ACNP - Italian Periodicals Catalogue

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Results: 1-9 |

Results: 9

Molecular regulation of lymphangiogenesis and targets for tissue oedema

Authors: Karkkainen, MJ Jussila, L Ferrell, RE Finegold, DN Alitalo, K

Citation: Mj. Karkkainen et al., Molecular regulation of lymphangiogenesis and targets for tissue oedema, TRENDS MO M, 7(1), 2001, pp. 18-22

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

Three novel activating mutations in the calcium-sensing receptor responsible for autosomal dominant hypocalcemia

Authors: Conley, YP Finegold, DN Peters, DG Cook, JS Oppenheim, DS Ferrell, RE

Citation: Yp. Conley et al., Three novel activating mutations in the calcium-sensing receptor responsible for autosomal dominant hypocalcemia, MOL GEN MET, 71(4), 2000, pp. 591-598

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

Familial nephrotic syndrome: Clinical spectrum and linkage to chromosome 19q13

Authors: Vats, A Nayak, A Ellis, D Randhawa, PS Finegold, DN Levinson, KL Ferrell, RE

Citation: A. Vats et al., Familial nephrotic syndrome: Clinical spectrum and linkage to chromosome 19q13, KIDNEY INT, 57(3), 2000, pp. 875-881

Indirect fluorescence detection of amino acids on electrophoretic microchips

Authors: Munro, NJ Huang, ZL Finegold, DN Landers, JP

Citation: Nj. Munro et al., Indirect fluorescence detection of amino acids on electrophoretic microchips, ANALYT CHEM, 72(13), 2000, pp. 2765-2773

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: 1-9 |