array-based comparative genomic hybridization analysis (Agilent technologies)
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array-based comparative genomic hybridization analysis
Array Based Comparative Genomic Hybridization Analysis, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/array-based+comparative+genomic+hybridization+analysis/pmc10965544-110-7-11
Average 90 stars, based on 1 article reviews
Array Based Comparative Genomic Hybridization Analysis, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/array-based+comparative+genomic+hybridization+analysis/pmc10965544-110-7-11
Average 90 stars, based on 1 article reviews
array-based comparative genomic hybridization analysis - by Bioz Stars,
2026-11
90/100 stars
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other:Article Title: Enrichment of ultraconserved elements among genomic imbalances causing mental delay and congenital anomalies Article Snippet: All the remaining cases were studied by array-based comparative Article Title: Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome). Article Snippet: No distinctive abnormalities were noted on comparative Hybridization:Article Title: Long-read sequencing reveals chromothripsis in a molecularly unsolved case of Cornelia de Lange syndrome Article Snippet: .. The high-resolution 1 x 1M array-based comparative Article Title: Decreased Expression of Vitamin D Receptor May Affect an Immune Response Via VDR – MIRNA 155 - SOCS1 Pathway in Primary Biliary Cirrhosis Article Snippet: FRI-344 DECREASED EXPRESSION OF VITAMIN D RECEPTOR MAY AFFECT AN IMMUNE RESPONSE VIAVDR – MIRNA155 SOCS1 PATHWAY IN PRIMARY BILIARY CIRRHOSIS A.K.. Podhorodecka, U. Wasik, P. Milkiewicz, M. Milkiewicz.. Department of Medical Biology Laboratory, Pomeranian Medical University, Szczecin; Liver and Internal Medicine Unit, Medical University of Warsaw, Warsaw; Department of Clinical and Molecular Biochemistry, Pomeranian Medical University, Szczecin, Poland E-mail: agnieszkakempinska@interia.eu Article Title: Diagnostic utility of array-based Comparative Genomic Hybridization in a clinical setting Article Snippet: .. Hence, all 37 cases were further analyzed using Agilent 60k oligonucleotide array-Comparative Article Title: Identification of copy number variants on human chromosome 22 in patients with a variety of clinical findings. Article Snippet: The aims of this study were to create a copy number variant (CNV) profile of human chromosome 22 and to establish a genotype-phenotype correlation for patients with genomic abnormalities on chromosome 22.. Thus, 1,654 consecutive pediatric patients with a diversity of clinical findings were evaluated by high-resolution chromosomal microarray analysis (CMA).. We identified 25 individuals with abnormal CNVs on chromosome 22, representing 1.5% of the cases analyzed in this cohort. Article Title: The Intra-Tumor Heterogeneity of C19MC miRNA Cluster Expression Mirrors the Presence of the Side Population in Hepatocellular Carcimnoa Article Snippet: EXOGENOUS ADMINISTRATION OF SERPINB3 INHIBITS CELL REPROGRAMMING E. Torchio, S. Quarta, S. Giulitti, C. Turato, A. Biasiolo, C. Luni, M. Ruvoletto, G. Villano, G.G.. Giobbe, P. Pontisso, N. Elvassore.. Department of Medicine, Internal Medicine and Hepatology, Regional Center for Hepatology (RCH); Department of Industrial Engineering, University of Padua; Venetian Institut of Molecular Medicine (VIMM), Padova, Italy E-mail: erikatorchio@gmail.com Article Title: Use of Array Comparative Genomic Hybridization for the Diagnosis of DiGeorge Syndrome in Saudi Arabian Population. Article Snippet: DiGeorge syndrome (DGS) is a genetic disorder known as a clinically variable syndrome with over 180 associated phenotypic features.. It is caused by a common human deletion in the 22q11.2 chromosomal region and currently is affecting approximately 1 in 4,000 individuals.. Despite the prevalence of inherited diseases mainly due to consanguineous marriages, the current diagnosis of DGS in Saudi Arabia is mainly based on conventional high-resolution chromosome banding (karyotyping) and FISH techniques. Translocation Assay:Article Title: Long-read sequencing reveals chromothripsis in a molecularly unsolved case of Cornelia de Lange syndrome Article Snippet: .. The high-resolution 1 x 1M array-based comparative Clone Assay:Article Title: Decreased Expression of Vitamin D Receptor May Affect an Immune Response Via VDR – MIRNA 155 - SOCS1 Pathway in Primary Biliary Cirrhosis Article Snippet: FRI-344 DECREASED EXPRESSION OF VITAMIN D RECEPTOR MAY AFFECT AN IMMUNE RESPONSE VIAVDR – MIRNA155 SOCS1 PATHWAY IN PRIMARY BILIARY CIRRHOSIS A.K.. Podhorodecka, U. Wasik, P. Milkiewicz, M. Milkiewicz.. Department of Medical Biology Laboratory, Pomeranian Medical University, Szczecin; Liver and Internal Medicine Unit, Medical University of Warsaw, Warsaw; Department of Clinical and Molecular Biochemistry, Pomeranian Medical University, Szczecin, Poland E-mail: agnieszkakempinska@interia.eu Article Title: The Intra-Tumor Heterogeneity of C19MC miRNA Cluster Expression Mirrors the Presence of the Side Population in Hepatocellular Carcimnoa Article Snippet: EXOGENOUS ADMINISTRATION OF SERPINB3 INHIBITS CELL REPROGRAMMING E. Torchio, S. Quarta, S. Giulitti, C. Turato, A. Biasiolo, C. Luni, M. Ruvoletto, G. Villano, G.G.. Giobbe, P. Pontisso, N. Elvassore.. Department of Medicine, Internal Medicine and Hepatology, Regional Center for Hepatology (RCH); Department of Industrial Engineering, University of Padua; Venetian Institut of Molecular Medicine (VIMM), Padova, Italy E-mail: erikatorchio@gmail.com Biomarker Discovery:Article Title: Identification of copy number variants on human chromosome 22 in patients with a variety of clinical findings. Article Snippet: The aims of this study were to create a copy number variant (CNV) profile of human chromosome 22 and to establish a genotype-phenotype correlation for patients with genomic abnormalities on chromosome 22.. Thus, 1,654 consecutive pediatric patients with a diversity of clinical findings were evaluated by high-resolution chromosomal microarray analysis (CMA).. We identified 25 individuals with abnormal CNVs on chromosome 22, representing 1.5% of the cases analyzed in this cohort. Article Title: Use of Array Comparative Genomic Hybridization for the Diagnosis of DiGeorge Syndrome in Saudi Arabian Population. Article Snippet: DiGeorge syndrome (DGS) is a genetic disorder known as a clinically variable syndrome with over 180 associated phenotypic features.. It is caused by a common human deletion in the 22q11.2 chromosomal region and currently is affecting approximately 1 in 4,000 individuals.. Despite the prevalence of inherited diseases mainly due to consanguineous marriages, the current diagnosis of DGS in Saudi Arabia is mainly based on conventional high-resolution chromosome banding (karyotyping) and FISH techniques. |