Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Bruce E Vogel"'
Autor:
Janet Ugolino, Kristina M Dziki, Annette Kim, Josephine J Wu, Bruce E Vogel, Mervyn J Monteiro
Publikováno v:
PLoS ONE, Vol 14, Iss 8, p e0220849 (2019)
Mutations in ATP13A2 cause Kufor-Rakeb syndrome (KRS), a juvenile form of Parkinson's disease (PD) with dementia. However, the mechanisms by which mutations in ATP13A2 cause KRS is not understood. The mutations lead to misfolding of the translated At
Externí odkaz:
https://doaj.org/article/2ca556a9c0fa4cc98b2e023881589e71
Autor:
Yongwang Zhong, Jiou Wang, Mark J Henderson, Peixin Yang, Brian M Hagen, Teepu Siddique, Bruce E Vogel, Han-Xiang Deng, Shengyun Fang
Publikováno v:
eLife, Vol 6 (2017)
Over 170 different mutations in the gene encoding SOD1 all cause amyotrophic lateral sclerosis (ALS). Available studies have been primarily focused on the mechanisms underlying mutant SOD1 cytotoxicity. How cells defend against the cytotoxicity remai
Externí odkaz:
https://doaj.org/article/7385a4b9f6ca41dc809a49f0ef1d3d6e
Publikováno v:
Microbiology Spectrum. 10
Our study demonstrates the ability of PBP4 to be an important mediator of β-lactam resistance in not only methicillin-susceptible Staphylococcus aureus (MSSA) background strains as previously demonstrated but also in MRSA strains. When present toget
Methicillin-Resistant Staphylococcus aureus (MRSA) are pathogenic bacteria that are infamously resistant to β-lactam antibiotics, a property attributed to the mecA gene. Recent studies have reported that mutations associated with the promoter region
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::feb278c85a3696541d3abbf4b9e06433
https://doi.org/10.1101/2022.06.17.496612
https://doi.org/10.1101/2022.06.17.496612
Autor:
Natalie, Acker, Harold, Smith, Claire, Devine, Sharon L, Oltjen, Sofia, Tsiropoulou, Zeljka, Smit-McBride, Karen, Lange, Oliver E, Blacque, Joanne A, Matsubara, Andrew, Gordus, Andy, Golden, Bruce E, Vogel
Publikováno v:
Proc Natl Acad Sci U S A
Age-related macular degeneration (AMD) is a leading cause of blindness among the elderly. Canonical disease models suggest that defective interactions between complement factor H (CFH) and cell surface heparan sulfate (HS) result in increased alterna
Autor:
Claire Devine, Karen I. Lange, Zeljka Smit-McBride, Sharon L. Oltjen, Andy Golden, Harold C. Smith, Sofia Tsiropoulou, Oliver E. Blacque, Joanne A Matsubara, Natalie Acker, Andrew Gordus, Bruce E. Vogel
Publikováno v:
Proceedings of the National Academy of Sciences. 118
Age-related macular degeneration (AMD) is a leading cause of blindness among the elderly. Canonical disease models suggest that defective interactions between complement factor H (CFH) and cell surface heparan sulfate (HS) result in increased alterna
Autor:
Peixin Yang, Teepu Siddique, Jiou Wang, Han Xiang Deng, Yongwang Zhong, Brian M. Hagen, Shengyun Fang, Bruce E. Vogel, Mark J. Henderson
Publikováno v:
eLife, Vol 6 (2017)
eLife
eLife
Over 170 different mutations in the gene encoding SOD1 all cause amyotrophic lateral sclerosis (ALS). Available studies have been primarily focused on the mechanisms underlying mutant SOD1 cytotoxicity. How cells defend against the cytotoxicity remai
Autor:
Mark J. Henderson, Jiou Wang, Peixin Yang, Teepu Siddique, Yongwang Zhong, Han Xiang Deng, Brian M. Hagen, Shengyun Fang, Bruce E. Vogel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d974e3cb4e18e0e686dc9fd99d6aca9e
https://doi.org/10.7554/elife.23759.021
https://doi.org/10.7554/elife.23759.021
An extracellular matrix protein prevents cytokinesis failure and aneuploidy in theC. elegansgermline
Publikováno v:
Cell Cycle. 10:1916-1920
Interactions between extracellular matrix (ECM) proteins and their transmembrane receptors mediate cytoskeletal reorganization and corresponding changes in cell shape during cell migration, adhesion, differentiation and polarization. Cytokinesis is t
Publikováno v:
Cell Research. 16:872-878
Hemicentins are conserved extracellular matrix proteins discovered in Caenorhabditis elegans, with orthologs in all vertebrate species including human and mouse. Hemicentins share a single, highly conserved amino-terminal von Willebrand A domain, fol