Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Hong Shi Kaleta"'
Autor:
Alyson Witt, Ethan M. Lange, David Rha, William Hagopian, Edna H. Ross, James E. Balow, Catherine Te, Richard M. Watanabe, Heather M. Stringham, Francis S. Collins, Richard C. McEachin, Zarir E. Karanjawala, Elizabeth R. Hauser, William L. Duren, Michael Boehnke, Thomas A. Buchanan, Timo T. Valle, Tasha E. Fingerlin, Richard N. Bergman, Jillian Blaschak-Harvan, Chun Li, Liisa Toivanen, Julie I. Knapp, Victoria L. Magnuson, Gabriele Vidgren, Leonid Segal, Delphine S. Ally, Anjene Musick, Jennie Chang, Stella J. Nylund, Arun M. Unni, Shane A. Shapiro, Peggy P. White, Karen L. Mohlke, Michael P. Epstein, Elza Demirchyan, Ben Shurtleff, Kristina Kudelko, Jaakko Tuomilehto, Joseph B. Rayman, Michael R. Erdos, Hong Shi Kaleta, Eva Tuomilehto-Wolf, Christian Welch, Carl D. Langefeld, Julie A. Douglas, Tiffany Musick, Joyce Tannenbaum, Carrie Pfahl, Ravi Sharaf, Kimmo Kohtamäki, Alistair So, Colin Martin, Jason Tovar, Soumitra Ghosh, Rachel Porter, Peter S. Chines, Edward H. Trager, Johan G. Eriksson, Ray Whiten, Kaisa Silander, Anabelle Morales-Mena, Gunther Birznieks, William Eldridge
Publikováno v:
The American Journal of Human Genetics. 67:1174-1185
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 we observe a weighted maximum LOD score (MLS) of 2.15 at map position 69.5 cM from pter and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0719c412274509a71d4aa0fa1bf5a5df
https://doi.org/10.1016/s0002-9297(07)62948-6
https://doi.org/10.1016/s0002-9297(07)62948-6
Autor:
Richard C. McEachin, Gabriele Vidgren, William Hagopian, Tasha E. Fingerlin, Shane A. Shapiro, Christian Welch, Colin Martin, William L. Duren, Michael Boehnke, Johan G. Eriksson, Gunther Birznieks, William Eldridge, Ray Whiten, Liisa Toivanen, Julie A. Douglas, Zarir E. Karanjawala, Francis S. Collins, Thomas A. Buchanan, Soumitra Ghosh, Carl D. Langefeld, Anjene Musick, Jennie Chang, Stella J. Nylund, Timo T. Valle, Alistair So, Catherine Te, Chun Li, Leonid Segal, Karen L. Mohlke, Carrie Pfahl, Ravi Sharaf, Edna H. Ross, Rachel Porter, Richard M. Watanabe, Joseph B. Rayman, Eva Tuomilehto-Wolf, Elza Demirchyan, David Rha, Joyce Tannenbaum, Victoria L. Magnuson, Elizabeth R. Hauser, Michael P. Epstein, Kimmo Kohtamäki, Richard N. Bergman, Delphine S. Ally, Alyson Witt, Edward H. Trager, Ben Shurtleff, Kristina Kudelko, Jaakko Tuomilehto, Peggy P. White, Julie I. Knapp, Michael R. Erdos, Kaisa Silander, Peter S. Chines, Hong Shi Kaleta, James E. Balow, Christian Ehnholm, Heather M. Stringham, Arun M. Unni, Tiffany Musick, Jason Tovar, Jillian Blaschak-Harvan, Anabelle Morales-Mena, Ethan M. Lange
Publikováno v:
The American Journal of Human Genetics. 67:1186-1200
Type 2 diabetes mellitus is a complex disorder encompassing multiple metabolic defects. We report results from an autosomal genome scan for type 2 diabetes-related quantitative traits in 580 Finnish families ascertained for an affected sibling pair a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60afb82ee87d3b201eb5e4c1a613b7db
https://doi.org/10.1016/s0002-9297(07)62949-8
https://doi.org/10.1016/s0002-9297(07)62949-8
Autor:
Richard N. Bergman, Johan G. Eriksson, Gunther Birznieks, Eva Tuomilehto-Wolf, William Eldridge, Victoria L. Magnuson, Colin Martin, William Hagopian, Delphine S. Ally, Christian Ehnholm, Soumitra Ghosh, Alistair So, Rachel Porter, Jillian Blaschak-Harvan, Arun M. Unni, Michael R. Erdos, James E. Balow, Gabriele Vidgren, Michael Boehnke, Ben Shurtleff, Kimmo Kohtamäki, Kristina Kudelko, Jaakko Tuomilehto, Elizabeth R. Hauser, Anjene Musick, Jennie Chang, Thomas A. Buchanan, Carl D. Langefeld, Shane A. Shapiro, Ravi Sharaf, Hong-Shi Kaleta, Timo T. Valle, Francis S. Collins, Tuula Tenkula, Joyce Tannenbaum, Leonid Segal, Peter S. Chines, Catherine Te, Richard M. Watanabe, Alyson Witt
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 96(5)
We are conducting a genome scan at an average resolution of 10 centimorgans (cM) for type 2 diabetes susceptibility genes in 716 affected sib pairs from 477 Finnish families. To date, our best evidence for linkage is on chromosome 20 with potentially
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ffe2748e75d7b9f00d0f8fe66f92274
https://pubmed.ncbi.nlm.nih.gov/10051618
https://pubmed.ncbi.nlm.nih.gov/10051618
Autor:
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., Hong Shi Kaleta, Lange, Ethan M., Chun Li, McEachin, Richard C.
Publikováno v:
American Journal of Human Genetics. Nov2000, Vol. 67 Issue 5.