Jacek Topczewski, Ph.D.
Affiliations: | Pediatrics | Northwestern University, Evanston, IL |
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"Jacek Topczewski"Mean distance: 17.85 (cluster 32)
Parents
Sign in to add mentor| Lila Solnica Krezel | post-doc | Northwestern School of Medicine (FlyTree) |
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Publications
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| Anderson RA, Schwalbach KT, Mui SR, et al. (2020) Zebrafish models of skeletal dysplasia induced by cholesterol biosynthesis deficiency. Disease Models & Mechanisms |
| Baumgartner EA, Compton ZJ, Evans S, et al. (2019) Identification of regulatory elements recapitulating early expression of L-plastin in the zebrafish enveloping layer and embryonic periderm. Gene Expression Patterns : Gep |
| Oyarbide U, Topczewski J, Corey SJ. (2019) Peering through zebrafish to understand inherited bone marrow failure syndromes. Haematologica. 104: 13-24 |
| Oyarbide Cuervas-Mons U, Snyderman M, Topczewski J, et al. (2019) Expression of Human SBDSR126T in Sbds Null Background Shows Eif6 Dysregulation: An Adult Zebrafish Model for Shwachman-Diamond Syndrome Blood. 134: 3737-3737 |
| Hu B, Gao Y, Davies L, et al. (2018) Glypican 4 and Mmp14 interact in regulating the migration of anterior endodermal cells by limiting extracellular matrix deposition. Development (Cambridge, England) |
| Pogoda HM, Riedl-Quinkertz I, Löhr H, et al. (2018) Direct activation of chordoblasts by retinoic acid is required for segmented centra mineralization during zebrafish spine development. Development (Cambridge, England) |
| Kell MJ, Riccio RE, Baumgartner EA, et al. (2018) Targeted deletion of the zebrafish actin-bundling protein L-plastin (lcp1). Plos One. 13: e0190353 |
| Oyarbide U, Kell MJ, Farinas J, et al. (2016) Gene Disruption of Zebrafish Sbds Phenocopies Human Shwachman-Diamond Syndrome but Suggests More Global and Lineage Defects Blood. 128: 336-336 |
| Sisson BE, Dale RM, Mui SR, et al. (2015) A role of glypican4 and wnt5b in chondrocyte stacking underlying craniofacial cartilage morphogenesis. Mechanisms of Development |
| Cvjetkovic N, Maili L, Weymouth KS, et al. (2015) Regulatory variant in FZD6 gene contributes to nonsyndromic cleft lip and palate in an African-American family. Molecular Genetics & Genomic Medicine. 3: 440-51 |