Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Walairat Laosinchai-Wolf"'
Autor:
Huiping Zhu, Gary J. Latham, Jessica L. Larson, Ya-Wen Huang, Caren Gentile, Henny H. Lemmink, Johanna Schleutker, Tsang-Ming Ko, Vivianna M. Van Deerlin, Kristin M. Abbott, Minna Toivonen, John N. Milligan, Walairat Laosinchai-Wolf, Stela Filipovic-Sadic
Publikováno v:
Journal of molecular diagnostics, 23(6), 753-764. ELSEVIER SCIENCE INC
J Mol Diagn
J Mol Diagn
Spinal muscular atrophy is a severe autosomal recessive disease caused by disruptions in the SMN1 gene. The nearly identical SMN2 gene copy number is associated with disease severity. SMN1 duplication markers, such as c.*3+80T>G and c.*211_*212del, c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92ec57853e976c37d5479aa151cdc6c1
https://research.rug.nl/en/publications/d7553b59-7a1d-4848-95cc-0efe7d7b1c4d
https://research.rug.nl/en/publications/d7553b59-7a1d-4848-95cc-0efe7d7b1c4d
Autor:
Ashima Sharma, Walairat Laosinchai-Wolf, Erika Mitchen, Deepa Eveleigh, Kortney Wilkinson-Busha, Jonathan Turner, Melissa Church, Adrian Lara, Carleen Gentry, Jaya Goyal, Ramakrishna Boyanapalli, Bernard Andruss, Gary Latham
Publikováno v:
Genetics in Medicine. 24:S154
Autor:
Kelnar, Kevin, Church, Melissa, Janovsky, Justin, Patel, Darshana, Lara, Adrian, Jefferson, Keri, Walairat Laosinchai-Wolf, Ringel, Lando, Ashton, Jacob D, Larson, Jessica L, Routsong, Ryan, Latham, Gary J, Milligan, John N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd7bad5931e063c185f42d8525392d03
Autor:
Walairat Laosinchai-Wolf, Ion Beldorth, Fei Yang, John B. Hedges, Jacquelyn J. Roth, Adam K. Ruskin, Keri L. Jefferson, Justin T Brown, Bernard F. Andruss, L Cai, Richard D. Press, Marie E. Fahey, Christopher D. Watt
Publikováno v:
The Journal of Molecular Diagnostics : JMD
This study describes the analytical performance of the QuantideX qPCR BCR-ABL IS Kit, the first Food and Drug Administration–cleared assay designed to monitor breakpoint cluster region–Abelson tyrosine-protein kinase 1 (BCR-ABL1) fusion transcrip
Autor:
Jaclyn Shingara, Kerri Keiger, Emmanuel Labourier, Jeffrey Shelton, Walairat Laosinchai-Wolf, Richard Conrad, David Brown, Patricia Powers
Publikováno v:
RNA. 11:1461-1470
MicroRNAs (miRNAs) are small, noncoding RNAs that regulate gene expression in both plants and animals. miRNA genes have been implicated in a variety of important biological processes, including development, differentiation, apoptosis, fat metabolism,
Autor:
Chris R. Novak, Marianna Goldrick, Cindy R. WalkerPeach, Marty R. Badgett, Walairat Laosinchai-Wolf, Andrew G. Hadd, Lesley A. Isgur
Publikováno v:
The Journal of Molecular Diagnostics. 6:348-355
The development of simple and rapid methods for the detection of the common genetic mutations associated with cystic fibrosis (CF) requires access to positive-control samples including the 5/7/9T variants of intron 8. We used PCR and a simple multipl
Autor:
Rupali Shinde, Emmanuel Labourier, Laura Langfield, Thomas J. Giordano, Sylvie Beaudenon-Huibregtse, Michelle Vinco, Walairat Laosinchai-Wolf
Publikováno v:
Human pathology. 45(7)
Molecular testing for oncogenic gene alterations provides clinically actionable information essential for the optimal management of follicular cell thyroid cancer. We aimed to establish the distribution and frequency of common oncogenic gene mutation
Autor:
Richard Sesboüé, David L. Smith, Sylvie Beaudenon-Huibregtse, Jean-Christophe Sabourin, Emmanuel Labourier, Walairat Laosinchai-Wolf, Aude Lamy
Publikováno v:
Archives of pathologylaboratory medicine. 138(3)
Context.—Current clinicopathologic assessment of malignant neoplastic diseases entails the analysis of specific genetic alterations that provide diagnostic, prognostic, or therapy-determining information.Objective.—To develop and validate a robus
Autor:
L Brusca, C Higgs, Q Wei, L. Friar, Emmanuel Labourier, Mike Griffiths, Walairat Laosinchai-Wolf, J Mason, A Masters, H Newell, Christopher D. Gocke, Judith E. Karp
Publikováno v:
Blood Cancer Journal
Modern management of leukemia and selection of optimal treatment approaches entails the analysis of multiple recurrent cytogenetic abnormalities with independent diagnostic or prognostic value. We report the first multicenter validation of a multiple
Publikováno v:
Cancer genetics. 205(10)
Molecular methods play a critical role in the accurate diagnosis of leukemia by complementing morphologic, cytochemical, immunophenotypic, and cytogenetic analyses. We developed a multiplex reverse transcription–polymerase chain reaction (RT-PCR) m