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Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH.
Jarbo C, Buckley PG, Piotrowski A, Mantripragada KK, Benetkiewicz M, Diaz de Ståhl T, Langford CF, Gregory SG, Dralle H, Gimm O, Bäckdahl M, Geli J, Larsson C, Westin G, Akerström G, Dumanski JP. Jarbo C, et al. Among authors: gimm o. Int J Cancer. 2006 Mar 1;118(5):1159-64. doi: 10.1002/ijc.21385. Int J Cancer. 2006. PMID: 16161042 Free article.
HRAS mutation prevalence and associated expression patterns in pheochromocytoma.
Stenman A, Welander J, Gustavsson I, Brunaud L, Bäckdahl M, Söderkvist P, Gimm O, Juhlin CC, Larsson C. Stenman A, et al. Among authors: gimm o. Genes Chromosomes Cancer. 2016 May;55(5):452-9. doi: 10.1002/gcc.22347. Epub 2016 Feb 23. Genes Chromosomes Cancer. 2016. PMID: 26773571 Free PMC article.
Role of SDHAF2 and SDHD in von Hippel-Lindau associated pheochromocytomas.
Kugelberg J, Welander J, Schiavi F, Fassina A, Bäckdahl M, Larsson C, Opocher G, Söderkvist P, Dahia PL, Neumann HP, Gimm O. Kugelberg J, et al. Among authors: gimm o. World J Surg. 2014 Mar;38(3):724-32. doi: 10.1007/s00268-013-2373-2. World J Surg. 2014. PMID: 24322175
Whole-exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene.
Juhlin CC, Stenman A, Haglund F, Clark VE, Brown TC, Baranoski J, Bilguvar K, Goh G, Welander J, Svahn F, Rubinstein JC, Caramuta S, Yasuno K, Günel M, Bäckdahl M, Gimm O, Söderkvist P, Prasad ML, Korah R, Lifton RP, Carling T. Juhlin CC, et al. Among authors: gimm o. Genes Chromosomes Cancer. 2015 Sep;54(9):542-54. doi: 10.1002/gcc.22267. Epub 2015 May 29. Genes Chromosomes Cancer. 2015. PMID: 26032282 Free PMC article.
179 results