Search Results - "Nisson, Paul"

A Human Homolog of the Saccharomyces cerevisiae REV3 Gene, which Encodes the Catalytic Subunit of DNA Polymerase ζ by Peter E. M. Gibbs, McGregor, W. Glenn, Maher, Veronica M., Nisson, Paul, Lawrence, Christopher W.

“…To get a better understanding of mutagenic mechanisms in humans, we have cloned and sequenced the human homolog of the Saccharomyces cerevisiae REV3 gene. The…”
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Neoplastic Transformation and Tumorigenesis Associated with Sam68 Protein Deficiency in Cultured Murine Fibroblasts by Liu, Keyi, Li, Limin, Nisson, Paul E., Gruber, Chris, Jessee, Joel, Cohen, Stanley N.

“…Sam68 is a multimeric 68-kDa RNA-binding nuclear protein of unknown function that interacts with, and is tyrosine-phosphorylated by, the oncogenic protein Src…”
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CCG repeats in cDNAs from human brain by KLEIDERLEIN, J. J, NISSON, P. E, JESSEE, J, LI, W.-B, BECKER, K. G, DERBY, M. L, ROSS, C. A, MARGOLIS, R. L

“…Expansion mutations of trinucleotide repeats and other units of unstable DNA have been proposed to account for at least some of the genetic susceptibility to a…”
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Reversible Tumorigenesis Induced by Deficiency of Vasodilator-Stimulated Phosphoprotein by Liu, Keyi, Li, Limin, Nisson, Paul E., Gruber, Chris, Jessee, Joel, Cohen, Stanley N.

“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Identification of a repeated sequence in the genome of the sea urchin which is traescribed by RNA polymerase III and contains the features of a retroposon by Nisson, Paul E., Hickey, Robert J., Boshar, Mark F., Crain, William R.

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Rapid and efficient cloning of Alu-PCR products using uracil DNA glycosylase by Nisson, P E, Rashtchian, A, Watkins, P C

“…By incorporating dUMP residues into the 5' end of PCR primers, one can generate products which, after treatment with uracil DNA glycosylase (UDG), contain 3'…”
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UV and chemical mutagenesis in rev7 mutants of yeast by Lawrence, C W, Nisson, P E, Christensen, R B

“…We have examined induced mutagenesis in rev7-1 mutants of Baker's yeast' Saccharomyces cerevisiae, using a variety of contrasting test systems and several…”
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Molecular cloning of PCR products by Finney, M, Nisson, P E, Rashtchian, A

“…It is often desirable to clone PCR products to establish a permanent source of cloned DNA for hybridization studies, to obtain high-quality DNA sequencing…”
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Isolation of exons from cloned DNA by exon trapping by Nisson, P E, Watkins, P C, Krizman, D B

“…Exon trapping is an RNA polymerase chain reaction (PCR) method to clone expressed sequences or exons directly from mammalian genomic DNA. The basic protocol in…”
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The exon trapping assay partly discriminates against alternatively spliced exons by Andreadis, Athena, Nisson, Paul E., Kosik, Kenneth S., Watkins, Paul C.

“…A cosmld containing eight exons of the gene coding for the microtubule-associated tau protein was subjected to the exon trapping assay. All the constitutive…”
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Protocols for trapping internal and 3'-terminal exons by Nisson, P E, Ally, A, Watkins, P C

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Use of random primer extension for concurrent amplification and nonradioactive labeling of nucleic acids by Mackey, J, Darfler, M, Nisson, P, Rashtchian, A

“…A method for efficient nonradioactive labeling of DNA with biotin using random primer extension has been developed. Under the conditions described, a…”
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Mutually exclusive expression of the Strongylocentrotus purpuratus Spc1 gene and its Lytechinus pictus homologue in cells of hybrid embryos by Nisson, Paul E., Gaudette, Michelle F., Brandhorst, Bruce P., Crain, William R.

“…ABSTRACT The expression of the Specl gene of Strongylocentrotus purpuratus and its Lytechinus pictus homologue LpSl was analyzed in reciprocal hybrid embryos…”
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Identification of the chromosome 14 origin of a C-negative marker associated with a 14q32 deletion by chromosome painting by Magnani, I, Sacchi, N, Darfler, M, Nisson, P E, Tornaghi, R, Fuhrman-Conti, A M

“…A constitutional chromosome 14 rearrangement was observed in a female with a psychodevelopmental disorder. Karyotype analysis using a variety of chromosome…”
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Spatial patterns of gene expression in preimplantation mouse embryos by Nisson, P E, Francis, S, Crain, W R

“…The distribution of total polyadenylated RNA and mRNAs from the beta-actin, fibronectin, and cytokeratin Endo A genes was examined in preimplantation mouse…”
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Mutually exclusive expression of the Strongylocentrotus purpuratus Spec1 gene and its Lytechinus pictus homologue in cells of hybrid embryos by Nisson, P E, Gaudette, M F, Brandhorst, B P, Crain, W R

“…The expression of the Spec1 gene of Strongylocentrotus purpuratus and its Lytechinus pictus homologue LpS1 was analyzed in reciprocal hybrid embryos of these…”
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Restricted expression of the Lytechinus pictus Spec1 gene homologue in reciprocal hybrid embryos with Strongylocentrotus purpuratus by Brandhorst, Bruce P., Filion, Mario, Nisson, Paul E., Crain, William R.

“…Hybrid embryos were derived from reciprocal crosses of Strongylocentrotus purpuratus and Lytechinus pictus sea urchins. The expression of proteins specific for…”
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Three Strongylocentrotus purpuratus actin genes show correct cell-specific expression in hybrid embryos of S. purpuratus and Lytechinus pictus by Nisson, P E, Dike, L E, Crain, W R

“…The cell-specific expression of three actin genes from the sea urchin species Strongylocentrotus purpuratus was examined in hybrid embryos of S. purpuratus and…”
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The timing of expression of four actin genes and an RNA polymerase III-transcribed repeated sequence is correct in hybrid embryos of the sea urchin species Strongylocentrotus purpuratus and Lytechinus pictus by Bullock, Bryant P., Nisson, Paul E., Crain, William R.

“…The accumulation of the mRNAs from four Strongylocentrotus purpuratus actin genes (the single muscle gene M, and three cytoskeletal genes CyI, CyIIIa, and…”
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Transcriptionally active chimeric gene derived from the fusion of the AML1 gene and a novel gene on chromosome 8 in t(8;21) leukemic cells by Nisson, P E, Watkins, P C, Sacchi, N

“…In the t(8;21)(q22;q22) of acute myelogenous leukemia (AML), the breakpoint on chromosome 21 disrupts the AML1 gene, generally in the intron between exons 5…”
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