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Page 1
VEGFR3 gene structure, regulatory region, and sequence polymorphisms.
Iljin K, Karkkainen MJ, Lawrence EC, Kimak MA, Uutela M, Taipale J, Pajusola K, Alhonen L, Halmekytö M, Finegold DN, Ferrell RE, Alitalo K. Iljin K, et al. Among authors: kimak ma. FASEB J. 2001 Apr;15(6):1028-36. doi: 10.1096/fj.00-0383com. FASEB J. 2001. PMID: 11292664
GJC2 missense mutations cause human lymphedema.
Ferrell RE, Baty CJ, Kimak MA, Karlsson JM, Lawrence EC, Franke-Snyder M, Meriney SD, Feingold E, Finegold DN. Ferrell RE, et al. Among authors: kimak ma. Am J Hum Genet. 2010 Jun 11;86(6):943-8. doi: 10.1016/j.ajhg.2010.04.010. Epub 2010 May 27. Am J Hum Genet. 2010. PMID: 20537300 Free PMC article.
Truncating mutations in FOXC2 cause multiple lymphedema syndromes.
Finegold DN, Kimak MA, Lawrence EC, Levinson KL, Cherniske EM, Pober BR, Dunlap JW, Ferrell RE. Finegold DN, et al. Among authors: kimak ma. Hum Mol Genet. 2001 May 15;10(11):1185-9. doi: 10.1093/hmg/10.11.1185. Hum Mol Genet. 2001. PMID: 11371511
HGF and MET mutations in primary and secondary lymphedema.
Finegold DN, Schacht V, Kimak MA, Lawrence EC, Foeldi E, Karlsson JM, Baty CJ, Ferrell RE. Finegold DN, et al. Among authors: kimak ma. Lymphat Res Biol. 2008;6(2):65-8. doi: 10.1089/lrb.2008.1524. Lymphat Res Biol. 2008. PMID: 18564920 Free PMC article.
Candidate gene analysis in primary lymphedema.
Ferrell RE, Kimak MA, Lawrence EC, Finegold DN. Ferrell RE, et al. Among authors: kimak ma. Lymphat Res Biol. 2008;6(2):69-76. doi: 10.1089/lrb.2007.1022. Lymphat Res Biol. 2008. PMID: 18564921
Connexin 47 mutations increase risk for secondary lymphedema following breast cancer treatment.
Finegold DN, Baty CJ, Knickelbein KZ, Perschke S, Noon SE, Campbell D, Karlsson JM, Huang D, Kimak MA, Lawrence EC, Feingold E, Meriney SD, Brufsky AM, Ferrell RE. Finegold DN, et al. Among authors: kimak ma. Clin Cancer Res. 2012 Apr 15;18(8):2382-90. doi: 10.1158/1078-0432.CCR-11-2303. Epub 2012 Feb 20. Clin Cancer Res. 2012. PMID: 22351697 Free PMC article.
Lymphedema-distichiasis syndrome and FOXC2 gene mutation.
Traboulsi EI, Al-Khayer K, Matsumoto M, Kimak MA, Crowe S, Wilson SE, Finegold DN, Ferrell RE, Meisler DM. Traboulsi EI, et al. Among authors: kimak ma. Am J Ophthalmol. 2002 Oct;134(4):592-6. doi: 10.1016/s0002-9394(02)01642-2. Am J Ophthalmol. 2002. PMID: 12383817
15 results