Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sarah J. Gignac"'
Autor:
Sarah J. Gignac, Katja R. MacCharles, Katherine Fu, Kywana Bonaparte, Gamze Akarsu, Thalia W. Barrett, Esther M. Verheyen, Joy M. Richman
Publikováno v:
Disease Models & Mechanisms, Vol 16, Iss 4 (2023)
Externí odkaz:
https://doaj.org/article/0b57a07629e241fc9d64d33b4d69f805
Autor:
Katherine Fu, Sarah J. Gignac, Sara Hosseini-Farahabadi, Joy M. Richman, Takashi Akazawa, Nathan Schuck
Publikováno v:
Hum Mol Genet
Heterozygous missense mutations in several genes in the WNT5A signaling pathway cause autosomal dominant Robinow syndrome 1 (DRS1). Our objective was to clarify the functional impact of a missense mutation in WNT5A on the skeleton, one of the main af
Publikováno v:
Journal of dental research. 96(11)
The study of rare genetic diseases provides valuable insights into human gene function. Here, we investigate dominant Robinow syndrome (RS), which affects the WNT5A signaling pathway. Autosomal dominant RS is caused by missense mutations in WNT5A or
Autor:
Deborah L. MacLatchy, Nguyen T.K. Vo, Sarah J. Gignac, Patricia M. Schulte, Lucy E. J. Lee, J. Andrew N. Alexander, Michael S. Mikhaeil
Publikováno v:
Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology. 175:15-27
The common killifish or mummichog (Fundulus heteroclitus) is an estuarine teleost increasingly used in comparative physiology, toxicology and embryology. Their ability to withstand extreme environmental conditions and ease of maintenance has made the
Publikováno v:
Mechanisms of Development. 145:S27-S28
Publikováno v:
Mechanisms of Development. 145:S147