FISH in genome research and molecular diagnostics
Tài liệu tham khảo
Landegent, 1985, Chromosomal localization of an unique gene by non-autoradiographic in situ hybridization, Nature, 317, 175, 10.1038/317175a0
Pinkel, 1986, Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization, Proc Natl Acad Sci USA, 83, 2934, 10.1073/pnas.83.9.2934
Lichter, 1990, High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones, Science, 247, 64, 10.1126/science.2294592
Wada, 1990, Human Xq24-Xq28: approaches to mapping with yeast artificial chromosomes, Am J Hum Genet, 46, 95
Kievits, 1990, Direct nonradioactive in situ hybridization of somatic cell hybrid DNA to human lymphocyte chromosomes, Cytometry, 11, 105, 10.1002/cyto.990110112
Takahashi, 1990, R-banding and nonisotopic in situ hybridization: precise localization of the human type II collagen gene (COL2A1), Hum Genet, 86, 14, 10.1007/BF00205165
Smit, 1991, Improved interpretation of complex chromosomal rearrangements by combined GTG banding and in situ suppression hybridization using chromosome-specific libraries and cosmid probes, Genes Chromosomes Cancer, 3, 239, 10.1002/gcc.2870030402
Nederlof, 1990, Multiple fluorescence in situ hybridization, Cytometry, 11, 126, 10.1002/cyto.990110115
Pinkel, 1988, Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocation of chromosome 4, Proc Natl Acad Sci USA, 85, 9138, 10.1073/pnas.85.23.9138
Carter, 1992, Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics, J Med Genet, 29, 299, 10.1136/jmg.29.5.299
Rack, 1993, Characterization of three de novo derivative chromosomes 16 by reverse chromosome painting and molecular analysis, Am J Hum Genet, 52, 987
Dauwerse, 1992, Multiple colors by fluorescence in situ hybridization using ratio Labelled DNA probes create a molecular karyotype, Hum Mol Genet, 1, 593, 10.1093/hmg/1.8.593
Lengauer, 1993, Chromosomal bar codes produced by multicolor fluorescence in situ hybridization with multiple YAC clones and whole chromosome painting probes, Hum Mol Genet, 2, 505, 10.1093/hmg/2.5.505
Guan, 1993, Generation of band-specific painting probes from a single microdissected chromosome, Hum Mol Genet, 2, 1117, 10.1093/hmg/2.8.1117
Craig, 1994, Distribution of CpG islands on mammalian chromosomes, Nature Genet, 7, 376, 10.1038/ng0794-376
Kallioniemi, 1992, Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors, Science, 258, 818, 10.1126/science.1359641
Speicher, 1993, Molecular cytogenetic analysis of formalin-fixed, paraffin-embedded solid tumors by comparative genomic hybridization after universal DNA-amplification, Hum Mol Genet, 2, 1907, 10.1093/hmg/2.11.1907
Du Manoir, 1993, Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization, Hum Genet, 90, 590, 10.1007/BF00202476
Engh, 1992, Estimating genomic distance from DNA sequence location in cell nuclei by a random walk model, Science, 257, 1410, 10.1126/science.1388286
Heng, 1992, High resolution mapping of mammalian genes by in situ hybridization to free chromatin, Proc Natl Acad Sci USA, 89, 9509, 10.1073/pnas.89.20.9509
Wiegant, 1992, High resolution in situ hybridization using DNA halo preparations, Hum Mol Genet, 1, 587, 10.1093/hmg/1.8.587
Parra, 1993, High resolution visual mapping of stretched DNA by fluorescent hybridization, Nature Genet, 5, 17, 10.1038/ng0993-17
Fidlerova, 1994, Two simple procedures for releasing chromatin from routinely fixed cells for fluorescence in situ hybridization, Cytogenet Cell Genet, 65, 203, 10.1159/000133632
Houseal, 1994, High resolution mapping of overlapping cosmids by fluorescence in situ hybridization, Cytometry, 15, 193, 10.1002/cyto.990150303
Heiskanen, 1994, High resolution mapping by FISH to extended DNA fibers prepared from agarose embedded cells, Biotechniques, 17, 928
Florijn, 1995, High resolution DNA FiberFISH genomic DNA mapping and colour barcoding of large genes, Hum Mol Genet, 4, 831, 10.1093/hmg/4.5.831
Dirks, 1993, Methodologies for specific intron and exon RNA localization in cultured cells by haptenized and fluorochromized probes, J Cell Sci, 104, 1187, 10.1242/jcs.104.4.1187
Raap, 1995, Ultrasensitive FISH using peroxidase-mediated deposition of biotin or fluorochrome tyramides, Hum Mol Genet, 4, 529, 10.1093/hmg/4.4.529
Simpson, 1994, Isolating fetal cells in maternal circulation for prenatal diagnosis, Prenat Diagn, 14, 1229, 10.1002/pd.1970141308
Ried, 1990, Carrier detection by in situ suppression hybridization with cosmid clones of the Duchenne/Becker muscular dystrophy (DMD/BMD) locus, Hum Genet, 85, 581, 10.1007/BF00193578
Valentijn, 1992, The growth arrest-specific gene GAS3 is duplicated in Charcot-Marie-Tooth disease type 1a, Nature Genet, 1, 166, 10.1038/ng0692-166
Knoll, 1993, Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: an overview, Am J Med Genet, 46, 2, 10.1002/ajmg.1320460103
Smith, 1993, Fluorescence in situ hybridisation and molecular studies used in the characterisation of a Robertsonian translocation (13q;15q) in Prader-Willi syndrome, Clin Genet, 43, 5, 10.1111/j.1399-0004.1993.tb04416.x
Kuwano, 1991, Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization, Am J Hum Genet, 49, 707
Gandelman, 1992, Molecular definition of the smallest region of deletion overlap in the Wolf-Hirschhorn syndrome, Am J Hum Genet, 51, 571
Breuning, 1993, Rubinstein-Taybi syndrome caused by submicroscopic deletions of chromosome 16, Am J Hum Genet, 52, 249
Desmaze, 1993, Physical mapping by FISH of the Di-George critical region (DGCR): involvement of the region in familial cases, Am J Hum Genet, 53, 1239
Ewart, 1993, Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome, Nature Genet, 5, 11, 10.1038/ng0993-11
Ward, 1993, Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: cinical experience with 4,500 specimens, Am J Hum Genet, 52, 854
Philip, 1995, Prenatal aneuploidy detection in interphase cells by fluorescence in situ hybridization (FISH), Prenat Diagn, 14, 1203, 10.1002/pd.1970141306
Drechsler, 1994, Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene, Hum Genet, 94, 331, 10.1007/BF00201588
Dauwerse, 1993, Cloning the breakpoint cluster region of the inv(16) in acute non-lymphocytic leukemia M4 Eo, Hum Mol Genet, 2, 1527, 10.1093/hmg/2.10.1527
Van der Reijden, 1993, A gene for a myosin peptide is disrupted by the inv(16)(p13q22) in acute nonlymphocytic leukemia M4Eo, Blood, 82, 2948, 10.1182/blood.V82.10.2948.2948
Liu, 1993, Fusion between transcription factor CBFß/PEBP2ß and a myosin heavy chain in acute myeloid leukemia, Science, 261, 1041, 10.1126/science.8351518
Marshall, 1995, A strategy for sequencing the genome 5 years early, Science, 267, 783, 10.1126/science.7846520