Zobrazeno 1 - 10
of 45
pro vyhledávání: '"EPAS1 Gene"'
Autor:
Jade P. Marrow, Razan Alshamali, Brittany A. Edgett, Melissa A. Allwood, Kyla L. S. Cochrane, Sara Al-Sabbag, Anmar Ayoub, Kjetil Ask, Gregory M. T. Hare, Keith R. Brunt, Jeremy A. Simpson
Publikováno v:
Frontiers in Physiology, Vol 15 (2024)
Erythropoietin (EPO) exerts non-canonical roles beyond erythropoiesis that are developmentally, structurally, and physiologically relevant for the heart as a paracrine factor. The role for paracrine EPO signalling and cellular crosstalk in the adult
Externí odkaz:
https://doaj.org/article/6990942d25af46f7b4676d92858673c8
Autor:
Narongsak Nakwan, Surakameth Mahasirimongkol, Nusara Satproedprai, Tassamonwan Chaiyasung, Punna Kunhapan, Cheep Charoenlap, Kamonnut Singkhamanan, Chariyawan Charalsawadi
Publikováno v:
Jornal de Pediatria, Vol 98, Iss 4, Pp 383-389 (2022)
Objective: To explore possible genes related to the development of persistent pulmonary hypertension of the newborn (PPHN). Methods: The authors identified 285 single nucleotide polymorphisms (SNPs) of 11 candidate genes (BMPR2, EPAS1, PDE3A, VEGFA,
Externí odkaz:
https://doaj.org/article/7fdd30fb30de4594ad41ea01c3096055
Akademický článek
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Publikováno v:
Journal of Integrative Agriculture, Vol 14, Iss 4, Pp 741-748 (2015)
Endothelial PAS domain protein 1 gene (EPAS1) is a key transcription factor that activates the expression of oxygen-regulated genes. In this study, in order to better understand the effects of EPAS1 gene on hematologic parameters in yak, we firstly q
Externí odkaz:
https://doaj.org/article/1a07db6a0a344672af004514b7021366
Autor:
Surakameth Mahasirimongkol, Kamonnut Singkhamanan, Nusara Satproedprai, Chariyawan Charalsawadi, Punna Kunhapan, Narongsak Nakwan, Cheep Charoenlap, Tassamonwan Chaiyasung
Publikováno v:
Jornal de Pediatria v.98 n.4 2022
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Jornal de Pediatria, Volume: 98, Issue: 4, Pages: 383-389, Published: 25 JUL 2022
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Jornal de Pediatria, Volume: 98, Issue: 4, Pages: 383-389, Published: 25 JUL 2022
Objective: To explore possible genes related to the development of persistent pulmonary hypertension of the newborn (PPHN). Methods: The authors identified 285 single nucleotide polymorphisms (SNPs) of 11 candidate genes (BMPR2, EPAS1, PDE3A, VEGFA,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afb7f310a119585fc9844d75b7f2edb4
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572022000400383
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572022000400383
Publikováno v:
Journal of Integrative Agriculture, Vol 13, Iss 9, Pp 1990-1998 (2014)
Endothelial PAS domain protein 1 (EPAS1), also called hypoxia-inducible factor-2, is a key regulatory factor of hypoxic responses and plays an essential role in high-altitude adaptation in mammalian species. In this study, polymorphisms of EPAS1 were
Externí odkaz:
https://doaj.org/article/a79b36c95c6f4f0e88f1f518254e990f
Publikováno v:
Genes, vol. 12, no. 11, 1793, 2021.
Genes
Volume 12
Issue 11
Genes, Vol 12, Iss 1793, p 1793 (2021)
Genes
Volume 12
Issue 11
Genes, Vol 12, Iss 1793, p 1793 (2021)
Endothelial PAS domain-containing protein 1 (EPAS1), also HIF2α, is an alpha subunit of hypoxia-inducible transcription factor (HIF), which mediates cellular and systemic response to hypoxia. EPAS1 has an important role in the transcription of many
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::744d88cccb201763b8ef43619d22284b
https://repozitorij.uni-lj.si/IzpisGradiva.php?id=133323
https://repozitorij.uni-lj.si/IzpisGradiva.php?id=133323
Autor:
Hyun Guy Kang, Yi Jun Kim, Kyoung Min Lee, Yongsik Cho, Jin-Hong Kim, Moon Jong Chang, Chong Bum Chang, Donghyeon Cheon, Hyeon Seop Kim, Hyeonkyeong Kim, Donghyun Kang, Seung Baik Kang
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-16 (2020)
Nature Communications
Nature Communications
Chondrosarcomas, malignant cartilaginous neoplasms, are capable of transitioning to highly aggressive, metastatic, and treatment-refractory states, resulting in significant patient mortality. Here, we aim to uncover the transcriptional program direct
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Publikováno v:
European Journal of Haematology. 103:287-299
Familial erythrocytosis (FE) is a congenital disorder, defined by elevated red blood cell number, hemoglobin, and hematocrit. Among eight types of FE, type 4 is caused by variants in the EPAS1 gene. Two other hypoxia-inducible factor alpha (HIFA) sub