Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jennifer S. Yamaoka"'
Autor:
Aaron T. Gerds, Min Ken Liao, Keri M. Law, Stephen K. Taylor, Thomas Goyne, Dale L. Kling, Lloyd J. Simons, Jennifer S. Yamaoka, James R. Vyvyan, Matthew G. Pridgeon, Carrie R. Arnold, Nathan D. Ide
Publikováno v:
Tetrahedron: Asymmetry. 15:3819-3821
An enzyme was expressed in Escherichia coli from a cloned amidase gene. When characterized, it was more enantioselective than commercial amidases. Three pheromones were made using this biotransformation chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8af9d9fcf19463d328bf47a7c9c1ed38
https://doi.org/10.1016/j.tetasy.2004.09.038
https://doi.org/10.1016/j.tetasy.2004.09.038
Autor:
Susan E. Lyons, Jordan A. Shavit, Lisa D. LaPointe, Jennifer S. Yamaoka, Fengyun Su, Marianne A. Juarez, Christopher L. Cooke
Publikováno v:
Zebrafish. 4(3)
The zebrafish has become a powerful tool for analysis of vertebrate hematopoiesis. Zebrafish, unlike mammals, have a robust primitive myeloid pathway that generates both granulocytes and macrophages. It is not clear how this unique primitive myeloid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18c11d702829bc1d7ef5f1260be716f6
https://pubmed.ncbi.nlm.nih.gov/18041923
https://pubmed.ncbi.nlm.nih.gov/18041923
Autor:
Andrew Hanosh, Susan E. Lyons, David A. Buchner, Daniel Goldman, Makoto Kamei, Pamela A. Raymond, Seongcheol Kim, Nathan D. Lawson, Brant M. Weinstein, Pudur Jagadeeswaran, Fengyun Su, Jordan A. Shavit, David Ginsburg, Linda K. Barthel, Julio D. Amigo, Beth McGee, Jennifer S. Yamaoka
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 104(35)
The zebrafish is a powerful model for studying vascular development, demonstrating remarkable conservation of this process with mammals. Here, we identify a zebrafish mutant, redhead ( rhd mi149 ), that exhibits embryonic CNS hemorrhage with intact g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42931dd79c0fc6c73986beb7e39d17d6
https://pubmed.ncbi.nlm.nih.gov/17715297
https://pubmed.ncbi.nlm.nih.gov/17715297
Autor:
Paula L. Bockenstedt, Arlette Ruiz-Saez, Randal J. Kaufman, Katharine A. Downes, Gustavo Jarchum, Marian Olpinski, Norma B. de Bosch, Flora Peyvandi, Beth McGee, Hugo Guglielmone, Salvador Minoldo, Bernard Chatelain, Wolfgang Sperl, Jennifer S. Yamaoka, William C. Nichols, Bin Zhang, David Ginsburg, Edward G. D. Tuddenham
Mutations in LMAN1 (ERGIC-53) or MCFD2 cause combined deficiency of factor V and factor VIII (F5F8D). LMAN1 and MCFD2 form a protein complex that functions as a cargo receptor ferrying FV and FVIII from the endoplasmic reticulum to the Golgi. In this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af575f8969e1cbb96b657b468c169ee3
https://europepmc.org/articles/PMC1895703/
https://europepmc.org/articles/PMC1895703/
