Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Jessica Moline"'
Autor:
Petra Bullova, Alessio Giubellino, Martha Quezado, Maya Lodish, Deloris E. Koziol, Charalampos Lyssikatos, Elena Belyavskaya, Maria de la Luz Sierra, Karel Pacak, Nadia Rentia, Constantine A. Stratakis, Louis Dye, Christopher A. Wassif, Margarita Raygada, Antony Cougnoux, Louis J. Maher, Charis Eng, Panagiotis Mastorakos, Jessica Moline, Paraskevi Xekouki, Spyridon A. Mastroyannis, Carl D. Malchoff, Eva Szarek
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 100:E710-E719
Germline mutations in genes coding succinate dehydrogenase (SDH) subunits A, B, C, and D have been identified in familial paragangliomas (PGLs)/pheochromocytomas (PHEOs) and other tumors. We described a GH-secreting pituitary adenoma (PA) caused by S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20983772a26d3cb8983b293d1a66d8f7
https://doi.org/10.1210/jc.2014-4297
https://doi.org/10.1210/jc.2014-4297
Autor:
Arun D. Singh, Jessica Moline
Publikováno v:
Retinoblastoma: Clinical Advances and Emerging Treatment Strategies. :36-48
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bc01b6a666a83add0853c5a89ba9791
https://doi.org/10.2217/ebo.12.179
https://doi.org/10.2217/ebo.12.179
Autor:
Brandie Heald, Charis Eng, Andres A. Roma, Peter G. Rose, Bin Yang, Haider Mahdi, Chad M. Michener, Jessica Moline, Charles V. Biscotti
Publikováno v:
Gynecologic Oncology. 130:121-126
Lynch syndrome (LS) is a hereditary condition that increases the risk for endometrial and other cancers. Recognizing women at risk for LS based on personal/family history is burdensome and imprecise. Tumor testing using microsatellite instability (MS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::785dde50703fb7c285046d11f71f4df9
https://doi.org/10.1016/j.ygyno.2013.04.022
https://doi.org/10.1016/j.ygyno.2013.04.022
Publikováno v:
Familial Cancer. 12:1-18
The number of described cancer susceptibility syndromes continues to grow, as does our knowledge on how to manage these syndromes with the aim of early detection and cancer prevention. Oncologists now have greater responsibility to recognize patterns
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbd6f2d94229bb636f32e73340d83656
https://doi.org/10.1007/s10689-012-9584-9
https://doi.org/10.1007/s10689-012-9584-9
Publikováno v:
Genetics in Medicine. 14:616-619
Cowden syndrome results from germline mutations in the gene for phosphatase and tensin homologue deleted on chromosome 10 (PTEN) and from variants in succinate dehydrogenase B and D subunits. We hypothesized that succinate accumulation may be common
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24d6dfb065ec193bb46ee61ad1fdaf5c
https://doi.org/10.1038/gim.2011.63
https://doi.org/10.1038/gim.2011.63
Autor:
Jessica Moline, Charis Eng, Ying Ni, Jessica Mester, Jinlian Chen, Xin He, Mohammed S. Orloff, Matthew D. Ringel
Publikováno v:
Human Molecular Genetics
Cowden syndrome (CS), a Mendelian autosomal-dominant disorder, predisposes to breast, thyroid and other cancers. Germline mutations in phosphatase and tensin homolog (PTEN) have been recently reported in 23% of a large series of classic CS. Here, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7b4c07bc1a25b941940880ee2e2113e
http://europepmc.org/articles/PMC3276278
http://europepmc.org/articles/PMC3276278
Autor:
Chadi A. Calarge, Michael Tansey, Vicki L. Ellingrod, Del D. Miller, Laura Acion, Jessica Moline, Janet A. Schlechte
Publikováno v:
Pharmacogenetics and Genomics. 19:373-382
To investigate the association between hyperprolactinemia and variants of the dopamine D2 receptor (DRD2) gene in children and adolescents in long-term treatment with risperidone.Medically healthy 7 to 17-year-old patients chronically treated with ri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::024591d64483e49a5f7f3cc2092051c2
https://doi.org/10.1097/fpc.0b013e328329a60f
https://doi.org/10.1097/fpc.0b013e328329a60f
Autor:
Jessica Moline, Stephan F. Taylor, Del D. Miller, Timothy L. Holman, Vicki L. Ellingrod, Jane Kerr
Publikováno v:
Schizophrenia Research. 98:47-54
Introduction The metabolic syndrome and insulin resistance represent growing concerns related to atypical antipsychotic (AAP) use as their incidence in the schizophrenia population is two-to-four-fold higher than the general population. Reduced methy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::610b300c5ecb492060b6b2f7998742f8
https://doi.org/10.1016/j.schres.2007.09.030
https://doi.org/10.1016/j.schres.2007.09.030
Autor:
Vicki L. Ellingrod, Jessica Moline
Publikováno v:
Journal of Pharmacy Practice. 20:277-282
The goal for this issue of the Journal of Pharmacy Practice is to provide an overview of pharmacogenomics and highlight research done in select therapeutic areas such as oncology, psychiatry, cardiology, and HIV, although pharmacogenomics is taking c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9e0a21d7749da54d11856fd825edf3b
https://doi.org/10.1177/0897190007304820
https://doi.org/10.1177/0897190007304820
Publikováno v:
Schizophrenia Research. 77:253-260
Purpose The excitatory neurotransmitter glutamate has become an important area of focus for schizophrenia researchers. Polymorphisms in the type-three metabotropic glutamate receptor gene (GRM3) have been associated with the pathogenesis of schizophr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9641b14cd93b2963c7ede833cb215d36
https://doi.org/10.1016/j.schres.2005.04.001
https://doi.org/10.1016/j.schres.2005.04.001