Risultati della ricerca - Maxime Bouchard

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  1. 1
    Plumbing in the embryo: developmental defects of the urinary tracts

    Plumbing in the embryo: developmental defects of the urinary tracts di Noriko Uetani, Maxime Bouchard

    Pubblicazione 2009
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  2. 2
    GATA transcription factors in development and disease

    GATA transcription factors in development and disease di Mathieu Tremblay, Oraly Sanchez-Ferras, Maxime Bouchard

    Pubblicazione 2018
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  3. 3
    Nephric lineage specification by Pax2 and Pax8

    Nephric lineage specification by Pax2 and Pax8 di Maxime Bouchard, Abdallah Souabni, Markus Mandler, Annette Neubüser, Meinrad Busslinger

    Pubblicazione 2002
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  4. 4
    Pax2 and Pax8 Regulate Branching Morphogenesis and Nephron Differentiation in the Developing Kidney

    Pax2 and Pax8 Regulate Branching Morphogenesis and Nephron Differentiation in the Developing Kidney di Melina Narlis, David Grote, Yaned Gaitan, Sami Kamel Boualia, Maxime Bouchard

    Pubblicazione 2007
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  5. 5
    Nephric duct insertion is a crucial step in urinary tract maturation that is regulated by a<i>Gata3-Raldh2-Ret</i>molecular network in mice

    Nephric duct insertion is a crucial step in urinary tract maturation that is regulated by a<i>Gata3-Raldh2-Ret</i>molecular network in mice di Ian Chia, David Grote, Michael Marcotte, Ekaterina Batourina, Cathy Mendelsohn, Maxime Bouchard

    Pubblicazione 2011
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  6. 6
    Pax2 and Pax8 cooperate in mouse inner ear morphogenesis and innervation

    Pax2 and Pax8 cooperate in mouse inner ear morphogenesis and innervation di Maxime Bouchard, Dominique de Caprona, Meinrad Busslinger, Pin‐Xian Xu, Bernd Fritzsch

    Pubblicazione 2010
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  7. 7
    Yap and Taz are required for Ret-dependent urinary tract morphogenesis

    Yap and Taz are required for Ret-dependent urinary tract morphogenesis di Antoine Reginensi, Masato Hoshi, Sami Kamel Boualia, Maxime Bouchard, Sanjay Jain, Helen McNeill

    Pubblicazione 2015
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  8. 8
    Maturation of ureter-bladder connection in mice is controlled by LAR family receptor protein tyrosine phosphatases

    Maturation of ureter-bladder connection in mice is controlled by LAR family receptor protein tyrosine phosphatases di Noriko Uetani, Kristen Bertozzi, Mélanie J. Chagnon, Wiljan Hendriks, Michel L. Tremblay, Maxime Bouchard

    Pubblicazione 2009
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  9. 9
    A core transcriptional network composed of Pax2/8, Gata3 and Lim1 regulates key players of pro/mesonephros morphogenesis

    A core transcriptional network composed of Pax2/8, Gata3 and Lim1 regulates key players of pro/mesonephros morphogenesis di Sami Kamel Boualia, Yaned Gaitan, Mathieu Tremblay, Richa Sharma, Julie Cardin, Artur Kania, Maxime Bouchard

    Pubblicazione 2013
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  10. 10
    Gata3 Acts Downstream of β-Catenin Signaling to Prevent Ectopic Metanephric Kidney Induction

    Gata3 Acts Downstream of β-Catenin Signaling to Prevent Ectopic Metanephric Kidney Induction di David Grote, Sami Kamel Boualia, Abdallah Souabni, Calli E. Merkel, Xuan Chi, Frank Costantini, Thomas J. Carroll, Maxime Bouchard

    Pubblicazione 2008
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  11. 11
    Oviduct epithelial cells constitute two developmentally distinct lineages that are spatially separated along the distal-proximal axis

    Oviduct epithelial cells constitute two developmentally distinct lineages that are spatially separated along the distal-proximal axis di Matthew J. Ford, Keerthana Harwalkar, Alain Pacis, Helen Maunsell, Yu Chang Wang, Dunarel Badescu, Katie Teng, Nobuko Yamanaka, Maxime Bouchard, Jiannis Ragoussis, Yojiro Yamanaka

    Pubblicazione 2021
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  12. 12
    Lineage Specification of Parietal Epithelial Cells Requires β-Catenin/Wnt Signaling

    Lineage Specification of Parietal Epithelial Cells Requires β-Catenin/Wnt Signaling di Stephan Grouls, Diana M. Iglesias, Nicolas Wentzensen, Marcus J. Moeller, Maxime Bouchard, Rolf Kemler, Paul Goodyer, Felix Niggli, Hermann-Josef Gröne, Wilhelm Kriz, Robert Koesters

    Pubblicazione 2011
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  13. 13
    Inhibition of Mammalian Target of Rapamycin Augments Lipopolysaccharide-Induced Lung Injury and Apoptosis

    Inhibition of Mammalian Target of Rapamycin Augments Lipopolysaccharide-Induced Lung Injury and Apoptosis di Jill A. Fielhaber, Scott F. Carroll, Anders Bondo Dydensborg, Mitra Shourian, Alexandra Triantafillopoulos, Sharon Harel, Sabah N. A. Hussain, Maxime Bouchard, Salman T. Qureshi, Arnold S. Kristof

    Pubblicazione 2012
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  14. 14
    Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly

    Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly di Daniela A. Braun, Jia Rao, Géraldine Mollet, David Schapiro, Marie-Claire Daugeron, Weizhen Tan, Olivier Gribouval, Olivia Boyer, Patrick Revy, Tilman Jobst‐Schwan, Johanna Magdalena Schmidt, Jennifer A. Lawson, Denny Schanze, Shazia Ashraf, Jeremy F.P. Ullmann, Charlotte A. Hoogstraten, Nathalie Boddaert, Bruno Collinet, Gaëlle Martin, Dominique Liger, Svjetlana Lovric, Mónica Furlano, Ida Chiara Guerrera, Oraly Sanchez-Ferras, Jennifer Hu, Anne‐Claire Boschat, Sylvia Sanquer, Björn Menten, Sarah Vergult, Nina De Rocker, Merlin Airik, Tobias Hermle, Shirlee Shril, Eugen Widmeier, Heon Yung Gee, Won‐Il Choi, Carolin E. Sadowski, Werner L. Pabst, Jillian K. Warejko, Ankana Daga, Tamara Basta, Verena Matejas, Karin Scharmann, Sandra D. Kienast, Babak Behnam, Brendan Beeson, Amber Begtrup, M. Bruce, Gaik-Siew Ch’ng, Shuan‐Pei Lin, Jui-Hsing Chang, Chao‐Huei Chen, Megan T. Cho, Patrick M. Gaffney, Patrick Gipson, Chyong-Hsin Hsu, Jameela A. Kari, Yu-Yuan Ke, Cathy Kiraly‐Borri, Wai-ming Lai, Emmanuelle Lemyre, Rebecca O. Littlejohn, Amira Masri, Mastaneh Moghtaderi, Kazuyuki Nakamura, Fatih Özaltın, Marleen Praet, Chitra Prasad, Agnieszka Prytula-Ebels, Elizabeth Roeder, Patrick Rump, Rhonda E. Schnur, Takashi Shiihara, Manish D. Sinha, Neveen A. Soliman, Kenza Soulami, David A. Sweetser, Wen‐Hui Tsai, Jeng-Daw Tsai, Rezan Topaloĝlu, Udo Vester, David H. Viskochil, Nithiwat Vatanavicharn, Jessica L. Waxler, Klaas J. Wierenga, Matthias T. F. Wolf, Sik-Nin Wong, Sebastian A. Leidel, Gessica Truglio, Peter C. Dedon, Annapurna Poduri, Shrikant Mane, Richard P. Lifton, Maxime Bouchard, Pekka Kannus, David Chitayat, Daniella Magen, Bert Callewaert, Herman van Tilbeurgh, Martin Zenker

    Pubblicazione 2017
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  15. 15
    Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations

    Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations di Dervla M. Connaughton, Rufeng Dai, Danielle Owen, Jonathan Marquez, Nina Mann, Adda L. Graham-Paquin, Makiko Nakayama, Étienne Coyaud, Estelle Laurent, Jonathan St‐Germain, Lot Snijders Blok, Arianna Vino, Verena Klämbt, Konstantin Deutsch, Chen-Han Wilfred Wu, Caroline M. Kolvenbach, Franziska Kause, Isabel Ottlewski, Ronen Schneider, Thomas M. Kitzler, Amar J. Majmundar, Florian Buerger, Ana C. Onuchic-Whitford, Youying Mao, Amy Kolb, Daanya Salmanullah, Evan Chen, Amelie T. van der Ven, Jia Rao, Hadas Ityel, Steve Seltzsam, Johanna M. Rieke, Jing Chen, Asaf Vivante, Daw‐Yang Hwang, Stefan Kohl, Gabriel C. Dworschak, Tobias Hermle, Mariëlle Alders, Tobias Bartolomaeus, Stuart B. Bauer, Michelle A. Baum, Eva H. Brilstra, Thomas D. Challman, Jacob Zyskind, Carrie E. Costin, Katrina M. Dipple, Floor A.M. Duijkers, Marcia Ferguson, David Fitzpatrick, Roger Fick, Ian Glass, Peter J. Hulick, Antonie D. Kline, Ilona Krey, Selvin Kumar, Lu W, Elysa J. Marco, Ingrid M. Wentzensen, Heather C. Mefford, Konrad Platzer, Inna Povolotskaya, Juliann M. Savatt, Н. В. Щербакова, Prabha Senguttuvan, Audrey Squire, Deborah R. Stein, Isabelle Thiffault, V. Yu. Voinova, Michael J. Somers, Michael A. Ferguson, Avram Z. Traum, Ghaleb H. Daouk, Ankana Daga, Nancy Rodig, Paulien A. Terhal, Ellen van Binsbergen, Loai Eid, Velibor Tasić, Hila Milo Rasouly, Tze Y. Lim, Dina Ahram, Ali G. Gharavi, Heiko Reutter, Heidi L. Rehm, Daniel G. MacArthur, Monkol Lek, Kristen M. Laricchia, Richard P. Lifton, Hong Xu, Shrikant Mane, Simone Sanna‐Cherchi, Andrew D. Sharrocks, Brian Raught, Simon E. Fisher, Maxime Bouchard, Mustafa K. Khokha, Shirlee Shril, Friedhelm Hildebrandt

    Pubblicazione 2020
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