Zobrazeno 1 - 10
of 41
pro vyhledávání: '"HMOX2"'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Jane I. Khudyakov, Elizabeth R. Piotrowski, Anna D. Keith, José Pablo Vázquez-Medina, Michael S. Tift, Anna B. Pearson, Daniel E. Crocker
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Frontiers in Physiology
Frontiers in Physiology
Marine mammals such as northern elephant seals (NES) routinely experience hypoxemia and ischemia-reperfusion events to many tissues during deep dives with no apparent adverse effects. Adaptations to diving include increased antioxidants and elevated
Ability to tolerate low salinity is a key factor affecting the distribution of the Chinese shrimp (Fenneropenaeus chinensis). Although previous studies have investigated the mechanisms underlying adaptations to low salinity in some crustaceans, littl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::234232786ad5af6a4420cd9984354a14
https://doi.org/10.1101/2020.11.12.379511
https://doi.org/10.1101/2020.11.12.379511
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 19
International Journal of Molecular Sciences, Vol 21, Iss 7123, p 7123 (2020)
Volume 21
Issue 19
International Journal of Molecular Sciences, Vol 21, Iss 7123, p 7123 (2020)
Heme oxygenase (HO) consists of inducible (HO-1) and constitutive (HO-2) isoforms that are encoded by Hmox1 and Hmox2 genes, respectively. As an anti-inflammatory and antioxidant molecule, HO participates in the development of metabolic diseases. Whe
Autor:
Sijia Tian, Jinhua Zheng, Xinglong Yang, Quanzhen Zhao, Ran An, Yanming Xu, Hongyan Huang, Yalan Chen
Publikováno v:
Neuroscience Letters. 642:119-122
Studies have reported conflicting results about possible associations between variants in heme oxygenase ( HMOX ) genes and risk of Parkinson’s disease (PD) in Caucasians, and little is known about these associations in Asians. We genotyped the sin
Autor:
Hyung-Ho Ha, Sungjin Park, Jungyeol Lee, Xiao Liu, Nam-Young Kang, Jong-Jin Kim, Seong Soon Kim, Zhenxun Wang, Lu Wang, Haw-Young Kwon, Yong-An Lee, So Young Choi, Seong Cheol Hong, Animesh Samanta, Myung Ae Bae, Young Hyun Yu, Wai Leong Tam, Jun-Seok Lee, Young-Tae Chang, Junyoung Kim, Bing Lim, Jia Hui Jane Lee, Beomsue Kim, Dongdong Su
Publikováno v:
Journal of the American Chemical Society
Tumor initiating cells (TIC) are resistant to conventional anticancer therapy and associated with metastasis and relapse in cancer. Although various TIC markers and their antibodies have been proposed, it is limited to the use of antibodies for in vi
Publikováno v:
European neurology. 81(1-2)
Backgrounds: Several recent case-control studies have suggested some candidate genes being responsible for causing the restless legs syndrome (RLS). However, the association between those genes and the risk for RLS among the Asian population has not
Publikováno v:
The FASEB Journal. 32
Autor:
Anna Sklodowska, Daniel Wysokinski, Jerzy Szaflik, Marta Chmielewska, Jacek P. Szaflik, Malgorzata Zaras, Katarzyna Wozniak, Janusz Blasiak, Ewelina Synowiec
Publikováno v:
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
Scopus-Elsevier
Scopus-Elsevier
Summary Background Age-related macular degeneration (AMD) is a primary cause of blindness among the elderly in developed countries. The nature of AMD is complex and includes both environmental and hereditary factors. Oxidative stress is thought to be
Autor:
Pedro Ayuso, Sara Ortega-Cubero, Pau Pastor, Elena García-Martín, Hortensia Alonso-Navarro, José A. G. Agúndez, Julián Benito-León, Tomás López-Alburquerque, Félix Javier Jiménez-Jiménez, Gara Esguevillas
Publikováno v:
European journal of clinical investigation. 47(5)
BACKGROUND Several reports found a relationship between increased serum lead levels and the risk for essential tremor (ET), especially in carriers of the minor allele of the single nucleotide polymorphism (SNP) rs1800435 in the aminolevulinate dehydr