Zobrazeno 1 - 10
of 16
pro vyhledávání: '"J Shawn Jones"'
Autor:
Nicholas J. Keeling, Christine M. Formea, J Shawn Jones, Emily Glogowski, Jyothsna Giri, Nina Gonzaludo, Sara L Rogers
Publikováno v:
Pharmacogenomics. 21(11)
Pharmacogenomics test coverage and reimbursement are major obstacles to clinical uptake. Several early adopter programs have been successfully initiated through dedicated investments by federal and institutional research funding. As a result of resea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4bce28df4f03f145e8e94b456b84a5f
https://pubmed.ncbi.nlm.nih.gov/32748688
https://pubmed.ncbi.nlm.nih.gov/32748688
Autor:
Jennifer N. Eichmeyer, Sara L Rogers, Tara J. Schmidlen, Raluca N Kurz, Emily Glogowski, Erica Schnettler, J Shawn Jones, Jyothsna Giri, Christine M. Formea
Publikováno v:
Pharmacogenomics. 21(11)
In this Perspective, the authors discuss the state of pharmacogenomics testing addressing a number of advances, challenges and barriers, including legal ramifications, changes to the regulatory landscape, coverage of testing and the implications of d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe014be115b8b01e3e81553a4c7da5e3
https://pubmed.ncbi.nlm.nih.gov/32635876
https://pubmed.ncbi.nlm.nih.gov/32635876
Publikováno v:
American journal of pharmaceutical education. 79(8)
Objective. To examine whether playing a board game can assist PharmD students in learning autonomic nervous system (ANS) pharmacology. Design. Of 72 students enrolled in a required second-year pharmacology course, 22 students volunteered to play the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4d3d1c16b0473b62476f3dd1e26f88b
https://pubmed.ncbi.nlm.nih.gov/26689278
https://pubmed.ncbi.nlm.nih.gov/26689278
Autor:
Mala Pande, Christopher I. Amos, Xiangjun Gu, Patrick M. Lynch, Qingyi Wei, Imelda M. Campos, Miguel A. Rodriguez-Bigas, Marsha L. Frazier, Jinyun Chen, J. Shawn Jones
Publikováno v:
Cancer Epidemiology, Biomarkers & Prevention. 15:886-891
Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant syndrome of familial malignancies resulting from germ-line mutations in DNA mismatch repair genes. Colorectal and endometrial cancers are most frequently observed. A polymorph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fcf8135a45443c1e5fcfc327cec6ae8
https://doi.org/10.1158/1055-9965.epi-05-0644
https://doi.org/10.1158/1055-9965.epi-05-0644
Autor:
Patrick M. Lynch, Christopher I. Amos, J. Shawn Jones, Xiangjun Gu, Miguel A. Rodriguez-Bigas, Marsha L. Frazier
Publikováno v:
Cancer Causes & Control. 16:749-753
We examined a G-to-A single nucleotide polymorphism of the ATM gene, to determine if it influences hereditary non-polyposis colorectal cancer (HNPCC) age of onset. HNPCC is caused by mutations in mismatch repair genes, especially hMLH1 and hMSH2. ATM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c9d3f09756f5c1551f7acc5e85be31f
https://doi.org/10.1007/s10552-005-1540-7
https://doi.org/10.1007/s10552-005-1540-7
Autor:
Christopher I. Amos, Xuedong Chi, Patrick M. Lynch, J. Shawn Jones, Marsha L. Frazier, Xiangjun Gu
Publikováno v:
Clinical Cancer Research. 10:5845-5849
Purpose: Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant syndrome of familial malignancies. Colorectal and endometrial cancers are most frequently observed. The syndrome results mainly from germ-line mutations in DNA mismat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a29cf620d07619779f8f3e335a4e567
https://doi.org/10.1158/1078-0432.ccr-03-0590
https://doi.org/10.1158/1078-0432.ccr-03-0590
Autor:
J. Shawn Jones, Xiangjun Gu, Imelda M. Campos, Patrick M. Lynch, Christopher I. Amos, Marsha L. Frazier
Publikováno v:
Cancer Epidemiology, Biomarkers & Prevention. 13:676-678
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc2439ed8cd730098c396fe67947e519
https://doi.org/10.1158/1055-9965.676.13.4
https://doi.org/10.1158/1055-9965.676.13.4
Autor:
Chongjuan Wei, Christopher I. Amos, Marsha L. Frazier, Jinyun Chen, Patrick M. Lynch, J. Shawn Jones, Subrata Sen
Publikováno v:
Molecular carcinogenesis. 46(4)
Aurora-A kinase is considered a potential cancer susceptibility gene that encodes a centrosome-associated, cell cycle-regulated serine/threonine kinase. We studied two single nucleotide polymorphisms (SNP) in the coding region of Aurora-A, 91T-to-A (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec25b1796f2b62ef9c9169d257bdbcf4
https://pubmed.ncbi.nlm.nih.gov/17219423
https://pubmed.ncbi.nlm.nih.gov/17219423
Autor:
Miguel A. Rodriguez-Bigas, Xiangjun Gu, Imelda M. Campos, Marsha L. Frazier, Maja Zecevic, Patrick M. Lynch, J. Shawn Jones, Christopher I. Amos
Publikováno v:
Journal of the National Cancer Institute. 98(2)
Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant disorder caused by germline mutations in DNA mismatch repair (MMR) genes. Insulin-like growth factor-I (IGF-I) is involved in colorectal carcinogenesis, and elevated plasma IG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcb097ae14e9c0a63036aac5892cbf22
https://pubmed.ncbi.nlm.nih.gov/17105989
https://pubmed.ncbi.nlm.nih.gov/17105989
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