Bryan Mackenzie
Overview
Explore the profile of Bryan Mackenzie including associated specialties, affiliations and a list of published articles.
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Articles
30
Citations
1675
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Recent Articles
1.
Azucenas C, Ruwe T, Bonamer J, Qiao B, Ganz T, Jormakka M, et al.
Am J Physiol Cell Physiol
. 2023 Mar;
324(5):C1110-C1118.
PMID: 36939203
Ferroportin (Fpn)-expressed at the plasma membrane of macrophages, enterocytes, and hepatocytes-mediates the transfer of cellular iron into the blood plasma. Under the control of the iron-regulatory hormone hepcidin, Fpn serves...
2.
Noel J, Ramser S, Pitstick L, Bonamer J, Mackenzie B, Seu K, et al.
Sci Rep
. 2022 Jan;
12(1):1235.
PMID: 35075211
M-CSF receptor signaling supports the development and survival of mononuclear phagocytes and is thought to play a role in post burn anemia by promoting myeloid lineage bias. We found M-CSF...
3.
Deshpande C, Azucenas C, Qiao B, Nomura N, Xin V, Font J, et al.
FEBS Open Bio
. 2020 Nov;
11(1):26-34.
PMID: 33190422
Ferroportin (Fpn) is an essential mammalian iron transporter that is negatively regulated by the hormone hepcidin. Our current molecular understanding of Fpn-mediated iron efflux and regulation is limited due to...
4.
Deshpande C, Ruwe T, Shawki A, Xin V, Vieth K, Valore E, et al.
Nat Commun
. 2018 Aug;
9(1):3075.
PMID: 30082682
Ferroportin (Fpn)-the only known cellular iron exporter-transports dietary and recycled iron into the blood plasma, and transfers iron across the placenta. Despite its central role in iron metabolism, our molecular...
5.
Aschemeyer S, Qiao B, Stefanova D, Valore E, Sek A, Ruwe T, et al.
Blood
. 2017 Dec;
131(8):899-910.
PMID: 29237594
Nonclassical ferroportin disease (FD) is a form of hereditary hemochromatosis caused by mutations in the iron transporter ferroportin (Fpn), resulting in parenchymal iron overload. Fpn is regulated by the hormone...
6.
Shawki A, Engevik M, Kim R, Knight P, Baik R, Anthony S, et al.
Am J Physiol Gastrointest Liver Physiol
. 2016 Jul;
311(3):G423-30.
PMID: 27390324
Divalent metal-ion transporter-1 (DMT1), the principal mechanism by which nonheme iron is taken up at the intestinal brush border, is energized by the H(+)-electrochemical potential gradient. The provenance of the...
7.
Shawki A, Anthony S, Nose Y, Engevik M, Niespodzany E, Barrientos T, et al.
Am J Physiol Gastrointest Liver Physiol
. 2015 Aug;
309(8):G635-47.
PMID: 26294671
Divalent metal-ion transporter-1 (DMT1) is a widely expressed iron-preferring membrane-transport protein that serves a critical role in erythroid iron utilization. We have investigated its role in intestinal metal absorption by...
8.
Carvalho S, Barreira da Silva R, Shawki A, Castro H, Lamy M, Eide D, et al.
Mol Microbiol
. 2015 Feb;
96(3):581-95.
PMID: 25644708
Cellular zinc homeostasis ensures that the intracellular concentration of this element is kept within limits that enable its participation in critical physiological processes without exerting toxic effects. We report here...
9.
Mitchell C, Shawki A, Ganz T, Nemeth E, Mackenzie B
Am J Physiol Cell Physiol
. 2013 Dec;
306(5):C450-9.
PMID: 24304836
Iron homeostasis is achieved by regulating the intestinal absorption of the metal and its recycling by macrophages. Iron export from enterocytes or macrophages to blood plasma is thought to be...
10.
Shawki A, Knight P, Maliken B, Niespodzany E, Mackenzie B
Curr Top Membr
. 2012 Nov;
70:169-214.
PMID: 23177986
Divalent metal-ion transporter-1 (DMT1) is a widely expressed, iron-preferring membrane transport protein. Animal models establish that DMT1 plays indispensable roles in intestinal nonheme-iron absorption and iron acquisition by erythroid precursor...