Arama Sonuçları - "microarray"

Analysis of Circadian Clock Gene Expression in Human Skin Explants Yazar: William Cvammen, Michael G. Kemp

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Mutual Balance between Vasohibin-1 and Soluble VEGFR-1 in Endothelial Cells Yazar: Yasufumi Sato, Hiroki Miyashita, Akihide Ohkuchi, Hirotada Suzuki

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Case Report: Paternal Uniparental Isodisomy and Heterodisomy of Chromosome 16 With a Normal Phenotype Yazar: Xu Zhang, Li Liu, Yang Liu, Xin Pan

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Searching for biomarkers in the progression from polycystic ovary syndrome to endometrial carcinoma Yazar: Zhenzhen Lu, Ying Gao

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Concurrent OPA1 mutation and chromosome 3q deletion leading to Behr syndrome: a case report Yazar: Ting Zeng, Linyan Liao, Yi Guo, Xuxu Liu, Xiaobo Xiong, Yu Zhang, Shi Cen, Honghui Li, Shuzhang Wei

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Presence of Uterine Leiomyomas Has No Significant Impact on Gene Expression Profile in the Scalp of Patients with Central Centrifugal Cicatricial Alopecia Yazar: Taylor A. Jamerson, C. Conover Talbot, Jr, Yemisi Dina, Crystal Aguh

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Circuits Regulating Superoxide and Nitric Oxide Production and Neutralization in Different Cell Types: Expression of Participating Genes and Changes Induced by Ionizing Radiation Yazar: Patryk Bil, Sylwia Ciesielska, Roman Jaksik, Joanna Rzeszowska-Wolny

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Personalized medicine: A step forward in dental treatment Yazar: Surbhi, Anand Kumar, Archna Nagpal, Puneeta Vohra

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Low Rates of Genetic Testing in Children With Developmental Delays, Intellectual Disability, and Autism Spectrum Disorders Yazar: John Peabody MD, PhD, Lisa DeMaria MA, Diana Tamandong-LaChica MD, Jhiedon Florentino MS, Maria Czarina Acelajado MD, Trever Burgon PhD

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Current Topics in Pharmacological Research on Bone Metabolism: Molecular Basis of Ectopic Bone Formation Induced by Mechanical Stress Yazar: Ken-Ichi Furukawa

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Prenatal Diagnosis of a Mosaic Paternal Uniparental Disomy for Chromosome 14: A Case Report of Kagami-Ogata Syndrome Yazar: Fenxia Li, Siping Liu, Bei Jia, Ruifeng Wu, Qingxian Chang

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Functional analysis of tumor metastasis: modeling colon cancer Yazar: Philip Y. Wai, Srinevas K. Reddy, Paul C. Kuo

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Exome sequencing identifies novel and known mutations in families with intellectual disability Yazar: Memoona Rasheed, Valeed Khan, Ricardo Harripaul, Maimoona Siddiqui, Madiha Amin Malik, Zahid Ullah, Muhammad Zahid, John B. Vincent, Muhammad Ansar

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Targeted haplotyping in pharmacogenomics using Oxford Nanopore Technologies' adaptive sampling Yazar: Koen Deserranno, Laurentijn Tilleman, Kaat Rubben, Dieter Deforce, Filip Van Nieuwerburgh

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Prenatal diagnosis of isochromosome 20q in a fetus with vertebral anomaly and rocker-bottom feet Yazar: Aline Receveur, Sophie Brisset, Jelena Martinovic, Anne Bazin, Laurence Lhomann, Claire Colmant, Dominique Pineau, Valérie Gautier, Lucie Tosca, Gérard Tachdjian

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Genomic Diagnosis for Pediatric Disorders: Revolution and Evolution Yazar: Emilie Lalonde, Stefan Rentas, Fumin Lin, Matthew C. Dulik, Cara M. Skraban, Nancy B. Spinner

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Transcriptomic Insights into the Effect of Melatonin in <i>Saccharomyces cerevisiae</i> in the Presence and Absence of Oxidative Stress Yazar: Mercè Sunyer-Figueres, Jennifer Vázquez, Albert Mas, María-Jesús Torija, Gemma Beltran

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2q37 deletion syndrome in a Colombian patient with macrocephaly: a case report Yazar: Sebastian Giraldo-Ocampo, Harry Pachajoa

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Effects of Scrophularia ningpoensis Hemsl. on Inhibition of Proliferation, Apoptosis Induction and NF-κB Signaling of Immortalized and Cancer Cell Lines Yazar: Thomas Efferth, Xiao Shen, Henry Johannes Greten, Tolga Eichhorn

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Recent advances and perspectives of nucleic acid detection for coronavirus Yazar: Minzhe Shen, Ying Zhou, Jiawei Ye, Abdu Ahmed Abdullah AL-maskri, Yu Kang, Su Zeng, Sheng Cai

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