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  Journal Articles
• A CGG-Repeat Expansion Mutation inZNF713Causes FRA7A: Association with Autistic Spectrum Disorder in two Families  Journal Articles
• A FISH study of chromosome fusion in the ICF syndrome: involvement of paracentric heterochromatin but not of the centromeres themselves.  Journal Articles
• A cell-specific regulatory region of the human ABO blood group gene regulates the neighborhood gene encoding odorant binding protein 2B  Journal Articles
• A genome assembly-integrated dog 1 Mb BAC microarray: a cytogenetic resource for canine cancer studies and comparative genomic analysis  Journal Articles
• A new association of congenital hydrocephalus, albinism, megalocornea, and retinal coloboma in a syndromic child: A clinical and genetic study  Journal Articles
• Acute Lymphoblastic Leukemia in a Patient With Constitutional Chromosome 1pter-p36.31 Duplication and 1q43-qter Deletion  Journal Articles
• Alternative Lengthening of Telomeres Is Characterized by High Rates of Telomeric Exchange  Journal Articles
• Amplification of telomerase (hTERT) gene is a poor prognostic marker in non-small-cell lung cancer  Journal Articles
• An approach to small lymph node biopsies: pearls and pitfalls of reporting in the real world  Journal Articles
• An uncommon 3.4-Mb interstitial deletion at 3q29  Journal Articles
• Assignment of bovine trophinin (TRO) to the q arm of the X chromosome by fluorescence in situ hybridization  Journal Articles
• Assignment of the bovine attractin (ATRN) gene to chromosome 13q21→q22 by in situ hybridization  Journal Articles
• 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  Journal Articles
• Canadian Anaplastic Lymphoma Kinase Study: A Model for Multicenter Standardization and Optimization of ALK Testing in Lung Cancer  Journal Articles
• Canadian ROS proto-oncogene 1 study (CROS) for multi-institutional implementation of ROS1 testing in non-small cell lung cancer  Journal Articles
• Chromosome content and ultrastructure of radiation-induced micronuclei  Journal Articles
• Chromosome divergence during evolution of the tetraploid clawed frogs, Xenopus mellotropicalis and Xenopus epitropicalis as revealed by Zoo-FISH  Journal Articles
• Comparison of HER2 Dual-Color and Fluorescence In Situ Hybridization in Breast Cancer  Journal Articles
• Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements  Journal Articles
• 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  Journal Articles
• Cyclin B-dependent kinase 1 regulates human TRF1 to modulate the resolution of sister telomeres  Journal Articles
• Cytogenetic Prognostication Within Medulloblastoma Subgroups  Journal Articles
• Cytogenetic comparison of saola <i>(Pseudoryx nghetinhensis)</i> and cattle <i>(Bos taurus)</i> using G- and Q-banding and FISH  Journal Articles
• DMG26  Journal Articles
• De novo 1q32q44 duplication and distal 1q trisomy syndrome  Journal Articles
• De novo deletion 12q: Report of a patient with 12q24.31q24.33 deletion  Journal Articles
• Defining a 0.5-Mb Region of Genomic Gain on Chromosome 6p22 in Bladder Cancer by Quantitative-Multiplex Polymerase Chain Reaction  Journal Articles
• Deletion 9q34.3 syndrome: genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly  Journal Articles
• Discordance between Immunohistochemistry and Erb-B2 Receptor Tyrosine Kinase 2 mRNA to Determine Human Epidermal Growth Factor Receptor 2 Low Status for Breast Cancer  Journal Articles
• Effects of a gluten-free diet on gut microbiota and immune function in healthy adult human subjects  Journal Articles
• Effects of hTERT on metal ion-induced genomic instability  Journal Articles
• Epigenetic Regulation of Tumor Necrosis Factor Alpha  Journal Articles
• Familial Evans Syndrome  Journal Articles
• Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletion  Journal Articles
• Fluorescence <i>in Situ</i> Hybridization Studies on Breast Tumor Samples for Distinguishing Between Different Subsets of Breast Cancer  Journal Articles
• Fluorescence in situ hybridization gene amplification analysis of EGFR and HER2 in patients with malignant salivary gland tumors treated with lapatinib  Journal Articles
• Fumarase deficiency: a rare disorder on the crossroads of clinical and metabolic genetics, neurology and cancer  Journal Articles
• Genetic considerations in recurrent congenital diaphragmatic hernia in two siblings  Journal Articles
• Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations  Journal Articles
• HER2 Testing in a Population-Based Study of Patients With Metastatic Breast Cancer Treated With Trastuzumab  Journal Articles
• Herceptest: Her2 expression and gene amplification in non-small cell lung cancer  Journal Articles
• Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency  Journal Articles
• Human Chromosome 7: DNA Sequence and Biology  Journal Articles
• Human coronaviruses disassemble processing bodies  Journal Articles
• Identification of a Low-Risk Luminal A Breast Cancer Cohort That May Not Benefit From Breast Radiotherapy  Journal Articles
• Identification of a Novel Group of Bacteria in Sludge from a Deteriorated Biological Phosphorus Removal Reactor  Journal Articles
• Improvements in Radiographic Progression-Free Survival Stratified by ERG Gene Status in Metastatic Castration-Resistant Prostate Cancer Patients Treated with Abiraterone Acetate  Journal Articles
• 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  Journal Articles
• Interplay Between Human Leukocyte Antigen Genes and the Microbial Colonization Process of the Newborn Intestine  Journal Articles
• Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome  Journal Articles
• Is Isolated Palatal Anomaly an Indication to Screen for 22q11 Region Deletion?  Journal Articles
• Isodicentric Yq mosaicism presenting as infertility and maturation arrest without altered SRY and AZF regions  Journal Articles
• Localization by FISH of the 31 Texas nomenclature type I markers to both Q- and R-banded bovine chromosomes  Journal Articles
• Low‐depth sequencing for copy number abnormalities in multiple myeloma supersedes fluorescent in situ hybridization in scope and resolution  Journal Articles
• Lymphatic vessels identified in failed corneal transplants with neovascularisation  Journal Articles
• Mapping of the human adenylosuccinate lyase (ADSL) gene to chromosome 22q13.1→q13.2  Journal Articles
• Microbial Architecture of Environmental Sulfur Processes: A Novel Syntrophic Sulfur-Metabolizing Consortia  Journal Articles
• Molecular breakpoint mapping of 6q11‐q14 interstitial deletions in seven patients  Journal Articles
• Molecular cytogenetic analysis of a series of 23 DiGeorge syndrome patients by fluorescence in situ hybridization.  Journal Articles
• Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects  Journal Articles
• Morphology of acute promyelocytic leukemia with cytogenetic or molecular evidence for the diagnosis: Characterization of additional microgranular variants  Journal Articles
• Novel roles of cardiac-derived erythropoietin in cardiac development and function  Journal Articles
• Partial monosomy 1q43 and partial trisomy 20q13.2: a case report  Journal Articles
• Persons with Quebec platelet disorder have a tandem duplication of PLAU, the urokinase plasminogen activator gene  Journal Articles
• 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  Journal Articles
• Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases.  Journal Articles
• Prenatal diagnosis by FISH of a 22q11 deletion in two families.  Journal Articles
• Primitive Neuroectodermal Tumors of the Female Genital Tract  Journal Articles
• Probing PML body function in ALT cells reveals spatiotemporal requirements for telomere recombination  Journal Articles
• RETIRED: Use of Array Genomic Hybridization Technology in Prenatal Diagnosis in Canada  Journal Articles
• Rearrangement of human cell homologous chromosome domains in response to ionizing radiation  Journal Articles
• Recurrent genomic rearrangements in primary testicular lymphoma.  Journal Articles
• Renal cell carcinoma with mixed features of papillary and clear cell cytomorphology: a fluorescent in situ hybridization study  Journal Articles
• Ring chromosome 22 and autism: Report and review  Journal Articles
• Role of KRAS and EGFR As Biomarkers of Response to Erlotinib in National Cancer Institute of Canada Clinical Trials Group Study BR.21  Journal Articles
• Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2  Journal Articles
• Target‐Induced Catalytic Assembly of Y‐Shaped DNA and Its Application for In Situ Imaging of MicroRNAs  Journal Articles
• Telomere maintenance by telomerase and by recombination can coexist in human cells  Journal Articles
• Telomeres in the Haemopoietic System  Journal Articles
• The Gene Encoding p120cas, a Novel Catenin, Localizes on Human Chromosome 11q11 (CTNND) and Mouse Chromosome 2 (Catns)  Journal Articles
• The Transcriptionally Competent U2 Gene Is Necessary and Sufficient for Adenovirus Type 12 Induction of the Fragile Site at 17q21-22  Journal Articles
• The endocycle controls nurse cell polytene chromosome structure during Drosophila oogenesis  Journal Articles
• The proto-oncogene C-KIT maps to canid B-chromosomes  Journal Articles
• The shortest telomeres drive karyotype evolution in transformed cells  Journal Articles
• Therapy for relapsed multiple myeloma  Journal Articles
• 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  Journal Articles
• Trisomy 18 as the first chromosome abnormality in a medullary breast cancer  Journal Articles
• Unusual dicentric chromosome 22 associated with a 22q13 deletion  Journal Articles
• Use of a Multitarget Fluorescence In Situ Hybridization Assay to Diagnose Bladder Cancer in Patients With Hematuria  Journal Articles
• Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation  Journal Articles
• Wolf-Hirschorn syndrome resulting from partial monosomy 4p/trisomy 9p  Journal Articles
• ‘Putting our heads together’: insights into genomic conservation between human and canine intracranial tumors  Journal Articles