Search Results - "Nylund, S J"

Substrate nucleotide-determined non-templated addition of adenine by Taq DNA polymerase: implications for PCR-based genotyping and cloning by Magnuson, V L, Ally, D S, Nylund, S J, Karanjawala, Z E, Rayman, J B, Knapp, J I, Lowe, A L, Ghosh, S, Collins, F S

“…The Applied Biosystems PRISM fluorescence-based genotyping system as well as the Invitrogen TA Cloning vector system are influenced by the tendency of Taq DNA…”
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Mapping genes for NIDDM. Design of the Finland-United States Investigation of NIDDM Genetics (FUSION) Study by VALLE, T, TUOMILEHTO, J, TUOMILEHTO-WOLF, E, EHNHOLM, C, BLASCHAK, J, LANGEFELD, C. D, WATANABE, R. M, MAGNUSON, V, ALLY, D. S, HAGOPIAN, W. A, ROSS, E, BUCHANAN, T. A, BERGMAN, R. N, COLLINS, F, BOEHNKE, M, GHOSH, S, HAUSER, E. R, ERIKSSON, J, NYLUND, S. J, KOHTAMAKI, K, TOIVANEN, L, VIDGREN, G

“…Mapping genes for NIDDM. Design of the Finland-United States Investigation of NIDDM Genetics (FUSION) Study. T Valle , J Tuomilehto , R N Bergman , S Ghosh , E…”
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Metaphase fluorescence in situ hybridization (FISH) in the follow-up of 60 patients with haemopoietic malignancies by Nylund, S J, Ruutu, T, Saarinen, U, Knuutila, S

“…Metaphase DNA fluorescence in situ hybridization (metaphase-FISH) was performed on follow-up samples from 60 patients suffering from haemopoietic malignancies…”
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Detection of minimal residual disease using fluorescence DNA in situ hybridization: a follow-up study in leukemia and lymphoma patients by Nylund, S J, Ruutu, T, Saarinen, U, Larramendy, M L, Knuutila, S

“…We used fluorescence DNA in situ hybridization (FISH) to detect chromosomal abnormalities as an indicator of minimal residual disease in follow-up samples from…”
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Ploidy in bone marrow cells from healthy donors: a MAC (morphology antibody chromosomes) study by Larramendy, M L, Nylund, S J, Wessman, M, Ruutu, T, Knuutila, S

“…The ploidy of human bone marrow cells belonging to the megakaryocytic, granulocytic-monocytic and erythrocytic lineages was studied by in situ hybridization…”
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The W64R variant of the β3-adrenergic receptor is not associated with Type II diabetes or obesity in a large Finnish sample by GHOSH, S, LANGEFELD, C. D, TUOMILEHTO, J, COLLINS, F. S, BOEHNKE, M, ALLY, D, WATANABE, R. M, HAUSER, E. R, MAGNUSON, V. L, NYLUND, S. J, VALLE, T, ERIKSSON, J, BERGMAN, R. N

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Simultaneous detection of high-resolution R-banding and fluorescence in situ hybridization signals after fluorouracil-induced cellular synchronization by Larramendy, M L, Nylund, S J, Armstrong, E, Knuutila, S

“…A method for simultaneous detection of fluorescence in situ hybridization of DNA probes and high resolution fluorescent R banding is described. Human…”
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Analysis of genotype and phenotype on the same interphase or mitotic cell. A manual of MAC (morphology antibody chromosomes) methodology by Knuutila, S, Nylund, S J, Wessman, M, Larramendy, M L

“…The purpose of this paper is to serve as a MAC (Morphology Antibody Chromosome) manual describing combined methodologies that allow simultaneous and/or…”
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Cell lineage involvement of recurrent chromosomal abnormalities in hematologic neoplasms by Knuutila, S, Teerenhovi, L, Larramendy, M L, Elonen, E, Franssila, K O, Nylund, S J, Timonen, T, Heinonen, K, Mahlamäki, E, Winqvist, R

“…Analysis of most hematologic neoplasms indicates the involvement of one or more cell lineages in the bone marrow and/or the blood but rules out the involvement…”
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A large sample of finnish diabetic sib-pairs reveals no evidence for a non-insulin-dependent diabetes mellitus susceptibility locus at 2qter by Ghosh, S, Hauser, E R, Magnuson, V L, Valle, T, Ally, D S, Karanjawala, Z E, Rayman, J B, Knapp, J I, Musick, A, Tannenbaum, J, Te, C, Eldridge, W, Shapiro, S, Musick, T, Martin, C, So, A, Witt, A, Harvan, J B, Watanabe, R M, Hagopian, W, Eriksson, J, Nylund, S J, Kohtamaki, K, Tuomilehto-Wolf, E, Boehnke, M

“…In the first reported positive result from a genome scan for non-insulin-dependent diabetes mellitus (NIDDM), Hanis et al. found significant evidence of…”
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Cell lineage involvement in four patients with myelodysplastic syndrome and t(1;7) or trisomy 8 studied by simultaneous immunophenotyping and fluorescence in situ hybridization by Nylund, S J, Verbeek, W, Larramendy, M L, Ruutu, T, Heinonen, K, Hallman, H, Knuutila, S

“…Four patients with myelodysplastic syndrome (MDS), one with t(1;7) and three with trisomy 8, were studied by immunophenotyping and fluorescence in situ…”
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The Finland–United States Investigation of Non–Insulin-Dependent Diabetes Mellitus Genetics (FUSION) Study. I. An Autosomal Genome Scan for Genes That Predispose to Type 2 Diabetes by Ghosh, Soumitra, Watanabe, Richard M., Valle, Timo T., Hauser, Elizabeth R., Magnuson, Victoria L., Langefeld, Carl D., Ally, Delphine S., Mohlke, Karen L., Silander, Kaisa, Kohtamäki, Kimmo, Chines, Peter, Balow, James, Birznieks, Gunther, Chang, Jennie, Eldridge, William, Erdos, Michael R., Karanjawala, Zarir E., Knapp, Julie I., Kudelko, Kristina, Martin, Colin, Morales-Mena, Anabelle, Musick, Anjene, Musick, Tiffany, Pfahl, Carrie, Porter, Rachel, Rayman, Joseph B., Rha, David, Segal, Leonid, Shapiro, Shane, Sharaf, Ravi, Shurtleff, Ben, So, Alistair, Tannenbaum, Joyce, Te, Catherine, Tovar, Jason, Unni, Arun, Welch, Christian, Whiten, Ray, Witt, Alyson, Blaschak-Harvan, Jillian, Douglas, Julie A., Duren, William L., Epstein, Michael P., Fingerlin, Tasha E., Kaleta, Hong Shi, Lange, Ethan M., Li, Chun, McEachin, Richard C., Stringham, Heather M., Trager, Edward, White, Peggy P., Eriksson, Johan, Toivanen, Liisa, Vidgren, Gabriele, Nylund, Stella J., Tuomilehto-Wolf, Eva, Ross, Edna H., Demirchyan, Elza, Hagopian, William A., Buchanan, Thomas A., Tuomilehto, Jaakko, Bergman, Richard N., Collins, Francis S., Boehnke, Michael

“…We performed a genome scan at an average resolution of 8 cM in 719 Finnish sib pairs with type 2 diabetes. Our strongest results are for chromosome 20, where…”
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The Finland–United States Investigation of Non–Insulin-Dependent Diabetes Mellitus Genetics (FUSION) Study. II. An Autosomal Genome Scan for Diabetes-Related Quantitative-Trait Loci by Watanabe, Richard M., Ghosh, Soumitra, Langefeld, Carl D., Valle, Timo T., Hauser, Elizabeth R., Magnuson, Victoria L., Mohlke, Karen L., Silander, Kaisa, Ally, Delphine S., Chines, Peter, Blaschak-Harvan, Jillian, Douglas, Julie A., Duren, William L., Epstein, Michael P., Fingerlin, Tasha E., Kaleta, Hong Shi, Lange, Ethan M., Li, Chun, McEachin, Richard C., Stringham, Heather M., Trager, Edward, White, Peggy P., Balow, James, Birznieks, Gunther, Chang, Jennie, Eldridge, William, Erdos, Michael R., Karanjawala, Zarir E., Knapp, Julie I., Kudelko, Kristina, Martin, Colin, Morales-Mena, Anabelle, Musick, Anjene, Musick, Tiffany, Pfahl, Carrie, Porter, Rachel, Rayman, Joseph B., Rha, David, Segal, Leonid, Shapiro, Shane, Sharaf, Ravi, Shurtleff, Ben, So, Alistair, Tannenbaum, Joyce, Te, Catherine, Tovar, Jason, Unni, Arun, Welch, Christian, Whiten, Ray, Witt, Alyson, Kohtamäki, Kimmo, Ehnholm, Christian, Eriksson, Johan, Toivanen, Liisa, Vidgren, Gabriele, Nylund, Stella J., Tuomilehto-Wolf, Eva, Ross, Edna H., Demirchyan, Elza, Hagopian, William A., Buchanan, Thomas A., Tuomilehto, Jaakko, Bergman, Richard N., Collins, Francis S., Boehnke, Michael

“…Type 2 diabetes mellitus is a complex disorder encompassing multiple metabolic defects. We report results from an autosomal genome scan for type 2…”
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The W64R variant of the beta3-adrenergic receptor is not associated with type II diabetes or obesity in a large Finnish sample by Ghosh, S, Langefeld, C D, Ally, D, Watanabe, R M, Hauser, E R, Magnuson, V L, Nylund, S J, Valle, T, Eriksson, J, Bergman, R N, Tuomilehto, J, Collins, F S, Boehnke, M

“…Recent studies have suggested an association between Type II (non-insulin-dependent) diabetes mellitus-related phenotypes and a cytosine-to-thymidine…”
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The W64R variant of the β 3 -adrenergic receptor is not associated with Type II diabetes or obesity in a large Finnish sample by Ghosh, S., Langefeld, C. D., Ally, D., Watanabe, R. M., Hauser, E. R., Magnuson, V. L., Nylund, S. J., Valle, T., Eriksson, J., Bergman, R. N., Tuomilehto, J., Collins, F. S., Boehnke, M.

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The W64R variant of the [beta]3-adrenergic receptor is not associated with Type II diabetes or obesity in a large Finnish sample by Ghosh, S, Langefeld, C D, Ally, D, Watanabe, R M, Hauser, E R, Magnuson, V L, Nylund, S J, Valle, T, Eriksson, J, Bergman, R N, J. Tuomilehto, Collins, F S, Boehnke, M

“…Recent studies have suggested an association between Type II (non-insulin-dependent) diabetes mellitus-related phenotypes and a cytosine-to-thymidine…”
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Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers by Ghosh, S, Karanjawala, ZE, Hauser, E R, Ally, D, Knapp, JI, Rayman, J B, Musick, A, Tannenbaum, J, Te, C

“…Large-scale genotyping is required to generate dense identity-by-descent maps to map genes for human complex disease. In some studies the number of genotypes…”
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Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION (Finland-U.S. Investigation of NIDDM Genetics) Study Group by Ghosh, S, Karanjawala, Z E, Hauser, E R, Ally, D, Knapp, J I, Rayman, J B, Musick, A, Tannenbaum, J, Te, C, Shapiro, S, Eldridge, W, Musick, T, Martin, C, Smith, J R, Carpten, J D, Brownstein, M J, Powell, J I, Whiten, R, Chines, P, Nylund, S J, Magnuson, V L, Boehnke, M, Collins, F S

“…Large-scale genotyping is required to generate dense identity-by-descent maps to map genes for human complex disease. In some studies the number of genotypes…”
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Clinical molecular cytogenetics by Knuutila, S, Wessman, M, Nylund, S J, Ruutu, T, Keinänen, M

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