Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Silke Nowak"'
Autor:
Kan, Zhuo, Diana, Naalden, Silke, Nowak, Nguyen, Xuan Huy, Lander, Bauters, Godelieve, Gheysen
Publikováno v:
Molecular Plant Pathology
Summary C‐type lectins (CTLs), a class of multifunctional proteins, are numerous in nematodes. One CTL gene, Mg01965, shown to be expressed in the subventral glands, especially in the second‐stage juveniles of the root‐knot nematode Meloidogyne
Autor:
Silke Nowak
Publikováno v:
Kirchliche Zeitgeschichte. 20:316-335
Zusammenfassung Silke Nowak untersucht die Formensprache, welche die Dichterin Gertrud Kolmar in der nationalsozialistischen Diktatur entwickelt und weist auf etwas Irritierendes hin: Auf der einen Seite schreibt Kolmar Gedichte in der Tradition der
Autor:
Markus J. van Roosmalen, Ellen van Binsbergen, Olivier Vanakker, Marie-José H. van den Boogaard, Mieke M. van Haelst, Sarah Vergult, Masoumeh Tavakoli-Yaraki, Marielle E M Swinkels, Silke Nowak, Kathleen Claes, Filip Roelens, Wigard P. Kloosterman, Karen Duran, Franki Speleman, Bruce Poppe, Björn Menten, Geert Mortier, Tom Sante, Edwin Cuppen, Nathalie Van der Aa
Publikováno v:
European journal of human genetics, 22(5), 652-659. Nature Publishing Group
European journal of human genetics
European Journal of Human Genetics, 22(5), 652-9. Nature Publishing Group
Vergult, S, Van Binsbergen, E, Sante, T, Nowak, S, Vanakker, O, Claes, K, Poppe, B, Van der Aa, N, van Roosmalen, M J, Duran, K, Tavakoli-Yaraki, M, Swinkels, M, van den Boogaard, M-J, van Haelst, M, Roelens, F, Speleman, F, Cuppen, E, Mortier, G, Kloosterman, W P & Menten, B 2014, ' Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations ', European Journal of Human Genetics, vol. 22, no. 5, pp. 652-9 . https://doi.org/10.1038/ejhg.2013.220
European journal of human genetics
European Journal of Human Genetics, 22(5), 652-9. Nature Publishing Group
Vergult, S, Van Binsbergen, E, Sante, T, Nowak, S, Vanakker, O, Claes, K, Poppe, B, Van der Aa, N, van Roosmalen, M J, Duran, K, Tavakoli-Yaraki, M, Swinkels, M, van den Boogaard, M-J, van Haelst, M, Roelens, F, Speleman, F, Cuppen, E, Mortier, G, Kloosterman, W P & Menten, B 2014, ' Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations ', European Journal of Human Genetics, vol. 22, no. 5, pp. 652-9 . https://doi.org/10.1038/ejhg.2013.220
Recently, microarrays have replaced karyotyping as a first tier test in patients with idiopathic intellectual disability and/or multiple congenital abnormalities (ID/MCA) in many laboratories. Although in about 14-18% of such patients, DNA copy-numbe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d634159ad2ef7c0d38275ac1a901f9e8
https://pure.amc.nl/en/publications/mate-pair-sequencing-for-the-detection-of-chromosomal-aberrations-in-patients-with-intellectual-disability-and-congenital-malformations(3b5e8830-4ec0-4ca9-ab42-c6a800c0463f).html
https://pure.amc.nl/en/publications/mate-pair-sequencing-for-the-detection-of-chromosomal-aberrations-in-patients-with-intellectual-disability-and-congenital-malformations(3b5e8830-4ec0-4ca9-ab42-c6a800c0463f).html
Autor:
Dieter Burdorf, Eckhard Schumacher, Armin Schäfer, Marcel Beyer, Urs Allemann, Hans-Jost Frey, Michael Gratz, Wolfram Groddeck, Hans-Joachim Hahn, Steffen Popp, Theresia Prammer, Johann Reißer, Monika Rinck, Norbert Christian Wolf, Thomas Kempf, Cornelia Ortlieb, Silke Nowak, Katharina Krüger, Uta Degner, Evi Ziegler c/o EDV Fotowerk Huber
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::039947fd6b30b1f95f9f847f6a86e754
https://doi.org/10.30965/9783846756072
https://doi.org/10.30965/9783846756072
Autor:
Silke Nowak
Publikováno v:
Zeitschrift für deutsche Philologie.
Autor:
Silke Nowak
Publikováno v:
Zeitschrift für deutsche Philologie.