M
Michal J. Nagiec
Researcher at Cornell University
Publications - 19
Citations - 1254
Michal J. Nagiec is an academic researcher from Cornell University. The author has contributed to research in topics: Phosphorylation & Kinase. The author has an hindex of 15, co-authored 18 publications receiving 1081 citations. Previous affiliations of Michal J. Nagiec include Houston Methodist Hospital & Baylor College of Medicine.
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Journal ArticleDOI
Genome Sequence of a Serotype M28 Strain of Group A Streptococcus: Potential New Insights into Puerperal Sepsis and Bacterial Disease Specificity
Nicole M. Green,Nicole M. Green,Nicole M. Green,Shizhen Zhang,Stephen F. Porcella,Michal J. Nagiec,Kent D. Barbian,Stephen B. Beres,Rance B Lefebvre,James M. Musser,James M. Musser +10 more
TL;DR: The genome of a genetically representative strain of serotype M28 strains has genes encoding a novel array of prophage virulence factors, cell-surface proteins, and other molecules likely to contribute to host-pathogen interactions.
Journal ArticleDOI
Molecular genetic anatomy of inter- and intraserotype variation in the human bacterial pathogen group A Streptococcus
Stephen B. Beres,Ellen W. Richter,Michal J. Nagiec,Paul Sumby,Stephen F. Porcella,Frank R. DeLeo,James M. Musser +6 more
TL;DR: A serotype M3 clone significantly underrepresented among necrotizing fasciitis cases has a unique frameshift mutation that truncates MtsR, a transcriptional regulator controlling expression of genes encoding iron-acquisition proteins, which provided unprecedented detail about the molecular anatomy of bacterial strain genotype-patient phenotype relationships.
Journal ArticleDOI
Regulation of Cell Signaling Dynamics by the Protein Kinase-Scaffold Ste5
Nan Hao,Sujata Nayak,Marcelo Behar,Ryan H. Shanks,Michal J. Nagiec,Beverly Errede,Jeff Hasty,Timothy C. Elston,Henrik G. Dohlman +8 more
TL;DR: It is proposed that scaffold proteins serve to modulate the temporal and dose-response behavior of the MAP kinase, and thus help cells respond to a gradient or mate efficiently with distant partners.
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Quantitative phosphoproteomic analysis reveals system-wide signaling pathways downstream of SDF-1/CXCR4 in breast cancer stem cells
Tingfang Yi,Bo Zhai,Yonghao Yu,Yoshikawa Kiyotsugu,Thomas Raschle,Manuel Etzkorn,Hee Chan Seo,Michal J. Nagiec,Rafael E. Luna,Ellis L. Reinherz,John Blenis,Steven P. Gygi,Gerhard Wagner +12 more
TL;DR: A system-wide view of phosphorylation events downstream of SDF-1/CXCR4 signaling in breast CSCs is given, providing a resource for the study of CSC-targeted cancer therapy and identifying several previously unidentified phosphoproteins and signaling pathways in Breast cancer stem cells.
Journal ArticleDOI
mTORC1 Promotes Metabolic Reprogramming by the Suppression of GSK3-Dependent Foxk1 Phosphorylation.
Long He,Ana P. Gomes,Xin Wang,Sang-Oh Yoon,Sang-Oh Yoon,Gina Lee,Gina Lee,Michal J. Nagiec,Michal J. Nagiec,Sungyun Cho,Andre Chavez,Tasnia Islam,Yonghao Yu,John M. Asara,Bo Yeon Kim,John Blenis,John Blenis,John Blenis +17 more
TL;DR: It is reported that the transcription factor forkhead/winged helix family k1 (Foxk1) is a mediator of mTORC1-regulated gene expression and is likely to be critical for metabolic diseases where improper m TORC1 signaling plays an important role.