Hsin-Yi H. Ho, Ph.D.

Affiliations: 
Harvard University, Cambridge, MA, United States 
Area:
Cell Cycle, Cytoskeleton, Systems Biology
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"Hsin-Yi Ho"

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Marc W. Kirschner grad student 2004 Harvard
 (Regulatory mechanisms of Cdc42-mediated actin assembly.)
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Publications

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Konopelski Snavely SE, Srinivasan S, Dreyer CA, et al. (2023) Non-canonical WNT5A-ROR signaling: New perspectives on an ancient developmental pathway. Current Topics in Developmental Biology. 153: 195-227
Konopelski Snavely SE, Susman MW, Kunz RC, et al. (2021) Proteomic analysis identifies the E3 ubiquitin ligase Pdzrn3 as a regulatory target of Wnt5a-Ror signaling. Proceedings of the National Academy of Sciences of the United States of America. 118
Zhang H, Sathyamurthy A, Liu F, et al. (2019) Agrin-Lrp4-Ror2 signaling regulates adult hippocampal neurogenesis in mice. Elife. 8
Tao H, Zhu M, Lau K, et al. (2019) Oscillatory cortical forces promote three dimensional cell intercalations that shape the murine mandibular arch. Nature Communications. 10: 1703
VanderVorst K, Dreyer CA, Konopelski SE, et al. (2019) Wnt/PCP Signaling Contribution to Carcinoma Collective Cell Migration and Metastasis. Cancer Research
Weissenböck M, Latham R, Nishita M, et al. (2019) Genetic interactions between Ror2 and Wnt9a, Ror1 and Wnt9a and Ror2 and Ror1 - phenotypic analysis of the limb skeleton and palate in compound mutants. Genes to Cells : Devoted to Molecular & Cellular Mechanisms
Willert K, Ho HH, Liebner S. (2019) Decision letter: Molecular determinants in Frizzled, Reck, and Wnt7a for ligand-specific signaling in neurovascular development Elife
Zhang H, Sathyamurthy A, Liu F, et al. (2019) Author response: Agrin-Lrp4-Ror2 signaling regulates adult hippocampal neurogenesis in mice Elife
Mansour TA, Lucot K, Konopelski SE, et al. (2018) Whole genome variant association across 100 dogs identifies a frame shift mutation in DISHEVELLED 2 which contributes to Robinow-like syndrome in Bulldogs and related screw tail dog breeds. Plos Genetics. 14: e1007850
Wojcik MH, Okada K, Prabhu SP, et al. (2018) De novo variant in KIF26B is associated with pontocerebellar hypoplasia with infantile spinal muscular atrophy. American Journal of Medical Genetics. Part A
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