Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Kenneth M K Mark"'
Publikováno v:
PLoS Pathogens, Vol 20, Iss 1, p e1011919 (2024)
[This corrects the article DOI: 10.1371/journal.ppat.1008581.].
Externí odkaz:
https://doaj.org/article/d2ee2c1dc6164d729cc23229967b16ba
Autor:
Cassandra M Burke, Kenneth M K Mark, Daniel J Walsh, Geoffrey P Noble, Alexander D Steele, Abigail B Diack, Jean C Manson, Joel C Watts, Surachai Supattapone
Publikováno v:
PLoS Pathogens, Vol 16, Iss 9, p e1008875 (2020)
Prions are unorthodox pathogens that cause fatal neurodegenerative diseases in humans and other mammals. Prion propagation occurs through the self-templating of the pathogenic conformer PrPSc, onto the cell-expressed conformer, PrPC. Here we study th
Externí odkaz:
https://doaj.org/article/56f2eed8818d434daa5cbc4eb00e3299
Publikováno v:
PLoS Pathogens, Vol 16, Iss 5, p e1008581 (2020)
Prions are unorthodox infectious agents that replicate by templating misfolded conformations of a host-encoded glycoprotein, collectively termed PrPSc. Prion diseases are invariably fatal and currently incurable, but oral drugs that can prolong incub
Externí odkaz:
https://doaj.org/article/c92a3a166e8d426b933c5f13166ab88f
Autor:
Cassandra M Burke, Daniel J Walsh, Kenneth M K Mark, Nathan R Deleault, Koren A Nishina, Umberto Agrimi, Michele A Di Bari, Surachai Supattapone
Publikováno v:
PLoS Pathogens, Vol 16, Iss 4, p e1008495 (2020)
Prion diseases are caused by the misfolding of a host-encoded glycoprotein, PrPC, into a pathogenic conformer, PrPSc. Infectious prions can exist as different strains, composed of unique conformations of PrPSc that generate strain-specific biological
Externí odkaz:
https://doaj.org/article/406d5eb819124d0c8c142131103deceb
Autor:
Sarah R Beattie, Kenneth M K Mark, Arsa Thammahong, Laure Nicolas Annick Ries, Sourabh Dhingra, Alayna K Caffrey-Carr, Chao Cheng, Candice C Black, Paul Bowyer, Michael J Bromley, Joshua J Obar, Gustavo H Goldman, Robert A Cramer
Publikováno v:
PLoS Pathogens, Vol 13, Iss 4, p e1006340 (2017)
Aspergillus fumigatus is responsible for a disproportionate number of invasive mycosis cases relative to other common filamentous fungi. While many fungal factors critical for infection establishment are known, genes essential for disease persistence
Externí odkaz:
https://doaj.org/article/40beb8360aa749b996a4d96db9aef212
Autor:
Cassandra M. Burke, Abigail B. Diack, Alexander D. Steele, Jean Manson, Surachai Supattapone, Daniel J. Walsh, Joel C. Watts, Geoffrey P. Noble, Kenneth M. K. Mark
Publikováno v:
Burke, C M, Mark, K M K, Walsh, D J, Noble, G P, Steele, A D, Diack, A, Manson, J, Watts, J C & Supattapone, S 2020, ' Identification of a Homology-Independent Linchpin Domain Controlling Mouse and Bank Vole Prion Protein Conversion ', PLoS Pathogens . https://doi.org/10.1371/journal.ppat.1008875
PLoS Pathogens, Vol 16, Iss 9, p e1008875 (2020)
PLoS Pathogens
PLoS Pathogens, Vol 16, Iss 9, p e1008875 (2020)
PLoS Pathogens
Prions are unorthodox pathogens that cause fatal neurodegenerative diseases in humans and other mammals. Prion propagation occurs through the self-templating of the pathogenic conformer PrPSc, onto the cell-expressed conformer, PrPC. Here we study th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dac70061a80920de52ee6430caffe230
https://hdl.handle.net/20.500.11820/9aec28ec-3889-447a-887f-a78d26e6edc5
https://hdl.handle.net/20.500.11820/9aec28ec-3889-447a-887f-a78d26e6edc5
Autor:
Kenneth M. K. Mark, Nathan R. Deleault, Umberto Agrimi, Koren Nishina, Daniel J. Walsh, Surachai Supattapone, Michele Angelo Di Bari, Cassandra M. Burke
Publikováno v:
PLoS Pathogens, Vol 16, Iss 4, p e1008495 (2020)
PLoS Pathogens
PLoS Pathogens
Prion diseases are caused by the misfolding of a host-encoded glycoprotein, PrPC, into a pathogenic conformer, PrPSc. Infectious prions can exist as different strains, composed of unique conformations of PrPSc that generate strain-specific biological
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-11 (2017)
BMC Cancer
BMC Cancer
Background Neoadjuvant chemotherapy is a key component of breast cancer treatment regimens and pathologic complete response to this therapy varies among patients. This is presumably due to differences in the molecular mechanisms that underlie each tu
Autor:
Todd W. Miller, Arminja N. Kettenbach, Jonathan D. Marotti, Yue Wang, Youdinghuan Chen, Chao Cheng, Kenneth M. K. Mark, Brock C. Christensen, Lucas A. Salas
Publikováno v:
Breast Cancer Research : BCR
Breast Cancer Research, Vol 21, Iss 1, Pp 1-13 (2019)
Breast Cancer Research, Vol 21, Iss 1, Pp 1-13 (2019)
Background BRCA1-mutated cancers exhibit deficient homologous recombination (HR) DNA repair, resulting in extensive copy number alterations and genome instability. HR deficiency can also arise in tumors without a BRCA1 mutation. Compared with other b
Autor:
Michael D. Cole, Tamutenda Chidawanyika, Elizabeth Sergison, Surachai Supattapone, Kenneth M. K. Mark
Publikováno v:
Cell Death Discovery
Cell Death Discovery, Vol 4, Iss 1, Pp 1-13 (2018)
Cell Death Discovery, Vol 4, Iss 1, Pp 1-13 (2018)
Endoplasmic reticulum (ER) stress from accumulated misfolded proteins in the ER can activate the unfolded protein response (UPR). The UPR acts either to restore proteostasis or to activate cell death pathways if the stress cannot be resolved. The key