Papadopoulos, Sarantos: Untersuchungen genomischer Veränderungen von Mammakarzinomzellen mittels Random Amplified Polymorphic DNA



Bishop, J. M.: "Cancer: the rise of the genetic paradigm," Genes Dev, 1995, 11, 9, S. 1309-15,

Fearon, E. R.; Vogelstein, B.: "A genetic model for colorectal tumorigenesis," Cell, 1990, 5, 61, S. 759-67,

Jeffreys, A. J.; Wilson, V.; Thein, S. L.: "Hypervariable 'minisatellite' regions in human DNA," Nature, 1985, 6006, 314, S. 67-73,

Thein, S.L., Jeffreys,A.J.: "Detection of somatic changes in human cancer DNA by DNA fingerprint analysis," British Journal of Cancer, 1987, 55, S. 353-356,

Smit, V. T.; Cornelisse, C. J.; De Jong, D.; Dijkshoorn, N. J.; Peters, A. A.; Fleuren, G. J.: "Analysis of tumor heterogeneity in a patient with synchronously occurring female genital tract malignancies by DNA flow cytometry, DNA fingerprinting, and immunohistochemistry," Cancer, 1988, 6, 62, S. 1146-52,

Vogelstein, B. , Fearon,E>R>: "Allelotype of colorectal carcinoma," Science, 1989, 244, S. 207-211,

Malkhosyan, S.; Yasuda, J.; Soto, J. L.; Sekiya, T.; Yokota, J.; Perucho, M.: "Molecular karyotype (amplotype) of metastatic colorectal cancer by unbiased arbitrarily primed PCR DNA fingerprinting," Proc Natl Acad Sci U S A, 1998, 17, 95, S. 10170-5,

Spira, J.; Wiener, F.; Ohno, S.; Klein, G.: "Is trisomy cause or consequence of murine T cell leukemia development? Studies on Robertsonian translocation mice," Proc Natl Acad Sci U S A, 1979, 12, 76, S. 6619-21,

Mitelman, F.; Mertens, F.; Johansson, B.: "A breakpoint map of recurrent chromosomal rearrangements in human neoplasia [see comments]," Nat Genet, 1997, 15 Spec No, S. 417-74,

Lisitsyn, N. A.; Lisitsina, N. M.; Dalbagni, G.; Barker, P.; Sanchez, C. A.; Gnarra, J.; Linehan, W. M.; Reid, B. J.; Wigler, M. H.: "Comparative genomic analysis of tumors: detection of DNA losses and amplification," Proc Natl Acad Sci U S A, 1995, 1, 92, S. 151-5,

Kallioniemi, A.; Kallioniemi, O. P.; Sudar, D.; Rutovitz, D.; Gray, J. W.; Waldman, F.; Pinkel, D.: "Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors," Science, 1992, 5083, 258, S. 818-21,

Williams, J. G.; Kubelik, A. R.; Livak, K. J.; Rafalski, J. A.; Tingey, S. V.: "DNA polymorphisms amplified by arbitrary primers are useful as genetic markers," Nucleic Acids Res, 1990, 22, 18, S. 6531-5,

Venugopal, G., Mohapatra, S., Salo, D., Mohapatra, S.: "Multiple Mismatch Annealing: Basis for Random Amplified Polymorphic DNA Fingerprinting.," Biochemical and Biophysical Research Communications, 1993, 3, 197, S. 1382-1387,

Welsh, J.; McClelland, M.: "Fingerprinting genomes using PCR with arbitrary primers," Nucleic Acids Res, 1990, 24, 18, S. 7213-8,

Caetano-Anolles, G.; Bassam, B. J.; Gresshoff, P. M.: "DNA amplification fingerprinting using very short arbitrary oligonucleotide primers," Biotechnology (N Y), 1991, 6, 9, S. 553-7,

Peinado, M. A.; Malkhosyan, S.; Velazquez, A.; Perucho, M.: "Isolation and characterization of allelic losses and gains in colorectal tumors by arbitrarily primed polymerase chain reaction," Proc Natl Acad Sci U S A, 1992, 21, 89, S. 10065-9,

Sobral, B.W.S., Honeycutt, R.J.: "High output genetic mapping of polyploids using PCR-generated markers.," Theor Appl Genet, 1993, 86, S. 105-112,

Russell, J. R.; Hosein, F.; Johnson, E.; Waugh, R.; Powell, W.: "Genetic differentiation of cocoa (Theobroma cacao L.) populations revealed by RAPD analysis," Mol Ecol, 1993, 2, 2, S. 89-97,

Dweikat, I., Mackenzie, S., Levy, M., Ohm, H.: "Pedigree assessment using RAPD-DGGE in cereal crop species.," Theor. Appl. Genet., 1993, 85, S. 497-505,

Akopyanz, N.; Bukanov, N. O.; Westblom, T. U.; Kresovich, S.; Berg, D. E.: "DNA diversity among clinical isolates of Helicobacter pylori detected by PCR-based RAPD fingerprinting," Nucleic Acids Res, 1992, 19, 20, S. 5137-42,

Kersulyte, D.; Woods, J. P.; Keath, E. J.; Goldman, W. E.; Berg, D. E.: "Diversity among clinical isolates of Histoplasma capsulatum detected by polymerase chain reaction with arbitrary primers," J Bacteriol, 1992, 22, 174, S. 7075-9,

Steindel, M.; Dias Neto, E.; de Menezes, C. L.; Romanha, A. J.; Simpson, A. J.: "Random amplified polymorphic DNA analysis of Trypanosoma cruzi strains," Mol Biochem Parasitol, 1993, 1, 60, S. 71-9,

Kambhampati, S.; Black, W. C. th; Rai, K. S.: "Random amplified polymorphic DNA of mosquito species and populations (Diptera: Culicidae): techniques, statistical analysis, and applications," J Med Entomol, 1992, 6, 29, S. 939-45,

Gwakisa, P. S.; Kemp, S. J.; Teale, A. J.: "Characterization of Zebu cattle breeds in Tanzania using random amplified polymorphic DNA markers," Anim Genet, 1994, 2, 25, S. 89-94,

Kresovich, S., Williams, J. G. K., MeFerson, J. R., Routman, E. J., Schaal, B. A.: "Characterization of genetic identities and relationships of Brassica oleracea L. via a random amplified polymorphic DNA assay.," Theor Appl Genet, 1992, 85, S. 190-196,

Dooley, J. J.; Harrison, S. P.; Mytton, L. R.; Dye, M.; Cresswell, A.; Skot, L.; Beeching, J. R.: "Phylogenetic grouping and identification of Rhizobium isolates on the basis of random amplified polymorphic DNA profiles," Can J Microbiol, 1993, 7, 39, S. 665-73,

Riedy, M. F.; Hamilton, W. J. d; Aquadro, C. F.: "Excess of non-parental bands in offspring from known primate pedigrees assayed using RAPD PCR," Nucleic Acids Res, 1992, 4, 20, S. 918,

Sineo, L.; Martini, R.; Borghi, G.; Failli, M.: "Analysis of genetic markers by random amplified polymorphic DNA polymerase chain reaction (RAPD-PCR)," Boll Chim Farm, 1993, 6, 132, S. 201-2,

Weinberg, H.-S.: "Molecular changes in the offspring of liquidators who emigrated to Israel from the Chernobyl disaster area," Enviromental Health Perspectives, 1997, 105, S. 1479-1481,

Arribas, R.: "Assessment of genomic damage in colorectal cancer by DNA fingerprinting:prognostic applications," Journal of clinical oncology, 1997, 10, 15, S. 3230-3240,

Offerhaus, G.J.A.: "The relationship of DNA aneuploidy to molecular genetic alterations in colorectal carcinoma," Gastroenterology, 1992, 102, S. 1612-1619,

Ionov, Y.; Peinado, M. A.; Malkhosyan, S.; Shibata, D.; Perucho, M.: "Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis," Nature, 1993, 6429, 363, S. 558-61,

Saitoh, Y.; Bruner, J. M.; Levin, V. A.; Kyritsis, A. P.: "Identification of allelic loss on chromosome arm 6p in human astrocytomas by arbitrarily primed polymerase chain reaction," Genes Chromosomes Cancer, 1998, 3, 22, S. 165-70,

Kohno, T.; Morishita, K.; Takano, H.; Shapiro, D. N.; Yokota, J.: "Homozygous deletion at chromosome 2q33 in human small-cell lung carcinoma identified by arbitrarily primed PCR genomic fingerprinting," Oncogene, 1994, 1, 9, S. 103-8,

Achille, A.; Biasi, M. O.; Zamboni, G.; Bogina, G.; Magalini, A. R.; Pederzoli, P.; Perucho, M.; Scarpa, A.: "Chromosome 7q allelic losses in pancreatic carcinoma," Cancer Res, 1996, 16, 56, S. 3808-13,

Kawakami, K.; Yasuda, J.; Shiraishi, M.; Kayama, T.; Doi, K.; Perucho, M.; Sekiya, T.: "Detection of DNA abnormalities by arbitrarily primed PCR fingerprinting: allelic losses in chromosome 10q in lung cancers," Biochem Biophys Res Commun, 1998, 1, 251, S. 153-7,

Maeda, T: "Analysis of genomic instability in squamous cell carcinoma of the head and neck using the random amplified polymorphic DNA method," Cancer Letters, 1999, 138, S. 183-188,

Okazaki, T.; Takita, J.; Kohno, T.; Handa, H.; Yokota, J.: "Detection of amplified genomic sequences in human small-cell lung carcinoma cells by arbitrarily primed-PCR genomic fingerprinting," Hum Genet, 1996, 3, 98, S. 253-8,

Kuchiki, H.: "Detection of DNA abnormalities by arbitrarily primed PCR fingerprinting:amplification of the MDM2 gene in a mediastinum fibrosarcoma," Biochemical and Biophysical Research Communications, 1999, 258, S. 271-277,

de Juan, C.: "DNA amplification on chromosome 6p12 in non-small-cell-lung-cancer detected by arbitrarily primed polymerase chain reaction," International Journal of cancer, 1999, 84, S. 344-349,

Dil, Afroze; Misra, A.; Sulaiman, I. M.; Sinha, S.; Sarkar, C.; Mahapatra, A. K.; Hasnain, S. E.: "Genetic alterations in brain tumors identified by RAPD analysis," Gene, 1998, 1, 206, S. 45-8,

Yasuda, J.; Kashiwabara, H.; Kawakami, K.; Uematsu, K.; Sugano, K.; Perucho, M.; Sekiya, T.: "Detection of microsatellite instability in cancers by arbitrarily primed-PCR fingerprinting using a fluorescently labeled primer (FAP- PCR)," Biol Chem, 1996, 9, 377, S. 563-70,

Kohno, T.; Kawanishi, M.; Inazawa, J.; Yokota, J.: "Identification of CpG islands hypermethylated in human lung cancer by the arbitrarily primed-PCR method," Hum Genet, 1998, 3, 102, S. 258-64,

Koebner, R. M.: "Predigestion of DNA template improves the level of polymorphism of random amplified polymorphic DNAs in wheat," Genet Anal, 1995, 1, 12, S. 63-7,

Sood, A. K.; Buller, R. E.: "Genomic instability in ovarian cancer: a reassessment using an arbitrarily primed polymerase chain reaction," Oncogene, 1996, 11, 13, S. 2499-504,

Deb, P.: "Search for retroviral related DNA polymorphisms using RAPD PCR in Schizophrenia," Biochimica et Biophysica Acta, 1999, 1453, S. 216-220,

Kinzler, K. W.; Vogelstein, B.: "Lessons from hereditary colorectal cancer," Cell, 1996, 2, 87, S. 159-70,

Lahiri, D. K.; Nurnberger, J. I., Jr.: "A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies," Nucleic Acids Res, 1991, 19, 19, S. 5444,

Walsh, P. S.; Metzger, D. A.; Higuchi, R.: "Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material," Biotechniques, 1991, 4, 10, S. 506-13,

Barlow, D.P.: "DNA Isolation for PFGE," Methods in Molecular Biology: Pulsed Field Gel Electrophoresis(Edited by Burmeister,M. and Ulanovsky,L.), Humana Press, Totorra ,NJ, 1992, 12, S. 111-112,

Burckhardt, J.: "Amplification of DNA from whole blood," PCR Methods Appl, 1994, 4, 3, S. 239-43,

Chester, N.; Marshak, D. R.: "Dimethyl sulfoxide-mediated primer Tm reduction: a method for analyzing the role of renaturation temperature in the polymerase chain reaction," Anal Biochem, 1993, 2, 209, S. 284-90,

Sarkar, G.; Kapelner, S.; Sommer, S. S.: "Formamide can dramatically improve the specificity of PCR," Nucleic Acids Res, 1990, 24, 18, S. 7465,

Varadaraj, K.; Skinner, D. M.: "Denaturants or cosolvents improve the specificity of PCR amplification of a G + C-rich DNA using genetically engineered DNA polymerases," Gene, 1994, 1, 140, S. 1-5,

Weissensteiner, T.; Lanchbury, J. S.: "Strategy for controlling preferential amplification and avoiding false negatives in PCR typing," Biotechniques, 1996, 6, 21, S. 1102-8,

Baskaran, N.; Kandpal, R. P.; Bhargava, A. K.; Glynn, M. W.; Bale, A.; Weissman, S. M.: "Uniform amplification of a mixture of deoxyribonucleic acids with varying GC content," Genome Res, 1996, 7, 6, S. 633-8,

Rees, W. A., Yager, T. D., Korte, J., von Hippel, P. H.: "Betaine Can Eliminate the Base Pair Composition Dependence of DNA Melting.," Biochemistry, 1993, 32, S. 137-144,

Henke, W.; Herdel, K.; Jung, K.; Schnorr, D.; Loening, S. A.: "Betaine improves the PCR amplification of GC-rich DNA sequences," Nucleic Acids Res, 1997, 19, 25, S. 3957-8,

Carninci, P.; Nishiyama, Y.; Westover, A.; Itoh, M.; Nagaoka, S.; Sasaki, N.; Okazaki, Y.; Muramatsu, M.; Hayashizaki, Y.: "Thermostabilization and thermoactivation of thermolabile enzymes by trehalose and its application for the synthesis of full length cDNA," Proc Natl Acad Sci U S A, 1998, 2, 95, S. 520-4,

Mullis, K. B.: "The polymerase chain reaction in an anemic mode: how to avoid cold oligodeoxyribonuclear fusion," PCR Methods Appl, 1991, 1, 1, S. 1-4,

D'Aquila, R. T.; Bechtel, L. J.; Videler, J. A.; Eron, J. J.; Gorczyca, P.; Kaplan, J. C.: "Maximizing sensitivity and specificity of PCR by pre-amplification heating," Nucleic Acids Res, 1991, 13, 19, S. 3749,

Yap, E. P.; McGee, J. O.: "Short PCR product yields improved by lower denaturation temperatures," Nucleic Acids Res, 1991, 7, 19, S. 1713,

Sardelli, A.: "Plateau Effect-Understanding PCR Limitations," Amplifications, 1993, 9, S. 1-5,

Cease, K. B.; Potcova, C. A.; Lohff, C. J.; Zeigler, M. E.: "Optimized PCR using Vent polymerase," PCR Methods Appl, 1994, 5, 3, S. 298-300,

Premaratne, S.; Helms, M.; Mower, H. F.: "Enhancement of ethidium bromide fluorescence in double-stranded DNA reacted with chloroacetaldehyde," Biotechniques, 1993, 3, 15, S. 394-6,

Comes, A.M., Humbert,J.F. ,Laurent,F.: "Rapid cloning of PCR-derived RAPD probes," Biotechniques, 1997, 2, 23, S. 210-212,

Bell, D. A.; DeMarini, D. M.: "Excessive cycling converts PCR products to random-length higher molecular weight fragments," Nucleic Acids Res, 1991, 18, 19, S. 5079,

Park, Y. H.; Kohel, R. J.: "Effect of concentration of MgCl2 on random-amplified DNA polymorphism," Biotechniques, 1994, 4, 16, S. 652-6,

Douglas, A.; Atchison, B.: "Degradation of DNA during the denaturation step of PCR," PCR Methods Appl, 1993, 2, 3, S. 133-4,

Gustafson, C. E.; Alm, R. A.; Trust, T. J.: "Effect of heat denaturation of target DNA on the PCR amplification," Gene, 1993, 2, 123, S. 241-4,

Schweder, M. E.; Shatters, R. G., Jr.; West, S. H.; Smith, R. L.: "Effect of transition interval between melting and annealing temperatures on RAPD analyses," Biotechniques, 1995, 1, 19, S. 38, 40-2,

Sommer, R.; Tautz, D.: "Minimal homology requirements for PCR primers," Nucleic Acids Res, 1989, 16, 17, S. 6749,

Schierwater, B.; Ender, A.: "Different thermostable DNA polymerases may amplify different RAPD products," Nucleic Acids Res, 1993, 19, 21, S. 4647-8,

Penner, G. A.; Bush, A.; Wise, R.; Kim, W.; Domier, L.; Kasha, K.; Laroche, A.; Scoles, G.; Molnar, S. J.; Fedak, G.: "Reproducibility of random amplified polymorphic DNA (RAPD) analysis among laboratories," PCR Methods Appl, 1993, 4, 2, S. 341-5,

MacPherson, J. M.; Eckstein, P. E.; Scoles, G. J.; Gajadhar, A. A.: "Variability of the random amplified polymorphic DNA assay among thermal cyclers, and effects of primer and DNA concentration," Mol Cell Probes, 1993, 4, 7, S. 293-9,

Meunier, J. R.; Grimont, P. A.: "Factors affecting reproducibility of random amplified polymorphic DNA fingerprinting," Res Microbiol, 1993, 5, 144, S. 373-9,

Kubelik, A. R.; Szabo, L. J.: "High-GC primers are useful in RAPD analysis of fungi," Curr Genet, 1995, 4, 28, S. 384-9,

Sengstag, C.: "The role of mitotic recombination in carcinogenesis," Crit Rev Toxicol, 1994, 4, 24, S. 323-53,

Gupta, P. K.; Sahota, A.; Boyadjiev, S. A.; Bye, S.; Shao, C.; O'Neill, J. P.; Hunter, T. C.; Albertini, R. J.; Stambrook, P. J.; Tischfield, J. A.: "High frequency in vivo loss of heterozygosity is primarily a consequence of mitotic recombination," Cancer Res, 1997, 6, 57, S. 1188-93,

Lichten, M.; Goldman, A. S.: "Meiotic recombination hotspots," Annu Rev Genet, 1995, 29, S. 423-44,

Tracy, R. B.; Chedin, F.; Kowalczykowski, S. C.: "The recombination hot spot chi is embedded within islands of preferred DNA pairing sequences in the E. coli genome [letter]," Cell, 1997, 2, 90, S. 205-6,

Bell, S. J.; Chow, Y. C.; Ho, J. Y. K.; Forsdyke, D. R.: "Correlation of chi orientation with transcription indicates a fundamental relationship between recombination and transcription [published erratum appears in Gene 1999 Apr 29;231(1-2):213]," Gene, 1998, 2, 216, S. 285-92,

Sowerby, S. J.; Kennedy, M. A.; Fitzgerald, P. H.; Morris, C. M.: "DNA sequence analysis of the major breakpoint cluster region of the BCR gene rearranged in Philadelphia-positive human leukemias," Oncogene, 1993, 6, 8, S. 1679-83,

Chissoe, S. L.; Bodenteich, A.; Wang, Y. F.; Wang, Y. P.; Burian, D.; Clifton, S. W.; Crabtree, J.; Freeman, A.; Iyer, K.; Jian, L.; et al.: "Sequence and analysis of the human ABL gene, the BCR gene, and regions involved in the Philadelphia chromosomal translocation," Genomics, 1995, 1, 27, S. 67-82,

Jaeger, U.; Karth, G. D.; Knapp, S.; Friedl, J.; Laczika, K.; Kusec, R.: "Molecular mechanism of the t(14;18)--a model for lymphoid-specific chromosomal translocations," Leuk Lymphoma, 1994, 3-4, 14, S. 197-202,

Wyatt, R. T.; Rudders, R. A.; Zelenetz, A.; Delellis, R. A.; Krontiris, T. G.: "BCL2 oncogene translocation is mediated by a chi-like consensus," J Exp Med, 1992, 6, 175, S. 1575-88,

Marshall, B.; Isidro, G.; Boavida, M. G.: "Insertion of a short Alu sequence into the hMSH2 gene following a double cross over next to sequences with chi homology [published erratum appears in Gene 1997 Sep 15;197(1-2):413]," Gene, 1996, 1, 174, S. 175-9,

Korenberg, J. R.; Rykowski, M. C.: "Human genome organization: Alu, lines, and the molecular structure of metaphase chromosome bands," Cell, 1988, 3, 53, S. 391-400,

Lehrman, M. A.; Russell, D. W.; Goldstein, J. L.; Brown, M. S.: "Alu-Alu recombination deletes splice acceptor sites and produces secreted low density lipoprotein receptor in a subject with familial hypercholesterolemia," J Biol Chem, 1987, 7, 262, S. 3354-61,

Ariga, T.; Carter, P. E.; Davis, A. E. d: "Recombinations between Alu repeat sequences that result in partial deletions within the C1 inhibitor gene," Genomics, 1990, 4, 8, S. 607-13,

Nystrom-Lahti, M.; Kristo, P.; Nicolaides, N. C.; Chang, S. Y.; Aaltonen, L. A.; Moisio, A. L.; Jarvinen, H. J.; Mecklin, J. P.; Kinzler, K. W.; Vogelstein, B.; et al.: "Founding mutations and Alu-mediated recombination in hereditary colon cancer," Nat Med, 1995, 11, 1, S. 1203-6,

Legius, E.; Marchuk, D. A.; Collins, F. S.; Glover, T. W.: "Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis," Nat Genet, 1993, 2, 3, S. 122-6,

Puget, N.; Torchard, D.; Serova-Sinilnikova, O. M.; Lynch, H. T.; Feunteun, J.; Lenoir, G. M.; Mazoyer, S.: "A 1-kb Alu-mediated germ-line deletion removing BRCA1 exon 17," Cancer Res, 1997, 5, 57, S. 828-31,

Smith, T. M.; Lee, M. K.; Szabo, C. I.; Jerome, N.; McEuen, M.; Taylor, M.; Hood, L.; King, M. C.: "Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1," Genome Res, 1996, 11, 6, S. 1029-49,

Levran, O., Doggett, N. A., Auerbach, A. D.: "Identification of Alu-Mediated Deletions in the Fanconi Anemia Gene FAA.," Human Mutation, 1998, 12, S. 145-152,

Munroe, D. J.: "IRS-Bubble PCR: An Effective Method for Representative Amplification of Human Genomic DNA Sequences from Complex Sources," Methods, 1996, 1, 9, S. 106-12,

Inoue, H.; Ishii, H.; Alder, H.; Snyder, E.; Druck, T.; Huebner, K.; Croce, C. M.: "Sequence of the FRA3B common fragile region: implications for the mechanism of FHIT deletion," Proc Natl Acad Sci U S A, 1997, 26, 94, S. 14584-9,

Munroe, D. J.; Haas, M.; Bric, E.; Whitton, T.; Aburatani, H.; Hunter, K.; Ward, D.; Housman, D. E.: "IRE-bubble PCR: a rapid method for efficient and representative amplification of human genomic DNA sequences from complex sources," Genomics, 1994, 3, 19, S. 506-14,

Eichler, E. E.: "Repetitive conundrums of centromere structure and function," Hum Mol Genet, 1999, 2, 8, S. 151-5,

Eichler, E. E.; Hoffman, S. M.; Adamson, A. A.; Gordon, L. A.; McCready, P.; Lamerdin, J. E.; Mohrenweiser, H. W.: "Complex beta-satellite repeat structures and the expansion of the zinc finger gene cluster in 19p12," Genome Res, 1998, 8, 8, S. 791-808,

Eichler, E. E.: "Masquerading repeats: paralogous pitfalls of the human genome [published erratum appears in Genome Res 1998 Oct;8(10):1095]," Genome Res, 1998, 8, 8, S. 758-62,

Kalitsis, P. , Choo,K.H.A.: "Centromere DNA of higher eukaryotes," The Centromere(Editor: K.H.A.Choo),Oxford University Press, 1997, S. 97-108,

Lee, C.; Wevrick, R.; Fisher, R. B.; Ferguson-Smith, M. A.; Lin, C. C.: "Human centromeric DNAs," Hum Genet, 1997, 3-4, 100, S. 291-304,

Eshleman, J. R.; Markowitz, S. D.: "Microsatellite instability in inherited and sporadic neoplasms," Curr Opin Oncol, 1995, 1, 7, S. 83-9,

Wahls, W. P.: "Meiotic recombination hotspots: shaping the genome and insights into hypervariable minisatellite DNA change," Curr Top Dev Biol, 1998, 37, S. 37-75,

Nuernberg, P., Zischler, H., Fuhrmann, E., Thiel, G., Losanova, T., Kinzel, D., Nisch, G., Witkowski, R., Epplen, J. T.: "Coamplification of Simple Repetitive DNA Fingerprint Fragments and the EGFR Gene in Human Gliomas.," Genes, Chromosomes & Cancer, 1991, 3, S. 79-88,

Blackburn, E. H.: "Structure and function of telomeres," Nature, 1991, 6319, 350, S. 569-73,

JW, Ijdo; Baldini, A.; Ward, D. C.; Reeders, S. T.; Wells, R. A.: "Origin of human chromosome 2: an ancestral telomere-telomere fusion," Proc Natl Acad Sci U S A, 1991, 20, 88, S. 9051-5,

Hastie, N. D.; Allshire, R. C.: "Human telomeres: fusion and interstitial sites," Trends Genet, 1989, 10, 5, S. 326-31,

Silver, A.; Cox, R.: "Telomere-like DNA polymorphisms associated with genetic predisposition to acute myeloid leukemia in irradiated CBA mice," Proc Natl Acad Sci U S A, 1993, 4, 90, S. 1407-10,

Bouffler, S.; Silver, A.; Cox, R.: "The role of DNA repeats and associated secondary structures in genomic instability and neoplasia," Bioessays, 1993, 6, 15, S. 409-12,

Cuthbert, G.; McCullough, S.; Finney, R.; Breese, G.; Bown, N.: "Jumping translocation at 11q23 with MLL gene rearrangement and interstitial telomeric sequences," Genes Chromosomes Cancer, 1999, 4, 24, S. 295-8,

Krawczak, M.; Cooper, D. N.: "Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment," Hum Genet, 1991, 5, 86, S. 425-41,

Schon, E. A.; Rizzuto, R.; Moraes, C. T.; Nakase, H.; Zeviani, M.; DiMauro, S.: "A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA," Science, 1989, 4902, 244, S. 346-9,

Mount, St. M.: "A catalogue of splice junction sequens," Nucleic Acids Research, 1982, 2, 10,

Stone, B.; Wharton, W.: "Targeted RNA fingerprinting: the cloning of differentially-expressed cDNA fragments enriched for members of the zinc finger gene family," Nucleic Acids Res, 1994, 13, 22, S. 2612-8,

Schmid, S.L., McNiven,M.A., De Camilli,P.: "Dynamin and its partners:a progress report," Current Opinion in Cell Cycle, 1998, 10, S. 504-512,

Urrutia, R.; Henley, J. R.; Cook, T.; McNiven, M. A.: "The dynamins: redundant or distinct functions for an expanding family of related GTPases?," Proc Natl Acad Sci U S A, 1997, 2, 94, S. 377-84,

Scaife, R.; Margolis, R. L.: "Biochemical and immunochemical analysis of rat brain dynamin interaction with microtubules and organelles in vivo and in vitro," J Cell Biol, 1990, 6 Pt 2, 111, S. 3023-33,

Guan, X. Y.; Meltzer, P. S.; Dalton, W. S.; Trent, J. M.: "Identification of cryptic sites of DNA sequence amplification in human breast cancer by chromosome microdissection [see comments]," Nat Genet, 1994, 2, 8, S. 155-61,

Newman-Smith, E. D.; Shurland, D. L.; van der Bliek, A. M.: "Assignment of the dynamin-1 gene (DNM1) to human chromosome 9q34 by fluorescence in situ hybridization and somatic cell hybrid analysis," Genomics, 1997, 2, 41, S. 286-9,

Hornigold, N.; Devlin, J.; Davies, A. M.; Aveyard, J. S.; Habuchi, T.; Knowles, M. A.: "Mutation of the 9q34 gene TSC1 in sporadic bladder cancer," Oncogene, 1999, 16, 18, S. 2657-61,

© Die inhaltliche Zusammenstellung und Aufmachung dieser Publikation sowie die elektronische Verarbeitung sind urheberrechtlich geschützt. Jede Verwertung, die nicht ausdrücklich vom Urheberrechtsgesetz zugelassen ist, bedarf der vorherigen Zustimmung. Das gilt insbesondere für die Vervielfältigung, die Bearbeitung und Einspeicherung und Verarbeitung in elektronische Systeme.

DiML DTD Version 2.0
Zertifizierter Dokumentenserver
der Humboldt-Universität zu Berlin
HTML - Version erstellt am:
Wed Sep 5 16:50:29 2001