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784 results

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Page 1
Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas.
Schmidt L, Duh FM, Chen F, Kishida T, Glenn G, Choyke P, Scherer SW, Zhuang Z, Lubensky I, Dean M, Allikmets R, Chidambaram A, Bergerheim UR, Feltis JT, Casadevall C, Zamarron A, Bernues M, Richard S, Lips CJ, Walther MM, Tsui LC, Geil L, Orcutt ML, Stackhouse T, Lipan J, Slife L, Brauch H, Decker J, Niehans G, Hughson MD, Moch H, Storkel S, Lerman MI, Linehan WM, Zbar B. Schmidt L, et al. Among authors: decker j. Nat Genet. 1997 May;16(1):68-73. doi: 10.1038/ng0597-68. Nat Genet. 1997. PMID: 9140397
Novel mutations of the MET proto-oncogene in papillary renal carcinomas.
Schmidt L, Junker K, Nakaigawa N, Kinjerski T, Weirich G, Miller M, Lubensky I, Neumann HP, Brauch H, Decker J, Vocke C, Brown JA, Jenkins R, Richard S, Bergerheim U, Gerrard B, Dean M, Linehan WM, Zbar B. Schmidt L, et al. Among authors: decker j. Oncogene. 1999 Apr 8;18(14):2343-50. doi: 10.1038/sj.onc.1202547. Oncogene. 1999. PMID: 10327054
Clinical utility gene card for: von Hippel-Lindau (VHL).
Decker J, Neuhaus C, Macdonald F, Brauch H, Maher ER. Decker J, et al. Eur J Hum Genet. 2014 Apr;22(4). doi: 10.1038/ejhg.2013.180. Epub 2013 Aug 28. Eur J Hum Genet. 2014. PMID: 23982691 Free PMC article. No abstract available.
Characteristic genomic imbalances in pediatric pheochromocytoma.
Hering A, Guratowska M, Bucsky P, Claussen U, Decker J, Ernst G, Hoeppner W, Michel S, Neumann H, Parlowsky T, Loncarevic I. Hering A, et al. Among authors: decker j. Genes Chromosomes Cancer. 2006 Jun;45(6):602-7. doi: 10.1002/gcc.20323. Genes Chromosomes Cancer. 2006. PMID: 16518846
Outcome of peripheral blood stem cell mobilization in advanced phases of CML is dependent on the type of chemotherapy applied.
Fischer T, Neubauer A, Mohm J, Huhn D, Busemann C, Link H, Arseniev L, Büssing B, Novotny J, Ganser A, Duyster J, Bunjes D, Westermeier T, Flohr T, Desprès D, Gamm H, Decker J, Derigs G, Aulitzky W, Huber C. Fischer T, et al. Among authors: decker j. Ann Hematol. 1998 Jul-Aug;77(1-2):21-6. doi: 10.1007/s002770050406. Ann Hematol. 1998. PMID: 9760148 Clinical Trial.
Mutation screening for the prothrombin variant G20210A by melting point analysis with the Light Cycler system: atypical results, detection of the variant C20209T and possible clinical implications.
Wylenzek C, Trübenbach J, Gohl P, Wildhardt G, Alkins S, Fausett MB, Decker J, Steinberger D. Wylenzek C, et al. Among authors: decker j. Clin Lab Haematol. 2005 Oct;27(5):343-6. doi: 10.1111/j.1365-2257.2005.00720.x. Clin Lab Haematol. 2005. PMID: 16178919
784 results