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Autor:
Castro, C. (Carla) N. (Noemi), Rosenzwajg, M. (Michelle), Carapito, R. (Raphaël), Shahrooei, M. (Mohammad), Konantz, M. (Martina), Khan, A. (Amjad), Miao, Z. (Zhichao), Gross, M. (Miriam), Tranchant, T. (Thibaud), Radosavljevic, M. (Mirjana), Paul, N. (Nicodème), Stemmelen, T. (Tristan), Pitoiset, F. (Fabien), Hirschler, A. (Aurélie), Nespola, B. (Benoit), Molitor, A. (Anne), Rolli, V. (Veronique), Pichot, A. (Angelique), Faletti, L. (Laura) E. (Eva), Rinaldi, B. (Bruno), Friant, S. (Sylvie), Mednikov, M. (Mark), Karauzum, H. (Hatice), Javad Aman, M. (M), Carapito, C. (Christine), Lengerke, C. (Claudia), Ziaee, V. (Vahid), Eyaid, W. (Wafaa), Ehl, S. (Stephan), Alroqi, F. (Fayhan), Parvaneh, N. (Nima), Bahram, S. (Seiamak)
The Nck-associated protein 1-like (NCKAP1L) gene, alternatively called hematopoietic protein 1 (HEM-1), encodes a hematopoietic lineage-specific regulator of the actin cytoskeleton. Nckap1l-deficient mice have anomalies in lymphocyte development, pha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4060::9daa33981bcca0594a5b08517aa590e3