Zobrazeno 1 - 10
of 107
pro vyhledávání: '"McGowan, SJ"'
Autor:
Tooze, RS, Miller, KA, Swagemakers, SMA, Calpena, E, McGowan, SJ, Boute, O, Collet, C, Johnson, D, Laffargue, F, de Leeuw, N, Morton, JV, Noons, P, Ockeloen, CW, Phipps, JM, Tan, TY, Timberlake, AT, Vanlerberghe, C, Wall, SA, Weber, A, Wilson, LC, Zackai, EH, Mathijssen, IMJ, Twigg, SRF, Wilkie, AOM
Publikováno v:
Genetics in Medicine, 25(9):100883. Lippincott Williams & Wilkins
Purpose Studies previously implicated PRRX1 in craniofacial development, including demonstration of murine Prrx1 expression in the pre-osteogenic cells of the cranial sutures. We investigated the role of heterozygous missense and loss-of-function var
Autor:
Reijnders, MRF, Miller, KA, Alvi, M, Goos, JAC, Lees, MM, de Burca, A, Henderson, A, Kraus, A, Mikat, B, de Vries, BBA, Isidor, B, Kerr, B, Marcelis, C, Schluth-Bolard, C, Deshpande, C, Ruivenkamp, CAL, Wieczorek, D, Deciphering Developmental Disorders Study, Baralle, D, Blair, EM, Engels, H, Lüdecke, H-J, Eason, J, Santen, GWE, Clayton-Smith, J, Chandler, K, Tatton-Brown, K, Payne, K, Helbig, K, Radtke, K, Nugent, KM, Cremer, K, Strom, TM, Bird, LM, Sinnema, M, Bitner-Glindzicz, M, van Dooren, MF, Alders, M, Koopmans, M, Brick, L, Kozenko, M, Harline, ML, Klaassens, M, Steinraths, M, Cooper, NS, Edery, P, Yap, P, Terhal, PA, van der Spek, PJ, Lakeman, P, Taylor, RL, Littlejohn, RO, Pfundt, R, Mercimek-Andrews, S, Stegmann, APA, Kant, SG, McLean, S, Joss, S, Swagemakers, SMA, Douzgou, S, Wall, SA, Küry, S, Calpena, E, Koelling, N, McGowan, SJ, Twigg, SRF, Mathijssen, IMJ, Nellaker, C, Brunner, HG, Wilkie, AOM
Publikováno v:
American Journal of Human Genetics, 102(6), 1195-1203
American journal of human genetics, vol 102, iss 6
American journal of human genetics, vol 102, iss 6
Next-generation sequencing is a powerful tool for the discovery of genes related to neurodevelopmental disorders (NDDs). Here, we report the identification of a distinct syndrome due to de novo or inherited heterozygous mutations in Tousled-like kina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::623bf0658c2dd1fcad885b720f5373c3
http://hdl.handle.net/1887/79379
http://hdl.handle.net/1887/79379
Autor:
Twigg, SR, Babbs, C, van den Elzen, ME, Goriely, A, Taylor, S, McGowan, SJ, Giannoulatou, E, Lonie, L, Ragoussis, J, Sadighi Akha, E, Knight, SJ, Zechi-Ceide, RM, Hoogeboom, JA, Pober, BR, Toriello, HV, Wall, SA, Rita Passos-Bueno, M, Brunner, HG, Mathijssen, IM, Wilkie, AO
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, 22, 1654-62
Human Molecular Genetics, 22, 8, pp. 1654-62
Human Molecular Genetics, 22(8), 1654-1662. Oxford University Press
Human Molecular Genetics, 22, 1654-62
Human Molecular Genetics, 22, 8, pp. 1654-62
Human Molecular Genetics, 22(8), 1654-1662. Oxford University Press
Contains fulltext : 118112.pdf (Publisher’s version ) (Open Access) Craniofrontonasal syndrome (CFNS), an X-linked disorder caused by loss-of-function mutations of EFNB1, exhibits a paradoxical sex reversal in phenotypic severity: females character
Autor:
Twigg, SR, Lloyd, D, Jenkins, D, Elçioglu, NE, Cooper, CD, Al-Sannaa, N, Annagür, A, Gillessen-Kaesbach, G, Hüning, I, Knight, SJ, Goodship, JA, Keavney, BD, Beales, PL, Gileadi, O, McGowan, SJ, Wilkie, AO
Publikováno v:
The American Journal of Human Genetics; Vol 91
Carpenter syndrome is an autosomal-recessive multiple-congenital- malformation disorder characterized by multisuture craniosynostosis and polysyndactyly of the hands and feet; many other clinical features occur, and the most frequent include obesity,
Autor:
Twigg, SRF, Wilkie, AOM, Hufnagel, RB, Miller, KA, Zhou, Y, McGowan, SJ, Taylor, J, Craft, J, Taylor, JC, Santoro, SL, Huang, T, Hopkin, RJ, Brady, AF, Clayton-Smith, J, Clericuzio, CL, Grange, DK, Groesser, L, Hafner, C, Horn, D, Temple, IK, Dobyns, WB, Curry, CJ, Jones, MC
Curry-Jones syndrome (CJS) is a multisystem disorder characterized by patchy skin lesions, polysyndactyly, diverse cerebral malformations, unicoronal craniosynostosis, iris colobomas, microphthalmia, and intestinal malrotation with myofibromas or ham
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::398df20c096adb044cf30378bd57dea9
https://doi.org/10.1016/j.ajhg.2016.04.007
https://doi.org/10.1016/j.ajhg.2016.04.007
Autor:
Giannoulatou, E, McVean, G, Taylor, IB, McGowan, SJ, Maher, GJ, Iqbal, Z, Pfeifer, SP, Turner, I, Wright, EMMB, Shorto, J, Itani, A, Turner, K, Gregory, L, Buck, D, Rajpert-De Meyts, E, Looijenga, LHJ (Leendert), Kerr, B, Wilkie, AOM, Goriely, A
Publikováno v:
Proceedings of the National Academy of Sciences of the U.S.A., 110(50), 20152-20157. National Academy of Sciences
The RAS proto-oncogene Harvey rat sarcoma viral oncogene homolog (HRAS) encodes a small GTPase that transduces signals from cell surface receptors to intracellular effectors to control cellular behavior. Although somatic HRAS mutations have been desc
Autor:
Sharma, VP, Fenwick, AL, Brockop, MS, McGowan, SJ, Goos, JAC, Hoogeboom, AJM, Brady, AF, Jeelani, O, Lynch, SA, Mulliken, JB, Murray, DJ, Phipps, JM, Sweeney, E, Tomkins, SE, Wilson, LC, Bennett, S, Cornall, RJ, Broxholme, J, Kanapin, A, Donnelly, P, Johnson, D, Wall, SA, van der Spek, PJ, Mathijssen, IMJ, Maxson, RE, Twigg, SRF, Wilkie, AOM
Publikováno v:
LANCET. 381
Autor:
Sharma, VP, Fenwick, AL, Brockop, MS, McGowan, SJ, Goos, Jacqueline, Hoogeboom, Jeannette, Brady, AF, Jeelani, NO, Lynch, SA, Mulliken, JB, Murray, DJ, Phipps, JM, Sweeney, E, Tomkins, SE, Wilson, LC, Bennett, S, Cornall, RJ, Broxholme, J, Kanapin, A, Johnson, D, Wall, SA, van der Spek, Peter, Mathijssen, Irene, Maxson, RE, Twigg, SRF, Wilkie, AOM
Publikováno v:
Nature Genetics, 45(10), 1261-1261. Nature Publishing Group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::3c378f73639266fba82ca9afa9d8a40a
https://pure.eur.nl/en/publications/d6818304-01e9-4cc2-8d39-d8df1a863353
https://pure.eur.nl/en/publications/d6818304-01e9-4cc2-8d39-d8df1a863353
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.