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pro vyhledávání: '"Elizabeth Jewlal"'
Publikováno v:
Developmental dynamics : an official publication of the American Association of AnatomistsREFERENCES. 250(12)
Background We compared skull shape and variation among genetically modified mice that exhibit different levels of connexin43 (Cx43) channel function, to determine whether Cx43 contributes to craniofacial phenotypic robustness. Specifically, we used t
Autor:
Katherine E. Willmore, Dale W. Laird, Kevin J. Barr, Alyssa C. Moore, Jessica J. Wu, Elizabeth Jewlal
Publikováno v:
Bone and Joint Institute
© 2020, Springer Science+Business Media, LLC, part of Springer Nature. Mutations in the gene encoding the gap-junctional protein connexin43 (Cx43) are the cause of the human disease oculodentodigital dysplasia (ODDD). The mandible is often affected
Publikováno v:
The FASEB Journal. 33
Publikováno v:
The FASEB Journal. 33
Autor:
Silvia Penuela, Elizabeth Jewlal, Brooke L. O’Donnell, Julia M. Abitbol, John J. Kelly, C. B. Wakefield, Katherine E. Willmore, Brian L. Allman, Kevin J. Barr
Publikováno v:
Anatomy and Cell Biology Publications
© 2019, Springer-Verlag GmbH Germany, part of Springer Nature. Abstract: Pannexins (Panxs), large-pore channel forming glycoproteins, are expressed in a wide variety of tissues including the skin, bone, and cochlea. To date, the use of single knock-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::866752f20f0dad876252bbc916793add
https://ir.lib.uwo.ca/anatomypub/131
https://ir.lib.uwo.ca/anatomypub/131
Autor:
David D'Souza, Heather Shaddick, Elizabeth Jewlal, Mark T. Corkum, Akira Sugimoto, Nikhilesh Patil, Eric Leung, Michel Prefontaine, Jacob McGee
Publikováno v:
Cureus
Introduction: While Papanicolaou (Pap) smears have resulted in a significant decline in cervical cancer incidence and mortality, our clinical experience indicates some women still present with locally advanced cervical cancer (LACC) despite having re
Autor:
Katherine E. Willmore, Dale W. Laird, Elizabeth Jewlal, Sommer G.E. Jarvis, Gregory M. Kelly, Kevin J. Barr, Jae Eun Lee
Publikováno v:
Bone. 136:115365
Oculodentodigital dysplasia (ODDD) is a disease caused by mutations in the GJA1 gene that encodes the gap-junctional protein connexin43 (Cx43). ODDD affects multiple organs, but craniofacial anomalies are typical. However, details on the timing of ph
Publikováno v:
The FASEB Journal. 34:1-1