Raelson相关文献与解析，生知库 | 链接生命科学的每一步

Cheek, Lakota; Schmicker, Robert H; Crowe, Remle; Goren, Emily; West, Amanda; McMullan, Jason; Raelson, Colin; Poole, Jeanne; Adams, Karen; Hoering, Antje; Myers, Brent; Nichol, Graham

发表日期：2025

文献求助收藏

Highly Active Antiretroviral Therapy (HAART) - "Sulfonyl", and anal cancer outcomes from patients living with HIV: a retrospective cohort

高效抗逆转录病毒疗法（HAART）——“磺胺类”药物与艾滋病毒感染者肛门癌预后：一项回顾性队列研究

期刊:Infectious Agents and Cancer

影响因子:2.8

doi:10.1186/s13027-025-00666-y

Miranda, Raelson Rodrigues; Rocha, Erika Andrade; de Almeida Robatto, Amanda Acioli; Galhera, Denis Artico; Victor, Carolina Ribeiro; Imbrahim, Karim Yaqub; Moniz, Camila Motta Venchiarutti

Study Protocol: A Cross-Sectional Examination of Socio-Demographic and Ecological Determinants of Nutrition and Disease Across Madagascar

研究方案：马达加斯加营养与疾病的社会人口学和生态决定因素的横断面研究

期刊:Frontiers in Public Health

影响因子:3.4

doi:10.3389/fpubh.2020.00500

Golden, Christopher D; Rice, Benjamin L; Randriamady, Hervet J; Vonona, Arisoa Miadana; Randrianasolo, Jean Frederick; Tafangy, Ambinintsoa Nirina; Andrianantenaina, Mamy Yves; Arisco, Nicholas J; Emile, Gauthier N; Lainandrasana, Faustin; Mahonjolaza, Robuste Fenoarison Faraniaina; Raelson, Hermann Paratoaly; Rakotoarilalao, Vololoniaina Ravo; Rakotomalala, Anjaharinony Andry Ny Aina; Rasamison, Alex Dominique; Mahery, Rebaliha; Tantely, M Luciano; Girod, Romain; Annapragada, Akshaya; Wesolowski, Amy; Winter, Amy; Hartl, Daniel L; Hazen, James; Metcalf, C Jessica E

发表日期：2020

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A Variant in the Nicotinic Acetylcholine Receptor Alpha 3 Subunit Gene Is Associated With Hypertension Risks in Hypogonadic Patients

烟碱乙酰胆碱受体 α3 亚基基因变异与性腺功能低下患者的高血压风险相关

期刊:Frontiers in Genetics

影响因子:2.8

doi:10.3389/fgene.2020.539862

Tao Wu, Yujia Wang, Wei Shi, Bi-Qi Zhang, John Raelson, Yu-Mei Yao, Huan-Dong Wu, Zao-Xian Xu, Francois-Christophe Marois-Blanchet, Jonathan Ledoux, Rikard Blunck, Jian-Zhong Sheng, Shen-Jiang Hu, Hongyu Luo, Jiangping Wu

EPHA4 regulates vascular smooth muscle cell contractility and is a sex-specific hypertension risk gene in individuals with type 2 diabetes

EPHA4 调节血管平滑肌细胞收缩力，是 2 型糖尿病患者中性别特异性高血压风险基因

期刊:Journal of Hypertension

影响因子:3.3

doi:10.1097/HJH.0000000000001948

Zeqin Zhang, Johanne Tremblay, John Raelson, Tamar Sofer, Lizhong Du, Qiang Fang, Maria Argos, Francois-Christophe Marois-Blanchet, Yu Wang, Lingling Yan, John Chalmers, Mark Woodward, Stephen Harrap, Pavel Hamet, Hongyu Luo, Jiangping Wu

High-resolution melting for detecting KRAS mutations in colorectal cancer

高分辨率熔解检测结直肠癌中的 KRAS 突变

期刊:Biomedical Reports

影响因子:2.3

doi:10.3892/br.2019.1254

Raelson Rodrigues Miranda, Tiago Donizetti Silva, Nora Manoukian Forones

Analysis of the association of EPHB6, EFNB1 and EFNB3 variants with hypertension risks in males with hypogonadism

EPHB6、EFNB1 和 EFNB3 变异与男性性腺功能低下患者高血压风险的关联分析

期刊:Scientific Reports

影响因子:3.8

doi:10.1038/s41598-018-32836-x

Tao Wu, Bi-Qi Zhang, John Raelson, Yu-Mei Yao, Huan-Dong Wu, Zao-Xian Xu, Francois-Christophe Marois-Blanchet, Muhammad Ramzan Tahir, Yujia Wang, W Edward Bradley, Hongyu Luo, Jiangping Wu, Jian-Zhong Sheng, Shen-Jiang Hu

PROX1 gene CC genotype as a major determinant of early onset of type 2 diabetes in slavic study participants from Action in Diabetes and Vascular Disease: Preterax and Diamicron MR Controlled Evaluation study

PROX1基因CC基因型是斯拉夫研究参与者中2型糖尿病早期发病的主要决定因素（来自糖尿病和血管疾病行动：培哚普利和格列美脲缓释片对照评估研究）

期刊:Journal of Hypertension

影响因子:4.1

doi:10.1097/HJH.0000000000001241

Hamet, Pavel; Haloui, Mounsif; Harvey, François; Marois-Blanchet, François-Christophe; Sylvestre, Marie-Pierre; Tahir, Muhammad-Ramzan; Simon, Paul H G; Kanzki, Beatriz Sonja; Raelson, John; Long, Carole; Chalmers, John; Woodward, Mark; Marre, Michel; Harrap, Stephen; Tremblay, Johanne

Evidence from single nucleotide polymorphism analyses of ADVANCE study demonstrates EFNB3 as a hypertension risk gene

来自 ADVANCE 研究的单核苷酸多态性分析证据表明，EFNB3 是一个高血压风险基因。

期刊:Scientific Reports

影响因子:3.9

doi:10.1038/srep44114

Tremblay, Johanne; Wang, Yujia; Raelson, John; Marois-Blanchet, Francois-Christophe; Wu, Zenghui; Luo, Hongyu; Bradley, Edward; Chalmers, John; Woodward, Mark; Harrap, Stephen; Hamet, Pavel; Wu, Jiangping

Validating genetic markers of response to recombinant human growth hormone in children with growth hormone deficiency and Turner syndrome: the PREDICT validation study

验证生长激素缺乏症和特纳综合征患儿对重组人生长激素反应的遗传标记：PREDICT验证研究

期刊:European Journal of Endocrinology

影响因子:5.2

doi:10.1530/EJE-16-0357

Stevens, Adam; Murray, Philip; Wojcik, Jerome; Raelson, John; Koledova, Ekaterina; Chatelain, Pierre; Clayton, Peter

Rurality and Area Deprivation and Outcomes After Out-of-Hospital Cardiac Arrest

农村地区和贫困程度与院外心脏骤停后的预后

Highly Active Antiretroviral Therapy (HAART) - "Sulfonyl", and anal cancer outcomes from patients living with HIV: a retrospective cohort

高效抗逆转录病毒疗法（HAART）——“磺胺类”药物与艾滋病毒感染者肛门癌预后：一项回顾性队列研究

Study Protocol: A Cross-Sectional Examination of Socio-Demographic and Ecological Determinants of Nutrition and Disease Across Madagascar

研究方案：马达加斯加营养与疾病的社会人口学和生态决定因素的横断面研究

A Variant in the Nicotinic Acetylcholine Receptor Alpha 3 Subunit Gene Is Associated With Hypertension Risks in Hypogonadic Patients

烟碱乙酰胆碱受体 α3 亚基基因变异与性腺功能低下患者的高血压风险相关

EPHA4 regulates vascular smooth muscle cell contractility and is a sex-specific hypertension risk gene in individuals with type 2 diabetes

EPHA4 调节血管平滑肌细胞收缩力，是 2 型糖尿病患者中性别特异性高血压风险基因

High-resolution melting for detecting KRAS mutations in colorectal cancer

高分辨率熔解检测结直肠癌中的 KRAS 突变

Analysis of the association of EPHB6, EFNB1 and EFNB3 variants with hypertension risks in males with hypogonadism

EPHB6、EFNB1 和 EFNB3 变异与男性性腺功能低下患者高血压风险的关联分析

PROX1 gene CC genotype as a major determinant of early onset of type 2 diabetes in slavic study participants from Action in Diabetes and Vascular Disease: Preterax and Diamicron MR Controlled Evaluation study

PROX1基因CC基因型是斯拉夫研究参与者中2型糖尿病早期发病的主要决定因素（来自糖尿病和血管疾病行动：培哚普利和格列美脲缓释片对照评估研究）

Evidence from single nucleotide polymorphism analyses of ADVANCE study demonstrates EFNB3 as a hypertension risk gene

来自 ADVANCE 研究的单核苷酸多态性分析证据表明，EFNB3 是一个高血压风险基因。

Validating genetic markers of response to recombinant human growth hormone in children with growth hormone deficiency and Turner syndrome: the PREDICT validation study

验证生长激素缺乏症和特纳综合征患儿对重组人生长激素反应的遗传标记：PREDICT验证研究