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Results: 1-7 |
Results: 7
Truncating mutations in FOXC2 cause multiple lymphedema syndromes
Authors: Finegold, DN Kimak, MA Lawrence, EC Levinson, KL Cherniske, EM Pober, BR Dunlap, JW Ferrell, RE
Citation: Dn. Finegold et al., Truncating mutations in FOXC2 cause multiple lymphedema syndromes, HUM MOL GEN, 10(11), 2001, pp. 1185-1189
VEGFR3 gene structure, regulatory region, and sequence polymorphisms
Authors: Iljin, K Karkkainen, MJ Lawrence, EC Kimak, MA Uutela, M Taipale, J Pajusola, K Alhonen, L Halmekyto, M Finegold, DN Ferrell, RE Alitalo, K
Citation: K. Iljin et al., VEGFR3 gene structure, regulatory region, and sequence polymorphisms, FASEB J, 15(6), 2001, pp. 1028-1036
A model for gene therapy of human hereditary lymphedema
Authors: 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
Citation: Mj. Karkkainen et al., A model for gene therapy of human hereditary lymphedema, P NAS US, 98(22), 2001, pp. 12677-12682
Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema
Authors: Karkkainen, MJ Ferrell, RE Lawrence, EC Kimak, MA Levinson, KL McTigue, MA Alitalo, K Finegold, DN
Citation: Mj. Karkkainen et al., Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema, NAT GENET, 25(2), 2000, pp. 153-159
Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma
Authors: Baysal, BE Ferrell, RE Willett-Brozick, JE Lawrence, EC Myssiorek, D Bosch, A van der Mey, A Taschner, PEM Rubinstein, WS Myers, EN Richard, CW Cornelisse, CJ Devilee, P Devlin, B
Citation: Be. Baysal et al., Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma, SCIENCE, 287(5454), 2000, pp. 848-851
Frequent sequence variation in the human myostatin (GDF8) gene as a markerfor analysis of muscle-related phenotypes
Authors: Ferrell, RE Conte, V Lawrence, EC Roth, SM Hagberg, JM Hurley, BF
Citation: Re. Ferrell et al., Frequent sequence variation in the human myostatin (GDF8) gene as a markerfor analysis of muscle-related phenotypes, GENOMICS, 62(2), 1999, pp. 203-207
Hereditary lymphedema: evidence for linkage and genetic heterogeneity
Authors: Ferrell, RE Levinson, KL Esman, JH Kimak, MA Lawrence, EC Barmada, MM Finegold, DN
Citation: Re. Ferrell et al., Hereditary lymphedema: evidence for linkage and genetic heterogeneity, HUM MOL GEN, 7(13), 1998, pp. 2073-2078
Risultati: 1-7 |