Výsledky vyhledávání - Roessler, E
- Zobrazuji výsledky 1 - 13 z 13
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The interleukin 2 receptor (IL-2R): the IL-2R alpha subunit alters the function of the IL-2R beta subunit to enhance IL-2 binding and signaling by mechanisms that do not require bi... Autor Grant, A J, Roessler, E, Ju, G, Tsudo, M, Sugamura, K, Waldmann, T A
Vydáno 1992Text -
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A Hypomorphic Allele in the FGF8 Gene Contributes to Holoprosencephaly and Is Allelic to Gonadotropin-Releasing Hormone Deficiency in Humans Autor Arauz, R.F., Solomon, B.D., Pineda-Alvarez, D.E., Gropman, A.L., Parsons, J.A., Roessler, E., Muenke, M.
Vydáno 2010Text -
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A lymphokine, provisionally designated interleukin T and produced by a human adult T-cell leukemia line, stimulates T-cell proliferation and the induction of lymphokine-activated k... Autor Burton, J D, Bamford, R N, Peters, C, Grant, A J, Kurys, G, Goldman, C K, Brennan, J, Roessler, E, Waldmann, T A
Vydáno 1994Text -
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The interleukin (IL) 2 receptor beta chain is shared by IL-2 and a cytokine, provisionally designated IL-T, that stimulates T-cell proliferation and the induction of lymphokine-act... Autor Bamford, R N, Grant, A J, Burton, J D, Peters, C, Kurys, G, Goldman, C K, Brennan, J, Roessler, E, Waldmann, T A
Vydáno 1994Text -
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Exome Sequencing and High-Density Microarray Testing in Monozygotic Twin Pairs Discordant for Features of VACTERL Association Autor Solomon, B.D., Pineda-Alvarez, D.E., Hadley, D.W., Hansen, N.F., Kamat, A., Donovan, F.X., Chandrasekharappa, S.C., Hong, S.-K., Roessler, E., Mullikin, J.C.
Vydáno 2013Text -
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Loss-of-Function Mutations in Growth Differentiation Factor-1 (GDF1) Are Associated with Congenital Heart Defects in Humans Autor Karkera, J. D. , Lee, J. S. , Roessler, E. , Banerjee-Basu, S. , Ouspenskaia, M. V. , Mez, J. , Goldmuntz, E. , Bowers, P. , Towbin, J. , Belmont, J. W. , Baxevanis, A. D. , Schier, A. F. , Muenke, M.
Vydáno 2007Text -
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TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and Phenotype Autor Keaton, A.A., Solomon, B.D., Kauvar, E.F., El-Jaick, K.B., Gropman, A.L., Zafer, Y., Meck, J.M., Bale, S.J., Grange, D.K., Haddad, B.R., Gowans, G.C., Clegg, N.J, Delgado, M.R., Hahn, J.S., Pineda-Alvarez, D.E., Lacbawan, F., Vélez, J.I., Roessler, E., Muenke, M.
Vydáno 2011Text -
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A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD Autor Jain, M, Vélez, J I, Acosta, M T, Palacio, L G, Balog, J, Roessler, E, Pineda, D, Londoño, A C, Palacio, J D, Arbelaez, A, Lopera, F, Elia, J, Hakonarson, H, Seitz, C, Freitag, C M, Palmason, H, Meyer, J, Romanos, M, Walitza, S, Hemminger, U, Warnke, A, Romanos, J, Renner, T, Jacob, C, Lesch, K-P, Swanson, J, Castellanos, F X, Bailey-Wilson, J E, Arcos-Burgos, M, Muenke, M
Vydáno 2012Text -
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Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function Autor Lacbawan, F, Solomon, B D, Roessler, E, El-Jaick, K, Domené, S, Vélez, J I, Zhou, N, Hadley, D, Balog, J Z, Long, R, Fryer, A, Smith, W, Omar, S, McLean, S D, Clarkson, K, Lichty, A, Clegg, N J, Delgado, M R, Levey, E, Stashinko, E, Potocki, L, VanAllen, M I, Clayton-Smith, J, Donnai, D, Bianchi, D W, Juliusson, P B, Njølstad, P R, Brunner, H G, Carey, J C, Hehr, U, Müsebeck, J, Wieacker, P F, Postra, A, Hennekam, R C M, van den Boogaard, M-J H, van Haeringen, A, Paulussen, A, Herbergs, J, Schrander-Stumpel, C T R M, Janecke, A R, Chitayat, D, Hahn, J, McDonald-McGinn, D M, Zackai, E H, Dobyns, W B, Muenke, M
Vydáno 2009Text