Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 41 Records) |
Query Trace: SERPING1[original query] |
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Association of genetic polymorphisms and age-related macular degeneration in Chinese population. Investigative ophthalmology & visual science 2012 53 (7): 4262-9. Tian Jun, Yu Wenzhen, Qin Xueying, Fang Kai, Chen Qing, Hou Jing, Li Juan, Chen Dafang, Hu Yonghua, Li Xiaox |
Association of genetic polymorphisms with response to bevacizumab for neovascular age-related macular degeneration in the Chinese population. Pharmacogenomics 2012 May 13 (7): 779-87. Tian Jun, Qin Xueying, Fang Kai, Chen Qing, Hou Jing, Li Juan, Yu Wenzhen, Chen Dafang, Hu Yonghua, Li Xiaox |
Mutations analysis of C1 inhibitor coding sequence gene among Portuguese patients with hereditary angioedema. Molecular immunology 2013 Apr 53 (4): 431-4. Martinho A, Mendes J, Simões O, Nunes R, Gomes J, Dias Castro E, Leiria-Pinto P, Ferreira M B, Pereira C, Castel-Branco M G, Pais |
Association of CFH and SERPING1 polymorphisms with anterior uveitis. The British journal of ophthalmology 2013 Nov 97 (11): 1475-80. Yang Ming-ming, Lai Timothy Y Y, Tam Pancy O S, Chiang Sylvia W Y, Ng Tsz Kin, Rong Shi Song, Pang Chi P |
Relationship between SERPING1 rs2511989 polymorphism and age-related macular degeneration risk: a meta-analysis. Molecular vision 2014 20 1434-42. Ma Yan-Bo, Fu Shao-Ying, Ma Yan-Hua, Liu Hong-Li |
F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema. Allergy 2015 Aug . Speletas M, Szilágyi Á, Csuka D, Koutsostathis N, Psarros F, Moldovan D, Magerl M, Kompoti M, Varga L, Maurer M, Farkas H, Germenis A |
Association between SERPING1 rs2511989 polymorphism and age-related macular degeneration: Meta-analysis. International journal of ophthalmology 2015 8 (2): 385-94. Dong Yi, Li Ze-Dong, Fang Xin-Yu, Shi Xue-Feng, Chen Song, Tang X |
Ethnic differences in the association of SERPING1 with age-related macular degeneration and polypoidal choroidal vasculopathy. Scientific reports 2015 5 9424. Liu Ke, Lai Timothy Y Y, Ma Li, Lai Frank H P, Young Alvin L, Brelen Marten E, Tam Pancy O S, Pang Chi Pui, Chen Li J |
Discovery of coding genetic variants influencing diabetes-related serum biomarkers and their impact on risk of type 2 diabetes. The Journal of clinical endocrinology and metabolism 2015 Apr 100 (4): E664-71. Ahluwalia Tarunveer Singh, Allin Kristine Højgaard, Sandholt Camilla Helene, Sparsø Thomas Hempel, Jørgensen Marit Eika, Rowe Michael, Christensen Cramer, Brandslund Ivan, Lauritzen Torsten, Linneberg Allan, Husemoen Lise Lotte, Jørgensen Torben, Hansen Torben, Grarup Niels, Pedersen Ol |
Genetic Investigation of Complement Pathway Genes in Type 2 Diabetic Retinopathy: An Inflammatory Perspective. Mediators of inflammation 2016 2016 1313027. Yang Ming Ming, Wang Jun, Ren Hong, Sun Yun Duan, Fan Jiao Jie, Teng Yan, Li Yan |
Associations of the Polymorphisms in DHRS4, SERPING1, and APOR Genes with Postmortem pH in Berkshire Pigs. Animal biotechnology 2017 Oct 28 (4): 288-293. Hwang Jung Hye, An Sang Mi, Kwon Seul Gi, Park Da Hye, Kim Tae Wan, Kang Deok Gyung, Yu Go Eun, Kim Il-Suk, Park Hwa Chun, Ha Jeongim, Kim Chul Wo |
A hereditary angioedema screening on an index case: Turkey. Asian Pacific journal of allergy and immunology 2018 8 37 (3): 154-161. Ozkars Mehmet Yasar, Keskin Ozlem, Bayram Nazan, Keskin Mehmet, Bayram Hasan, Sahin Yavuz, Kucukosmanoglu Ercan, Attila Nurhan, Kirik Serkan Kir |
First Analysis of SERPING1 Gene in Patients with Hereditary Angioedema in Colombia Reveals Two Genotypic Variants in a Highly Symptomatic Individual. Journal of clinical immunology 2018 Apr . Rodríguez Jairo A, Narváez Carlos |
Exome sequencing in large, multiplex bipolar disorder families from Cuba. PloS one 2018 13 (10): e0205895. Maaser Anna, Forstner Andreas J, Strohmaier Jana, Hecker Julian, Ludwig Kerstin U, Sivalingam Sugirthan, Streit Fabian, Degenhardt Franziska, Witt Stephanie H, Reinbold Céline S, Koller Anna C, Raff Ruth, Heilmann-Heimbach Stefanie, Fischer Sascha B, , Herms Stefan, Hoffmann Per, Thiele Holger, Nürnberg Peter, Löhlein Fier Heide, Orozco-Díaz Guillermo, Carmenate-Naranjo Deinys, Proenza-Barzaga Niurka, Auburger Georg W J, Andlauer Till F M, Cichon Sven, Marcheco-Teruel Beatriz, Mors Ole, Rietschel Marcella, Nöthen Markus |
Evaluation of the association of C5 with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy. Eye and vision (London, England) 2019 11 6 34. Liu Ke, Ma Li, Lai Timothy Y Y, Brelen Marten E, Tam Pancy O S, Tham Clement C, Pang Chi Pui, Chen Li J |
A hereditary angioedema screening in two villages, based on an index case, and identification of a novel mutation, "1033G>T", at the SERPING1 gene. Postepy dermatologii i alergologii 2019 10 36 (4): 403-411. Ozkars Mehmet Yasar, Kesk?n Ozlem, Bayram Nazan, Onay Huseyin, Kesk?n Mehmet, Bayram Hasan, Sah?n Yavuz, Küçükosmano?lu Ercan, K?r?k Serk |
Angiotensin-Converting Enzyme Inhibitor-Associated Angioedema: From Bed to Bench. Journal of investigational allergology & clinical immunology 2019 10 30 (4): 272-280. Carucci L, Bova M, Petraroli A, Ferrara A L, Sutic A, de Crescenzo G, Cordisco G, Margaglione M, Gambardella J, Spadaro G, Genovese A, Loffredo |
Genetic Study of Hereditary Angioedema Type I and Type II (First Report from Iranian Patients: Describing Three New Mutations). Immunological investigations 2020 9 51 (1): 170-181. Nabilou Susan, Pak Fatemeh, Alizadeh Zahra, Fazlollahi Mohammad Reza, Houshmand Masoud, Ayazi Maryam, Mohammadzadeh Iraj, Bemanian Mohammad Hasan, Fayezi Abbas, Nabavi Mohammad, Saghafi Shiva, Mohammadian Sajedeh, Kokhaei Parviz, Moin Mostafa, Pourpak Zah |
A Comparative Analysis of the Lipoprotein(a) and Low-Density Lipoprotein Proteomic Profiles Combining Mass Spectrometry and Mendelian Randomization. CJC open 2021 5 3 (4): 450-459. Bourgeois Raphaëlle, Girard Arnaud, Perrot Nicolas, Guertin Jakie, Mitchell Patricia L, Couture Christian, Gotti Clarisse, Bourassa Sylvie, Poggio Paolo, Mass Elvira, Capoulade Romain, Scipione Corey A, Després Audrey-Anne, Couture Patrick, Droit Arnaud, Pibarot Philippe, Boffa Michael B, Thériault Sébastien, Koschinsky Marlys L, Mathieu Patrick, Arsenault Benoit |
CFH I62V as a Putative Genetic Marker for Posner-Schlossman Syndrome. Frontiers in immunology 2021 3 12 608723. Yang Ming Ming, Sun Hong Yan, Meng Ting, Qiu Shan Hu, Zeng Qi Qiao, Ng Tsz Kin, Jiang Li, Deng Ting Ming, Zeng Ai Neng, Wang Jun, Luo Xiao Li |
The effect of systemic levels of TNF-alpha and complement pathway activity on outcomes of VEGF inhibition in neovascular AMD. Eye (London, England) 2021 Nov . Khan Adnan H, Pierce Charles O, De Salvo Gabriella, Griffiths Helen, Nelson Marie, Cree Angela J, Menon Geeta, Lotery Andrew |
Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke.
Journal of the American Heart Association 2021 Oct e022482. Leskelä Jaakko, Toppila Iiro, Härma Mari-Anne, Palviainen Teemu, Salminen Aino, Sandholm Niina, Pietiäinen Milla, Kopra Elisa, Pais de Barros Jean-Paul, , Lassenius Mariann I, Kumar Anmol, Harjutsalo Valma, Roslund Kajsa, Forsblom Carol, Loukola Anu, Havulinna Aki S, Lagrost Laurent, Salomaa Veikko, Groop Per-Henrik, Perola Markus, Kaprio Jaakko, Lehto Markku, Pussinen Pirkko |
In Search of an Association Between Genotype and Phenotype in Hereditary Angioedema due to C1-INH Deficiency. Clinical reviews in allergy & immunology 2021 1 61 (1): 1-14. Loli-Ausejo David, López-Lera Alberto, Drouet Christian, Lluncor Marina, Phillips-Anglés Elsa, Pedrosa María, Cabañas Rosario, Caballero Tere |
Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema Genes. Frontiers in genetics 2022 8 13 914376. Mathey Carina M, Maj Carlo, Scheer Annika B, Fazaal Julia, Wedi Bettina, Wieczorek Dorothea, Amann Philipp M, Löffler Harald, Koch Lukas, Schöffl Clemens, Dickel Heinrich, Ganjuur Nomun, Hornung Thorsten, Forkel Susann, Greve Jens, Wurpts Gerda, Hallberg Pär, Bygum Anette, Von Buchwald Christian, Karawajczyk Malgorzata, Steffens Michael, Stingl Julia, Hoffmann Per, Heilmann-Heimbach Stefanie, Mangold Elisabeth, Ludwig Kerstin U, Rasmussen Eva R, Wadelius Mia, Sachs Bernhardt, Nöthen Markus M, Forstner Andreas |
Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE). Frontiers in allergy 2022 7 3 868185. Parsopoulou Faidra, Loules Gedeon, Zamanakou Maria, Csuka Dorottya, Szilagyi Agnes, Kompoti Maria, Porebski Grzegorz, Psarros Fotis, Magerl Markus, Valerieva Anna, Staevska Maria, Obtulowicz Krystyna, Maurer Marcus, Speletas Matthaios, Farkas Henriette, Germenis Anastasios |
Mutation update of SERPING1 related to hereditary angioedema in the Chinese population. Hereditas 2022 Jul 159 (1): 28. Wang Xue, Lei Shubin, Xu Yingyang, Liu Shuang, Zhi Yuxia |
High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis. Journal of personalized medicine 2022 10 12 (10): . Tesolin Paola, Bertinetto Francesca Eleonora, Sonaglia Arianna, Cappellani Stefania, Concas Maria Pina, Morgan Anna, Ferrero Norma Maria, Zabotti Alen, Gasparini Paolo, Amoroso Antonio, Quartuccio Luca, Girotto Giorg |
Systematic Approach Revealed SERPING1 Splicing-Affecting Variants to be Highly Represented in the Czech National HAE Cohort. Journal of clinical immunology 2023 8 . Hana Grombirikova, Viktor Bily, Premysl Soucek, Michal Kramarek, Roman Hakl, Lucie Ballonova, Barbora Ravcukova, Dita Ricna, Karolina Kozena, Lucie Kratochvilova, Marta Sobotkova, Radana Zachova, Pavel Kuklinek, Pavlina Kralickova, Irena Krcmova, Jana Hanzlikova, Martina Vachova, Olga Krystufkova, Eva Dankova, Milos Jesenak, Martina Novackova, Michal Svoboda, Jiri Litzman, Tomas Freiberg |
Screening for type II hereditary angioedema-the "poor man's c1-inhibitor function". The journal of allergy and clinical immunology. Global 2023 11 3 (1): 100179. Ankur Kumar Jindal, Valerie Chiang, Prabal Barman, Archan Sil, Sanchi Chawla, Elaine Y L Au, Amit Rawat, Philip H |
Occurrence of SARS-CoV-2 viremia is associated with genetic variants of genes related to COVID-19 pathogenesis. Frontiers in medicine 2023 10 10 1215246. Emilia Roy-Vallejo, Sara Fernández De Córdoba-Oñate, Pablo Delgado-Wicke, Ana Triguero-Martínez, Nuria Montes, Rosa Carracedo-Rodríguez, Nelly Zurita-Cruz, Ana Marcos-Jiménez, Amalia Lamana, José María Galván-Román, Gonzalo Villapalos García, Pablo Zubiaur, Marianela Ciudad, Laura Rabes, Marta Sanz, Carlos Rodríguez, Almudena Villa, Jesús Álvarez Rodríguez, Celeste Marcos, Julia Hernando, Paula Díaz-Fernández, Francisco Abad, Ignacio de Los Santos, Diego A Rodríguez Serrano, Rosario García-Vicuña, Carmen Suárez Fernández, Rosa P Gomariz, Cecilia Muñoz-Calleja, Elena Fernández-Ruiz, Isidoro González-Álvaro, Laura Cardeñoso, , Ana Barrios, Jesús Sanz, Pedro Casado, Ángela Gutiérrez, Azucena Bautista, Pilar Hernández, Nuria Ruiz Giménez, Berta Moyano, Paloma Gil, María Jesús Delgado, Pedro Parra, Beatriz Sánchez, Carmen Sáez, Marta Fernández Rico, Cristina Arévalo Román, Santos Castañeda, Irene Llorente, Eva G Tomero, Noelia García Castañeda, Miren Uriarte, Leticia Fontán García-Rodrigo, Diego Domingo García, Teresa Alarcón Cavero, María Auxiliadora Semiglia Chong, Ainhoa Gutiérrez Cobos, Francisco Sánchez-Madrid, Enrique Martín Gayo, Ildefonso Sánchez-Cerrillo, Pedro Martínez-Fleta, Celia López-Sanz, Ligia Gabrie, Luciana Del Campo Guerola, Reyes Tejedor, Julio Ancochea, Elena García Castillo, Elena Ávalos, Ana Sánchez-Azofra, Tamara Alonso, Carolina Cisneros, Claudia Valenzuela, Francisco Javier García Pérez, Rosa María Girón, Javier Aspa, Celeste Marcos, M Del Perpetuo Socorro Churruca, Enrique Zamora, Adrián Martínez, Mar Barrio Mayo, Rosalina Henares Espi, Rosa Méndez, David Arribas, Marta Chicot Llano, Begoña González, Begoña Quicios, Pablo Patiño, Marina Trigueros, Cristina Dominguez Peña, David Jiménez Jiménez, Pablo Villamayor, Alfonso Canabal, Rafael de la Cámara, Javier Ortiz, Isabel Iturra |
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- Page last updated:Apr 22, 2024
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