Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sarah L. Teakel"'
Autor:
Bashar M. Thejer, Partho P. Adhikary, Amandeep Kaur, Sarah L. Teakel, Ashleigh Van Oosterum, Ishith Seth, Marina Pajic, Katherine M. Hannan, Megan Pavy, Perlita Poh, Jalal A. Jazayeri, Thiri Zaw, Dana Pascovici, Marina Ludescher, Michael Pawlak, Juan C. Cassano, Lynne Turnbull, Mitra Jazayeri, Alexander C. James, Craig P. Coorey, Tara L. Roberts, Simon J. Kinder, Ross D. Hannan, Ellis Patrick, Mark P. Molloy, Elizabeth J. New, Tanja N. Fehm, Hans Neubauer, Ewa M. Goldys, Leslie A. Weston, Michael A. Cahill
Publikováno v:
BMC Molecular and Cell Biology, Vol 21, Iss 1, Pp 1-24 (2020)
Abstract Background Progesterone Receptor Membrane Component 1 (PGRMC1) is expressed in many cancer cells, where it is associated with detrimental patient outcomes. It contains phosphorylated tyrosines which evolutionarily preceded deuterostome gastr
Externí odkaz:
https://doaj.org/article/2bd658d87bfa450aac0f899967a1efce
Autor:
Bashar M. Thejer, Partho P. Adhikary, Sarah L. Teakel, Johnny Fang, Paul A. Weston, Saliya Gurusinghe, Ayad G. Anwer, Martin Gosnell, Jalal A. Jazayeri, Marina Ludescher, Lesley-Ann Gray, Michael Pawlak, Robyn H. Wallace, Sameer D. Pant, Marie Wong, Tamas Fischer, Elizabeth J. New, Tanja N. Fehm, Hans Neubauer, Ewa M. Goldys, Jane C. Quinn, Leslie A. Weston, Michael A. Cahill
Publikováno v:
BMC Molecular and Cell Biology, Vol 21, Iss 1, Pp 1-19 (2020)
Abstract Background Progesterone receptor membrane component 1 (PGRMC1) is often elevated in cancers, and exists in alternative states of phosphorylation. A motif centered on PGRMC1 Y180 was evolutionarily acquired concurrently with the embryological
Externí odkaz:
https://doaj.org/article/d57b2568cb0049e990fdf5278618e4ac
Autor:
Manjeet Kumar, Sarah L. Teakel, Crystall Swarbrick, Intifar S. Chowdhury, David C. Thorn, Margaret Sunde, John A. Carver, Jade K. Forwood
Publikováno v:
The FEBS Journal.
Autor:
Ross D. Hannan, Tanja Fehm, Partho P. Adhikary, Ishith Seth, Ewa M. Goldys, Alexander James, Marina Pajic, Elizabeth J. New, Juan C. Cassano, Megan Pavy, Craig P. Coorey, Leslie A. Weston, Mitra Jazayeri, Sarah L. Teakel, Simon J. Kinder, Lynne Turnbull, Mark P. Molloy, Ashleigh Van Oosterum, Dana Pascovici, Ellis Patrick, Hans Neubauer, Michael Pawlak, Tara L. Roberts, Michael A. Cahill, Bashar M. Thejer, Jalal A. Jazayeri, Amandeep Kaur, Katherine M. Hannan, Marina Ludescher, Thiri Zaw, Perlita Poh
Publikováno v:
BMC Molecular and Cell Biology
BMC Molecular and Cell Biology, Vol 21, Iss 1, Pp 1-24 (2020)
BMC Molecular and Cell Biology, Vol 21, Iss 1, Pp 1-24 (2020)
Background Progesterone Receptor Membrane Component 1 (PGRMC1) is expressed in many cancer cells, where it is associated with detrimental patient outcomes. It contains phosphorylated tyrosines which evolutionarily preceded deuterostome gastrulation a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4de00d56a22e934f8adfe291e000118
Autor:
Michealla Marama, Michael A. Cahill, David Aragão, Sofiya Tsimbalyuk, Jade K. Forwood, Sarah L. Teakel
We recently reported that the membrane associated progesterone receptor (MAPR) protein family (mammalian members: PGRMC1, PGRMC2, NEUFC and NENF) originated from a new class of prokaryotic cytochrome b5 (cytb5) domain proteins, called cytb5M (MAPR-li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::886ebebf41431ff356275cddfaea43d2
https://doi.org/10.1101/2021.11.30.470528
https://doi.org/10.1101/2021.11.30.470528
Autor:
M. Marama, S. Y. Gerdes, Sarah L. Teakel, Daniel Tamarit, Thijs J. G. Ettema, David Aragão, Jade K. Forwood, Michael A. Cahill
The multiple functions of PGRMC1, the archetypal heme-binding eukaryotic MAPR family member, include steroidogenic regulation, membrane trafficking, and steroid responsiveness. The interrelationships between these functions are currently poorly under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af62ea1bc2b24d45ea59fcfaaae0f36c
https://doi.org/10.1101/2021.11.17.468889
https://doi.org/10.1101/2021.11.17.468889
Autor:
Lesley-Ann Gray, Partho P. Adhikary, Saliya Gurusinghe, Ewa M. Goldys, Fang J, Jalal A. Jazayeri, Leslie A. Weston, Sarah L. Teakel, Paul A. Weston, Jane Quinn, Hans Neubauer, Tamás Fischer, Michael A. Cahill, Robyn Heather Wallace, Michael Pawlak, Elizabeth J. New, Ayad G. Anwer, Marie Wong, Martin E. Gosnell, Bashar M. Thejer, Sameer D. Pant, Marina Ludescher, Tanja Fehm
Publikováno v:
BMC Molecular and Cell Biology, Vol 21, Iss 1, Pp 1-19 (2020)
BMC Molecular and Cell Biology
BMC Molecular and Cell Biology
Background Progesterone receptor membrane component 1 (PGRMC1) is often elevated in cancers, and exists in alternative states of phosphorylation. A motif centered on PGRMC1 Y180 was evolutionarily acquired concurrently with the embryological gastrula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be16e693c3cce2f7aa639ad93a48ace6
https://doi.org/10.21203/rs.2.20008/v1
https://doi.org/10.21203/rs.2.20008/v1
Autor:
Bashar M. Thejer, Gereon Poschmann, Michael A. Cahill, Hans Neubauer, Marina Ludescher, Sarah L. Teakel, Jade K. Forwood
Publikováno v:
Biochemical and biophysical research communications. 524(1)
PGRMC1 is a protein from the MAPR family with a range of cellular functions. PGRMC1 has been described to play a role in fertility, neuroprotection, steroidogenesis, membrane trafficking and in cancer cell biology. PGRMC1 represents a likely key regu
Autor:
Partho P. Adhikary, Juan C. Cassano, Bashar M. Thejer, Alexander James, Ross D. Hannan, Katherine M. Hannan, Michael Pawlak, Ellis Patrick, Simon J. Kinder, Amandeep Kaur, Marina Ludescher, Elizabeth J. New, Ashleigh Van Oosterum, Ewa M. Goldys, Dana Pascovici, Ishith Seth, Lynne Turnbull, Jalal A. Jazayeri, Mark P. Molloy, Megan Pavy, Craig P. Coorey, Mitra Jazayeri, Thiri Zaw, Perlita Poh, Sarah L. Teakel, Leslie A. Weston, Hans Neubauer, Tara L. Roberts, Marina Pajic, Michael A. Cahill, Tanja Fehm
Background: Progesterone Receptor Membrane Component 1 (PGRMC1) is expressed in many cancer cells, where it is associated with detrimental patient outcomes. Multiple different functions and cellular locations have been attributed to PGRMC1 in a varie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebd5b95fd7918a256bd5c09bc3526dff