Zobrazeno 1 - 10
of 948
pro vyhledávání: '"GUCY1A3"'
Autor:
Parham Nejati, Saba Naseri, Maryam Eini, Reza Alibakhshi, Sousan Mahmoudi, Lida Haghnazari, Nazanin Jalilian
Publikováno v:
Journal of Mazandaran University of Medical Sciences, Vol 33, Iss 219, Pp 16-26 (2023)
Background and purpose: Hypertension is a global health challenge due to its high prevalence and increased risk of cardiovascular disease. It is a multifactorial disease in which both genetic and environmental factors are involved. So far, a number o
Externí odkaz:
https://doaj.org/article/f7de717c883b498dafdc72c3666ff1d1
Publikováno v:
Lipids in Health and Disease, Vol 18, Iss 1, Pp 1-6 (2019)
Abstract Background Previous genome-wide association studies have found two single nucleotide polymorphisms (SNP) rs7692387 and rs1842896 located on or near the GUCY1A3 gene were associated with coronary artery disease (CAD). GUCY1A3 was considered t
Externí odkaz:
https://doaj.org/article/102fade90d1548f7be355c5a3ec34377
Autor:
Virgile Clergue-Duval, Louise Nicolas-Sacy, Emily Karsinti, El-Hadi Zerdazi, Jean-Louis Laplanche, Georges Brousse, Andries T. Marees, Eske M. Derks, Patrick Henry, Frank Bellivier, Florence Vorspan, Vanessa Bloch
Publikováno v:
Frontiers in Psychiatry, Vol 12 (2021)
Introduction: Cocaine users often present with repetitive events of cocaine-associated chest pain (CACP), clinically resembling acute coronary syndromes. The aim of the study is to describe the specific risk factors for CACP.Method: Cocaine users (n
Externí odkaz:
https://doaj.org/article/9c368532da6647569cd61595225fb281
Autor:
Yohei Mineharu, Susumu Miyamoto
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Moyamoya disease is an idiopathic chronically progressive cerebrovascular disease, which causes both ischemic and hemorrhagic stroke. Genetic studies identified RNF213/Mysterin and GUCY1A3 as disease-causing genes. They were also known to be associat
Externí odkaz:
https://doaj.org/article/5be143b18b624796bb9f80a2d1a734fc
Autor:
Krishan K. Vishnolia, Aleksandar Rakovic, Celine Hoene, Karim Tarhbalouti, Zouhair Aherrahrou, Jeanette Erdmann
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Soluble guanylyl cyclase (sGC) protein is a heterodimer formed by two subunits encoded by GUCY1A1 and GUCY1B1 genes. The chromosomal locus 4q32.1 harbors both of these genes, which has been previously significantly associated with coronary artery dis
Externí odkaz:
https://doaj.org/article/6e8ae3b21bcb401097c3a34b8dd6e473
Akademický článek
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Akademický článek
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Publikováno v:
BMC Complementary Medicine and Therapies, Vol 20, Iss 1, Pp 1-12 (2020)
BMC Complementary Medicine and Therapies
BMC Complementary Medicine and Therapies
Background The tanshinones and phenolic acids in Salvia miltiorrhiza (also named Danshen) have been confirmed for the treatment of coronary heart disease (CHD), but the action mechanisms remain elusive. Methods In the current study, the co-expression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9920caa8c886394efdab8ee904a07560
https://doaj.org/article/32831bba74554755be62137e1ed1d63d
https://doaj.org/article/32831bba74554755be62137e1ed1d63d
Publikováno v:
Lipids in Health and Disease, Vol 18, Iss 1, Pp 1-6 (2019)
Lipids in Health and Disease
Lipids in Health and Disease
Background Previous genome-wide association studies have found two single nucleotide polymorphisms (SNP) rs7692387 and rs1842896 located on or near the GUCY1A3 gene were associated with coronary artery disease (CAD). GUCY1A3 was considered to be invo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ed6d38c07f0a25c7dc52509b2af6781
https://doaj.org/article/102fade90d1548f7be355c5a3ec34377
https://doaj.org/article/102fade90d1548f7be355c5a3ec34377
Autor:
Susumu Miyamoto, Yohei Mineharu
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Frontiers in Neurology
Frontiers in Neurology
Moyamoya disease is an idiopathic chronically progressive cerebrovascular disease, which causes both ischemic and hemorrhagic stroke. Genetic studies identified RNF213/Mysterin and GUCY1A3 as disease-causing genes. They were also known to be associat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::352d627933b762bcedaa2481b9672d60
https://doi.org/10.3389/fneur.2021.687088
https://doi.org/10.3389/fneur.2021.687088