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Journal articles on the topic 'Allure report'

Author: Grafiati

Published: 28 May 2022

Last updated: 31 July 2025

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1

Kurian, Alka. "Film festival report: Lost along the margins, Seattle's South Asian Film Festival, allure and agony." Studies in South Asian Film & Media 3, no. 1 (2012): 51–55. http://dx.doi.org/10.1386/safm.3.1.51_7.

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Patil, Rahul. "Full mouth prosthetic rehabilitation using hobo’s philosophy: A case report." IP Annals of Prosthodontics and Restorative Dentistry 9, no. 3 (2023): 179–86. http://dx.doi.org/10.18231/j.aprd.2023.035.

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The face, which is the part of the body that is most exposed, has the mouth as a prominent feature. The allure of the teeth draws all eyes. Some patients with collapsed bites were required to have all of their teeth extracted and replaced with traditional complete dentures because rehabilitation techniques' efficacy was questioned in the 20th century. The occlusal surfaces of a patient's teeth will gradually deteriorate over the course of their lifetime. But excessive occlusal wear can result in pulpal injury, occlusal discord, functional impairment, and aesthetic deformity. Thanks to improvem

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COSTRELL, ROBERT M. "Accounting for the rise in unfunded public pension liabilities: faulty counterfactuals and the allure of simple gain/loss summations." Journal of Pension Economics and Finance 17, no. 1 (2016): 23–45. http://dx.doi.org/10.1017/s1474747216000159.

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AbstractThis paper provides a methodological critique of an influential method for assessing the impact on the Unfunded Accrued Liabilities (UAL) of the gap between assumed and actual investment returns over extended periods, and offers a sound replacement. The method in question simply sums over time the components of the annual actuarial gain/loss report. This implicitly assumes that in the counterfactual exercise, the interest on the additional UAL is covered dollar-for-dollar by amortization. But under actual funding formulas amortization usually varies less than interest. This means there

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Amar, Tsulis Iq’bal Khairul, Alfia Magfirona, Zaini Munawar, and Budi Priyanto. "Investigation of Project Delays: Towards a Sustainable Toll Road Project." E3S Web of Conferences 517 (2024): 05014. http://dx.doi.org/10.1051/e3sconf/202451705014.

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Private investment in toll roads is anticipated to surge due to their potential to cover operational and developmental costs through toll fees. However, the allure for investors and lenders hinges on achieving long-term sustainability, a challenging feat in the context of frequent project implementation delays, especially in Indonesia’s toll road construction. This study delves into the primary obstacles thwarting timely project completion, drawing insights from the literature to gauge their significance in ensuring the sustainability of toll road projects. Based on a 5-point Likert scale ques

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Guala, Dimitri, Christoph Ogris, Nikola Müller, and Erik L. L. Sonnhammer. "Genome-wide functional association networks: background, data & state-of-the-art resources." Briefings in Bioinformatics 21, no. 4 (2019): 1224–37. http://dx.doi.org/10.1093/bib/bbz064.

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Abstract The vast amount of experimental data from recent advances in the field of high-throughput biology begs for integration into more complex data structures such as genome-wide functional association networks. Such networks have been used for elucidation of the interplay of intra-cellular molecules to make advances ranging from the basic science understanding of evolutionary processes to the more translational field of precision medicine. The allure of the field has resulted in rapid growth of the number of available network resources, each with unique attributes exploitable to answer dif

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Vujičić, Lejla. "History in the void: Giuseppe Samonà’s 1967 proposal for Montecitorio competition." JOURNAL OF ARCHITECTURE AND URBANISM 48, no. 2 (2024): 100–108. http://dx.doi.org/10.3846/jau.2024.20743.

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Giuseppe Samonà was one of the most influential figures in 20th century Italian architecture and urban culture. In 1967, Samonà and his team submitted a competition proposal for the extension of the Camera dei deputati in Rome, considered by many to be one of the most significant and conceptually mature projects of his career. By examining the design and the report appended to the competition submittal the author explores the concept of the void that is the backbone of the project and finds that it has a twofold interpretation. Apart from the obvious physical manifestation of emptying, the voi

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Pooran, Steve, and Wazim R. Sharif. "Students’ Attitude towards Agricultural Science in the Hinterland Regions of Guyana." European Modern Studies Journal 8, no. 1 (2024): 194–99. http://dx.doi.org/10.59573/emsj.8(1).2024.17.

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This research investigates the attitudes of students towards Agricultural Science in the Hinterland Regions of Guyana, aiming to grasp their perspectives and aid educators in crafting dynamic lessons to instill a positive perception of the subject. It serves as a valuable resource for policymakers and curriculum developers, shedding light on the subject's importance and effective engagement strategies. Additionally, it delves into the correlation between gender and students' viewpoints on learning Agricultural Science. Utilizing a questionnaire, data was gathered from 100 students and su

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Akbar, Fuad Husain, Hasta Handayani Idrus, Tuti Ningseh, Mustafa Bin Jaapar, Putri Rejeki, and Riki Kristanto. "The Growth of Medical Tourism Combines Health Innovation with Global Mobility." Journal of Dentistry and Oral Research 8, no. 1 (2019): 1–8. https://doi.org/10.52338/jodor.2024.4246.

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Objectives: The study investigates the expanding field of dental tourism within the broader context of medical tourism, exploring the factors that drive its growth, its economic implications, and the satisfaction of patients who seek dental care abroad. Methods: Employing the PRISMA systematic review method, the authors searched academic databases for articles published from 2015 to 2024, using keywords related to dental and medical tourism. The search yielded numerous articles, from which eight were selected based on relevance and quality criteria. Results: The review found that dental touris

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Daniel, Piotr, Justyna Składanek, Michał Leśkiewicz, Karina Otręba, Joanna Cieszkowska, and Karolina Czupryńska. "Why is surgery not popular among medical students and young doctors? - Review of literature." Journal of Education, Health and Sport 73 (June 4, 2024): 51721. http://dx.doi.org/10.12775/jehs.2024.73.51721.

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Introduction: Contemporary medicine is witnessing significant advancements in conservative treatment modalities. However, surgery remains paramount for radical cancer treatment and emergent conditions such as trauma, peritonitis, gastrointestinal obstruction, and cholecystitis. Despite the essential role of surgeons, there is a global trend indicating waning interest among medical students in pursuing surgical specialties. Concurrently, practicing surgeons report heightened levels of professional burnout, and many regions face a looming shortage of surgical professionals, posing a threat to he

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R, Mysiuk, Yuzevych V, and Mysiuk I. "Api test automation of search functionality with artificial intelligence." Artificial Intelligence 27, jai2022.27(1) (2022): 269–74. http://dx.doi.org/10.15407/jai2022.01.269.

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One of the steps in software development is to test the software product. With the development of technology, the testing process has improved to automated testing, which reduces the impact of the human factor on error and speeds up testing. The main software products for testing are considered to be web applications, web services, mobile applications and performance testing. According to the testing pyramid, when testing web services, you need to develop more test cases than when testing a web application. Because automation involves writing software code for testing, the use of ready-made to

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Haggart, Kerri, Janet Hoek, and Mei-Ling Blank. "Flavor Capsule Variants’ Performance in a “Dark Market”: Implications for Standardized Packaging." Nicotine & Tobacco Research 22, no. 5 (2018): 853–56. http://dx.doi.org/10.1093/ntr/nty158.

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Abstract Background By increasing excise taxes, eliminating tobacco marketing, and requiring standardized (plain) packaging of tobacco products, governments internationally have reduced smoking’s allure. Yet product innovations, such as flavor capsule variants (FCVs), remain unregulated and may appeal to non-smokers. We examined the growth of FCVs in a country with a progressive policy environment. Methods Each year, New Zealand tobacco companies must provide details of the number of cigarette sticks released for each brand and variant to the Ministry of Health. We used this information to ana

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Chirayu, Pal*1 &. Dhanur Motwani*2 Atindra Patel3. "THE STUDY AND SURVEY POINT UP MASSIVE DATA, UTILIZATION AND TECHNIQUES USED IN HIGHER EDUCATION SYSTEM." INTERNATIONAL JOURNAL OF ENGINEERING SCIENCES & RESEARCH TECHNOLOGY 7, no. 8 (2018): 599–607. https://doi.org/10.5281/zenodo.1403414.

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Data mining and big data analytics have the ability and potential to metamorphosis and transfigure the present day pedagogy, teaching, andragogy and the fact-finding for student’s benefits. Evolution of big data will serve as the beginning for a new era in education and scrutinization and exploration in education. The forefront and leading-edge critique traverse the contemporary state of big data analytics. This paper aims to study the implications for edification and development for today and the next day. Data mining and data analytics have clutched great impetus in the past few years

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Syeed, Sayyid M. "EDITORIAL." American Journal of Islam and Society 8, no. 1 (1991): v—vii. http://dx.doi.org/10.35632/ajis.v8i1.2640.

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We report with great sadness the death of Victor Danner, a friend ofIslam and Muslims, a graduate of Georgetown and Harvard, and Chairmanof the Department of Near Eastern Languages and Cultures at Indiana University,BloomingtOn, Indiana. Darner's latest publication was The Islamic Traditiontion: An Introduction. W have been inviting Muslim anti non-Mush scholarsfrom time to time to present their responses to the International Instituteof Islamic Thought’s caIl for the Islamization of Knowledge. So far, we havebeen very lucky to have had the opportunity to listen to the late Fazlur Rahman,Sayye

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Tjaden, Patricia, and Nancy Thoennes. "The Role of Stalking in Domestic Violence Crime Reports Generated by the Colorado Springs Police Department." Violence and Victims 15, no. 4 (2000): 427–41. http://dx.doi.org/10.1891/0886-6708.15.4.427.

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A review of 1,785 domestic violence crime reports generated by the Colorado Springs Police Department found that 1 in 6 (16.5 percent) contained evidence the suspect stalked the victim. Female victims were significantly more likely than male victims to allege stalking by their partners (18.3 vs. 10.5 percent). Most stalkers were former rather than current intimates. Regardless of victims’ gender, reports with stalking allegations were significantly less likely to mention physical abuse or victim injury in the presenting condition, to involve households with children, or to involve victims and

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Schneiderman, David. "SYMPOSIUM REPORT: AFTER ALLAIRE AND BELANGER-CAMPEAU." Constitutional Forum / Forum constitutionnel 3, no. 1 - 4 (2011): 1991. http://dx.doi.org/10.21991/c9s94q.

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Vulturar, Romana, Adina Chiş, Melinda Hambrich, Beatrice Kelemen, Loredana Ungureanu, and Andrei C. Miu. "Allelic distribution of BDNF Val66Met polymorphism in healthy Romanian volunteers." Translational Neuroscience 7, no. 1 (2016): 31–34. http://dx.doi.org/10.1515/tnsci-2016-0006.

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AbstractPopulation stratification of functional gene polymorphisms is a potential confounding factor in genetic association studies. The Val66Met (rs6265) single-nucleotide polymorphism in the brain-derived neurotrophic factor gene (BDNF) exhibits one of the highest variabilities in terms of allelic distribution between populations. The present study reports the distribution of BDNF Val66Met alleles in a sample of healthy volunteers (N = 1124) selected from the Romanian population. Frequencies were 80.74% for the Val allele and 19.26% for the Met allele. The data from this study extends effort

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Hedman, Minttu, and Jukka U. Palo. "Long D13S317 variant allele: A cautionary case report." Forensic Science International: Genetics 14 (January 2015): 38–41. http://dx.doi.org/10.1016/j.fsigen.2014.08.016.

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Malachkova, N. V., and Miteb Al-Jarrah Osama Mohammad. "Study of the effect of RS1800629 TNF polymorphism on the course of age-related macular degeneration through the prism of ANTI-VEGF therapy." Reports of Vinnytsia National Medical University 26, no. 2 (2022): 267–73. http://dx.doi.org/10.31393/reports-vnmedical-2022-26(2)-16.

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Annotation. Age-related macular degeneration (AMD) includes pathological changes in the deep layers of the retina, macula, and surrounding blood vessels, leading to loss of central vision. The wet form of nosology is the leading cause of irreversible blindness in developed countries among people over 60, where more than 30 million people suffer from the disease. The number of patients in the United States is expected to increase from 9.1 million in 2010 to 17.8 million in 2050. New therapeutic strategies and the development of new practical methods for identifying patients at high risk of trea

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Costa, Magdaline, Peter Grant, Gillian Rice, Simon Futers, and Robert Medcalf. "Human Endothelial Cell-derived Nuclear Proteins that Recognise Polymorphic DNA Elements in the von Willebrand Factor Gene Promoter Include YY1." Thrombosis and Haemostasis 86, no. 08 (2001): 672–79. http://dx.doi.org/10.1055/s-0037-1616103.

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SummaryFour common base-change polymorphisms have been found in the von Willebrand factor gene promoter: (-1793 C/G, -1234 T/C, -1185 G/A and -1051 A/G). All four polymorphisms are in strong linkage dis-equilibrium and recent reports have indicated these polymorphisms are associated with plasma vWF:Ag levels suggesting that one or more of these elements influence regulation of the vWF gene. We report that human endothelial cell-derived trans-acting factors display allelic preferences in binding activity to each polymorphic site. The common A allele variant of the –1051 polymorphism and the rar

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Jezek, D. A., F. E. Lower, D. R. Wagenknecht, et al. "Report of a new DRB1*13 allele: DRB1*1336." Tissue Antigens 57, no. 6 (2001): 548–50. http://dx.doi.org/10.1034/j.1399-0039.2001.057006548.x.

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LeClere, Sherry, Chenxi Wu, Philip Westra, and R. Douglas Sammons. "Cross-resistance to dicamba, 2,4-D, and fluroxypyr in Kochia scoparia is endowed by a mutation in an AUX/IAA gene." Proceedings of the National Academy of Sciences 115, no. 13 (2018): E2911—E2920. http://dx.doi.org/10.1073/pnas.1712372115.

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The understanding and mitigation of the appearance of herbicide-resistant weeds have come to the forefront of study in the past decade, as the number of weed species that are resistant to one or more herbicide modes of action is on the increase. Historically, weed resistance to auxin herbicides has been rare, but examples, such as Kochia scoparia L. Schrad (kochia), have appeared, posing a challenge to conventional agricultural practices. Reports of dicamba-resistant kochia populations began in the early 1990s in areas where auxin herbicides were heavily utilized for weed control in corn and w

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Ahmad, Sajjad, Sadaqat ALi, Nasir Siddique, Qazi Laeeque Ahmad, Muhammad Amjad, and Mohammad Ashraf Tahir. "A Unique Allele Variant at STR Locus D2S1338 in a Paternity Testing Case." 99 3, no. 1 (2021): 109–17. http://dx.doi.org/10.26735/abhs9965.

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Background: The relationship testing through DNA profiling may undesirably be affected by the rare allele variants, tri-allelic pattern and null alleles. Therefore, it is vital to report such anomalies. We report a paternity testing in a sexual assault case studied at Punjab Forensic Science Agency, Lahore Pakistan showing a unique allele variant in mother and child. Methods: DNA was extracted from the buccal swabs of reference samples using organic extraction method and DNA profiling was done for 15 autosomal STRs and amelogenin using Identifiler Plus kit. Results: A novel out of marker range

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Denga, O. V., and A. O. Osadcha. "Study of the association of gene polymorphism associated with sports success and risk of occupational diseases in young football players." Reports of Vinnytsia National Medical University 26, no. 2 (2022): 179–83. http://dx.doi.org/10.31393/reports-vnmedical-2022-26(2)-02.

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Annotation. Advances in sports genetics have opened up new opportunities in determining the propensity to perform physical activity of varying intensity and duration, as well as in the diagnosis and prevention of pathologies of athletes whose development is associated with excessive training loads. Detection of gene polymorphism makes it possible to develop personalized schemes for the prevention of various pathologies in athletes. The aim of the study was to study the genetic polymorphisms of the genes ACE (Ins/Del), ACTN3 (R577X), AMPD (Gln12Ter), UCP2 (Arg/Gly) in young football players, wh

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Dubaniewicz, A. "Analysis of DQB1 allele frequencies in pulmonary tuberculosis: preliminary report." Thorax 58, no. 10 (2003): 890–91. http://dx.doi.org/10.1136/thorax.58.10.890.

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Chamberlain, Kristen, James W. Smith, Diana Moffatt, Jane Moore, Donald Arnold, and John G. Kelton. "The HPA-15 (Gov) Platelet Alloantigen System: Allele Frequencies in the Canadian Population." Blood 106, no. 11 (2005): 2180. http://dx.doi.org/10.1182/blood.v106.11.2180.2180.

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Abstract Human platelet antigens (HPAs) are genetically defined polymorphisms expressed on plasma membrane proteins. Alloimmunization following exposure to the incompatible antigen during pregnancy, or following transfusion or transplantation, can cause severe thrombocytopenia and bleeding. The Gov-a/Gov-b biallelic system is expressed on CD109, a 175kD glyco sylphosphatidylinositol-anchored glycoprotein found on platelets, endothelial cells, and activated T-cells (Kelton, 1990; Smith, 1995). Alloimmunization to Gov-a/b is implicated in neonatal alloimmune thrombocytopenia (NAT) and post-trans

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Lobashevsky, Andrew L., Deidre H. Fallon, and William C. Goggins. "P125 HLA allele specific antibodies: What should be entered in Unet, antigen, allele or epitope (case report)?" Human Immunology 79 (October 2018): 154. http://dx.doi.org/10.1016/j.humimm.2018.07.182.

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Monteiro Leitão, Roberto, Marco Orsini, Mariana Pontes do Nascimento Mateus, Renan Falconi, Antônio Marcos da Silva Catarino, and Gilberto Canedo Martins Jr. "Spinocerebellar ataxia type 7: A case report." International Journal of Case Reports and Images 15, no. 2 (2024): 53–57. http://dx.doi.org/10.5348/101470z01rl2024cr.

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Introduction: Spinocerebellar ataxia type 7 is part of a rare group of neurodegenerative diseases, characterized by lesions in the brainstem, cerebellum, spinal cord, and retina, manifesting as motor disturbances associated with signs of pyramidal involvement and amaurosis. The dysfunction is caused by autosomal dominant genetic alterations, with disease severity and the age of symptom onset being directly linked to the patient’s genetic expression. Case Report: We present the case of a 24-year-old woman, previously healthy, who denied smoking, drinking alcohol, or taking any other drugs. She

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Palahniuk, H. O., I. P. Pashkova, M. O. Matokhniuk, S. V. Franchuk, and V. M. Zhebel. "C-natriuretic peptide – as an indicator of persistent increase in blood pressure in men with hypertension." Reports of Vinnytsia National Medical University 26, no. 2 (2022): 248–53. http://dx.doi.org/10.31393/reports-vnmedical-2022-26(2)-13.

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Annotation. According to multiple studies hypertension (AH) is a multifactorial disease. It is recognized that one of the key mechanisms of persistent increase in blood pressure (BP) is the imbalance between vasoconstriction and vasodilation and endothelial dysfunction (ED) is one of the leading links in the pathogenesis of AH. The consequence of ED is a persistent vasoconstrictor reaction which results in myocardial remodeling in the form of left ventricular hypertrophy (LVH) and the subsequent development of congestive heart failure (CHF). One of the most important representatives of the gro

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Monteiro, Catarina, Ana Gonçalves, Jorge Oliveira, et al. "Thrombocytopenia-Absent Radius Syndrome: Descriptions of Three New Cases and a Novel Splicing Variant in RBM8A That Expands the Spectrum of Null Alleles." International Journal of Molecular Sciences 23, no. 17 (2022): 9621. http://dx.doi.org/10.3390/ijms23179621.

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Thrombocytopenia-absent radius (TAR) syndrome is a rare congenital disorder characterized by the bilateral absence of the radius and thrombocytopenia, and sometimes by other skeletal, gastrointestinal, cardiac, and renal abnormalities. The underlying genetic defect is usually the compound inheritance of a microdeletion in 1q21.1 (null allele) and a low-frequency, non-coding single nucleotide variant (SNV) in the RBM8A gene (hypomorphic allele). We report three new cases from two unrelated families. The two siblings presented the common genotype, namely the compound heterozygosity for a 1q21.1

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Barnell, Erica K., Kenneth F. Newcomer, Zachary L. Skidmore, et al. "Impact of a 40-Gene Targeted Panel Test on Physician Decision Making for Patients With Acute Myeloid Leukemia." JCO Precision Oncology, no. 5 (January 2021): 191–203. http://dx.doi.org/10.1200/po.20.00182.

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PURPOSE Physicians treating hematologic malignancies increasingly order targeted sequencing panels to interrogate recurrently mutated genes. The precise impact of these panels on clinical decision making is not well understood. METHODS Here, we report our institutional experience with a targeted 40-gene panel (MyeloSeq) that is used to generate a report for both genetic variants and variant allele frequencies for the treating physician (the limit of mutation detection is approximately one AML cell in 50). RESULTS In total, 346 sequencing reports were generated for 325 patients with suspected h

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Kniazkova, P. V., and V. Yu Harbuzova. "Analysis of the redistribution of rs4977574-polymorphic variants of the ANRIL gen in patients with acute coronary syndrome of different sex." Reports of Vinnytsia National Medical University 26, no. 1 (2022): 108–12. http://dx.doi.org/10.31393/reports-vnmedical-2022-26(1)-20.

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Annotation. The aim of the study was to analyze the distribution of rs4977574-polymorphic variants of the ANRIL gene in patients with acute coronary syndrome of different sex. The venous blood of 234 patients with acute coronary syndrome (ACS) and 195 people without cardiac pathology was used for the study. DNA was isolated from whole venous blood using the GeneJET Whole Blood Genomic DNA Purification Mini Kit (ThermoFisher Scientific, USA). rs4977574 ANRIL gene polymorphism was studied by real-time PCR reaction in the presence of TaqMan assay C_31720978_30. Statistical analysis of the study w

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Kniazkova, P. V., and V. Yu Harbuzova. "Analysis of the redistribution of rs4977574-polymorphic variants of the ANRIL gen in patients with acute coronary syndrome of different sex." Reports of Vinnytsia National Medical University 26, no. 1 (2022): 108–12. http://dx.doi.org/10.31393/reports-vnmedical-2022-26(1)-20.

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Annotation. The aim of the study was to analyze the distribution of rs4977574-polymorphic variants of the ANRIL gene in patients with acute coronary syndrome of different sex. The venous blood of 234 patients with acute coronary syndrome (ACS) and 195 people without cardiac pathology was used for the study. DNA was isolated from whole venous blood using the GeneJET Whole Blood Genomic DNA Purification Mini Kit (ThermoFisher Scientific, USA). rs4977574 ANRIL gene polymorphism was studied by real-time PCR reaction in the presence of TaqMan assay C_31720978_30. Statistical analysis of the study w

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Kniazkova, P. V., and V. Yu Harbuzova. "Analysis of the redistribution of rs4977574-polymorphic variants of the ANRIL gen in patients with acute coronary syndrome of different sex." Reports of Vinnytsia National Medical University 26, no. 1 (2022): 108–12. http://dx.doi.org/10.31393/reports-vnmedical-2022-26(1)-20.

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Annotation. The aim of the study was to analyze the distribution of rs4977574-polymorphic variants of the ANRIL gene in patients with acute coronary syndrome of different sex. The venous blood of 234 patients with acute coronary syndrome (ACS) and 195 people without cardiac pathology was used for the study. DNA was isolated from whole venous blood using the GeneJET Whole Blood Genomic DNA Purification Mini Kit (ThermoFisher Scientific, USA). rs4977574 ANRIL gene polymorphism was studied by real-time PCR reaction in the presence of TaqMan assay C_31720978_30. Statistical analysis of the study w

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Melnyk, O. V., N. O. Sorokina, H. V. Lischishyn, et al. "The role of PPARGC1A and the RS8192678 polymorphism in determining the performance of athletes." Reports of Vinnytsia National Medical University 26, no. 3 (2022): 497–501. http://dx.doi.org/10.31393/reports-vnmedical-2022-26(3)-26.

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Annotation. The impact of genetics on physiology and sports performance is one of the most controversial areas of sports medicine. Studies have shown that in addition to wild-type genes, almost 200 gene polymorphisms affect athletic performance, and more than 20 polymorphisms can determine the status of elite athletes. Sports results are manifested to a greater extent not only due to environmental factors, but also due to the athlete's own genotype, so the purpose of our review article is to study the effects of the PPARGC1A gene and its rs8192678 polymorphism on sports characteristics. For th

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Zainuddin, Nur Aina’a Mardhiah, Ahmed A. Saleh Falah, Muhammad Haniff Mokti, Rozalina Zakaria, Zulzilawati Jusoh, and Wei Ru Wong. "Investigation on the Effect of Fluorescence Material based on D-Shaped Hollow Core Photonic Crystal Fiber." Journal of Physics: Conference Series 2627, no. 1 (2023): 012012. http://dx.doi.org/10.1088/1742-6596/2627/1/012012.

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Abstract In this paper, we report the outcomes when fluorescence material coated the hollow core (inner part) of D-shaped photonic crystal fiber (PCF) that has internal diameter (ID), 10 μm. Fluorescence involves the emission of light by a substance that has absorbed light or other electromagnetic radiation. The coated material namely, allene has contributed significantly to the output of transmission spectra at the visible region. The changes in transmission wavelength are remarked when certain parameters vary along the study. The air hole deposited with allene exhibits strong electromagnetic

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Teive, Hélio A. Ghizoni, Fabio Massaiti Iwamoto, Carlos Henrique Camargo, Iscia Lopes-Cendes, and Lineu Cesar Werneck. "Machado-Joseph disease versus hereditary spastic paraplegia: case report." Arquivos de Neuro-Psiquiatria 59, no. 3B (2001): 809–11. http://dx.doi.org/10.1590/s0004-282x2001000500030.

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Machado-Joseph disease (MJD) is the most common autosomal dominant spinocerebellar ataxia and presents great phenotypic variability. MJD presenting with spastic paraparesis was recently described in Japanese patients. We report the case of 41-year-old woman with the phenotype of complicated hereditary spastic paraplegia. Her father died at the age of 56 years due to an undiagnosed progressive neurological disease that presented parkinsonism. She had an expanded allele with 66 CAG repeats and a normal allele with 22 repeats in the gene of MJD. MJD should be considered in the differential diagno

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Zhou, Mingtao, Shengfei Wang, Aishun Ding, et al. "First polyallene-based well-defined amphiphilic diblock copolymer via RAFT polymerization." Polymer Chemistry 12, no. 21 (2021): 3088–95. http://dx.doi.org/10.1039/d1py00509j.

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Adiputra, Putu Anda Tusta, I. Gede Putu Supadmanaba, I. Gede Krisna Arim Sadeva, Anak Agung Bagus Putra Indrakusuma, Putri Ayu Wulandari, and Desak Made Wihandani. "Case Report: The Relationship of CCND1 RS614367 Polymorphism with Clinicopathological Features." Biomedical and Pharmacology Journal 16, no. 3 (2023): 1855–59. http://dx.doi.org/10.13005/bpj/2765.

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Recent studies have shown that the CCND1 rs614367 polymorphism increases the risk of breast cancer and its invasive nature. However, studies evaluating the relationship of the CCND1 rs614367 polymorphism based on the clinicopathology of breast cancer patients in Indonesia were still limited. This study is aimed to determine the CCND1 rs614367 polymorphism in breast cancer and its relationship with the patient's clinicopathology. Methods: This study was a cross-sectional study on 45 samples of breast cancer patients. After collecting demographic and clinical data, PCR and sequencing will be per

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Bian, Xue-Yu, Mark R. Thomas, M. Saif Rasheed, et al. "A Recessive Allele (tgr-1) Conditioning Tomato Resistance to Geminivirus Infection Is Associated with Impaired Viral Movement." Phytopathology® 97, no. 8 (2007): 930–37. http://dx.doi.org/10.1094/phyto-97-8-0930.

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Begomoviruses (the family Geminiviridae) are transmitted by the whitefly Bemisia tabaci and contain monopartite or bipartite circular single-stranded (ss)DNA genomes. They have emerged as severe problems in the production of agricultural and horticultural crops worldwide. Here, we report the identification of a tomato breeding line, FLA653, that confers a high level of resistance to Tomato leaf curl virus (TLCV, monopartite). Genetic analysis indicated that the resistance is controlled by a single recessive allele named tgr-1, which is in contrast to previous reports that multiple genetic fact

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Azam, Pirkarami, Rasouli Sousan, and Khoshlahjeh Motamed Nasim. "Mechanism of Degradation of Acidic Dyes in Industrial Effluents by a Nano-photo Catalytic Process with a Study of Intermediate Compounds." Pharmaceutical and Chemical Journal 3, no. 2 (2016): 149–56. https://doi.org/10.5281/zenodo.13749255.

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The dye stuff lost in the textile industry poses a major problem to wastewater sources. This paper reports an investigation into the effect of a number of operating factors on the removal of Allura Red AC from an aqueous solution through photocatalysis Advanced Oxidation Processes (AOPs) are effective processes in treating waters polluted by a variety of harmful pollutants. This paper discusses about effect of the number of factors on removal of Allura Red AC from an aqueous solution using a photcatalytic process. The photcatalyst used in this solution was WO3/TiO2. Optimal dose of the photoca

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Sinnreich, Michael, Christian Therrien, and George Karpati. "Lariat branch point mutation in the dysferlin gene with mild limb-girdle muscular dystrophy." Neurology 66, no. 7 (2006): 1114–16. http://dx.doi.org/10.1212/01.wnl.0000204358.89303.81.

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The authors report a genotype-phenotype correlation in a limb-girdle muscular dystrophy 2B family. Two severely affected sisters were homozygous for a dysferlin null mutation. Their mildly affected compound heterozygous mother harbored, in addition to one null allele, an in-frame exon-skipping allele caused by a novel lariat branch point mutation. The dysferlin molecule arising from the latter allele appeared to partially complement the null mutation, likely accounting for the mother's mild phenotype.

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Paradkar, Minal U., Swarup A. V. Shah, Alpa J. Dherai, Dhanashri Shetty, and Tester F. Ashavaid. "Distribution of CYP2D6 genotypes in the Indian population – preliminary report." Drug Metabolism and Personalized Therapy 33, no. 3 (2018): 141–51. http://dx.doi.org/10.1515/dmpt-2018-0011.

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Abstract Background Cytochrome P450 2D6 (CYP2D6) allelic distribution exhibits differences amongst worldwide populations. There is lack of data from Mumbai, Western India, on the major CYP2D6 alleles *2, *3, *4, *5, *10 and *41, and gene multiplication alleles. Hence, the present study was undertaken to determine the distribution of these clinically relevant CYP2D6 alleles. Methods Fifty-two healthy individuals were screened using TaqMan SNP genotyping and copy number variation (CNV) assays by real-time polymerase chain reaction. Results The allele frequencies of CYP2D6*2, *3, *4, *5, *10 and

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Bahrij, D. A., O. L. Starzhyns'ka, and V. M. Zhebel. "Phenotypic realization of single nucleotide polymorphism rs950880 of IL1RL1 gene in healthy inhabitants of Vinnytsia region." Reports of Vinnytsia National Medical University 25, no. 3 (2021): 364–68. http://dx.doi.org/10.31393/reports-vnmedical-2021-25(3)-02.

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Annotation. Soluble growth stimulating factor (sST2) is a new biomarker that has recently been used quite successfully in cardiology. However, the possible genetic component of peptide production has not been sufficiently studied. The aim of the study was to assess the plasma level of sST2 and other aspects of the phenotypic implementation of single nucleotide polymorphism (SNP) rs950880 of the IL1RL1 gene in men without cardiovascular disease in the Podillia region, Ukraine. 70 men who met the criteria for inclusion/non-inclusion in the study were examined, general clinical, laboratory and in

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Esmaeili, Behnaz, Behnaz Bayat, Atefe Alirezaee, Mona Delkhah, Mohammad Reza Mehdizadeh, and Zahra Pourpak. "Human Neutrophil Antigen Genotype and Allele Frequencies in Iranian Blood Donors." Journal of Immunology Research 2022 (February 7, 2022): 1–11. http://dx.doi.org/10.1155/2022/4387555.

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Objective. Human neutrophil antigens (HNAs) can be targeted by HNA-allo antibodies and cause a variety of clinical conditions such as transfusion-related acute lung injury (TRALI) and neonatal alloimmune neutropenia (NAIN). The current study is aimed at identifying the genotype and allele frequencies of HNAs in Iranian blood donors. Methods. A total of 150 blood samples were obtained from healthy blood donors. HNA-1, HNA-3, HNA-4, and HNA-5 were genotyped, using the polymerase chain reaction sequence-specific primer (PCR-SSP) technique. The expression of the HNA-2 antigen on the neutrophil sur

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Afshar-Kharghan, Vahid, Chester Q. Li, Mohammad Khoshnevis-Asl, and José A. López. "Kozak Sequence Polymorphism of the Glycoprotein (GP) Ib Gene Is a Major Determinant of the Plasma Membrane Levels of the Platelet GP Ib-IX-V Complex." Blood 94, no. 1 (1999): 186–91. http://dx.doi.org/10.1182/blood.v94.1.186.413k19_186_191.

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Despite the known importance of the sequences surrounding ATG start codons (Kozak sequences) for efficient translation of proteins, few reports have appeared that describe the natural variations in these sequences. Here, we report a human polymorphism in the Kozak sequence of the platelet adhesion receptor, glycoprotein (GP) Ib, a component of the GP Ib-IX-V complex, which mediates the initial adhesion of platelets to the blood vessel wall following injury. The polymorphism is based on the presence of either thymine (T) or cytosine (C) at position −5 from the initiator ATG in the GP Ib gene.

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Grandchamp, Bernard, Gilles Hetet, Caroline Kannengiesser, et al. "A novel type of congenital hypochromic anemia associated with a nonsense mutation in the STEAP3/TSAP6 gene." Blood 118, no. 25 (2011): 6660–66. http://dx.doi.org/10.1182/blood-2011-01-329011.

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Abstract STEAP3/TSAP6 encodes a ferrireductase that is involved in the acquisition of iron by developing erythroblasts and steap3/tsap6 null-mice display severe microcytic anemia. We report a family in which 3 siblings born to healthy parents display transfusion-dependent hypochromic anemia. A nonsense STEAP3/TSAP6 was identified in the siblings at the heterozygous state. This mutation was inherited from their father while no mutation was found in their mother. A large variability of expression was found between normal alleles in a control population, confirming a previous report that STEAP3/T

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Willows, Jamie, Maryam Al Badi, Chloe Richardson, Noel Edwards, Sarah Rice, and John A. Sayer. "Case Report: Investigation and molecular genetic diagnosis of familial hypomagnesaemia: a case report." F1000Research 8 (May 15, 2019): 666. http://dx.doi.org/10.12688/f1000research.19006.1.

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Genetic mutations causing familial hypomagnesaemia syndromes are well-recognised. Affected patients can present with severe symptoms of hypomagnesaemia, such as seizures or cardiac arrhythmia. We report an affected child, from a consanguineous family, who presented in the first weeks of life with seizures secondary to hypomagnesaemia, without other associated clinical features. We performed whole exome sequencing in the affected child and segregation analysis within the family, which revealed a novel homozygous missense mutation in TRPM6, which was confirmed as a heterozygous allele in both pa

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Marya, CM, Bhavna Gupta, and Rajesh Anegundi. "Xeroderma Pigmentosa; Review and Case Report." Journal of Oral Health and Community Dentistry 1, no. 2 (2007): 43–45. http://dx.doi.org/10.5005/johcd-1-2-43.

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ABSTRACT Xeroderma Pigmentosa is caused by an autosomal recessive allele. It is characterized by dry, pigmented skin, spidery blood vessels in the skin, skin cancers, and sometimes other abnormalities of both the eyes and brain. A harsh reaction to sunlight, such as severe sunburn and blistering at only a slight exposure, is a notable symptom and should be distinguished within the first year or two of life. The majority of the people who are born with these disorders die by early adulthood due to malignant cancers. This article reports a case of 6-year-old child suffering from XP with dental i

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Perrotta, S., E. Miraglia del Giudice, N. Alloisio, et al. "Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74)." Blood 83, no. 11 (1994): 3346–49. http://dx.doi.org/10.1182/blood.v83.11.3346.3346.

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Abstract We report a new mutation responsible for nonhemolytic hereditary elliptocytosis (HE). The proband displayed an impaired spectrin self- association and an increase of the alpha I 74-kD fragment (alpha I/74 abnormality). The responsible mutation occurred in exon 2 of spectrin alpha-gene: alpha 34 Arg-->Trp (CGG-->TGG), defining spectrin Genova. In Trans to allele alpha Genova, the proband disclosed allele alpha LELY, a common low-expression allele of spectrin alpha-gene. It was recognized through particular peptide maps as well as characteristic mutations in exon 40 and intron 45,

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Perrotta, S., E. Miraglia del Giudice, N. Alloisio, et al. "Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74)." Blood 83, no. 11 (1994): 3346–49. http://dx.doi.org/10.1182/blood.v83.11.3346.bloodjournal83113346.

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We report a new mutation responsible for nonhemolytic hereditary elliptocytosis (HE). The proband displayed an impaired spectrin self- association and an increase of the alpha I 74-kD fragment (alpha I/74 abnormality). The responsible mutation occurred in exon 2 of spectrin alpha-gene: alpha 34 Arg-->Trp (CGG-->TGG), defining spectrin Genova. In Trans to allele alpha Genova, the proband disclosed allele alpha LELY, a common low-expression allele of spectrin alpha-gene. It was recognized through particular peptide maps as well as characteristic mutations in exon 40 and intron 45, respecti

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