Search Results - "Balow Jr, J."

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  1. 1

    Analysis of CARD15 NOD2 haplotypes fails to identify common variants associated with rheumatoid arthritis susceptibility by Addo, A., Le, J., Li, W., Aksentijevich, I., Balow Jr, J., Lee, A., Gregersen, P. K., Kastner, D. L., Remmers, E. F.

    Published in Scandinavian journal of rheumatology (01-06-2005)
    “…Objectives: The CARD15 NOD2 gene product plays an important role in host response to bacterial lipopolysaccharides and bacterial muramyl dipeptide via…”
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    Journal Article
  2. 2

    Mapping of a Gene Causing Familial Mediterranean Fever to the Short Arm of Chromosome 16 by Pras, Elon, Pras, Mordechai, Aksentijevich, Ivona, Gruberg, Luis, Balow, James E, Prosen, Leandrea, Dean, Michael, Steinberg, Alfred D, Kastner, Daniel L

    Published in The New England journal of medicine (04-06-1992)
    “…Familial Mediterranean fever is a disorder characterized by intermittent attacks of fever with abdominal pain, pleurisy, or arthritis; its symptoms are not…”
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  3. 3

    Linkage disequilibrium mapping places the gene causing familial Mediterranean fever close to D16S246 by LEVY, E. N, YANG SHEN, GUMUCIO, D, PRAS, M, SHOHAT, M, ROTTER, J. I, FISCHEL-GHODSIAN, N, RICHARDS, R. I, KASTNER, D. L, KUPELIAN, A, KRUGLYAK, L, AKSENTIJEVICH, I, PRAS, E, BALOW, J. E, LINZER, B, XIAOGUANG CHEN, SHELTON, D. A

    Published in American journal of human genetics (01-03-1996)
    “…This report presents refined genetic mapping data for the gene causing familial Mediterranean fever (FMF), a recessively inherited disorder of inflammation. We…”
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  4. 4

    Evidence for linkage of the gene causing familial Mediterranean fever to chromosome 17q in non-Ashkenazi Jewish families : second locus or type I error ? by AKSENTIJEVICH, I, GRUBERG, L, PRAS, E, BALOW, J. E, KOVO, M, GAZIT, E, DEAN, M, PRAS, M, KASTNER, D. L

    Published in Human genetics (01-07-1993)
    “…Familial Mediterranean fever (FMF) is an autosomal recessive disorder of unknown pathogenesis, characterized by recurrent, self-limited attacks of fever with…”
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  5. 5

    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

    Published in American journal of human genetics (01-11-2000)
    “…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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  6. 6

    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

    Published in American journal of human genetics (01-11-2000)
    “…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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    Ancient Missense Mutations in a New Member of the RoRet Gene Family Are Likely to Cause Familial Mediterranean Fever by Aksentijevich, I, Centola, M, Deng, Zuoming, Sood, R, Balow, JE Jr, Wood, G, Zaks, N, Mansfield, E, Chen, Xiang, Eisenberg, S, Vedula, A, Shafran, N, Raben, N, Pras, E, Pras, M

    Published in Cell (22-08-1997)
    “…Familial Mediterranean fever (FMF) is a recessively inherited disorder characterized by dramatic episodes of fever and serosal inflammation. This report…”
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    Clinical differences between North African and Iraqi Jews with familial Mediterranean fever by Pras, Eran, Livneh, Avi, Balow Jr, James E., Pras, Elon, Kastner, Daniel L., Pras, Mordechai, Langevitz, Pnina

    Published in American journal of medical genetics (13-01-1998)
    “…Familial Mediterranean fever (FMF) is an autosomal recessive disease causing attacks of fever and serositis. The gene causing this disease, designated MEFV,…”
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    Journal Article
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