Zobrazeno 1 - 10
of 24
pro vyhledávání: '"David H.-F. Teng"'
Autor:
Mark A. Poritz, Anne J. Blaschke, Carrie L. Byington, Lindsay Meyers, Kody Nilsson, David E. Jones, Stephanie A. Thatcher, Thomas Robbins, Beth Lingenfelter, Elizabeth Amiott, Amy Herbener, Judy Daly, Steven F. Dobrowolski, David H. -F. Teng, Kirk M. Ririe
Publikováno v:
PLoS ONE, Vol 6, Iss 11 (2011)
Externí odkaz:
https://doaj.org/article/96631b77deda413c8b218bf44403a887
Autor:
Mark A Poritz, Anne J Blaschke, Carrie L Byington, Lindsay Meyers, Kody Nilsson, David E Jones, Stephanie A Thatcher, Thomas Robbins, Beth Lingenfelter, Elizabeth Amiott, Amy Herbener, Judy Daly, Steven F Dobrowolski, David H-F Teng, Kirk M Ririe
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26047 (2011)
The ideal clinical diagnostic system should deliver rapid, sensitive, specific and reproducible results while minimizing the requirements for specialized laboratory facilities and skilled technicians. We describe an integrated diagnostic platform, th
Externí odkaz:
https://doaj.org/article/e7ad8b4b51a1448aad5d2451b0503fca
Autor:
Jason H. Richardson, Prasan Kankaew, James C McAvin, Boonsong Jaichapor, David H.-F. Teng, James A. Swaby, Shuenn-Jue Wu, Jittawadee Murphy, David L. Maserang, Russell E. Coleman, Panadda Krairojananan, Patcharee Kongtak, Robert Crisp, Timothy Davis, Sajeewane Ekanayake, Subhamoy Pal
Publikováno v:
Military Medicine. 180:937-942
Dengue fever occurs in localized outbreaks and can significantly erode troop strength and mission readiness. Timely identification of dengue virus (DENV) provides for rapid and appropriate patient management decisions, such as medical evacuation and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f00c78d04ff7be5aed85ee176a3753aa
https://doi.org/10.7205/milmed-d-14-00428
https://doi.org/10.7205/milmed-d-14-00428
Autor:
Burt Richards, Mark A. Poritz, Bruce D. Roth, Bob Risley, David H.-F. Teng, Tanya Sandrock, Harry A. Austin, Mark Stump, Karen Repetny, Forrest Hsu, Alexander Kamb, Sanghee Yoo, Marianne K.-H. Kim
Publikováno v:
Molecular Therapy. 4(5):398-406
Pseudotyped retroviral vectors combine the advantages of broad host range, high expression, stable chromosomal integration, and ease of preparation. These vectors greatly facilitate delivery into mammalian cells of sequences encoding individual pepti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9760df3e9d1ebfec337fe543371bde43
Autor:
David H. F. Teng, Yuan Chen, Sean V. Tavtigian, Lubing Lian, Alexander K. C. Wong, Phoung C. Ha
Publikováno v:
Genomics. 74:352-364
We have performed a homozygous deletion screen on 268 candidate genes in 90 human tumor cell lines derived from multiple types of cancers. Most of the candidate genes investigated have been proposed to be involved in cellular processes that are germa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf0769acdc428b369c4a45558f896bb4
https://doi.org/10.1006/geno.2001.6551
https://doi.org/10.1006/geno.2001.6551
Autor:
Marc Desrochers, Alun Thomas, Marianne Schroeder, Priya Dayananth, Arlene Carillo, Amy Pederson, Rong Hu, Jodi Mcarthur-Morrison, Teresa Janecki, Kirsten Laity, Audrey Beck, Diana Iliev, Yang Chen, David A. Frank, David H. F. Teng, Ann Marie Woodland, Martine Dumont, Jeff Swensen, Richard D. Smith, Julia Reid, Vicki Abtin, Sarah C. Snyder, James M. Farnham, Sam Richards, Brandon Penn, Sean V. Tavtigian, Brad Swedlund, Siavash Ghaffari, Martine Tranchant, Lisa A. Cannon-Albright, Amber Leavitt, Cheryl Frye, Jacques Simard, Michelle Baumgard, Kelly T. Peterson, Nicola J. Camp, Mark H. Skolnick, Fernand Labrie, Edward N. Kort, Johanna M. Rommens, Jamila Gupte, Gilles Leblanc, Susan L. Neuhausen
Publikováno v:
Nature Genetics. 27:172-180
It is difficult to identify genes that predispose to prostate cancer due to late age at diagnosis, presence of phenocopies within high-risk pedigrees and genetic complexity. A genome-wide scan of large, high-risk pedigrees from Utah has provided evid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0104713bbd578aded836768bf147d1a6
https://doi.org/10.1038/84808
https://doi.org/10.1038/84808
Autor:
Alexander Kamb, David H.-F. Teng, Andrew Maxfield, Christine Dunn, Ludmilla Zharkikh, Jon Karpilow, Burt Richards
Publikováno v:
Somatic Cell and Molecular Genetics. 25:191-205
Quality bioassays are central to all approaches directed at understanding or perturbing the function of proteins. One type of cell-based bioassay involves an engineered reporter whose transcriptional activity serves as a readout for upstream signals
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::217d320df2fb8a6060a48eb4e6a4b684
https://doi.org/10.1023/a:1019206625658
https://doi.org/10.1023/a:1019206625658
Autor:
Patricia A. Ormonde, David H. F. Teng, Simin Berry, Paul L. Bartel, Yuan Chen, Priya Dayananth, Ralph Pero, Grant Salada, Alexander K. C. Wong, Phuong C. Ha, Sean V. Tavtigian, Lubing Lian, Quentin Lawrence
Publikováno v:
Oncogene. 17:2279-2285
There are several lines of evidence indicating that the carboxy-terminal region of the tumor suppressor protein BRCA1 is a functionally significant domain. Using the yeast two-hybrid and in vitro biochemical assays, we show that a protein, CtIP, inte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::345be616ebcab8411a3e69197a951a24
https://doi.org/10.1038/sj.onc.1202150
https://doi.org/10.1038/sj.onc.1202150
Autor:
Cheryl Frye, Peter A. Steck, Michelle Baumgard, Bradley D. Swedlund, Samar A. Jasser, W. K. A. Yung, Rong Hu, Mark A. Pershouse, Azra H. Ligon, David H. F. Teng, Huai Lin, Lauren A. Langford, Sean V. Tavtigian, Thaylon Davis, T. Hattier
Publikováno v:
Nature Genetics. 15:356-362
Deletions involving regions of chromosome 10 occur in the vast majority (> 90%) of human glioblastoma multiformes. A region at chromosome 10q23-24 was implicated to contain a tumour suppressor gene and the identification of homozygous deletions in fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7d0f8a1525861e9b5288ca1c1a8c324
https://doi.org/10.1038/ng0497-356
https://doi.org/10.1038/ng0497-356
Autor:
Russell Bell, Fernand Labrie, Jodi Mcarthur-Morrison, S.C. Snyder, Robert Kehrer, Linda Steele, Thaylon Davis, K. Nguyen, Martine Dumont, J.T. Mitchell, Alun Thomas, Teresa Janecki, Mark H. Skolnick, Lisa A. Cannon-Albright, M. Stringfellow, Chantal Samson, David H. F. Teng, Alexander Kamb, T. Hattier, Barbara L. Weber, Sofia D. Merajver, Dominique Stoppa-Lyonnet, Hiroaki Shizuya, David E. Goldgar, Marianne Schroeder, T.D. Tran, Ping Jiang, Carole Bélanger, Jorunn E. Eyfjord, Simin Berry, Jacques Simard, J.-F. Leblanc, Martine Tranchant, Steinunn Thorlacius, Qian Chen, Robert Bogden, Yi Peng, Jane Weaver-Feldhaus, Sean V. Tavtigian, Fergus J. Couch, Cheryl Frye, Johanna M. Rommens, Alexander K. C. Wong, Srikanth Jammulapati, C. Stroup, Bradley D. Swedlund, Susan L. Neuhausen, Donna M Shattuck-Eidens, Kenneth Offit, J. Swense
Publikováno v:
Nature Genetics. 12:333-337
Breast carcinoma is the most common malignancy among women in developed countries. Because family history remains the strongest single predictor of breast cancer risk, attention has focused on the role of highly penetrant, dominantly inherited genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2ed0a2178f423da973579178b301888
https://doi.org/10.1038/ng0396-333
https://doi.org/10.1038/ng0396-333