Generation and characterization of a human chromosome 9 cosmid library
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C. L. Jackson | D. Housman | D. Ward | D. Taruscio | A. Baldini | A. Buckler | D. Britt | Deborah E. Britt | S. Graw | Alan J. Buckler | Domenica Taruscio
[1] J. Sambrook,et al. Molecular Cloning: A Laboratory Manual , 2001 .
[2] J. Haines,et al. Construction of a GT polymorphism map of human 9q. , 1992, Genomics.
[3] C. Robert Cloninger,et al. A genetic study of platelet adenylate cyclase activity: evidence for a single major locus effect in fluoride-stimulated activity. , 1991, American journal of human genetics.
[4] T. Shows,et al. The 1991 catalog of mapped genes and report of the nomenclature committee (Part 1 of 5) , 1991 .
[5] D. Ward,et al. In situ hybridization banding of human chromosomes with Alu-PCR products: a simultaneous karyotype for gene mapping studies. , 1991, Genomics.
[6] D C Ward,et al. Differential distribution of long and short interspersed element sequences in the mouse genome: chromosome karyotyping by fluorescence in situ hybridization. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[7] D. Ledbetter,et al. Rapid isolation of DNA probes within specific chromosome regions by interspersed repetitive sequence polymerase chain reaction. , 1990, Genomics.
[8] C. L. Jackson,et al. Monochromosomal rodent-human hybrids from microcell fusion of human lymphoblastoid cells containing an inserted dominant selectable marker. , 1990, Genomics.
[9] R. Larson,et al. Deletions of interferon genes in acute lymphoblastic leukemia. , 1990, The New England journal of medicine.
[10] G Hermanson,et al. High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones. , 1990, Science.
[11] D. Ledbetter,et al. Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[12] Stanley Fahn,et al. Human gene for torsion dystonia located on chromosome 9q32-q34 , 1989, Neuron.
[13] C. Burks,et al. The distribution of interspersed repetitive DNA sequences in the human genome. , 1989, Genomics.
[14] J. Weber,et al. Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. , 1989, American journal of human genetics.
[15] M. Farrall,et al. Mapping of mutation causing Friedreich's ataxia to human chromosome 9 , 1988, Nature.
[16] A. Houghton,et al. Loss of heterozygosity at autosomal and X-linked loci during tumor progression in a patient with melanoma. , 1987, Cancer research.
[17] S. Povey,et al. EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9 , 1987, The Lancet.
[18] A. Bird. CpG-rich islands and the function of DNA methylation , 1986, Nature.
[19] J. Milbrandt,et al. Organization of a Chinese hamster ovary dihydrofolate reductase gene identified by phenotypic rescue , 1983, Molecular and cellular biology.
[20] A. Feinberg,et al. Hypomethylation of ras oncogenes in primary human cancers. , 1983, Biochemical and biophysical research communications.
[21] R. Weinberg,et al. Isolation of a transforming sequence from a human bladder carcinoma cell line , 1982, Cell.
[22] C. Schmid,et al. Renaturation rate studies of a single family of interspersed repeated sequences in human deoxyribonucleic acid. , 1981, Biochemistry.
[23] F. Sanger,et al. DNA sequencing with chain-terminating inhibitors. , 1977, Proceedings of the National Academy of Sciences of the United States of America.
[24] M. Siniscalco,et al. Simultaneous identification of chromatid replication and of human chromosomes in metaphases of man-mouse somatic cell hybrids. (With 1 color plate). , 1977, Cytogenetics and Cell Genetics.
[25] F. Ruddle,et al. Differential staining of interspecific chromosomes in somatic cell hybrids by alkaline Giemsa stain , 1976, Somatic cell genetics.
[26] E. Southern. Detection of specific sequences among DNA fragments separated by gel electrophoresis. , 1975, Journal of molecular biology.
[27] K BOCZKOWSKI,et al. CHROMOSOMAL ENDOREDUPLICATION IN A CASE OF TURNER'S SYNDROME WITH 44/XX KARYOTYPE. , 1965, Lancet.
[28] G. Church,et al. Genomic sequencing. , 1993, Methods in molecular biology.