Výsledky vyhledávání - Paris Ataliotis

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  1. 1
    Establishment of conditionally immortalized epithelial cell lines from both colon and small intestine of adult H-2Kb-tsA58 transgenic mice.

    Establishment of conditionally immortalized epithelial cell lines from both colon and small intestine of adult H-2Kb-tsA58 transgenic mice. Autor R Whitehead, P E VanEeden, Mark Noble, Paris Ataliotis, Parmjit Jat

    Vydáno 1993
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  2. 2
    Direct derivation of conditionally immortal cell lines from an H-2Kb-tsA58 transgenic mouse.

    Direct derivation of conditionally immortal cell lines from an H-2Kb-tsA58 transgenic mouse. Autor Parmjit Jat, Mark Noble, Paris Ataliotis, Yujiro Tanaka, N Yannoutsos, Lesli H. Larsen, D Kioussis

    Vydáno 1991
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  3. 3
    Desmosomal glycoproteins II and III. Cadherin-like junctional molecules generated by alternative splicing

    Desmosomal glycoproteins II and III. Cadherin-like junctional molecules generated by alternative splicing Autor Andrew E. Parker, Grant N. Wheeler, J Arnemann, Sara C. Pidsley, Paris Ataliotis, C. Thomas, David A. Rees, Anthony I. Magee, Roger S. Buxton

    Vydáno 1991
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  4. 4
    Tbx1 regulation of myogenic differentiation in the limb and cranial mesoderm

    Tbx1 regulation of myogenic differentiation in the limb and cranial mesoderm Autor Akbar Dastjerdi, Lesley Robson, Rebecca Walker, Julia Hadley, Zhen Zhang, Marc Rodríguez‐Niedenführ, Paris Ataliotis, Antonio Baldini, Peter Scambler, Philippa H. Francis‐West

    Vydáno 2006
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  5. 5
    Desmosomal glycoprotein DGI, a component of intercellular desmosome junctions, is related to the cadherin family of cell adhesion molecules.

    Desmosomal glycoprotein DGI, a component of intercellular desmosome junctions, is related to the cadherin family of cell adhesion molecules. Autor Grant N. Wheeler, Andrew E. Parker, C. Thomas, Paris Ataliotis, D Poynter, J Arnemann, A.J. Rutman, Sara C. Pidsley, Fiona M. Watt, David A. Rees

    Vydáno 1991
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  6. 6
    <i>Tbx1</i> haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome

    <i>Tbx1</i> haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome Autor Richard Paylor, Beate Glaser, Annalisa Mupo, Paris Ataliotis, Corinne M. Spencer, Angela Sobotka, Chelsey Sparks, Chul-Hee Choi, John S. Oghalai, Sarah Curran, Kieran C. Murphy, Stephen Monks, Nigel Williams, Michael O’Donovan, Michael J. Owen, Peter Scambler, Elizabeth Lindsay

    Vydáno 2006
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  7. 7
    WDR11‐mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome

    WDR11‐mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome Autor Y. Kim, Daniel P. S. Osborn, Ji‐Young Lee, Masatake Araki, Kimi Araki, Timothy J. Mohun, Johanna Känsäkoski, Nina Brandstack, Hyun–Taek Kim, Francesc Miralles, Cheol‐Hee Kim, Nigel A. Brown, Hyung‐Goo Kim, Juan Pedro Martı́nez-Barberá, Paris Ataliotis, Taneli Raivio, Lawrence C. Layman, Soo‐Hyun Kim

    Vydáno 2017
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