Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Norman, Gerry"'
Autor:
Francis Barany, Philip B. Paty, Jurg Ott, Daniel A. Notterman, William L. Gerald, Kenneth Offit, Michael F. Christman, Bert Gold, Tomas Kirchhoff, Josephine Hoh, Norman Gerry, Robert F. Stengel, Jinru Shia, Zhaoshi Zeng, Sarah F. Giardina, Richard Shattock, Shuang Wang, Gunter S. Schemmann, Manny D. Bacolod
Supplementary Information from The Signatures of Autozygosity among Patients with Colorectal Cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae2a7f812aee774fa76f2e8cabce9d0e
https://doi.org/10.1158/0008-5472.22373711.v1
https://doi.org/10.1158/0008-5472.22373711.v1
Autor:
Francis Barany, Philip B. Paty, Jurg Ott, Daniel A. Notterman, William L. Gerald, Kenneth Offit, Michael F. Christman, Bert Gold, Tomas Kirchhoff, Josephine Hoh, Norman Gerry, Robert F. Stengel, Jinru Shia, Zhaoshi Zeng, Sarah F. Giardina, Richard Shattock, Shuang Wang, Gunter S. Schemmann, Manny D. Bacolod
Previous studies have shown that among populations with a high rate of consanguinity, there is a significant increase in the prevalence of cancer. Single nucleotide polymorphism (SNP) array data (Affymetrix, 50K XbaI) analysis revealed long regions o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08a903f77c2a09d974b64174de8865eb
https://doi.org/10.1158/0008-5472.c.6497177.v1
https://doi.org/10.1158/0008-5472.c.6497177.v1
Autor:
Mark N. Polizzotto, Jacqueline Nordwall, Abdel G. Babiker, Andrew Phillips, David M. Vock, Nnakelu Eriobu, Vivian Kwaghe, Roger Paredes, Lourdes Mateu, Srikanth Ramachandruni, Rajeev Narang, Mamta K. Jain, Susana M. Lazarte, Jason V. Baker, Anne E.P. Frosch, Garyfallia Poulakou, Konstantinos N. Syrigos, Gretchen S. Arnoczy, Natalie A. McBride, Philip A. Robinson, Farjad Sarafian, Sanjay Bhagani, Hassan S. Taha, Thomas Benfield, Sean T.H. Liu, Anastasia Antoniadou, Jens Ulrik Stæhr Jensen, Ioannis Kalomenidis, Adityo Susilo, Prasetyo Hariadi, Tomas O. Jensen MD, Jose Luis Morales-Rull, Marie Helleberg, Sreenath Meegada, Isik S. Johansen, Daniel Canario, Eduardo Fernández-Cruz, Simeon Metallidis, Amish Shah, Aki Sakurai, Nikolaos G. Koulouris, Robin Trotman, Amy C. Weintrob, Daria Podlekareva, Usman Hadi, Kathryn M. Lloyd, Birgit Thorup Røge, Sho Saito, Kelly Sweerus, Jakob J. Malin, Christoph Lübbert, Jose Muñoz, Matthew J. Cummings, Marcelo H. Losso, Dan Turner, Kathryn Shaw-Saliba, Robin Dewar, Helene Highbarger, Perrine Lallemand, Tauseef Rehman, Norman Gerry, Dona Arlinda, Christina C. Chang, Birgit Grund, Michael R. Holbrook, Horace P. Holley, Fleur Hudson, Laura A. McNay, Daniel D. Murray, Sarah L. Pett, Megan Shaughnessy, Mary C. Smolskis, Giota Touloumi, Mary E. Wright, Mittie K. Doyle, Sharon Popik, Christine Hall, Roshan Ramanathan, Huyen Cao, Elsa Mondou, Todd Willis, Joseph V. Thakuria, Leman Yel, Elizabeth Higgs, Virginia L. Kan, Jens D. Lundgren, James D. Neaton, H. Clifford Lane
Publikováno v:
Lancet (London, England)
Background Passive immunotherapy using hyperimmune intravenous immunoglobulin (hIVIG) to SARS-CoV-2, derived from recovered donors, is a potential rapidly available, specific therapy for an outbreak infection such as SARS-CoV-2. Findings from randomi
Autor:
Lori Diseati, Laura B. Scheinfeldt, Rachel S. Kasper, Ruixue Zhaoyang, Neda Gharani, Tara J. Schmidlen, Erynn S. Gordon, Cecili K. Sessions, Susan K. Delaney, Joseph P. Jarvis, Norman Gerry, Michael Christman
Publikováno v:
Journal of Personalized Medicine, Vol 5, Iss 1, Pp 36-49 (2015)
There is currently great interest in using genetic risk estimates for common disease in personalized healthcare. Here we assess melanoma risk-related preventive behavioral change in the context of the Coriell Personalized Medicine Collaborative (CPMC
Externí odkaz:
https://doaj.org/article/f5be952e25a044a29b4e40603cf0c0d6
Autor:
Angela J, Rogers, Deborah, Wentworth, Andrew, Phillips, Katy, Shaw-Saliba, Robin L, Dewar, Neil R, Aggarwal, Abdel G, Babiker, Weizhong, Chang, Nila J, Dharan, Victoria J, Davey, Elizabeth S, Higgs, Norman, Gerry, Adit A, Ginde, J W Awori, Hayanga, Helene, Highbarger, Jeroen L, Highbarger, Mamta K, Jain, Virginia, Kan, Kami, Kim, Perrine, Lallemand, Bradley G, Leshnower, Joseph K, Lutaakome, Gail, Matthews, Ahmad, Mourad, Eleftherios, Mylonakis, Ven, Natarajan, Maria L, Padilla, Lavannya M, Pandit, Roger, Paredes, Sarah, Pett, Srikanth, Ramachandruni, M Tauseef, Rehman, Brad T, Sherman, D Clark, Files, Samuel M, Brown, Michael A, Matthay, B Taylor, Thompson, James D, Neaton, H Clifford, Lane, Richard, Williams
Publikováno v:
ACTIV-3/TICO Study Group*, Nielsen, H, Thisted, R K, Petersen, K T & Juhl, M R 2022, ' The Association of Baseline Plasma SARS-CoV-2 Nucleocapsid Antigen Level and Outcomes in Patients Hospitalized With COVID-19 ', Annals of Internal Medicine, vol. 175, no. 10, pp. 1401-1410 . https://doi.org/10.7326/M22-0924
Background: Levels of plasma SARS-CoV-2 nucleocapsid (N) antigen may be an important biomarker in patients with COVID-19 and enhance our understanding of the pathogenesis of COVID-19. Objective: To evaluate whether levels of plasma antigen can predic
Autor:
Adebowale Adeyemo, Norman Gerry, Guanjie Chen, Alan Herbert, Ayo Doumatey, Hanxia Huang, Jie Zhou, Kerrie Lashley, Yuanxiu Chen, Michael Christman, Charles Rotimi
Publikováno v:
PLoS Genetics, Vol 5, Iss 7, p e1000564 (2009)
The evidence for the existence of genetic susceptibility variants for the common form of hypertension ("essential hypertension") remains weak and inconsistent. We sought genetic variants underlying blood pressure (BP) by conducting a genome-wide asso
Externí odkaz:
https://doaj.org/article/20a7da60efcc42948501239fd86c819c
Autor:
Lisa, Kalman, Jay, Leonard, Norman, Gerry, Jack, Tarleton, Christina, Bridges, Julie M, Gastier-Foster, Robert E, Pyatt, Eileen, Stonerock, Monique A, Johnson, C Sue, Richards, Iris, Schrijver, Tianhui, Ma, Vanessa Rangel, Miller, Yetsa, Adadevoh, Pat, Furlong, Christine, Beiswanger, Lorraine, Toji
Publikováno v:
The Journal of molecular diagnostics : JMD. 13(2)
Duchenne and Becker muscular dystrophies (DMD/BMD) are allelic X-linked recessive disorders that affect approximately 1 in 3500 and 1 in 20,000 male individuals, respectively. Approximately 65% of patients with DMD have deletions, 7% to 10% have dupl