Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 236 Records) |
| Query Trace: Disease and NOS3[original query] |
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| Genetic modulation of anemia severity, hemolysis level, and hospitalization rate in Angolan children with Sickle Cell Anemia. Molecular biology reports 2022 Sep . Germano Isabel, Santos Brígida, Delgadinho Mariana, Ginete Catarina, Lopes Pedro, Arez Ana Paula, Brito Miguel, Faustino Pau |
| The Association of PLAUR Genotype and Soluble suPAR Serum Level with COVID-19-Related Lung Damage Severity. International journal of molecular sciences 2022 12 23 (24): . Nekrasova Ludmila A, Shmakova Anna A, Samokhodskaya Larisa M, Kirillova Karina I, Stoyanova Simona S, Mershina Elena A, Nazarova Galina B, Rubina Kseniya A, Semina Ekaterina V, Kamalov Armais |
| Gene Sequencing Identifies Perturbation in Nitric Oxide Signaling as a Nonlipid Molecular Subtype of Coronary Artery Disease. Circulation. Genomic and precision medicine 2022 Oct 101161CIRCGEN121003598. Khera Amit V, Wang Minxian, Chaffin Mark, Emdin Connor A, Samani Nilesh J, Schunkert Heribert, Watkins Hugh, McPherson Ruth, Erdmann Jeanette, Elosua Roberto, Boerwinkle Eric, Ardissino Diego, Butterworth Adam S, Di Angelantonio Emanuele, Naheed Aliya, Danesh John, Chowdhury Rajiv, Krumholz Harlan M, Sheu Wayne H-H, Rich Stephen S, Rotter Jerome I, Chen Yii-der Ida, Gabriel Stacey, Lander Eric S, Saleheen Danish, Kathiresan Sek |
Stroke genetics informs drug discovery and risk prediction across ancestries.
Nature 2022 10 611 (7934): 115-123. Mishra Aniket, Malik Rainer, Hachiya Tsuyoshi, Jürgenson Tuuli, Namba Shinichi, Posner Daniel C, Kamanu Frederick K, Koido Masaru, Le Grand Quentin, Shi Mingyang, He Yunye, Georgakis Marios K, Caro Ilana, Krebs Kristi, Liaw Yi-Ching, Vaura Felix C, Lin Kuang, Winsvold Bendik Slagsvold, Srinivasasainagendra Vinodh, Parodi Livia, Bae Hee-Joon, Chauhan Ganesh, Chong Michael R, Tomppo Liisa, Akinyemi Rufus, Roshchupkin Gennady V, Habib Naomi, Jee Yon Ho, Thomassen Jesper Qvist, Abedi Vida, Cárcel-Márquez Jara, Nygaard Marianne, Leonard Hampton L, Yang Chaojie, Yonova-Doing Ekaterina, Knol Maria J, Lewis Adam J, Judy Renae L, Ago Tetsuro, Amouyel Philippe, Armstrong Nicole D, Bakker Mark K, Bartz Traci M, Bennett David A, Bis Joshua C, Bordes Constance, Børte Sigrid, Cain Anael, Ridker Paul M, Cho Kelly, Chen Zhengming, Cruchaga Carlos, Cole John W, de Jager Phil L, de Cid Rafael, Endres Matthias, Ferreira Leslie E, Geerlings Mirjam I, Gasca Natalie C, Gudnason Vilmundur, Hata Jun, He Jing, Heath Alicia K, Ho Yuk-Lam, Havulinna Aki S, Hopewell Jemma C, Hyacinth Hyacinth I, Inouye Michael, Jacob Mina A, Jeon Christina E, Jern Christina, Kamouchi Masahiro, Keene Keith L, Kitazono Takanari, Kittner Steven J, Konuma Takahiro, Kumar Amit, Lacaze Paul, Launer Lenore J, Lee Keon-Joo, Lepik Kaido, Li Jiang, Li Liming, Manichaikul Ani, Markus Hugh S, Marston Nicholas A, Meitinger Thomas, Mitchell Braxton D, Montellano Felipe A, Morisaki Takayuki, Mosley Thomas H, Nalls Mike A, Nordestgaard Børge G, O'Donnell Martin J, Okada Yukinori, Onland-Moret N Charlotte, Ovbiagele Bruce, Peters Annette, Psaty Bruce M, Rich Stephen S, Rosand Jonathan, Sabatine Marc S, Sacco Ralph L, Saleheen Danish, Sandset Else Charlotte, Salomaa Veikko, Sargurupremraj Muralidharan, Sasaki Makoto, Satizabal Claudia L, Schmidt Carsten O, Shimizu Atsushi, Smith Nicholas L, Sloane Kelly L, Sutoh Yoichi, Sun Yan V, Tanno Kozo, Tiedt Steffen, Tatlisumak Turgut, Torres-Aguila Nuria P, Tiwari Hemant K, Trégouët David-Alexandre, Trompet Stella, Tuladhar Anil Man, Tybjærg-Hansen Anne, van Vugt Marion, Vibo Riina, Verma Shefali S, Wiggins Kerri L, Wennberg Patrik, Woo Daniel, Wilson Peter W F, Xu Huichun, Yang Qiong, Yoon Kyungheon, , , , , , , , , , , , , , , , Millwood Iona Y, Gieger Christian, Ninomiya Toshiharu, Grabe Hans J, Jukema J Wouter, Rissanen Ina L, Strbian Daniel, Kim Young Jin, Chen Pei-Hsin, Mayerhofer Ernst, Howson Joanna M M, Irvin Marguerite R, Adams Hieab, Wassertheil-Smoller Sylvia, Christensen Kaare, Ikram Mohammad A, Rundek Tatjana, Worrall Bradford B, Lathrop G Mark, Riaz Moeen, Simonsick Eleanor M, Kõrv Janika, França Paulo H C, Zand Ramin, Prasad Kameshwar, Frikke-Schmidt Ruth, de Leeuw Frank-Erik, Liman Thomas, Haeusler Karl Georg, Ruigrok Ynte M, Heuschmann Peter Ulrich, Longstreth W T, Jung Keum Ji, Bastarache Lisa, Paré Guillaume, Damrauer Scott M, Chasman Daniel I, Rotter Jerome I, Anderson Christopher D, Zwart John-Anker, Niiranen Teemu J, Fornage Myriam, Liaw Yung-Po, Seshadri Sudha, Fernández-Cadenas Israel, Walters Robin G, Ruff Christian T, Owolabi Mayowa O, Huffman Jennifer E, Milani Lili, Kamatani Yoichiro, Dichgans Martin, Debette Stephan |
| The Role of Polymorphism in the Endothelial Homeostasis and Vitamin D Metabolism Genes in the Severity of Coronary Artery Disease. Biomedicines 2023 9 11 (9): . Anastasia Ponasenko, Anna Sinitskaya, Maxim Sinitsky, Maria Khutornaya, Olga Barbara |
| Analysis of endothelial gene polymorphisms in Spanish patients with vascular dementia and Alzheimer´s disease. Scientific reports 2023 8 13 (1): 13441. Raquel Manso-Calderón, Purificación Cacabelos-Pérez, M Dolores Sevillano-García, M Elisa Herrero-Prieto, Rogelio González-Sarmien |
| Glu298Asp variant of the endothelial nitric oxide synthase gene and acute coronary syndrome or premature coronary artery disease: A systematic review and meta-analysis. Nitric oxide : biology and chemistry 2023 7 138-139 85-95. Himanshu Rai, Sean Fitzgerald, J J Coughlan, Mark Spence, Roisin Colleran, Michael Joner, Robert A Byr |
| Whole-exome sequencing in moyamoya patients of Northern-European origin identifies gene variants involved in Nitric Oxide metabolism: A pilot study. Brain & spine 2023 6 3 101745. Markus K H Wiedmann, Ingunn V Steinsvåg, Tovy Dinh, Magnus D Vigeland, Pål G Larsson, Hanne Hjorthaug, Ying Sheng, Inger-Lise Mero, Kaja K Selm |
| Association between the Polymorphisms rs2070744, 4b/a and rs1799983 of the NOS3 Gene with Chronic Kidney Disease of Uncertain or Non-Traditional Etiology in Mexican Patients. Medicina (Kaunas, Lithuania) 2023 5 59 (5): . Alejandro Marín-Medina, José Juan Gómez-Ramos, Norberto Mendoza-Morales, Luis Eduardo Figuera-Villanue |
| Recent Progress in Genetics and Epigenetics Research on Diabetic Nephropathy in Malaysia. Journal of diabetes research 2023 5 2023 9053580. Norhashimah Abu Seman, Siti Haslina Othm |
| Protection against Ischemic Heart Disease: A Joint Role for eNOS and the K Channel. International journal of molecular sciences 2023 5 24 (9): . Paolo Severino, Andrea D'Amato, Massimo Mancone, Alberto Palazzuoli, Marco Valerio Mariani, Silvia Prosperi, Vincenzo Myftari, Carlo Lavalle, Giovanni Battista Forleo, Lucia Ilaria Birtolo, Viviana Caputo, Fabio Miraldi, Cristina Chimenti, Roberto Badagliacca, Viviana Maestrini, Raffaele Palmirotta, Carmine Dario Vizza, Francesco Fede |
| [Anthra-cycline-Induced Cardiotoxicity: the Role of Genetic Predictors]. Kardiologiia 2023 5 63 (4): 22-28. K V Kopeva, E V Grakova, S N Shilov, A A Popova, E N Berezikova, M N Neupokoeva, E T Ratushnyak, A T Teplyak |
| Effects of ADIPOQ and NOS3 SNPs/haplotypes on blood pressure control in patients with adherence to antihypertensive therapy. Pharmacogenomics 2023 4 . Cunha Warlley R, Agostini Lívia C, Dos Moreira Wellington Ms, M Teixeira Luiz Fernando, Vital Wendel C, da Silva Glenda N, Silva Nayara Nt, Luizon Marcelo R, Oliveira-Paula Gustavo H, Lima Angélica A, Belo Vanessa |
| Association of nitric oxide synthase gene polymorphism with asthma: A systematic review and meta-analysis. The clinical respiratory journal 2023 4 . Zeru Fan, Tao Liu, Wei |
| NOS3 (rs61722009) gene variants testing in prediction of COVID-19 pneumonia severity. Nitric oxide : biology and chemistry 2023 4 134-135 44-48. Fishchuk Liliia, Rossokha Zoia, Pokhylko Valeriy, Cherniavska Yuliia, Dubitska Olha, Vershyhora Viktoriia, Tsvirenko Svitlana, Kovtun Serhii, Gorovenko Natali |
| Whole-exome sequencing in searching for novel variants associated with the development of high altitude pulmonary edema. Gene 2023 3 870 147384. Chen Mingyue, Yi Faling, Qi Yijin, Zhao Beibei, Zhang Zhanhao, He Xue, Yuan Dongya, Jin Tian |
| Contribution of NOS3AS Variants to Susceptibility to Essential Hypertension: A Study in Kermanshah Province, Western Iran. Biochemical genetics 2023 3 . Karami Bahareh, Azimi Azam, Rahimi Zohreh, Mahmoudi Sousan, Jalilian Nazan |
| PREDICTING THE OCCURRENCE OF PRIMARY OPEN-ANGLE GLAUCOMA DEPENDING ON THE GENETIC POLYMORPHISM ENDOTHELIAL NO SYNTHASE (NOS3) GENE. Wiadomosci lekarskie (Warsaw, Poland : 1960) 2023 2 75 (12): 3087-3093. Isaiev Oleksii, Serdiuk Valerii, Ziablitsev Den |
| Association between NOS3 gene polymorphisms and genetic susceptibility to congenital heart Disease: A systematic review and meta-analysis. Cytokine 2023 11 173 156415. Kang Yi, Wei Wang, Xin Zhang, Xin Dong, Zhengye Fan, Yuhu Ma, Jie Gao, Xinyao Li, Tao Y |
| Genetic Modulation of HPV Infection and Cervical Lesions: Role of Oxidative Stress-Related Genes. Antioxidants (Basel, Switzerland) 2023 10 12 (10): . Ângela Inácio, Laura Aguiar, Beatriz Rodrigues, Patrícia Pires, Joana Ferreira, Andreia Matos, Inês Mendonça, Raquel Rosa, Manuel Bicho, Rui Medeiros, Maria Clara Bic |
| Matrix Gla Protein and Nitric Oxide Synthase-3 Genetic Variants in Chronic Kidney Disease and Their Relation with Cardiovascular Risk. International journal of nephrology 2024 9 2024 3850055. G Priyadarshini, Sreejith Parameswaran, Jayaprakash Sahoo, Sandhiya Selvarajan, Ananthakrishnan Ramesh, Medha Rajap |
| Nitric Oxide Synthase 3 Gene Polymorphisms and Their Association with Acute Myocardial Infarction and Chronic Stable Angina: A Case-Control Study from Northern India. International journal of applied & basic medical research 2024 9 14 (3): 174-181. Sunil Kumar, Deepak Juyal, Arun Pandey, Preeti Tomar, Vinay Sagar, Rakesh Yadav, Renu Saxe |
| Mitochondrial related variants associated with cardiovascular traits. Frontiers in physiology 2024 9 15 1395371. Marisa Cañadas-Garre, Joaquín J Maqueda, Blanca Baños-Jaime, Claire Hill, Ryan Skelly, Ruaidhri Cappa, Eoin Brennan, Ross Doyle, Catherine Godson, Alexander P Maxwell, Amy Jayne McKnig |
| The promoter polymorphism rs3918226 of endothelial nitric oxide synthase gene as a novel susceptibility marker for peripheral artery disease. Annals of vascular surgery 2024 7 . Sergey Zhabin, Victor Lazarenko, Iulia Azarova, Elena Klyosova, Daniil Bashkatov, Stanislav Kononov, Maxim Dolgintsev, Mikhail Churnosov, Maria Solodilova, Alexey Polonik |
| PTPRD gene variant rs10739150: A potential game-changer in hypertension diagnosis. PloS one 2024 6 19 (6): e0304950. Laith Al-Eit |
| Interaction between Caffeine Consumption & Genetic susceptibility in Parkinson's disease: a systematic review. Ageing research reviews 2024 6 102381. Yujuan Yang, Zhi-Dong Zhou, Ling Xiao Yi, Brendan Jen-Wei Tan, Eng-King T |
| Genetic Screening of Patients with Sporadic Alzheimer's Disease and Frontotemporal Lobar Degeneration in the Chinese Population. Journal of Alzheimer's disease : JAD 2024 5 . Yaoru Li, Ziying Yang, Yanxin Zhang, Fang Liu, Jing Xu, Yaping Meng, Gebeili Xing, Xuqin Ruan, Jun Sun, Nan Zha |
| Sex-Specific Susceptibility Loci Associated With Coronary Artery Aneurysms in Patients With Kawasaki Disease. Korean circulation journal 2024 5 . Jae-Jung Kim, Young Mi Hong, Sin Weon Yun, Kyung-Yil Lee, Kyung Lim Yoon, Myung-Ki Han, Gi Beom Kim, Hong-Ryang Kil, Min Seob Song, Hyoung Doo Lee, Kee Soo Ha, Hyun Ok Jun, Jeong Jin Yu, Gi Young Jang, Jong-Keuk Lee, |
| Leiomyoma and the importance of genetic variation on genes related to the vasculature system - C?S, MTHFR, NOS3, CYBA, and ACE1. European journal of obstetrics, gynecology, and reproductive biology 2024 1 294 65-70. Ângela Inácio, Laura Aguiar, Beatriz Rodrigues, Patrícia Pires, Joana Ferreira, Tiago Bilhim, João Pisco, Manuel Bicho, Maria Clara Bic |
| Identifying genetic susceptibility loci associated with human coronary artery disease. PloS one 2025 1 20 (1): e0315460. Aqsa Zahid, Andleeb Batool, Abdul Wajid, Yurong Wu, Chun Liang, Muhammad Ajmal Khan, Amin Ullah, Kashif Iqbal Sahibzada, Hong X |
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