekani, Parisa Ahmadfard, Mehdi Pasalar

“… Epidermolysis bullosa (EB) is an inherited disease that causes widespread symptoms characterized by extreme epithelial fragility. …”
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ARV1 p.Gln62Ter, a novel mutation linked to developmental and epileptic encephalopathy-38 by Mostafa Neissi, Ayoob Radhi Al-Zaalan, Misagh Mohammadi-Asl, Mojdeh Roghani, Javad Mohammadi-Asl, Kamele Jorfi

“…Abstract Developmental and epileptic encephalopathy is a rare and severe form of inherited neurodegenerative disorder characterized by various forms of seizures. …”
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Clinical Manifest X-Linked Recessive Adrenoleukodystrophy in a Female by Gyda Hlin Skuladottir Jack, Karolina Malm-Willadsen, Anja Frederiksen, Dorte Glintborg, Marianne Andersen

“…Adrenoleukodystrophy (ALD) is a rare X-linked inherited leukodystrophy with a reduced capacity for degradation of very long chain fatty acids (VLCFAs). …”
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Identification of a pathogenic SDHD mutation in a Chinese family with hereditary head and neck paraganglioma: implications for genetic counseling and management by Pu Wang, Liming Gao, Wenyang Zhang, Rui Guo, Yin Xia

“…Genetic counseling for the third generation revealed that only one child (III-4) carried the pathogenic mutation inherited from the patient’s third sister. Conclusion We identified a pathogenic mutation in SDHD in a Chinese HNPGL family, which is the second reported case of its kind. …”
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Whole exome analysis of primary immunodeficiency by E. S. Rahmani, Н. Azarpara, M. Karimipoor, Н. Rahimi

“…The human primary immunodeficiency diseases (PIDs) refer to a rare heterogeneous group of single-gene inherited disorders causing malfunctions in the immune system, and thus the affected patients have a predisposition to severe life-threatening infections. …”
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Patient-derived cornea organoid model to study metabolomic characterization of rare disease: aniridia-associated keratopathy by Ali Can Koc, Vedat Sari, Gamze Kocak, Tuba Recber, Emirhan Nemutlu, Daniel Aberdam, Sinan Güven

“…Abstract Background Aniridia is a rare panocular disease caused by gene mutation in the PAX6, which is essential for eye development. Aniridia is inherited in an autosomal dominant manner, but its phenotype can vary significantly among individuals with the same mutation. …”
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Spondylocostal Dysplasia in a 7-Year-Old Sri Lankan Girl Causing Restrictive Lung Disease: A Case Report and Review of the Literature by Phirarthana Kamalanathan, Meranthi Fernando, Rohan Jayawardena, A. Upasena, Shaman Rajindrajith, Sachith Mettananda

“…It is a recessively inherited disorder, and commonly identified disease-causing mutations are in DLL3 gene. …”
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Investigating the Clinical Characteristics and PITX3Mutations of a Large Chinese Family with Anterior Segment Mesenchymal Dysgenesis and Congenital Posterior Polar Cataract by Hui Dang, Min Peng, Weiyue Gu, Gang Ding, Yuqin Sun, Zhongkai Hao, Ning Wei, Xu Wang, Chenming Zhang, Aijun Deng

“…The congenital posterior polar cataract with or without anterior interstitial dysplasia (ASMD) of this family was inherited in an autosomal dominant manner, and the frameshift mutation (c.640_656dup) in the PITX3 gene was the cause of ocular abnormalities observed in this family. …”
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SOX5-Null Heterozygous Mutation in a Family with Adult-Onset Hyperkinesia and Behavioral Abnormalities by Michael Zech, Katharina Poustka, Sylvia Boesch, Riccardo Berutti, Tim M. Strom, Wolfgang Grisold, Werner Poewe, Juliane Winkelmann

“…The mutation was found to be inherited to the patient’s son who manifested abnormal behavior including diminished social functioning, paranoid ideation, and anxiety since adolescence. …”
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Ionospheric Disturbances Over the Indian Sector During 8 September 2017 Geomagnetic Storm: Plasma Structuring and Propagation by L. Alfonsi, C. Cesaroni, L. Spogli, M. Regi, A. Paul, S. Ray, S. Lepidi, D. Di Mauro, H. Haralambous, C. Oikonomou, P. R. Shreedevi, A. K. Sinha

“…Our results provide evidence of independent EPBs appearance freshly generated and inherited from a migrating plasma structure. The EPB (or EPBs) occurring in the south of India is/are freshly generated just above the magnetic equator, and is/are likely triggered by the sudden increase of EEJ just before the local sunset, acting as a pre‐reversal enhancement. …”
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Multiple Components of the VHL Tumor Suppressor Complex Are Frequently Affected by DNA Copy Number Loss in Pheochromocytoma by David A. Rowbotham, Katey S. S. Enfield, Victor D. Martinez, Kelsie L. Thu, Emily A. Vucic, Greg L. Stewart, Kevin L. Bennewith, Wan L. Lam

“…Pheochromocytomas (PCC) are rare tumors that arise in chromaffin tissue of the adrenal gland. PCC are frequently inherited through predisposing mutations in genes such as the von Hippel-Lindau (VHL) tumor suppressor. …”
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BCL-2 inhibitors in hematological malignancies: biomarkers that predict response and management strategies by Mariam Markouli, Maria N. Pagoni, Panagiotis Diamantopoulos

“…We further analyze the tumor characteristics that result in the development of intrinsic or inherited resistance to BCL-2 inhibitors. Finally, we focus on the biomarkers that can be used to predict responses to treatment in the name of personalized medicine, with the goal of exploring alternative strategies to overcome resistance.…”
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