Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Zawerton A"'
Autor:
Albtoush, Nansy, Queisser, Kimberly A., Zawerton, Ash, Lauer, Mark E., Beswick, Ellen J., Petrey, Aaron C
Publikováno v:
In Matrix Biology August 2023 121:149-166
Autor:
Zawerton, Ash, Mignot, Cyril, Sigafoos, Ashley, Blackburn, Patrick R., Haseeb, Abdul, McWalter, Kirsty, Ichikawa, Shoji, Nava, Caroline, Keren, Boris, Charles, Perrine, Marey, Isabelle, Tabet, Anne-Claude, Levy, Jonathan, Perrin, Laurence, Hartmann, Andreas, Lesca, Gaetan, Schluth-Bolard, Caroline, Monin, Pauline, Dupuis-Girod, Sophie, Guillen Sacoto, Maria J., Schnur, Rhonda E., Zhu, Zehua, Poisson, Alice, El Chehadeh, Salima, Alembik, Yves, Bruel, Ange-Line, Lehalle, Daphné, Nambot, Sophie, Moutton, Sébastien, Odent, Sylvie, Jaillard, Sylvie, Dubourg, Christèle, Hilhorst-Hofstee, Yvonne, Barbaro-Dieber, Tina, Ortega, Lucia, Bhoj, Elizabeth J., Masser-Frye, Diane, Bird, Lynne M., Lindstrom, Kristin, Ramsey, Keri M., Narayanan, Vinodh, Fassi, Emily, Willing, Marcia, Cole, Trevor, Salter, Claire G., Akilapa, Rhoda, Vandersteen, Anthony, Canham, Natalie, Rump, Patrick, Gerkes, Erica H., Klein Wassink-Ruiter, Jolien S., Bijlsma, Emilia, Hoffer, Mariëtte, Vargas, Marcelo, Wojcik, Antonina, Cherik, Florian, Francannet, Christine, Rosenfeld, Jill A., Machol, Keren, Scott, Daryl A., Bacino, Carlos A., Wang, Xia, Clark, Gary D., Bertoli, Marta, Zwolinski, Simon, Thomas, Rhys H., Akay, Ela, Chang, Richard C., Bressi, Rebekah, Sanchez Russo, Rossana, Srour, Myriam, Russell, Laura, Goyette, Anne-Marie E., Dupuis, Lucie, Mendoza-Londono, Roberto, Karimov, Catherine, Joseph, Maries, Nizon, Mathilde, Cogné, Benjamin, Kuechler, Alma, Piton, Amélie, Klee, Eric W., Lefebvre, Véronique *, Clark, Karl J., Depienne, Christel *
Publikováno v:
In Genetics in Medicine March 2020 22(3):524-537
Autor:
Petrey, Aaron C., Obery, Dana R., Kessler, Sean P., Zawerton, Ash, Flamion, Bruno, de la Motte, Carol A. *
Publikováno v:
In Blood 29 August 2019 134(9):765-775
Autor:
Zawerton, Ash, Yao, Baojin, Yeager, J. Paige, Pippucci, Tommaso, Haseeb, Abdul, Smith, Joshua D., Wischmann, Lisa, Kühl, Susanne J., Dean, John C.S., Pilz, Daniela T., Holder, Susan E., McNeill, Alisdair, Graziano, Claudio, Lefebvre, Véronique
Publikováno v:
In The American Journal of Human Genetics 7 February 2019 104(2):246-259
Autor:
Ashley N. Sigafoos, Salima El Chehadeh, Marcia C. Willing, Ela Akay, Florian Cherik, Anne-Marie E. Goyette, Vinodh Narayanan, Diane Masser-Frye, Catherine Karimov, Rhonda E. Schnur, Rebekah Bressi, Rhys H. Thomas, Gary D. Clark, Tina Barbaro-Dieber, Jill A. Rosenfeld, Carlos A. Bacino, Maria J. Guillen Sacoto, Laura Russell, Kristin Lindstrom, Caroline Schluth-Bolard, Xia Wang, Yvonne Hilhorst-Hofstee, Marcelo Vargas, Zehua Zhu, Ash Zawerton, Boris Keren, Mariëtte J.V. Hoffer, Isabelle Marey, Alice Poisson, Daphné Lehalle, Maries Joseph, Gaetan Lesca, Simon Zwolinski, Laurence Perrin, Rhoda Akilapa, Emilia K. Bijlsma, Christel Depienne, Amélie Piton, Claire G. Salter, Lucie Dupuis, Daryl A. Scott, Jolien S. Klein Wassink-Ruiter, Benjamin Cogné, Mathilde Nizon, Richard Chang, Kirsty McWalter, Myriam Srour, Perrine Charles, Anne-Claude Tabet, Natalie Canham, Sylvie Odent, Caroline Nava, Karl J. Clark, Elizabeth J. Bhoj, Jonathan Levy, Keri Ramsey, Yves Alembik, Lucia Ortega, Sophie Dupuis-Girod, Shoji Ichikawa, Christine Francannet, Marta Bertoli, Christèle Dubourg, Eric W. Klee, Ange-Line Bruel, Sebastien Moutton, Emily Fassi, Anthony Vandersteen, Abdul Haseeb, Antonina Wojcik, Patrick R. Blackburn, Lynne M. Bird, Patrick Rump, Véronique Lefebvre, Alma Kuechler, Sophie Nambot, Keren Machol, Cyril Mignot, Andreas Hartmann, Rossana Sanchez Russo, Erica H. Gerkes, Sylvie Jaillard, Roberto Mendoza-Londono, Trevor Cole, Pauline Monin
Publikováno v:
Genetics in Medicine
Genetics in Medicine, Nature Publishing Group, 2020, 22 (3), pp.524-537. ⟨10.1038/s41436-019-0657-0⟩
Genetics in medicine : official journal of the American College of Medical Genetics, vol 22, iss 3
Genetics in Medicine, 22(3), 524-537. Nature Publishing Group
Genet Med
Genetics in Medicine, 22(3), 524-537. NATURE PUBLISHING GROUP
Genetics in Medicine, Nature Publishing Group, 2020, 22 (3), pp.524-537. ⟨10.1038/s41436-019-0657-0⟩
Genetics in medicine : official journal of the American College of Medical Genetics, vol 22, iss 3
Genetics in Medicine, 22(3), 524-537. Nature Publishing Group
Genet Med
Genetics in Medicine, 22(3), 524-537. NATURE PUBLISHING GROUP
International audience; PURPOSE: Lamb-Shaffer syndrome (LAMSHF) is a neurodevelopmental disorder described in just over two dozen patients with heterozygous genetic alterations involving SOX5, a gene encoding a transcription factor regulating cell fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e572914cd3ed1c6195ff6874c9228a5a
https://doi.org/10.1038/s41436-019-0657-0
https://doi.org/10.1038/s41436-019-0657-0
Autor:
Bruno Flamion, Aaron C. Petrey, Dana R. Obery, Carol A. de la Motte, Sean P. Kessler, Ash Zawerton
Publikováno v:
Blood
Petrey, A C, Obery, D R, Kessler, S P, Zawerton, A, Flamion, B & de la Motte, C A 2019, ' Platelet hyaluronidase-2 regulates the early stages of inflammatory disease in colitis ', Blood, vol. 134, no. 9, pp. 765-775 . https://doi.org/10.1182/blood.2018893594
Petrey, A C, Obery, D R, Kessler, S P, Zawerton, A, Flamion, B & de la Motte, C A 2019, ' Platelet hyaluronidase-2 regulates the early stages of inflammatory disease in colitis ', Blood, vol. 134, no. 9, pp. 765-775 . https://doi.org/10.1182/blood.2018893594
Platelets are specialized cells essential for hemostasis that also function as crucial effectors capable of mediating inflammatory and immune responses. These sentinels continually survey their environment and discriminate between homeostatic and dan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dce46e21463339be151de85c7843f5b
https://pubmed.ncbi.nlm.nih.gov/31262781
https://pubmed.ncbi.nlm.nih.gov/31262781
Autor:
Susan E. Holder, Claudio Graziano, Véronique Lefebvre, Joshua D. Smith, Ash Zawerton, Lisa Wischmann, Susanne J. Kühl, John Dean, Tommaso Pippucci, J. Paige Yeager, Deciphering Developmental Disorders Study, Daniela T. Pilz, Baojin Yao, Abdul Haseeb, Alisdair McNeill
Publikováno v:
American journal of human genetics. 104(2)
SOX4, together with SOX11 and SOX12, forms group C of SRY-related (SOX) transcription factors. They play key roles, often in redundancy, in multiple developmental pathways, including neurogenesis and skeletogenesis. De novo SOX11 heterozygous mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fc470316e6d77206c7ec3a8e6181974
https://pubmed.ncbi.nlm.nih.gov/30951678
https://pubmed.ncbi.nlm.nih.gov/30951678
Publikováno v:
The Journal of Pain. 17:S49
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f569c16df2459a077110951d6dcc0259
https://doi.org/10.1016/j.jpain.2016.01.199
https://doi.org/10.1016/j.jpain.2016.01.199
Publikováno v:
The Journal of Pain. 16:S40
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abac5106795874875fdd4b0e6285f8cd
https://doi.org/10.1016/j.jpain.2015.01.173
https://doi.org/10.1016/j.jpain.2015.01.173
Publikováno v:
In The Journal of Pain April 2015 16(4) Supplement:S40-S40