Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Michael Brent Hawkins"'
Publikováno v:
Dev Dyn
BACKGROUND: The naturally occurring chicken mutant talpid(2) (ta(2)), best known for its limb and craniofacial defects, has long served as a valuable tool for developmental biologists studying growth and patterning of craniofacial structures and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8aadaf66b1ce3f6c3a23e6120055c3bf
https://doi.org/10.1002/dvdy.318
https://doi.org/10.1002/dvdy.318
Publikováno v:
Developmental Dynamics. 250
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4e71a42f0f2d4ff2d3ddc533f76437c
https://doi.org/10.1002/dvdy.414
https://doi.org/10.1002/dvdy.414
Autor:
Qiaowei Pan, Mauricio Losilla, Allyse M. Ferrara, Alex Dornburg, Tatsuya Ota, Kevin L. Childs, Yann Guiguen, Marine Milhes, Amy R. McCune, Ingo Braasch, Michael Brent Hawkins, Andrew W. Thompson, Emily Funk, Olivia E Fitch, Hugues Roest Crollius, Dustin J. Wcisel, Quenton C. Fontenot, Romain Feron, Brett Racicot, Elise Parey, Solomon R. David, Matthew P. Harris, Kazuhiko Kawasaki, Camille Berthelot, Jeffrey A. Yoder
The bowfin fish (Amia calva) diverged before the genome duplication in teleost fishes, and its archetypical body plan and slow rate of molecular evolution make it a key species for genomic exploration as a basal representative of the neopterygian fis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9901de8d8b0071d56cc6b07fa34a28ec
https://doi.org/10.21203/rs.3.rs-92055/v1
https://doi.org/10.21203/rs.3.rs-92055/v1
Autor:
Matthew P. Harris, Fransiska Malfait, Charlotte Gistelinck, Hanna De Saffel, Michael Brent Hawkins, Paul Witten, Ronald Y. Kwon, Patrick Sips, Katrin Henke, David R. Eyre, Andy Willaert, Brecht Guillemyn, Petra Vermassen, Paul Coucke, Sofie Symoens, Shannon Fisher, Anne De Paepe, Jan Willem Beck, MaryAnn Weis
Publikováno v:
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America
Significance Type I collagenopathies are a heterogenous group of connective tissue disorders, caused by genetic defects in type I collagen. Inherent to these disorders is a large clinical variability, of which the underlying molecular basis remains u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::180d0fc57ad73b64efa9e9db708fa9a0
https://doi.org/10.1073/pnas.1722200115
https://doi.org/10.1073/pnas.1722200115