Kết quả tìm kiếm - Anna Straatman-Iwanowska

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  1. 1
    Enteropathogenic Escherichia coli (EPEC) adhesion to intestinal epithelial cells: role of bundle-forming pili (BFP), EspA filaments and intimin

    Enteropathogenic Escherichia coli (EPEC) adhesion to intestinal epithelial cells: role of bundle-forming pili (BFP), EspA filaments and intimin Bằng Jennifer Cleary, Li‐Ching Lai, Robert K. Shaw, Anna Straatman-Iwanowska, Michael S. Donnenberg, Gad Frankel, Stuart Knutton

    Được phát hành 2004
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    Artigo
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  2. 2
    Two Faces of CwlM, an Essential PknB Substrate, in Mycobacterium tuberculosis

    Two Faces of CwlM, an Essential PknB Substrate, in Mycobacterium tuberculosis Bằng Obolbek Turapov, Francesca Forti, Baleegh A. Kadhim, Daniela Ghisotti, Jad Sassine, Anna Straatman-Iwanowska, Andrew R. Bottrill, Patrick J. Moynihan, Russell Wallis, Philippe Barthe, Martin Cohen‐Gonsaud, Paul Ajuh, Waldemar Vollmer, Galina V. Mukamolova

    Được phát hành 2018
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    Artigo
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  3. 3
    Mutation in the TCRα subunit constant gene (TRAC) leads to a human immunodeficiency disorder characterized by a lack of TCRαβ+ T cells

    Mutation in the TCRα subunit constant gene (TRAC) leads to a human immunodeficiency disorder characterized by a lack of TCRαβ+ T cells Bằng Neil V. Morgan, Sarah Goddard, Tony S. Cardno, David McDonald, Fatimah Rahman, D Barge, A. Ciupek, Anna Straatman-Iwanowska, Shanaz Pasha, Mary Guckian, Graham Anderson, Aarnoud Huissoon, Andrew J. Cant, Warren P. Tate, Sophie Hambleton, Eamonn R. Maher

    Được phát hành 2011
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    Artigo
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  4. 4
    Autosomal Recessive Keratoderma-Ichthyosis-Deafness (ARKID) Syndrome Is Caused by VPS33B Mutations Affecting Rab Protein Interaction and Collagen Modification

    Autosomal Recessive Keratoderma-Ichthyosis-Deafness (ARKID) Syndrome Is Caused by VPS33B Mutations Affecting Rab Protein Interaction and Collagen Modification Bằng Robert Gruber, Clare Rogerson, Christian Windpassinger, Blerida Banushi, Anna Straatman-Iwanowska, Joanna Hanley, Federico Forneris, Robert Strohal, Peter Ulz, Debra Crumrine, Gopinathan K. Menon, Stefan Blunder, Matthias Schmuth, Andreas Th. Müller, Holly Smith, Kevin Mills, Peter M. Kroisel, Andreas Janecke, Paul Gissen

    Được phát hành 2016
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    Revisão
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  5. 5
    Vps33b is crucial for structural and functional hepatocyte polarity

    Vps33b is crucial for structural and functional hepatocyte polarity Bằng Joanna Hanley, Dipok Kumar Dhar, Francesca Mazzacuva, Rebeca Fiadeiro, Jemima J. Burden, Anne-Marie Lyne, Holly Smith, Anna Straatman-Iwanowska, Blerida Banushi, Alex Virasami, Kevin Mills, Frédéric P. Lemaigre, A. S. Knisely, Steven J. Howe, Neil J. Sebire, Simon N. Waddington, Coen C. Paulusma, Peter T. Clayton, Paul Gissen

    Được phát hành 2017
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    Artigo
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  6. 6
    Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease

    Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease Bằng Neil V. Morgan, Mark R. Morris, Hakan Cangül, Diane Gleeson, Anna Straatman-Iwanowska, Nicholas P. Davies, Stephen Keenan, Shanaz Pasha, Fatimah Rahman, Dean Gentle, Maaike P.G. Vreeswijk, Peter Devilee, Margaret A. Knowles, Serdar Ceylaner, Richard C. Trembath, Carlos Dalence, Erol Kısmet, Vedat Köseoğlu, Hans‐Christoph Rossbach, Paul Gissen, David Tannahill, Eamonn R. Maher

    Được phát hành 2010
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    Artigo
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  7. 7
    Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization

    Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization Bằng Andrew R. Cullinane, Anna Straatman-Iwanowska, Andreas Zaucker, Yoshiyuki Wakabayashi, Christopher K Bruce, Guanmei Luo, Fatimah Rahman, Figen Gürakan, Eda Ütine, Tanju Özkan, Jonas Denecke, Jurica Vuković, Maja Di Rocco, Hanna Mandel, Hakan Cangül, Randolph P. Matthews, Steven G. Thomas, Joshua Z. Rappoport, Irwin M. Arias, Hartwig Wolburg, A. S. Knisely, Déirdre Kelly, Ferenc Müller, Eamonn R. Maher, Paul Gissen

    Được phát hành 2010
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    Artigo
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  8. 8
    Associations among genotype, clinical phenotype, and intracellular localization of trafficking proteins in ARC syndrome

    Associations among genotype, clinical phenotype, and intracellular localization of trafficking proteins in ARC syndrome Bằng Holly Smith, Romain Galmes, Ekaterina Gogolina, Anna Straatman-Iwanowska, Kim Reay, Blerida Banushi, Christopher K Bruce, Andrew R. Cullinane, René Romero, Richard Chang, O. Ackermann, Clarisse Baumann, Hakan Cangül, Fatma Çakmak Çelik, Canan Aygün, Richard J. Coward, Carlo Dionisi‐Vici, Barbara Sibbles, Carol Inward, Chong Ae Kim, Judith Klumperman, A. S. Knisely, Steve P. Watson, Paul Gissen

    Được phát hành 2012
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    Artigo
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  9. 9
    Regulation of post-Golgi LH3 trafficking is essential for collagen homeostasis

    Regulation of post-Golgi LH3 trafficking is essential for collagen homeostasis Bằng Blerida Banushi, Federico Forneris, Anna Straatman-Iwanowska, Adam Strange, Anne-Marie Lyne, Clare Rogerson, Jemima J. Burden, Wendy Heywood, Joanna Hanley, Ivan Doykov, Kees R. Straatman, Holly Smith, Danai Bem, Janos Kriston‐Vizi, Gema Ariceta, Maija Risteli, Chunguang Wang, R Ardill, Marcin Zaniew, Julita Latka-Grot, Simon N. Waddington, Stewen J. Howe, Francesco Ferraro, Asllan Gjinovci, Scott P. Lawrence, Mark Marsh, Mark Girolami, Laurent Bozec, Kevin Mills, Paul Gissen

    Được phát hành 2016
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    Artigo
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  10. 10
    Single-cell guided prenatal derivation of primary fetal epithelial organoids from human amniotic and tracheal fluids

    Single-cell guided prenatal derivation of primary fetal epithelial organoids from human amniotic and tracheal fluids Bằng M Gerli, Giuseppe Calà, Max Arran Beesley, Beatrice Sina, Lucinda Tullie, Kylin Yunyan Sun, Francesco Panariello, Federica Michielin, Joseph R. Davidson, Francesca Maria Russo, Brendan C. Jones, Dani Do Hyang Lee, Savvas Savvidis, Theodoros Xenakis, Ian C. Simcock, Anna Straatman-Iwanowska, Robert A. Hirst, Anna L. David, Christopher O’Callaghan, Alessandro Olivo, Simon Eaton, Stavros Loukogeorgakis, Davide Cacchiarelli, Jan Deprest, Vivian Li, Giovanni Giuseppe Giobbe, Paolo De Coppi

    Được phát hành 2024
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    Artigo
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