نتائج البحث

Nanoplasmonic Infrared Microarray Sensor Enabling Structural Protein Biomarker‐Based Drug Screening for Neurodegenerative Diseases.

• Authors : Kavungal, Deepthy^1,2 (AUTHOR); Morro, Enzo² (AUTHOR); Kumar, Senthil T^2,3 (AUTHOR)

• Source: Advanced Science. 10/20/2025, Vol. 12 Issue 39, p1-18. 18p.

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A multi-classification deep neural network for cancer type identification from high-dimension, small-sample and imbalanced gene microarray data.

• Authors : Zeng, Yifu^1,2 (AUTHOR); Zhang, Yixiang³ (AUTHOR); Xiao, Zikai¹ (AUTHOR)

• Source: Scientific Reports. 2/12/2025, Vol. 15 Issue 1, p1-19. 19p.

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Fast and Economic Microarray-Based Detection of Species-, Resistance-, and Virulence-Associated Genes in Clinical Strains of Vancomycin-Resistant Enterococci (VRE).

• Authors : Osadare, Ibukun Elizabeth^1,2 (AUTHOR) ; Monecke, Stefan^1,2 (AUTHOR) ; Abdilahi, Abdinasir^1,2 (AUTHOR)

• Source: Sensors (14248220). Oct2024, Vol. 24 Issue 19, p6476. 17p.

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Genetic findings of children with congenital heart diseases using chromosomal microarray and trio-based whole exome sequencing.

• Authors : Guo, Rui^1,2 (AUTHOR); Duan, Chunhong² (AUTHOR); Zarrei, Mehdi^3,4 (AUTHOR)

• Source: Scientific Reports. 7/26/2025, Vol. 15 Issue 1, p1-11. 11p.

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Meta-analysis of microarray data to identify potential signature genes and MiRNAs associated with the pathogenesis of asthma

• Authors : Asma Vafadar; Shayan Khalili Alashti; Saeed Khazayel

Subjects: Asthma; Microarray meta-analysis; Gene expression

• Source: Journal of Translational Medicine, Vol 23, Iss 1, Pp 1-20 (2025)

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Comparative analysis of hybrid-SNP microarray and nanopore sequencing for detection of large-sized copy number variants in the human genome

• Authors : Catarina Silva; José Ferrão; Bárbara Marques

Subjects: Third-generation sequencing; Whole genome sequencing; Nanopore Sequencing

• Source: Molecular Cytogenetics, Vol 18, Iss 1, Pp 1-15 (2025)

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Gold nanoparticle-decorated fluorine-doped tin oxide substrate for sensitive label-free OIRD microarray chips

• Authors : Yuda Ren; Meng Li; Xiaoyi Li

Subjects: Limit of Detection; Tin Compounds; Metal Nanoparticles

• Source: Analytical and Bioanalytical Chemistry. 416:3775-3783

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超声检查正常和异常的高龄孕妇胎儿染色体微阵列分析.

• Authors : 刘利娜¹; 吴和明¹; 郑志远¹

• Source: Guangdong Medical Journal. Apr2025, Vol. 46 Issue 4, p538-541. 4p.

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ACG-SFE: Adaptive cluster-guided simple, fast, and efficient feature selection for high-dimensional microarray data in binary classification.

• Authors : Tye, Yi Wei¹ (AUTHOR); Chew, XinYing¹ (AUTHOR) ; Yusof, Umi Kalsom² (AUTHOR)

• Source: PLoS ONE. 9/8/2025, Vol. 20 Issue 9, p1-38. 38p.

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The Diagnostic Utility of Prenatal Microarray in High-Risk Pregnancies: A Single-Center Experience in Enhancing Reproductive Care and Risk Stratification.

• Authors : Bakır, Abdullatif¹ (AUTHOR) ; Alay, Mustafa Tarık^1,2 (AUTHOR); Tekbaş, Umut Can^1,3 (AUTHOR)

• Source: Diagnostics (2075-4418). Sep2025, Vol. 15 Issue 17, p2129. 13p.

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An updated comparison of microarray and RNA-seq for concentration response transcriptomic study: case studies with two cannabinoids, cannabichromene and cannabinol

• Authors : Xiugong Gao; Miranda R. Yourick; Kayla Campasino

Subjects: BMC modeling; Cannabinoids; Sequence Analysis, RNA

• Source: BMC GenomicsBMC Genomics, Vol 26, Iss 1, Pp 1-20 (2025)

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Whole genome uniparental isodisomy detected using single nucleotide polymorphism (SNP) microarray in molar pregnancy: a case report

• Authors : Onyinye O. Okonkwo; Veronica Ortega; Sheila Kane

Subjects: Uniparental disomy (UPD); Complete hydatidiform mole (CHM); Single nucleotide polymorphism (SNP) microarray

• Source: Mol CytogenetMolecular Cytogenetics, Vol 18, Iss 1, Pp 1-7 (2025)

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Etiological diagnosis of miscarriage by combining use of chromosomal microarray analysis and whole-exome sequencing

• Authors : Jianlong Zhuang; Wanyu Fu; Ling Gu

Subjects: Chromosomal microarray analysis; Whole-exome sequencing; Etiological diagnosis

• Source: European Journal of Medical Research, Vol 30, Iss 1, Pp 1-9 (2025)

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A comparison of the TempO-Seq and Affymetrix microarray platform using RTqPCR validation.

• Authors : Wehr, Matthias M.¹ (AUTHOR) ; Reamon-Buettner, Stella Marie¹ (AUTHOR); Ritter, Detlef¹ (AUTHOR)

• Source: BMC Genomics. 7/3/2024, Vol. 25 Issue 1, p1-14. 14p.

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AN APPROPRIATE APPROACH ON THE IMPLICATIONS OF MICROARRAY TECHNOLOGY FOR ANIMAL GENETIC RESEARCH.

• Authors : DAVIDESCU, Madalina Alexandra¹; MADESCU, Bianca Maria¹; PANZARU, Claudia¹

• Source: Scientific Papers. Series D. Animal Science. 2024, Vol. 67 Issue 2, p23-30. 8p.

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Transdermal Administration of Nanobody Molecules using Hydrogel‐Forming Microarray Patch Technology: A Unique Delivery Approach.

• Authors : Hutton, Aaron R. J.¹ (AUTHOR); Kirkby, Melissa¹ (AUTHOR); Van Bogaert, Tom² (AUTHOR)

• Source: Macromolecular Materials & Engineering. Jun2024, Vol. 309 Issue 6, p1-13. 13p.

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Evaluating Microarray Pharmacogenetic Testing in Cancer Patients

• Authors : Atrium Health Levine Cancer Institute

• Source: Evaluating the Use of Microarray Pharmacogenetic Testing in Patients With Cancer

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An Evolutional Neural Network Framework for Classification of Microarray Data

• Authors : Evari, Maryam Eshraghi; Sulaiman, Md Nasir; Behjat, Amir Rajabi

Subjects: Computer Science - Neural and Evolutionary Computing; Computer Science - Artificial Intelligence; Quantitative Biology - Genomics

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PSG and Other Candidate Genes as Potential Biomarkers of Therapy Resistance in B-ALL: Insights from Chromosomal Microarray Analysis and Machine Learning.

• Authors : Surimova V; National Medical Research Center for Hematology, 125167 Moscow, Russia.; Intelligent Systems in Management and Automation Department, Moscow Technical University of Communications and Informatics, 111024 Moscow, Russia.

Subjects: Machine Learning* ; Drug Resistance, Neoplasm*/Drug Resistance, Neoplasm*/Drug Resistance, Neoplasm*/genetics ; Biomarkers, Tumor*/Biomarkers, Tumor*/Biomarkers, Tumor*/genetics

• Source: International journal of molecular sciences [Int J Mol Sci] 2025 Aug 01; Vol. 26 (15). Date of Electronic Publication: 2025 Aug 01.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067

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Prenatal identification of carrier status for autosomal recessive disorders on chromosomal microarray.

• Authors : Yu An¹; Orthlieb, Marlena²; Ramaswamy, Priya²

• Source: Perinatal Journal. Dec2023, Vol. 31 Issue 3, p244-249. 6p.

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Complementary role of echocardiography, karyotyping, and chromosomal microarray in congenital cardiac anomalies

• Authors : Jun Yin; Xiaomeng Zhang; Qingsong Wang

Subjects: congenital cardiac anomalies; echocardiography; chromosome karyotyping

• Source: Frontiers in Medicine, Vol 12 (2025)

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A retrospective study for the diagnostic value of chromosomal microarray analysis in fetuses with high-risk prenatal indications

• Authors : Hui Xiao; Junfang Xiao; Huan Zhang

Subjects: chromosomal microarray analysis; copy number variations; prenatal diagnosis

• Source: Frontiers in Genetics, Vol 16 (2025)

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High-throughput screening of monoclonal antibodies against carbapenemases using a multiplex protein microarray platform

• Authors : Sascha D. Braun; Martin Reinicke; Celia Diezel

Subjects: carbapenemase; protein microarray; monoclonal antibody

• Source: Frontiers in Microbiology, Vol 16 (2025)

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مالتیپل اسکلروزیس و مسیر سیگنال دهی MAPK یک مطالعه مبتنی بر ریز آرایه.

• Authors : میرزا علی مفضل جه^1,2,3; امیررضا دهقان⁴; اباذر روستازاده^1,3,5

• Source: Pars Journal of Medical Sciences. Feb2025, Vol. 22 Issue 4, p72-78. 7p.

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Multiple primary dermatofibrosarcoma protuberans tumors in a single patient with chromosomal microarray analysis: A case report and review

• Authors : Joseph S. Durgin; Carli P. Whittington; Mallory Joseph

Subjects: Male; Skin Neoplasms; Oncogene Proteins, Fusion

• Source: Journal of Cutaneous Pathology. 51:490-495

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