Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Peter G Farlie"'
Autor:
Kerry A Miller, Casey J Ah-Cann, Megan F Welfare, Tiong Y Tan, Kate Pope, Georgina Caruana, Mary-Louise Freckmann, Ravi Savarirayan, John F Bertram, Michael S Dobbie, John F Bateman, Peter G Farlie
Publikováno v:
PLoS Genetics, Vol 9, Iss 8, p e1003746 (2013)
Cilia are architecturally complex organelles that protrude from the cell membrane and have signalling, sensory and motility functions that are central to normal tissue development and homeostasis. There are two broad categories of cilia; motile and n
Externí odkaz:
https://doaj.org/article/f9538cbfee0b4876ad5196ec0eb6824d
Autor:
Georgina Caruana, Peter G Farlie, Adam H Hart, Stefan Bagheri-Fam, Megan J Wallace, Michael S Dobbie, Christopher T Gordon, Kerry A Miller, Belinda Whittle, Helen E Abud, Ruth M Arkell, Timothy J Cole, Vincent R Harley, Ian M Smyth, John F Bertram
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e55429 (2013)
Mice harbouring gene mutations that cause phenotypic abnormalities during organogenesis are invaluable tools for linking gene function to normal development and human disorders. To generate mouse models harbouring novel alleles that are involved in o
Externí odkaz:
https://doaj.org/article/4ef49950460e4f1d88f053a4f9e96464
Autor:
Kerry A Miller, Christopher T Gordon, Megan F Welfare, Georgina Caruana, John F Bertram, John F Bateman, Peter G Farlie
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e76342 (2013)
Fras1 is an extracellular matrix associated protein with essential roles in adhesion of epithelia and mesenchyme during early embryonic development. The adhesive function of Fras1 is achieved through interaction with a group of related proteins, Frem
Externí odkaz:
https://doaj.org/article/d720fb9778524eaeb3a67e6a17bb2ae2
Autor:
Peter G. Farlie, Nadia M. Davidson, Naomi L. Baker, Mai Raabus, Kelly N. Roeszler, Claire Hirst, Andrew Major, Mylene M. Mariette, David M. Lambert, Alicia Oshlack, Craig A. Smith
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-12 (2017)
The transcription factor Nkx2.5 is essential for heart development. Here, the authors identify a previously unknown expression domain for Nkx2.5 in the emu wing and explore its role in diminished wing bud development in the flightless emu, compared w
Externí odkaz:
https://doaj.org/article/d39fc2c1c3a943f48666365a2d6c0c28
Autor:
Damien Bates, Kumudhini Kugathasan, James P Roy, Steven A. Stacker, Peter G. Farlie, Dong Zhang, Margaret L. Kirby, Donald F. Newgreen, James L. Wilkinson, Michael M. Halford, You Fang Zhang, Darrin P Smith, Maria L Macheda
Publikováno v:
Growth Factors. 36:58-68
Ryk is a member of the receptor tyrosine kinase (RTK) family of proteins that control and regulate cellular processes. It is distinguished by binding Wnt ligands and having no detectable intrinsic protein tyrosine kinase activity suggesting Ryk is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72e17bec50bb20c2ed667e4c07a4b40c
https://doi.org/10.1080/08977194.2018.1491848
https://doi.org/10.1080/08977194.2018.1491848
Publikováno v:
Molecular Syndromology. 7:312-321
The complex anatomy of the skull and face arises from the requirement to support multiple sensory and structural functions. During embryonic development, the diverse component elements of the neuro- and viscerocranium must be generated independently
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::652d3e2220eb0689ecf53b7f6fa1c7ea
https://doi.org/10.1159/000450533
https://doi.org/10.1159/000450533
Autor:
Patrícia P.O. Rocha, Juliana G. Giannetti, Marzia Pollazzon, Alessandro Iodice, Maria Marinelli, Satz Mengensatzproduktion, Ilaria Kolobova, Elvis C. Mateo, Patrícia R. de M. Lima, Manuela Napoli, Ivan Ivanovski, Tiong Yang Tan, Martin Poot, Elga Fabia Belligni, Joziele de S. Lima, Siulan Vendramini-Pittoli, Livia Garavelli, Rafaella X. Pietra, Bruno F. Gamba, Carlo Fusco, Charles Coutton, Veronica Barbieri, Giovana da C. César, Roseli Maria Zechi-Ceide, Mariana Lacerda de Freitas, Luana Assis Ferreira, Paula Frassinetti Vasconcelos de Medeiros, Gabrielle S. Vianna, Michele da S. Gonçalves, Nicky Kilpatrick, Francesca Madia, Anthony J. Penington, Chiara Sartori, Jessie X. Xu, Nancy Mizue Kokitsu-Nakata, Manuela Mussini, Fernanda S. Jehee, Fabrizia Franchi, Maria E. Street, Carla Rosenberg, Patrick Yap, Liam Crapper, Antonio Richieri-Costa, Rejane A.C. Monteiro, Rosana R. Xavier, Ilenia Maini, Naomi L. Baker, Scott C. Bell, Maria Augusta N.P. Monteiro, Valdirene T. de Oliveira, Simonetta Rosato, Ana C.V. Krepischi Santos, Druckerei Stückle, Carl Ernst, Rosario Pascarella, Andréia M. Carvalho, Lucilene Arilho Ribeiro-Bicudo, Peter G. Farlie
Publikováno v:
Molecular Syndromology. 7:I-VI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db58d86090fdaf131c3502e161f58fd5
https://doi.org/10.1159/000452981
https://doi.org/10.1159/000452981
Autor:
Bryn Jones, Stephan Waldmueller, Elizabeth J. Bhoj, Erik G. Puffenberger, Hakon Hakonarson, Nanditha Das, Tiong Yang Tan, Claudia Gonzaga-Jauregui, Ioanna Skubas, Sarah J. Hatsell, Susannah Brydges, Stefanie Eggers, Karlla W. Brigatti, Kevin A. Strauss, Melissa G. Dominguez, Ron A. Deckelbaum, Angelika Riess, Gwenaël Le Guyader, Peter G. Farlie, Virginia Hughes, Peter J Simm, Tobias B. Haack, LiQin Xie, Katharina Steindl, Pascal Joset, Aris N. Economides, Dong Li, Fanny Pelluard, Michael Hofbeck, Chia-Jen Siao, Naomi L. Baker, John D. Overton, Anita Rauch, Valerie Mayne, Marc Sturm
Publikováno v:
American journal of human genetics. 101(6)
Bone morphogenetic protein 2 (BMP2) in chromosomal region 20p12 belongs to a gene superfamily encoding TGF-β-signaling proteins involved in bone and cartilage biology. Monoallelic deletions of 20p12 are variably associated with cleft palate, short s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::201c0fea7aa1fe2f57af20a24c97ef97
https://pubmed.ncbi.nlm.nih.gov/29198724
https://pubmed.ncbi.nlm.nih.gov/29198724
Autor:
Kerry A. Miller, John F. Bertram, Susan M. White, Tiong Yang Tan, Georgina Caruana, Andrew A Heggie, Ravi Savarirayan, Zornitza Stark, Megan F Welfare, John F. Bateman, Trent Burgess, Peter G. Farlie
Publikováno v:
Molecular Syndromology. 5:276-286
The 22q11.2 deletion syndrome (22q11DS) is thought to be a contiguous gene syndrome caused by haploinsufficiency for a variable number of genes with overlapping function during the development of the craniofacial, pharyngeal and cardiac structures. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ae40b2c6819aa9a5e5f84512825dd05
https://doi.org/10.1159/000368865
https://doi.org/10.1159/000368865
Autor:
Mathilde Huckert, Séraphin Nguefack, John F. Bateman, Renata Moldenhauer Minillo, Nara Sobreira, Vinciane Wouters, Corinne Stoetzel, Marie-Cécile Manière, Cedrik Tekendo-Ngongang, Virginie Laugel-Haushalter, Bee Chin Chen, Vincent Laugel, Kerry A. Miller, Rutger Meinsma, Kimberly F. Doheny, Cristina Has, Stefania Gimelli, Kurt N. Hetrick, Elisabeth Flori, Sophie Dahoun, Peter G. Farlie, David Valle, John B. Mulliken, Anne Dompmartin, Helen Mecili, Georgina Caruana, Martin Poot, Susan M. White, André B.P. van Kuilenburg, Laurence Myriam Boon, Decio Brunoni, Rowani Mohd Rawi, Agnès Bloch-Zupan, Ambroise Wonkam, Ilkka Kaitila, Raoul C.M. Hennekam, Druckerei Stückle, Judith Meijer, Megan F Welfare, Ana B. Alvarez Perez, Mustapha Amyere, Satz Mengensatzproduktion, Maria de Fátima de Faria Soares, John F. Bertram, Zornitza Stark, Odile Enjolras, Jean Muller, Ebtesam M. Abdalla, Miikka Vikkula, Tiong Yang Tan, Frédérique Sloan-Béna, Julie Jurgens, Catherine Godfraind, Pierre-Louis Docquier, Hua Ling, Ravi Savarirayan, Andrew A Heggie, Hélène Dollfus, Trent Burgess
Publikováno v:
Molecular Syndromology. 5:I-IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::728f4d75c99e719eb11cefff35acda4a
https://doi.org/10.1159/000370090
https://doi.org/10.1159/000370090