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Did you mean tract tucker (231 results)?
Mechanisms of X-chromosome inactivation.
Chang SC, Tucker T, Thorogood NP, Brown CJ. Chang SC, et al. Among authors: tucker t. Front Biosci. 2006 Jan 1;11:852-66. doi: 10.2741/1842. Front Biosci. 2006. PMID: 16146776 Review.
Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasms.
Kanagal-Shamanna R, Hodge JC, Tucker T, Shetty S, Yenamandra A, Dixon-McIver A, Bryke C, Huxley E, Lennon PA, Raca G, Xu X, Jeffries S, Quintero-Rivera F, Greipp PT, Slovak ML, Iqbal MA, Fang M. Kanagal-Shamanna R, et al. Among authors: tucker t. Cancer Genet. 2018 Dec;228-229:197-217. doi: 10.1016/j.cancergen.2018.07.003. Epub 2018 Oct 10. Cancer Genet. 2018. PMID: 30377088 Free article. Review.
ALK+ hyaline vascular Castleman disease: a new kid on the block.
Farinha P, Subtil A, Carr A, Kaba R, Rinsma R, Tucker T, Hayes M. Farinha P, et al. Among authors: tucker t. Histopathology. 2022 May;80(6):1007-1010. doi: 10.1111/his.14624. Epub 2022 Feb 22. Histopathology. 2022. PMID: 35137445 No abstract available.
Fine-needle aspiration of soft tissue myoepithelioma.
Wang G, Tucker T, Ng TL, Villamil CF, Hayes MM. Wang G, et al. Among authors: tucker t. Diagn Cytopathol. 2016 Feb;44(2):152-5. doi: 10.1002/dc.23399. Epub 2015 Dec 8. Diagn Cytopathol. 2016. PMID: 26644362
Use of Treatment-Focused Tumor Sequencing to Screen for Germline Cancer Predisposition.
Lau TTY, May CM, Sefid Dashti ZJ, Swanson L, Starks ER, Parker JDK, Moore RA, Tucker T, Bosdet I, Young SS, Santos JL, Compton K, Heidary N, Hoang L, Schrader KA, Sun S, Kwon JS, Tinker AV, Karsan A. Lau TTY, et al. Among authors: tucker t. J Mol Diagn. 2021 Sep;23(9):1145-1158. doi: 10.1016/j.jmoldx.2021.06.006. Epub 2021 Jun 29. J Mol Diagn. 2021. PMID: 34197922 Free article.
Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics Repository.
Mighton C, Smith AC, Mayers J, Tomaszewski R, Taylor S, Hume S, Agatep R, Spriggs E, Feilotter HE, Semenuk L, Wong H, Lazo de la Vega L, Marshall CR, Axford MM, Silver T, Charames GS, Di Gioacchino V, Watkins N, Foulkes WD, Clavier M, Hamel N, Chong G, Lamont RE, Parboosingh J, Karsan A, Bosdet I, Young SS, Tucker T, Akbari MR, Speevak MD, Vaags AK, Lebo MS, Lerner-Ellis J; Canadian Open Genetics Repository Working Group. Mighton C, et al. Among authors: tucker t. J Med Genet. 2022 Jun;59(6):571-578. doi: 10.1136/jmedgenet-2021-107738. Epub 2021 Apr 19. J Med Genet. 2022. PMID: 33875564 Free PMC article.
Integrating Tumor Sequencing Into Clinical Practice for Patients With Mismatch Repair-Deficient Lynch Syndrome Spectrum Cancers.
Dixon K, Asrat MJ, Bedard AC, Binnington K, Compton K, Cremin C, Heidary N, Lohn Z, Lovick N, McCullum M, Mindlin A, O'Loughlin M, Petersen T, Portigal-Todd C, Scott J, St-Martin G, Thompson J, Turnbull R, Mung SW, Hong Q, Bezeau M, Bosdet I, Tucker T, Young S, Yip S, Aubertin G, Blood KA, Nuk J, Sun S, Schrader KA. Dixon K, et al. Among authors: tucker t. Clin Transl Gastroenterol. 2021 Aug 16;12(8):e00397. doi: 10.14309/ctg.0000000000000397. Clin Transl Gastroenterol. 2021. PMID: 34397043 Free PMC article.
37 results