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Annita Achilleos, Ph.D. - Publications

Affiliations: 
2010 Basic Medical Science New York University, New York, NY, United States 
Area:
Cell Biology, Genetics, Human Development
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12 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Falcon KT, Watt KEN, Dash S, Zhao R, Sakai D, Moore EL, Fitriasari S, Childers M, Sardiu ME, Swanson S, Tsuchiya D, Unruh J, Bugarinovic G, Li L, Shiang R, ... Achilleos A, et al. Dynamic regulation and requirement for ribosomal RNA transcription during mammalian development. Proceedings of the National Academy of Sciences of the United States of America. 119: e2116974119. PMID 35881792 DOI: 10.1073/pnas.2116974119  0.321
2022 Chern T, Achilleos A, Tong X, Hill MC, Saltzman AB, Reineke LC, Chaudhury A, Dasgupta SK, Redhead Y, Watkins D, Neilson JR, Thiagarajan P, Green JBA, Malovannaya A, Martin JF, et al. Mutations in Hcfc1 and Ronin result in an inborn error of cobalamin metabolism and ribosomopathy. Nature Communications. 13: 134. PMID 35013307 DOI: 10.1038/s41467-021-27759-7  0.628
2020 Chern T, Achilleos A, Tong X, Hsu CW, Wong L, Poché RA. Mouse models to study the pathophysiology of combined methylmalonic acidemia and homocystinuria, cblC type. Developmental Biology. PMID 32941884 DOI: 10.1016/J.Ydbio.2020.09.005  0.617
2020 Achilleos A, Chern T, Tong X, Hill MC, Chaudhury A, Reineke LC, Neilson J, Sun J, Ray RS, Watkins D, Thiagarajan P, Dasgupta SK, James MF, Poché RA. CblX is a New Cobalamin Syndrome Affecting Craniofacial Development The Faseb Journal. 34: 1-1. DOI: 10.1096/Fasebj.2020.34.S1.05416  0.627
2016 Noack Watt KE, Achilleos A, Neben CL, Merrill AE, Trainor PA. The Roles of RNA Polymerase I and III Subunits Polr1c and Polr1d in Craniofacial Development and in Zebrafish Models of Treacher Collins Syndrome. Plos Genetics. 12: e1006187. PMID 27448281 DOI: 10.1371/Journal.Pgen.1006187  0.452
2016 Sakai D, Dixon J, Achilleos A, Dixon M, Trainor PA. Prevention of Treacher Collins syndrome craniofacial anomalies in mouse models via maternal antioxidant supplementation. Nature Communications. 7: 10328. PMID 26792133 DOI: 10.1038/Ncomms10328  0.407
2015 Achilleos A, Trainor PA. Mouse Models of Rare Craniofacial Disorders. Current Topics in Developmental Biology. 115: 413-58. PMID 26589934 DOI: 10.1016/Bs.Ctdb.2015.07.011  0.35
2015 Achilleos A, Huffman NT, Marcinkiewicyz E, Seidah NG, Chen Q, Dallas SL, Trainor PA, Gorski JP. MBTPS1/SKI-1/S1P proprotein convertase is required for ECM signaling and axial elongation during somitogenesis and vertebral development†. Human Molecular Genetics. 24: 2884-98. PMID 25652402 DOI: 10.1093/Hmg/Ddv050  0.41
2012 Achilleos A, Trainor PA. Neural crest stem cells: discovery, properties and potential for therapy. Cell Research. 22: 288-304. PMID 22231630 DOI: 10.1038/Cr.2012.11  0.317
2011 Achilleos A, Crane J, Bhatt S, Trainor P. Understanding neural crest cell development using Gcnf−/− mutant mice as a model system Developmental Biology. 356: 185. DOI: 10.1016/J.Ydbio.2011.05.224  0.372
2010 Achilleos A, Wehman AM, Nance J. PAR-3 mediates the initial clustering and apical localization of junction and polarity proteins during C. elegans intestinal epithelial cell polarization. Development (Cambridge, England). 137: 1833-42. PMID 20431121 DOI: 10.1242/Dev.047647  0.617
2007 Totong R, Achilleos A, Nance J. PAR-6 is required for junction formation but not apicobasal polarization in C. elegans embryonic epithelial cells. Development (Cambridge, England). 134: 1259-68. PMID 17314130 DOI: 10.1242/Dev.02833  0.621
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