Preliminary data regarding the influence of the COL1a1 rs2249492 polymorphism on the risk of malocclusion in the Romanian population by Adina Maria TOPÂRCEAN, Arina ACATRINEI, Ioana RUSU, Cristina MIRCEA, Dana FEȘTILĂ, Ondine Patricia LUCACIU, Radu Septimiu CÂMPIAN, Odette BODO, Beatrice KELEMEN, Mircea Constantin Dinu GHERGIE

“…Subsequent studies on larger sample sizes should include statistical analysis focused on associations between the rs2249492 allele and continuous phenotypic variation inside, but not restricted to Class II malocclusion, in order to acquire a more detailed picture of the interaction between the polymorphism and this complex condition. …”
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Genetic Navigation: A Narrative Review of XRCC1 Polymorphism Impact on Platinum-Based Chemotherapy Outcomes in NSCLC Patients by Permatasari LI, Afifah NN, Ishmatullah MH, Intania R, Halimah E, Barliana MI

“…This review aims to investigate the role of XRCC1 polymorphisms in platinum resistance, focusing on their impact on DNA repair efficiency. …”
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LncRNA RNF144A-AS1 gene polymorphisms and their influence on lung cancer patients in the Chinese Han population by Hongjiao Wu, Yuning Xie, Ang Li, Xiyao Liu, Liwen Guo, Fengjun Wu, Zhenbang Yang, Zhi Zhang, Xuemei Zhang

“…Lung cancer is primarily classified as NSCLC, which is distinguished by a wide range of genetic variations. This study focused on RNF144A-AS1, a relatively unexplored lncRNA, to explore the impact of its genetic polymorphisms on the susceptibility to NSCLC. …”
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A comprehensive consolidation of data on the connection between CDKN2A polymorphisms and the susceptibility to childhood acute lymphoblastic leukemia by Maryam Aghasipour, Fatemeh Asadian, Seyed Alireza Dastgheib, Abolhasan Alijanpour, Ali Masoudi, Maedeh Barahman, Mohammad Golshan-Tafti, Reza Bahrami, Amirmasoud Shiri, Hossein Aarafi, Kazem Aghili, Hossein Neamatzadeh

“…This investigation was undertaken to examine the correlation between CDKN2A polymorphisms and the risk of acute lymphoblastic leukemia in children. …”
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Genetic Associations of IL-2 (rs2069762) and EGR3 (rs3750192) Polymorphisms with Schizophrenia: A Meta-Analysis by Anu Shibi Anilkumar, Sheena Mariam Thomas, Ramakrishnan Veerabathiran

“…The inclusion criteria focused on studies linking IL-2, EGR3, and schizophrenia, requiring genotypic and allele frequency data. …”
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The Specific Dermatoses of Pregnancy by Paulina Polańska

“…They encompass four primary conditions: atopic eruption of pregnancy (AEP), polymorphic eruption of pregnancy (PEP), intrahepatic cholestasis of pregnancy (ICP), and pemphigoid gestationis (PG). …”
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Flora Checklist in the Bayanaul State National Nature Park, Kazakhstan with Special Focus on New Species of Conservation Interest by Zhumabekova Bibigul, Tarasovskaya Natalia, Klimenko Mikhail, Shakeneva Dinara, Assylbekova Gulmira, Shujaul Mulk Khan, Fazal Manan

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Selection for Growth Performance in <i>Oreochromis niloticus</i> Across Different Aquatic Environments Using Growth Hormone Gene Polymorphisms by Fawzia S. Ali, Simone T. Awad, Mohamed Ismail, Shabaan A. Hemeda, Abeer F. El Nahas, Eman M. Abbas, Ahmed Mamoon, Hani Nazmi, Ehab El-Haroun

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Glutathione S-transferase M1 (GSTM1) and T1 (GSTT1) null polymorphisms and the risk of hypertension: a meta-analysis. by Beihai Ge, Yadong Song, Yi Zhang, Xiaowen Liu, Yuxiang Wen, Xiaomei Guo

“…<h4>Background</h4>Some studies have recently focused on the association between glutathione S-transferase M1 (GSTM1) and glutathione S-transferase T1 (GSTT1) null polymorphisms and hypertension; however, results have been inconsistent.…”
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Investigation of the association of AGTR1 A1166C rs5186 and FTO rs9939609 polymorphisms with the obesity in children and adolescents by Alaa Hashim Abd Ali, Teplyakova E. D., Bocharova O. V., Karantysh G. V., Shkurat T. P.

“…Genotyping of A1166C polymorphisms of the AGTR1 rs5186 gene was performed using PCR allele-specific primers. …”
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Phylogeny of <i>Yersinia pestis</i> strains of the 4.ANT lineage from the Tuva mountains and adjacent plague foci by Elizaveta V. Stankovtseva, Eugeniy G. Oglodin, Dmitry B. Verzhutsky, Nadezhda S. Chervyakova, Ekaterina A. Naryshkina, Andrey V. Fedorov, Galina A. Eroshenko, Sergey V. Balakhonov, Vladimir V. Kutyrev

“…The Tuva mountain plague focus (TMPF) in Russia has been continuously epizootically active since its discovery in 1964. …”
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Molecular tool for efficient breeding of DOMINANT Greenshell laying hens and significant refinement of phenotypic selection focused on eggshell color by Kristina Beranova, Eva Jozova, Vojtech Anderle, Michael Rost, Lukas Zita, Pavel Beran, Helena Tyllerova Landova, Vladislav Curn, Milan Tyller

“…This study presents the results of genotyping the polymorphism of the O locus responsible for shell coloration and photometric measurement of eggshell color based on the CIELAb system, which was carried out on the unique Czech breeding population Dominant Greenshell. …”
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A functional polymorphism in the promoter region of microRNA-146a is associated with the risk of Alzheimer disease and the rate of cognitive decline in patients. by Lili Cui, You Li, Guoda Ma, Yan Wang, Yujie Cai, Shengyuan Liu, Yanyan Chen, Jia Li, Yuliu Xie, Gen Liu, Bin Zhao, Keshen Li

“…Although genetic studies have focused on the association between the miR146a gene and susceptibility to several diseases, no association study of miR146a variability with AD has been conducted. …”
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Dynamics of Cognitive Impairment in Older Adults Linked to Suicide-Related Single-Nucleotide Polymorphisms: A 3-Year Follow-Up Study by Yana Zorkina, Alexander Berdalin, Irina Morozova, Alisa Andryushchenko, Konstantin Pavlov, Olga Pavlova, Olga Abramova, Valeriya Ushakova, Angelina Zeltzer, Marat Kurmishev, Victor Savilov, Olga Karpenko, Georgy Kostyuk, Anna Morozova

“…Conclusions: The research focused on analyzing genetic factors of cognitive decline in healthy older adults without subjective cognitive decline. …”
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Lack of evidence from studies of soluble protein fragments that Knops blood group polymorphisms in complement receptor-type 1 are driven by malaria. by Patience B Tetteh-Quarcoo, Christoph Q Schmidt, Wai-Hong Tham, Richard Hauhart, Haydyn D T Mertens, Arthur Rowe, John P Atkinson, Alan F Cowman, J Alexandra Rowe, Paul N Barlow

“…Here, four variant short recombinant versions of CR1 were produced and analyzed, focusing on complement control protein modules (CCPs) 15-25 of its ectodomain. …”
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The rs243865 Polymorphism in Matrix Metalloproteinase-2 and its Association With Target Organ Damage in Patients With Resistant Hypertension: Cross-Sectional Study by An Tuan Huynh, Hoang Anh Vu, Ho Quoc Chuong, Tien Hoang Anh, An Viet Tran

“…Particular attention recently has focused on the role of matrix metalloproteinase-2 (MMP-2) gene polymorphisms, implicated in hypertensive target organ damage (TOD). …”
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Investigating the role of the brain-derived neurotrophic factor Val66Met polymorphism in repetitive mild traumatic brain injury outcomes in rats by Lauren P. Giesler, William T. O’Brien, Jesse Bain, Gershon Spitz, Emily J. Jaehne, Maarten van den Buuse, Sandy R. Shultz, Richelle Mychasiuk, Stuart J. McDonald

“…While demographic factors like age and sex influence outcomes, the understanding of genetic contributions, particularly the role of the brain-derived neurotrophic factor (BDNF) Val66Met polymorphism, remains limited. This study aimed to characterize acute effects of repetitive mTBI (rmTBI) in rats with the Val68Met SNP, the rodent equivalent of the human Val66Met, focusing on behavioral, fluid biomarker, and histological changes. …”
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Investigating the Role of Genetic Polymorphisms in External Apical Root Resorption Among Orthodontic Patients: Implications for Treatment Outcomes—A Literature Review by Christina Charisi, Vasileios Zisis, Konstantinos Poulopoulos, Stefanos Zisis, Athanasios Poulopoulos, Dieter Müßig

“…The search was conducted using MEDLINE (National Library of Medicine)-PubMed with restrictions concerning the date of publication. In particular, we focused on the period 2014–2024 using the following keywords: gene polymorphisms AND orthodontic treatment AND apical root resorption OR external apical root resorption. …”
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THE GENETIC SUSCEPTIBILITY TO ATHEROSCLEROSIS by T. V. Kozhanova, E. V. Neudakhin, S. S. Zhilina, T. I. Mescheryakova, A. A. Abramov, E. N. Lukash, A. G. Prityko

“…Multiple factors, including endothelial dysfunction, lipid metabolism defects, inflammation and immune responses, oxidative stress, cell proliferation, tissue remodeling and hemostatic defects are involved in the pathogenesis of atherosclerosis. In this review we focus and discuss on some of the major candidate genes and genetic polymorphisms associated with human atherosclerotic vascular diseases.…”
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Unravelling genetic diversity in pointed gourd (Trichosanthes dioica) genotypes from India’s Eastern plateau and hill region: Insights from morphological and molecular markers by Ankit Kumar Sinha, P. Bhavana, A.K. Singh, J.K. Ranjan, H. Choudhary, G.P. Mishra, K. Thamilarsi, Paresh Chaukhande, Reshma Shinde, Prakash Kumar, Jitendra Rajak, Sajiya Ekbal

“…Molecular analysis with sixteen polymorphic ISSR markers generated 96 bands, of which 76 were polymorphic (78.91%), with Polymorphism Information Content (PIC) ranging from 0.35 to 0.47. …”
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