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Page 1
A model for gene therapy of human hereditary lymphedema.
Karkkainen MJ, Saaristo A, Jussila L, Karila KA, Lawrence EC, Pajusola K, Bueler H, Eichmann A, Kauppinen R, Kettunen MI, Yla-Herttuala S, Finegold DN, Ferrell RE, Alitalo K. Karkkainen MJ, et al. Among authors: ferrell re. Proc Natl Acad Sci U S A. 2001 Oct 23;98(22):12677-82. doi: 10.1073/pnas.221449198. Epub 2001 Oct 9. Proc Natl Acad Sci U S A. 2001. PMID: 11592985 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. Am J Ophthalmol. 2002 Oct;134(4):592-6. doi: 10.1016/s0002-9394(02)01642-2. Am J Ophthalmol. 2002. PMID: 12383817
Age of onset in hereditary lymphedema.
Levinson KL, Feingold E, Ferrell RE, Glover TW, Traboulsi EI, Finegold DN. Levinson KL, et al. J Pediatr. 2003 Jun;142(6):704-8. doi: 10.1067/mpd.2003.235. J Pediatr. 2003. PMID: 12838201
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: ferrell re. FASEB J. 2001 Apr;15(6):1028-36. doi: 10.1096/fj.00-0383com. FASEB J. 2001. PMID: 11292664
Candidate gene analysis in primary lymphedema.
Ferrell RE, Kimak MA, Lawrence EC, Finegold DN. Ferrell RE, et al. Lymphat Res Biol. 2008;6(2):69-76. doi: 10.1089/lrb.2007.1022. Lymphat Res Biol. 2008. PMID: 18564921
737 results