UV irradiation triggers ubiquitin-dependent degradation of p21(WAF1) to promote DNA repair von Bendjennat, Mourad, Boulaire, Jérôme, Jascur, Thomas, Brickner, Howard, Barbier, Valerie, Sarasin, Alain, Fotedar, Arun, Fotedar, Rati

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Phenotypic severity scoring system and categorisation for prune belly syndrome: application to a pilot cohort of 50 living patients von Wong, Daniel G., Arevalo, Michelle K., Passoni, Niccolo Maria, Iqbal, Nida S., Jascur, Thomas, Kern, Adam J., Sanchez, Emma J., Satyanarayan, Arthi, Gattineni, Jyothsna, Baker, Linda A.

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Regulation of p21(WAF1/CIP1) stability by WISp39, a Hsp90 binding TPR protein von Jascur, Thomas, Brickner, Howard, Salles-Passador, Isabelle, Barbier, Valerie, El Khissiin, Abdelhamid, Smith, Brian, Fotedar, Rati, Fotedar, Arun

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Protein import into yeast mitochondria: the inner membrane import site protein ISP45 is the MPI1 gene product von Horst, M, Jeno, P, Kronidou, N.G, Bolliger, L, Oppliger, W, Scherer, P, Manning-Krieg, U, Jascur, T, Schatz, G

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Disrupted yeast mitochondria can import precursor proteins directly through their inner membrane von Hwang, S. (University of Basel, Basel, Switzerland), Jascur, T, Vestweber, D, Pon, L, Schatz, G

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Activation of ZAP-70 through Specific Dephosphorylation at the Inhibitory Tyr-292 by the Low Molecular Weight Phosphotyrosine Phosphatase (LMPTP) von Bottini, Nunzio, Stefanini, Lavinia, Williams, Scott, Alonso, Andres, Jascur, Thomas, Abraham, Robert T., Couture, Clément, Mustelin, Tomas

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Sequential translocation of an artificial precursor protein across the two mitochondrial membranes von JASCUR, T, GOLDENBERG, D. P, VETWEBER, D, SCHATZ, G

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Involvement of Phosphatidylinositol 3-Kinase in NFAT Activation in T Cells von Jascur, Thomas, Gilman, Jennifer, Mustelin, Tomas

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Regulation of the Lck SH2 Domain by Tyrosine Phosphorylation von Couture, C, Songyang, Z, Jascur, T, Williams, S, Tailor, P, Cantley, L C, Mustelin, T

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Regulation of p21 super(WAF1/CIP1) Stability by WISp39, a Hsp90 Binding TPR Protein von Jascur, T, Brickner, H, Salles-Passador, I, Barbier, V, El Khissiin, A, Smith, B, Fotedar, R, Fotedar, A

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Modification of Phosphatidylinositol 3-Kinase SH2 Domain Binding Properties by Abl- or Lck-mediated Tyrosine Phosphorylation at Tyr-688 von von Willebrand, M, Williams, S, Saxena, M, Gilman, J, Tailor, P, Jascur, T, Amarante-Mendes, G P, Green, D R, Mustelin, T

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Inhibition of Phosphatidylinositol 3‐Kinase Blocks T Cell Antigen Receptor/CD3‐Induced Activation of the Mitogen‐Activated Kinase Erk2 von Willebrand, Maria, Jascur, Thomas, Bonnefoy‐Bérard, Nathalie, Yano, Hiroshi, Altman, Amnon, Matsuda, Yuzuru, Mustelin, Tomas

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Bcr - Abl-mediated resistance to apoptosis is independent of PI 3-kinase activity von Amarante-Mendes, G P, Jascur, T, Nishioka, W K, Mustelin, T, Green, D R

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Involvement of Src‐homology‐2‐domain‐containing Protein‐tyrosine Phosphatase 2 in T Cell Activation von Tailor, Pankaj, Jascur, Thomas, Williams, Scott, Willebrand, Maria, Couture, Clément, Mustelin, Tomas

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Oligomerization and intracellular protein transport: dimerization of intestinal dipeptidylpeptidase IV occurs in the Golgi apparatus von Jascur, Thomas, Matter, Karl, Hauri, Hans Peter

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Reconstitution of T Cell Antigen Receptor‐Induced Erk2 Kinase Activation in Lck‐Negative JCaM1 Cells by Syk von Williams, Scott, Couture, Clément, Gilman, Jennifer, Jascur, Thomas, Deckert, Marcel, Altman, Amnon, Mustelin, Tomas

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Purification and characterization of an activated form of the protein tyrosine kinase Lck from an Escherichia coli expression system von Flint, Nicholas A., Amrein, Kurt E., Jascur, Thomas, Burn, Paul

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Monte Carlo studium spin3/2 Blume-Emery-Griffiths model na honeycomb lattice von Žukovič, Milan

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Curcumin mediates chemosensitization to 5-fluorouracil through miRNA-induced suppression of epithelial-to-mesenchymal transition in chemoresistant colorectal cancer von Toden, Shusuke, Okugawa, Yoshinaga, Jascur, Thomas, Wodarz, Dominik, Komarova, Natalia L, Buhrmann, Constanze, Shakibaei, Mehdi, Boland, C Richard, Goel, Ajay

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Prune belly syndrome in surviving males can be caused by Hemizygous missense mutations in the X-linked Filamin A gene von Iqbal, Nida S, Jascur, Thomas A, Harrison, Steven M, Edwards, Angelena B, Smith, Luke T, Choi, Erin S, Arevalo, Michelle K, Chen, Catherine, Zhang, Shaohua, Kern, Adam J, Scheuerle, Angela E, Sanchez, Emma J, Xing, Chao, Baker, Linda A

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