In Situ Hybridization, Fluorescence Concept

subject area of

• 15q11.2 microdeletion (BP1–BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: A series of 52 patients  Academic Article
• A CGG-Repeat Expansion Mutation inZNF713Causes FRA7A: Association with Autistic Spectrum Disorder in two Families  Academic Article
• A new association of congenital hydrocephalus, albinism, megalocornea, and retinal coloboma in a syndromic child: A clinical and genetic study  Academic Article
• Acute Lymphoblastic Leukemia in a Patient With Constitutional Chromosome 1pter-p36.31 Duplication and 1q43-qter Deletion  Academic Article
• Alternative Lengthening of Telomeres Is Characterized by High Rates of Telomeric Exchange  Academic Article
• Amplification of telomerase (hTERT) gene is a poor prognostic marker in non-small-cell lung cancer  Academic Article
• An approach to small lymph node biopsies: pearls and pitfalls of reporting in the real world  Academic Article
• An uncommon 3.4-Mb interstitial deletion at 3q29  Academic Article
• Assignment of bovine trophinin (TRO) to the q arm of the X chromosome by fluorescencein situhybridization  Academic Article
• Assignment of the bovine attractin (ATRN) gene to chromosome 13q21→q22 by in situ hybridization  Academic Article
• Balanced translocation t(3;18)(p13;q22.3) and points mutation in the ZNF407 gene detected in patients with both moderate non-syndromic intellectual disability and autism  Academic Article
• Blood pressure and anthropometrics of 4-y-old children born after preimplantation genetic screening: follow-up of a unique, moderately sized, randomized controlled trial  Academic Article
• Canadian Anaplastic Lymphoma Kinase Study: A Model for Multicenter Standardization and Optimization of ALK Testing in Lung Cancer  Academic Article
• Canadian ROS proto-oncogene 1 study (CROS) for multi-institutional implementation of ROS1 testing in non-small cell lung cancer  Academic Article
• Chromosome content and ultrastructure of radiation-induced micronuclei  Academic Article
• Chromosome divergence during evolution of the tetraploid clawed frogs, Xenopus mellotropicalis and Xenopus epitropicalis as revealed by Zoo-FISH  Academic Article
• Comparison of HER2 Dual-Color and Fluorescence In Situ Hybridization in Breast Cancer  Academic Article
• Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements  Academic Article
• Confocal image characterization of human papillomavirus DNA sequences revealed with Eu in HeLa cell nuclei stained with Hoechst 33342.  Academic Article
• Core binding factor beta (CBFB) haploinsufficiency due to an interstitial deletion at 16q21q22 resulting in delayed cranial ossification, cleft palate, congenital heart anomalies, and feeding difficulties but favorable outcome  Academic Article
• Cyclin B-dependent kinase 1 regulates human TRF1 to modulate the resolution of sister telomeres  Academic Article
• Cytogenetic Prognostication Within Medulloblastoma Subgroups  Academic Article
• Cytogenetic comparison of saola <i>(Pseudoryx nghetinhensis)</i> and cattle <i>(Bos taurus)</i> using G- and Q-banding and FISH  Academic Article
• DMG26  Academic Article
• De novo 1q32q44 duplication and distal 1q trisomy syndrome  Academic Article
• De novo deletion 12q: Report of a patient with 12q24.31q24.33 deletion  Academic Article
• Defining a 0.5-Mb Region of Genomic Gain on Chromosome 6p22 in Bladder Cancer by Quantitative-Multiplex Polymerase Chain Reaction  Academic Article
• Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly  Academic Article
• Discordance between Immunohistochemistry and Erb-B2 Receptor Tyrosine Kinase 2 mRNA to Determine Human Epidermal Growth Factor Receptor 2 Low Status for Breast Cancer  Academic Article
• Effects of a gluten-free diet on gut microbiota and immune function in healthy adult human subjects  Academic Article
• Effects of hTERT on metal ion-induced genomic instability  Academic Article
• Epigenetic Regulation of Tumor Necrosis Factor Alpha  Academic Article
• Familial Evans Syndrome  Academic Article
• Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletion  Academic Article
• Fluorescence <i>in Situ</i> Hybridization Studies on Breast Tumor Samples for Distinguishing Between Different Subsets of Breast Cancer  Academic Article
• Fluorescence in situ hybridization as an adjunct tool in the diagnosis of primary and metastatic renal cell carcinoma in fine needle aspiration specimens  Academic Article
• Fluorescence in situ hybridization gene amplification analysis of EGFR and HER2 in patients with malignant salivary gland tumors treated with lapatinib  Academic Article
• Fluorescencein situ hybridization of uncultured lymphocytes from cystic hygroma fluid: a potential approach for rapid prenatal diagnosis  Academic Article
• Fumarase deficiency: a rare disorder on the crossroads of clinical and metabolic genetics, neurology and cancer  Academic Article
• Genetic considerations in recurrent congenital diaphragmatic hernia in two siblings  Academic Article
• Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations  Academic Article
• HER2 Testing in a Population-Based Study of Patients With Metastatic Breast Cancer Treated With Trastuzumab  Academic Article
• HER2 and TOP2A as predictive markers for anthracycline-containing chemotherapy regimens as adjuvant treatment of breast cancer: a meta-analysis of individual patient data  Academic Article
• Herceptest: Her2 expression and gene amplification in non-small cell lung cancer  Academic Article
• Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency  Academic Article
• Human Chromosome 7: DNA Sequence and Biology  Academic Article
• Human coronaviruses disassemble processing bodies  Academic Article
• Identification of a Low-Risk Luminal A Breast Cancer Cohort That May Not Benefit From Breast Radiotherapy  Academic Article
• Identification of a Novel Group of Bacteria in Sludge from a Deteriorated Biological Phosphorus Removal Reactor  Academic Article
• Identification of early breast cancer patient cohorts who may benefit from lapatinib therapy  Academic Article
• Improvements in Radiographic Progression-Free Survival Stratified by ERG Gene Status in Metastatic Castration-Resistant Prostate Cancer Patients Treated with Abiraterone Acetate  Academic Article
• Interphase FISH analysis of PTEN in histologic sections shows genomic deletions in 68% of primary prostate cancer and 23% of high-grade prostatic intra-epithelial neoplasias  Academic Article
• Interplay Between Human Leukocyte Antigen Genes and the Microbial Colonization Process of the Newborn Intestine  Academic Article
• Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome  Academic Article
• Is Isolated Palatal Anomaly an Indication to Screen for 22q11 Region Deletion?  Academic Article
• Isodicentric Yq mosaicism presenting as infertility and maturation arrest without altered SRY and AZF regions  Academic Article
• Localization by FISH of the 31 Texas nomenclature type I markers to both Q- and R-banded bovine chromosomes  Academic Article
• Low‐depth sequencing for copy number abnormalities in multiple myeloma supersedes fluorescent in situ hybridization in scope and resolution  Academic Article
• Mapping of the human adenylosuccinate lyase (ADSL) gene to chromosome 22q13.1→q13.2  Academic Article
• Microbial Architecture of Environmental Sulfur Processes: A Novel Syntrophic Sulfur-Metabolizing Consortia  Academic Article
• Molecular breakpoint mapping of 6q11-q14 interstitial deletions in seven patients  Academic Article
• Molecular cytogenetic analysis of a series of 23 DiGeorge syndrome patients by fluorescence in situ hybridization.  Academic Article
• Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects  Academic Article
• Morphology of acute promyelocytic leukemia with cytogenetic or molecular evidence for the diagnosis: Characterization of additional microgranular variants  Academic Article
• Partial monosomy 1q43 and partial trisomy 20q13.2: a case report  Academic Article
• Persons with Quebec platelet disorder have a tandem duplication of PLAU, the urokinase plasminogen activator gene  Academic Article
• Phase II Study of Ganitumab, a Fully Human Anti–Type-1 Insulin-Like Growth Factor Receptor Antibody, in Patients With Metastatic Ewing Family Tumors or Desmoplastic Small Round Cell Tumors  Academic Article
• Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases.  Academic Article
• Predicting Anthracycline Benefit: TOP2A and CEP17—Not Only but Also  Academic Article
• Prenatal diagnosis by FISH of a 22q11 deletion in two families.  Academic Article
• Primitive Neuroectodermal Tumors of the Female Genital Tract  Academic Article
• Probing PML body function in ALT cells reveals spatiotemporal requirements for telomere recombination  Academic Article
• RETIRED: Use of Array Genomic Hybridization Technology in Prenatal Diagnosis in Canada  Academic Article
• Rearrangement of human cell homologous chromosome domains in response to ionizing radiation  Academic Article
• Renal cell carcinoma with mixed features of papillary and clear cell cytomorphology: a fluorescent in situ hybridization study  Academic Article
• Ring chromosome 22 and autism: Report and review  Academic Article
• Role of KRAS and EGFR As Biomarkers of Response to Erlotinib in National Cancer Institute of Canada Clinical Trials Group Study BR.21  Academic Article
• Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involvesFOXP2  Academic Article
• Target-Induced Catalytic Assembly of Y-Shaped DNA and Its Application for In Situ Imaging of MicroRNAs  Academic Article
• Telomere maintenance by telomerase and by recombination can coexist in human cells  Academic Article
• Telomeres in the Haemopoietic System  Academic Article
• The Gene Encoding p120cas, a Novel Catenin, Localizes on Human Chromosome 11q11 (CTNND) and Mouse Chromosome 2 (Catns)  Academic Article
• The endocycle controls nurse cell polytene chromosome structure during Drosophila oogenesis  Academic Article
• The proto-oncogene C-KIT maps to canid B-chromosomes  Academic Article
• The shortest telomeres drive karyotype evolution in transformed cells  Academic Article
• The transcriptionally competent U2 gene is necessary and sufficient for adenovirus type 12 induction of the fragile site at 17q21-22  Academic Article
• Topoisomerase II alpha protein and responsiveness of breast cancer to adjuvant chemotherapy with CEF compared to CMF in the NCIC CTG randomized MA.5 adjuvant trial  Academic Article
• Trisomy 18 as the first chromosome abnormality in a medullary breast cancer  Academic Article
• Unusual dicentric chromosome 22 associated with a 22q13 deletion  Academic Article
• Use of a Multitarget Fluorescence In Situ Hybridization Assay to Diagnose Bladder Cancer in Patients With Hematuria  Academic Article
• Wolf-Hirschorn syndrome resulting from partial monosomy 4p/trisomy 9p  Academic Article