Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jaime Wendt-Andrae"'
Autor:
Francoise Van den Bergh, Marshall W. Anderson, Jiang Wang, John D. Ebben, Michael Tschannen, Thomas J. Albert, Dong Hai Xiong, Jaime Wendt Andrae, Qi Zhang, Alex A. Adjei, Haiming Xu, Yian Wang, Xing Hua, Liang Wang, Mary Anne Watt, Peter Vedell, Yan Lu, Haijie Xiao, Ming You, Carl Morrison, Todd Richmond, Howard J. Jacob, Michael A. James, Pengyuan Liu, Rebecca R. Selzer, Feng Ding, Karen Head, Jigar Patel, Peng Cui, Sandra L. Starnes, Ken C. Lo, Jing Pan, Ping Yang
Publikováno v:
Carcinogenesis. 33:1270-1276
Lung cancer is the leading cause of cancer-related death, with non-small cell lung cancer (NSCLC) being the predominant form of the disease. Most lung cancer is caused by the accumulation of genomic alterations due to tobacco exposure. To uncover its
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2226b3c0f0baa7057f204b4dfd422df4
https://doi.org/10.1093/carcin/bgs148
https://doi.org/10.1093/carcin/bgs148
Autor:
Howard J. Jacob, Shirng-Wern Tsaih, John Parrington, Jaime Wendt Andrae, Shuang Jia, Andrew Wiederhold, Leah C. Solberg Woods, Pippa Simpson, James B. Meigs, Hong He, Antony Galione, Mary L. Kaldunski, Alexander Stoddard, Michael Tschannen, Shun-Hua Li, Martin J. Hessner, Katie Holl, Margarida Ruas da Silva, Raymond G. Hoffmann
Publikováno v:
Genetics
The genetic basis of type 2 diabetes remains incompletely defined despite the use of multiple genetic strategies. Multiparental populations such as heterogeneous stocks (HS) facilitate gene discovery by allowing fine mapping to only a few megabases,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77f3b8027b4c850d09fe77035ca54277
https://pubmed.ncbi.nlm.nih.gov/25236446
https://pubmed.ncbi.nlm.nih.gov/25236446
Autor:
David A. Margolis, Jennifer L. Geurts, Howard J. Jacob, Mary Shimoyama, George Kowalski, Paula E. North, Regan Veith, Brandon Wilk, David Dimmock, Altheia Roquemore-Goins, Barbara J. Joers, Robert M. Kliegman, Daniel Helbling, Kelly Abrams, Jozef Lazar, Shirng Wern Tsaih, Jeremy M. Harris, Jaime Wendt-Andrae, Gunter Scharer, Bradley K. Taylor, Michael Tschannen, David P. Bick, Kent Brodie, Jill Northup, Elizabeth A. Worthey, Kimberly A. Strong, Michael H. Farrell
Publikováno v:
Science Translational Medicine. 5
The price of whole-genome and -exome sequencing has fallen to the point where these methods can be applied to clinical medicine. Here, we outline the lessons we have learned in converting a sequencing laboratory designed for research into a fully fun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf2a3a28b5d53c4c77d9453ae9ccdc72
https://doi.org/10.1126/scitranslmed.3006468
https://doi.org/10.1126/scitranslmed.3006468
Autor:
Sonia L. Sugg, Jaime Wendt Andrae, Edwin Cuppen, Howard J. Jacob, Donna McAllister, Xujing Wang, Tatjana Adamovic, Victor Guryev
Publikováno v:
Cancer Research, 69(12), 5159-5167. AMER ASSOC CANCER RESEARCH
Cancer Research, 69(12), 5159-5167. American Association for Cancer Research Inc.
Cancer Research, 69(12), 5159-5167. American Association for Cancer Research Inc.
The presence of copy number variants in normal genomes poses a challenge to identify small genuine somatic copy number changes in high-resolution cancer genome profiling studies due to the use of unpaired reference DNA. Another problem is the well-kn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6261fe04db3b47f42b0d33ea14e592f
https://research.rug.nl/en/publications/4d3ce37f-c36b-4643-b8ee-3d243089440b
https://research.rug.nl/en/publications/4d3ce37f-c36b-4643-b8ee-3d243089440b
Genome-wide linkage analysis is a powerful tool for the identification of genes underlying single gene and complex genetic disorders. The most commonly used technique for performing genome wide scans for genetic studies in the rat is by analysis of s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9316cc7d5e9ebd70af4855c205b2491b
https://doi.org/10.1385/1-59259-850-1:131
https://doi.org/10.1385/1-59259-850-1:131
Publikováno v:
Methods in molecular medicine. 108
Genome-wide linkage analysis is a powerful tool for the identification of genes underlying single gene and complex genetic disorders. The most commonly used technique for performing genome wide scans for genetic studies in the rat is by analysis of s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::56924adef7dc2e2e0fbfcda31b959d48
https://pubmed.ncbi.nlm.nih.gov/16028680
https://pubmed.ncbi.nlm.nih.gov/16028680
Autor:
Dan Chen, Susan Bromberg, Jiaming Yu, Val C. Sheffield, Peter J. Tonellato, Jeff Nie, Anne E. Kwitek, Howard J. Jacob, Danilo C. Carlos, Todd E. Scheetz, Jeffrey Eckert, Angela Lemke, Thomas L. Casavant, Kimberly Orlebeke, Jo Gullings-Handley, M. Bento Soares, Jaime Wendt Andrae, Dean Pasko
Publikováno v:
Genome research. 14(4)
The laboratory rat is a major model organism for systems biology. To complement the cornucopia of physiological and pharmacological data generated in the rat, a large genomic toolset has been developed, culminating in the release of the rat draft gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43078fbc7faa5c846f19fd614243f274
https://pubmed.ncbi.nlm.nih.gov/15060019
https://pubmed.ncbi.nlm.nih.gov/15060019