Bryan T. Phillips, Ph.D.
Affiliations: | 2004 | Texas A & M University, College Station, TX, United States |
Area:
Genetics, Animal Physiology BiologyGoogle:
"Bryan Phillips"Parents
Sign in to add mentor| Bruce B. Riley | grad student | 2004 | Texas A & M | |
| (Molecular analysis of placodal development in zebrafish.) | ||||
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Publications
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| Michel MFV, Phillips BT. (2023) SYS-1/beta-catenin inheritance and regulation by Wnt-signaling during asymmetric cell division. Biorxiv : the Preprint Server For Biology |
| Vora SM, Fassler JS, Phillips BT. (2020) Centrosomes are Required for Proper β-catenin Processing and Wnt Response. Molecular Biology of the Cell. mbcE20020139 |
| Skuodas S, Clemons A, Hayes M, et al. (2020) The ABCF gene family facilitates disaggregation during animal development. Molecular Biology of the Cell. mbcE19080443 |
| Lam AK, Phillips BT. (2017) Wnt Signaling Polarizes C. elegans Asymmetric Cell Divisions During Development. Results and Problems in Cell Differentiation. 61: 83-114 |
| Vora SM, Phillips BT. (2016) The benefits of local depletion: The centrosome as a scaffold for ubiquitin-proteasome-mediated degradation. Cell Cycle (Georgetown, Tex.). 1-11 |
| Baldwin AT, Clemons AM, Phillips BT. (2016) Unique and redundant β-catenin regulatory roles of two Dishevelled paralogs during C. elegans asymmetric cell division. Journal of Cell Science. 129: 983-93 |
| Mila D, Calderon A, Baldwin AT, et al. (2015) Asymmetric Wnt Pathway Signaling Facilitates Stem Cell-Like Divisions via the Non-Receptor Tyrosine Kinase FRK-1 in Caenorhabditis elegans. Genetics |
| Vora S, Phillips BT. (2015) Centrosome-Associated Degradation Limits β-Catenin Inheritance by Daughter Cells after Asymmetric Division. Current Biology : Cb. 25: 1005-16 |
| Baldwin AT, Phillips BT. (2014) The tumor suppressor APC differentially regulates multiple β-catenins through the function of axin and CKIα during C. elegans asymmetric stem cell divisions. Journal of Cell Science. 127: 2771-81 |
| Puri P, Phillips BT, Suzuki H, et al. (2014) The transition from stem cell to progenitor spermatogonia and male fertility requires the SHP2 protein tyrosine phosphatase. Stem Cells (Dayton, Ohio). 32: 741-53 |