Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Evan Hermann"'
Autor:
Thais Oliveira, Evan Hermann, Daniel Lin, Winyoo Chowanadisai, Elizabeth Hull, McKale Montgomery
Publikováno v:
Redox Biology, Vol 47, Iss , Pp 102149- (2021)
Epithelial-to-mesenchymal transition (EMT) is an essential mechanism for development and wound healing, but in cancer it also mediates the progression and spread of aggressive tumors while increasing therapeutic resistance. Adoption of a mesenchymal
Externí odkaz:
https://doaj.org/article/cd005d5810d04c55a134738595db0e0b
Autor:
John Ice, Brenda J. Smith, Winyoo Chowanadisai, Amritpal Kaur, Evan Hermann, Edralin A. Lucas, Sanmi Alake, Dingbo Lin, Babajide Ojo
Publikováno v:
Curr Dev Nutr
OBJECTIVES: The anti-inflammatory cytokine, IL-10, plays an important role in reducing the risk of many inflammatory diseases. This study investigated the time and sex effects of IL-10 gene deletion on metabolic risk factors that contribute to the de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::006b57b493d7cfdd9e2d6da1d35eaf45
https://europepmc.org/articles/PMC8181497/
https://europepmc.org/articles/PMC8181497/
Autor:
Mckale Montgomery, Winyoo Chowanadisai, Emily Chambers, Evan Hermann, Danielle N. Davis, Dingbo Lin
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 12 (2021)
Frontiers in Genetics, Vol 12 (2021)
The SLC39A8 gene encodes a divalent metal transporter, ZIP8. SLC39A8 is associated with pleiotropic effects across multiple tissues, including the brain. We determine the different brain magnetic resonance imaging (MRI) phenotypes associated with SLC
Autor:
Laurie R. Thompson, Stephen L. Clarke, Winyoo Chowanadisai, Thais Oliveira, Evan Hermann, Mckale Montgomery
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 6751, p 6751 (2020)
International Journal of Molecular Sciences
Volume 21
Issue 18
International Journal of Molecular Sciences
Volume 21
Issue 18
The tumor suppressor gene TP53 is the most commonly mutated gene in human cancer. In addition to loss of tumor suppressor functions, mutations in TP53 promote cancer progression by altering cellular iron acquisition and metabolism. A newly identified
Autor:
Mckale Montgomery, Evan Hermann, Thais Oliveira, Stephen L. Clarke, Laurie R. Thompson, Winyoo Chowanadisai
Publikováno v:
Curr Dev Nutr
OBJECTIVES: The tumor suppressor gene TP53 is the most commonly mutated gene in human cancer, but mutations in TP53 do not just result in loss of tumor suppressor function, they can also promote cancer progression by altering cellular iron acquisitio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acf031bb71ecfbddeacc41e225d6d237
https://europepmc.org/articles/PMC7258668/
https://europepmc.org/articles/PMC7258668/
Publikováno v:
Cancer Research. 81:2006-2006
The essentiality of iron for cell growth and proliferation, coupled with its capacity to promote damaging free radical production, has made it a desirable target for cancer treatment and prevention. One such approach may be through the activation of
Autor:
Tizazu Tilla, Edralin A. Lucas, Brenda J. Smith, Dawd Gashu, Sanmi Alake, Evan Hermann, Amritpal Kaur, Levin Dotimas
Publikováno v:
Curr Dev Nutr
OBJECTIVES: This study evaluated whether wheat germ (WG) alone or in combination with antibiotics (Ab) will ameliorate metabolic and gut integrity and inflammatory markers in mice fed a Western diet (WD). METHODS: Six-wk-old male C57BL/6 mice were ra
Publikováno v:
Curr Dev Nutr
OBJECTIVES: The SLC39A8 gene encodes a divalent metal transporter, ZIP8. ZIP8 polymorphisms are associated with pleiotropic effects including altered risks for schizophrenia. Our objective is to determine the different brain MRI phenotypes associated
Autor:
Evan Hermann, Danielle N. Davis, Edralin A. Lucas, Mckale Montgomery, Winyoo Chowanadisai, Emily Chambers
Publikováno v:
Curr Dev Nutr
OBJECTIVES: Impaired metal homeostasis in the brain has been reported in neurodegenerative diseases such as Alzheimer's Disease and Parkinson's Disease and can be detected using magnetic resonance imaging (MRI). Many factors, including genetics, affe