Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Byron W H Mui"'
Autor:
Fahad K. Kidwai, Byron W. H. Mui, Konstantinia Almpani, Priyam Jani, Cyrus Keyvanfar, Kulsum Iqbal, Sriram S. Paravastu, Deepika Arora, Pamela Orzechowski, Randall K. Merling, Barbara Mallon, Vamsee D. Myneni, Moaz Ahmad, Paul Kruszka, Maximilian Muenke, Jeremiah Woodcock, Jeffrey W. Gilman, Pamela G. Robey, Janice S. Lee
Publikováno v:
Journal of Developmental Biology, Vol 9, Iss 4, p 39 (2021)
In this case report, we focus on Muenke syndrome (MS), a disease caused by the p.Pro250Arg variant in fibroblast growth factor receptor 3 (FGFR3) and characterized by uni- or bilateral coronal suture synostosis, macrocephaly without craniosynostosis,
Externí odkaz:
https://doaj.org/article/f1ce3cbb92f44d77abee4940f92d27f1
Autor:
Yankel Gabet, Brian Sworder, Nathan J. Burbach, Byron W H Mui, Luis F de Castro, Kenn Holmbeck, Agnes D. Berendsen, Sergei A. Kuznetsov, Natasha Cherman, Pamela Gehron Robey, Matthew D. Phillips, Kathryn Futrega
Publikováno v:
Bone Research
Bone Research, Vol 9, Iss 1, Pp 1-12 (2021)
Bone Research, Vol 9, Iss 1, Pp 1-12 (2021)
In a previous transcriptomic study of human bone marrow stromal cells (BMSCs, also known as bone marrow-derived “mesenchymal stem cells”), SFRP2 was highly over-represented in a subset of multipotent BMSCs (skeletal stem cells, SSCs), which recre
Autor:
Byron W H Mui, Jeremiah W. Woodcock, Randall K. Merling, Vamsee D. Myneni, Kulsum Iqbal, Fahad Kidwai, Pamela Orzechowski, Barbara S. Mallon, Jeffrey W. Gilman, Deepika Arora, Pamela Gehron Robey, Konstantinia Almpani, Paul Kruszka, Maximilian Muenke, Moaz Ahmad, Janice S. Lee, Sriram S Paravastu, Cyrus Keyvanfar, Priyam Jani
Publikováno v:
Journal of Developmental Biology, Vol 9, Iss 39, p 39 (2021)
Journal of Developmental Biology
Journal of Developmental Biology
In this case report, we focus on Muenke syndrome (MS), a disease caused by the p.Pro250Arg variant in fibroblast growth factor receptor 3 (FGFR3) and characterized by uni- or bilateral coronal suture synostosis, macrocephaly without craniosynostosis,
Autor:
Barbara S. Mallon, Paul Kruszka, Pamela Gehron Robey, Janice S. Lee, Ariel F. Martinez, Fahad Kidwai, Byron W H Mui, Deepika Arora, Maximilian Muenke
Publikováno v:
Stem Cell Res
Stem Cell Research, Vol 46, Iss, Pp 101823-(2020)
Stem Cell Research, Vol 46, Iss, Pp 101823-(2020)
Muenke syndrome is the leading genetic cause of craniosynostosis and results in a variety of disabling clinical phenotypes. To model the disease and study the pathogenic mechanisms, a human induced pluripotent stem cell (hiPSC) line was generated fro
Autor:
Byron W H Mui, Vamsee D. Myneni, Pamela Gehron Robey, Madison Hockaday, Randall K. Merling, Katarzyna Futrega, Luis Fernandez de Castro Diaz, Kulsum Iqbal, Fahad Kidwai, Dan S. Kaufman, Janice Lee, Deepika Arora, Sania Ali, Daniel Martin, Natasha Cherman, Moaz Ahmad
Publikováno v:
Stem Cells (Dayton, Ohio)
Human pluripotent stem cells (hPSCs) can provide a platform to model bone organogenesis and disease. To reflect the developmental process of the human skeleton, hPSC differentiation methods should include osteogenic progenitors (OPs) arising from thr
Publikováno v:
Investigative Ophthalmology & Visual Science
Purpose The roles of gap junction protein connexin 50 (Cx50) encoded by Gja8, during lens development are not fully understood. Connexin 50 knockout (KO) lenses have decreased proliferation of epithelial cells and altered fiber cell denucleation. We