Works matching DE "COMPARATIVE genomic hybridization"
Results: 1623
Genome-wide CTCF distribution in vertebrates defines equivalent sites that aid the identification of disease-associated genes.
- Published in:
- Nature Structural & Molecular Biology, 2011, v. 18, n. 6, p. 708, doi. 10.1038/nsmb.2059
- By:
- Publication type:
- Article
A simple method for enhancing hybridization efficiency in chromosome and array comparative genomic hybridization.
- Published in:
- Biotechnic & Histochemistry, 2011, v. 86, n. 3, p. 192, doi. 10.3109/10520291003666781
- By:
- Publication type:
- Article
A simple method for fixation and microdissection of frozen fresh tissue sections for molecular cytogenetic analysis of cancers.
- Published in:
- Biotechnic & Histochemistry, 2005, v. 80, n. 3/4, p. 147, doi. 10.1080/10520290500382806
- By:
- Publication type:
- Article
Preliminary analysis of genomic abnormalities in canine meningiomas.
- Published in:
- Veterinary & Comparative Oncology, 2008, v. 6, n. 3, p. 182, doi. 10.1111/j.1476-5829.2008.00159.x
- By:
- Publication type:
- Article
Molecular signatures for the phylum (class) Thermotogae and a proposal for its division into three orders ( Thermotogales, Kosmotogales ord. nov. and Petrotogales ord. nov.) containing four families ( Thermotogaceae, Fervidobacteriaceae fam. nov., Kosmotogaceae fam. nov. and Petrotogaceae fam. nov.) and a new genus Pseudothermotoga gen. nov. with five new combinations
- Published in:
- Antonie van Leeuwenhoek, 2014, v. 105, n. 1, p. 143, doi. 10.1007/s10482-013-0062-7
- By:
- Publication type:
- Article
Genetic diversity of Rhodopirellula strains.
- Published in:
- Antonie van Leeuwenhoek, 2013, v. 104, n. 4, p. 547, doi. 10.1007/s10482-013-0004-4
- By:
- Publication type:
- Article
Unique Retrotransposon LINE-1 Distribution at the Prader–Willi Angelman Syndrome Locus.
- Published in:
- Journal of Molecular Evolution, 2007, v. 65, n. 4, p. 475, doi. 10.1007/s00239-007-9043-7
- By:
- Publication type:
- Article
Comparative Genomics Reveals Long, Evolutionarily Conserved, Low-Complexity Islands in Yeast Proteins.
- Published in:
- Journal of Molecular Evolution, 2006, v. 63, n. 3, p. 415, doi. 10.1007/s00239-005-0291-0
- By:
- Publication type:
- Article
Fragile Bones Secondary to SMURF1 Gene Duplication.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Bridging the gap from prenatal karyotyping to whole-genome array comparative genomic hybridization in Hong Kong: survey on knowledge and acceptance of health-care providers and pregnant women.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Comprehensive genetic assessment of the human embryo: can empiric application of microarray comparative genomic hybridization reduce multiple gestation rate by single fresh blastocyst transfer?
- Published in:
- Archives of Gynecology & Obstetrics, 2012, v. 286, n. 3, p. 755, doi. 10.1007/s00404-012-2396-1
- By:
- Publication type:
- Article
Two predominant molecular subtypes of spinal meningioma: thoracic NF2-mutant tumors strongly associated with female sex, and cervical AKT1-mutant tumors originating ventral to the spinal cord.
- Published in:
- Acta Neuropathologica, 2022, v. 144, n. 5, p. 1053, doi. 10.1007/s00401-022-02474-9
- By:
- Publication type:
- Article
Molecular classification of diffuse cerebral WHO grade II/III gliomas using genome- and transcriptome-wide profiling improves stratification of prognostically distinct patient groups.
- Published in:
- Acta Neuropathologica, 2015, v. 129, n. 5, p. 679, doi. 10.1007/s00401-015-1409-0
- By:
- Publication type:
- Article
Oncogenic FAM131B-BRAF fusion resulting from 7q34 deletion comprises an alternative mechanism of MAPK pathway activation in pilocytic astrocytoma.
- Published in:
- Acta Neuropathologica, 2011, v. 121, n. 6, p. 763, doi. 10.1007/s00401-011-0817-z
- By:
- Publication type:
- Article
Machine Learning Based Big Data Processing Framework for Cancer Diagnosis Using Hidden Markov Model and GM Clustering.
- Published in:
- Wireless Personal Communications, 2018, v. 102, n. 3, p. 2099, doi. 10.1007/s11277-017-5044-z
- By:
- Publication type:
- Article
Imputation of non-genotyped individuals based on genotyped relatives: assessing the imputation accuracy of a real case scenario in dairy cattle.
- Published in:
- Genetics Selection Evolution, 2014, v. 46, p. 1, doi. 10.1186/1297-9686-46-6
- By:
- Publication type:
- Article
Genomic imbalances in childhood medulloblastoma by comparative genomic hybridization.
- Published in:
- Turkish Journal of Cancer, 2003, v. 33, n. 4, p. 177
- By:
- Publication type:
- Article
Experimental Design and Data Analysis for Array Comparative Genomic Hybridization.
- Published in:
- Cancer Investigation, 2008, v. 26, n. 9, p. 923, doi. 10.1080/07357900801993432
- By:
- Publication type:
- Article
Investigation of the diagnostic value of chromosome analysis and bacterial artificial chromosome-based array comparative genomic hybridization in prenatal diagnosis.
- Published in:
- Turkish Journal of Medical Sciences, 2015, v. 45, n. 6, p. 1263, doi. 10.3906/sag-1312-161
- By:
- Publication type:
- Article
The psychiatric phenotype of 15q11.2-q13.3 duplications.
- Published in:
- European Psychiatry, 2021, v. 64, p. S720, doi. 10.1192/j.eurpsy.2021.1908
- By:
- Publication type:
- Article
Late-Onset Sacsinopathy Diagnosed by Exome Sequencing and Comparative Genomic Hybridization.
- Published in:
- Journal of Neurogenetics, 2013, v. 27, n. 4, p. 176, doi. 10.3109/01677063.2013.831094
- By:
- Publication type:
- Article
The correlation between copy number variation in Chromosome 14 and DNA methylation in Saudi autistic children.
- Published in:
- European Review for Medical & Pharmacological Sciences, 2022, v. 26, n. 21, p. 7866
- By:
- Publication type:
- Article
Editorial Comment from Dr Kuroda to Male infertility in Sertoli cell‐only syndrome: An investigation of autosomal gene defects.
- Published in:
- International Journal of Urology, 2019, v. 26, n. 2, p. 298, doi. 10.1111/iju.13867
- By:
- Publication type:
- Article
Male infertility in Sertoli cell‐only syndrome: An investigation of autosomal gene defects.
- Published in:
- International Journal of Urology, 2019, v. 26, n. 2, p. 292, doi. 10.1111/iju.13863
- By:
- Publication type:
- Article
Editorial Comment from Dr Miyamoto to Male infertility in Sertoli cell‐only syndrome: An investigation of autosomal gene defects.
- Published in:
- International Journal of Urology, 2019, v. 26, n. 2, p. 298, doi. 10.1111/iju.13860
- By:
- Publication type:
- Article
Comparative genomic hybridization (CGH) of augmentation cystoplasties.
- Published in:
- International Journal of Urology, 2007, v. 14, n. 6, p. 539, doi. 10.1111/j.1442-2042.2006.01724.x
- By:
- Publication type:
- Article
The Use of CGH Arrays for Identifying Copy Number Variations in Children with Autism Spectrum Disorder.
- Published in:
- Brain Sciences (2076-3425), 2024, v. 14, n. 3, p. 273, doi. 10.3390/brainsci14030273
- By:
- Publication type:
- Article
Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong.
- Published in:
- Clinical & Translational Medicine, 2016, v. 5, n. 1, p. 1, doi. 10.1186/s40169-016-0098-1
- By:
- Publication type:
- Article
Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong.
- Published in:
- Clinical & Translational Medicine, 2016, v. 5, n. 1, p. 1, doi. 10.1186/s40169-016-0098-1
- By:
- Publication type:
- Article
Phylogenomics of the killer whale indicates ecotype divergence in sympatry.
- Published in:
- Heredity, 2015, v. 114, n. 1, p. 48, doi. 10.1038/hdy.2014.67
- By:
- Publication type:
- Article
Poster Abstracts.
- Published in:
- 2009
- Publication type:
- Abstract
Integrating copy number data of 64 iAMP21 BCP-ALL patients narrows the common region of amplification to 1.57 Mb.
- Published in:
- Frontiers in Oncology, 2023, v. 13, p. 1, doi. 10.3389/fonc.2023.1128560
- By:
- Publication type:
- Article
Common Variable Immunodeficiency and Neurodevelopmental Delay Due to a 13Mb Deletion on Chromosome 4 Including the NFKB1 Gene: A Case Report.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
A Retrospective Analysis of 10-Year Data Assessed the Diagnostic Accuracy and Efficacy of Cytogenomic Abnormalities in Current Prenatal and Pediatric Settings.
- Published in:
- Frontiers in Genetics, 2019, v. 10, p. 1, doi. 10.3389/fgene.2019.01162
- By:
- Publication type:
- Article
Reproductive History of a Woman With 8p and 18p Genetic Imbalance and Minor Phenotypic Abnormalities.
- Published in:
- Frontiers in Genetics, 2019, v. 10, p. 1, doi. 10.3389/fgene.2019.01164
- By:
- Publication type:
- Article
A Retrospective Analysis of 10-Year Data Assessed the Diagnostic Accuracy and Efficacy of Cytogenomic Abnormalities in Current Prenatal and Pediatric Settings.
- Published in:
- Frontiers in Genetics, 2019, v. 10, p. 1, doi. 10.3389/fgene.2019.01162
- By:
- Publication type:
- Article
Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes.
- Published in:
- Frontiers in Genetics, 2019, p. 1, doi. 10.3389/fgene.2019.00955
- By:
- Publication type:
- Article
Comparative Cytogenetics and Neo-Y Formation in Small-Sized Fish Species of the Genus Pyrrhulina (Characiformes, Lebiasinidae).
- Published in:
- Frontiers in Genetics, 2019, p. 1, doi. 10.3389/fgene.2019.00678
- By:
- Publication type:
- Article
IgG and IgA subclass mRNA-bearing plasma cells in periodontitis gingival tissue and immunoglobulin levels in the gingival crevicular fluid.
- Published in:
- Clinical & Experimental Immunology, 1997, v. 107, n. 1, p. 158, doi. 10.1046/j.1365-2249.1997.d01-891.x
- By:
- Publication type:
- Article
EXPLORING THE CHROMOSOMAL BLUEPRINT: THE PROMISE OF CYTOGENETICS IN UNRAVELING GENETIC MYSTERIES.
- Published in:
- International Journal of Pharmaceutical, Chemical & Biological Sciences, 2024, v. 14, n. 2, p. 1
- By:
- Publication type:
- Article
Array-based Comparative Genomic Hybridization and Its Application to Cancer Genomes and Human Genetics.
- Published in:
- Journal of Lung Cancer, 2011, v. 10, n. 2, p. 77, doi. 10.6058/jlc.2011.10.2.77
- By:
- Publication type:
- Article
A Novel Diagnostic Method for Thyroid Follicular Tumors Based on Immunofluorescence Analysis of p53-Binding Protein 1 Expression: Detection of Genomic Instability.
- Published in:
- Thyroid, 2019, v. 29, n. 5, p. 657, doi. 10.1089/thy.2018.0548
- By:
- Publication type:
- Article
Aberrant DNA methylation patterns in microsatellite stable human colorectal cancers define a new marker panel for the CpG island methylator phenotype.
- Published in:
- International Journal of Cancer, 2022, v. 150, n. 4, p. 617, doi. 10.1002/ijc.33831
- By:
- Publication type:
- Article
Enhanced DNA repair and genomic stability identify a novel HIV‐related diffuse large B‐cell lymphoma signature.
- Published in:
- International Journal of Cancer, 2019, v. 145, n. 11, p. 3078, doi. 10.1002/ijc.32381
- By:
- Publication type:
- Article
Characterization of six Merkel cell polyomavirus‐positive Merkel cell carcinoma cell lines: Integration pattern suggest that large T antigen truncating events occur before or during integration.
- Published in:
- International Journal of Cancer, 2019, v. 145, n. 4, p. 1020, doi. 10.1002/ijc.32280
- By:
- Publication type:
- Article
Anti-Hypothalamus and Anti-Pituitary Auto-antibodies in ROHHAD Syndrome: Additional Evidence Supporting an Autoimmune Etiopathogenesis.
- Published in:
- Hormone Research in Paediatrics, 2019, v. 92, n. 2, p. 124, doi. 10.1159/000499163
- By:
- Publication type:
- Article
A Novel Deletion in the Thyrotropin Beta-Subunit Gene Identified by Array Comparative Genomic Hybridization Analysis Causes Central Congenital Hypothyroidism in a Boy Originating from Turkey.
- Published in:
- Hormone Research in Paediatrics, 2014, v. 82, n. 3, p. 201, doi. 10.1159/000362413
- By:
- Publication type:
- Article
Advances in Understanding the Karyotype Evolution of Tetrapulmonata and Two Other Arachnid Taxa, Ricinulei and Solifugae.
- Published in:
- Genes, 2025, v. 16, n. 2, p. 207, doi. 10.3390/genes16020207
- By:
- Publication type:
- Article
Identification and Candidate Gene Evaluation of a Large Fast Neutron-Induced Deletion Associated with a High-Oil Phenotype in Soybean Seeds.
- Published in:
- Genes, 2024, v. 15, n. 7, p. 892, doi. 10.3390/genes15070892
- By:
- Publication type:
- Article
Robertsonian Translocation between Human Chromosomes 21 and 22, Inherited across Three Generations, without Any Phenotypic Effect.
- Published in:
- Genes, 2024, v. 15, n. 6, p. 722, doi. 10.3390/genes15060722
- By:
- Publication type:
- Article