Zobrazeno 1 - 10
of 579
pro vyhledávání: '"R, Mollicone"'
Autor:
S.M. White, R. Mollicone, M. Rozek, Z. Tümer, T. Opiola, J.-J. Candelier, C.R. Bonvicino, H. Winking, A. Hebinck, H. Kuiper, Ch. Zühlke, H. Yasue, J.M. Perez de la Lastra, S. Kiuchi, A. Pienkowska, N. Arnal, B. Gläser, C. Ngo, H. Mehenni, C. Steinlein, P.S. D’Andrea, R.P.M.A. Crooijmans, A. Eggen, C. Zijlstra, M. Yerle, U. Butzmann, S.E. Antonarakis, Y.E. Shahein, E. Anton, R. Korstanje, D.F. de Andres-Cara, N.A. de Haan, R. Heilig, B. Brenig, J. Egozcue, C. Delcros, M. Østergaard, G.F. Gillissen, A. Wandall, R. Kreutz, R.J. McKinlay Gardner, F. Piumi, M. Mahony, A. Robic, C. Ozouf-Costaz, N. Tommerup, T. Haaf, C. Rodellar, C. Szpirer, F. Vidal, P.A. Ioannou, P.M. Kroisel, C. Drögemüller, K. Buchet-Poyau, Y. Takagaki, T.L. Harboe, C. Wilhelm, F. Porto-Foresti, J. Barciszewski, A.C.M. Bonné, M.T. Roldan-Arjona, C. Rogel-Gaillard, H. Hiraiwa, Y. Muneta, M. Grzmil, P. Zaragoza, C. Bonillo, H.A. van Lith, J. Kunz, A. Dalski, O. Distl, F. Laccone, D. Milan, C. Windpassinger, T. Awata, H. Uenishi, J. Szpirer, R. Fries, A.A. Bosma, F. Foresti, M.F.Z. Daniel-Silva, H. Hayes, R. Roy, H. Omran, P. Pinton, S. Schlickum, E. Petek, E. Schwinger, L. Li, P. Coullin, C. Knorr, L.F.M. van Zutphen, J. Blanco, H.P. Klinger, A. Volz, J. Mißbach, I.B. Otazu, E. Northrop, C. Andersen, P. Burfeind, M. Den Bieman, M. Meins, R. Melkaoui, J. Beck, U. Radhakrishna, M. Gautier, R. Oriol, L.F. Almeida-Toledo, I. Nanda, K. Wagner, F. Habermann, V. Petrovic, M. Schmid, R. Yamamoto, P. Moore, P. van Vooren, G. Hauke, H. Zürcher, F. Hildebrandt, C.G. Ziegler, J. Koch, P. Laurent, J.L. Williams, M.A.M. Groenen, J.J. Garrido, C. Schelling, S. Yadav, C. Kosan, H.R. Slater
Publikováno v:
Cytogenetic and Genome Research. 97:261-275
Autor:
Kamiyama, Shin1,2 kammy@unii.ac.jp, Sone, Hideyuki1,2
Publikováno v:
Biologics. Sep2024, Vol. 4 Issue 3, p242-279. 38p.
Autor:
E. Petek, M. Rozek, Z. Tümer, S.E. Antonarakis, E. Anton, Ch. Zühlke, J.L. Williams, U. Butzmann, M.A.M. Groenen, E. Northrop, A.C.M. Bonné, J.M. Perez de la Lastra, H.R. Slater, N.A. de Haan, R. Heilig, C. Delcros, Y.E. Shahein, J.J. Garrido, F. Porto-Foresti, M. Østergaard, C. Steinlein, A. Robic, G.F. Gillissen, A. Volz, R.J. McKinlay Gardner, T.L. Harboe, B. Brenig, R. Korstanje, S.M. White, M. Den Bieman, R. Melkaoui, R. Kreutz, F. Piumi, J. Beck, D.F. de Andres-Cara, T. Haaf, C. Rodellar, U. Radhakrishna, M. Gautier, N. Tommerup, K. Wagner, I. Nanda, K. Buchet-Poyau, L.F. Almeida-Toledo, P.S. D’Andrea, P.M. Kroisel, M. Grzmil, C. Schelling, M. Mahony, C. Drögemüller, J. Barciszewski, M. Meins, F. Vidal, C. Zijlstra, S. Yadav, C. Bonillo, C. Kosan, V. Petrovic, J. Egozcue, F. Habermann, M. Schmid, R. Roy, A.A. Bosma, F. Foresti, C. Windpassinger, H. Uenishi, R. Yamamoto, H. Hiraiwa, A. Dalski, R. Mollicone, J. Szpirer, R. Fries, C. Wilhelm, R. Oriol, C. Ozouf-Costaz, M.F.Z. Daniel-Silva, H. Hayes, E. Schwinger, P. Coullin, C. Andersen, P. Pinton, M.T. Roldan-Arjona, C. Rogel-Gaillard, J.-J. Candelier, L.F.M. van Zutphen, H.A. van Lith, P.A. Ioannou, O. Distl, H. Omran, J. Kunz, S. Schlickum, T. Awata, L. Li, H. Kuiper, H.P. Klinger, P. van Vooren, S. Kiuchi, J. Mißbach, N. Arnal, A. Pienkowska, D. Milan, C. Ngo, H. Mehenni, R.P.M.A. Crooijmans, T. Opiola, B. Gläser, I.B. Otazu, C.R. Bonvicino, H. Winking, A. Hebinck, J. Blanco, A. Eggen, A. Wandall, C. Knorr, C. Szpirer, H. Zürcher, F. Hildebrandt, C.G. Ziegler, Y. Takagaki, J. Koch, P. Laurent, P. Burfeind, H. Yasue, P. Moore, M. Yerle, G. Hauke, Y. Muneta, P. Zaragoza, F. Laccone
Publikováno v:
Cytogenetic and Genome Research. 97:281-283
Publikováno v:
Romanian journal of physiology : physiological sciences. 35(1-2)
Publikováno v:
Vox sanguinis. 78
Formal genetics of ABO, H-h and Se-se systems illustrate that these three systems are genetically independentPopulation analysis of phenotypes and family segregation of the ABH related genetic markersInactivating mutations of FUT1 and FUT2 are compat
Publikováno v:
Human mutation. 16(6)
One Indonesian individual without detectable plasma alpha3-fucosyltransferase activity was identified with three point mutations, 730CG (L244V), 907CG (R303G), and 370CT (P124S), in the coding region of one FUT6 allele. Another individual, expressing
Publikováno v:
The Journal of biological chemistry. 274(18)
Alignment of 15 vertebrate alpha1,3-fucosyltransferases revealed one arginine conserved in all the enzymes employing exclusively type 2 acceptor substrates. At the equivalent position, a tryptophan was found in FUT3-encoded Lewis alpha1,3/1,4-fucosyl
Autor:
HART, JAN1, HARTOVÁ, VERONIKA1 nidlova@tf.czu.cz
Publikováno v:
Research in Agricultural Engineering. 2024, Vol. 70 Issue 3, p143-154. 12p.
Autor:
Zhang, Linyu1,2 (AUTHOR), Feng, Ying3 (AUTHOR), Zhang, Yue1,2 (AUTHOR), Sun, Xinrui1,2 (AUTHOR), Ma, Qianhong2,4 (AUTHOR) maqh@scu.edu.cn, Ma, Fang1,2 (AUTHOR) maqh@scu.edu.cn
Publikováno v:
Biomolecules (2218-273X). Jul2024, Vol. 14 Issue 7, p770. 16p.
Publikováno v:
Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine. 4(4)
Fucosyltransferases are involved in the last steps of the biosynthesis of ABH and Lewis oligosaccharide antigens. Seven human genes (FUT1 to FUT7) and one pseudogene (Sec 1) have been cloned and localized on different chromosomes (9q34.3; 11q21; 19p1