Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: CFD[original query] |
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Lack of association of CFD polymorphisms with advanced age-related macular degeneration. Molecular vision 2010 16 2273-8. Zeng Jiexi, Chen Yuhong, Tong Zongzhong, Zhou Xinrong, Zhao Chao, Wang Kevin, Hughes Guy, Kasuga Daniel, Bedell Matthew, Lee Clara, Ferreyra Henry, Kozak Igor, Haw Weldon, Guan Jean, Shaw Robert, Stevenson William, Weishaar Paul D, Nelson Mark H, Tang Luosheng, Zhang Ka |
Coding polymorphisms in the genes of the alternative complement pathway and abdominal aortic aneurysm. International journal of immunogenetics 2011 Jun 38 (3): 243-8. Bradley D T, Badger S A, Bown M J, Sayers R D, Hughes A |
Complement factor D in age-related macular degeneration. Investigative ophthalmology & visual science 2011 52 (12): 8828-34. Stanton Chloe M, Yates John R W, den Hollander Anneke I, Seddon Johanna M, Swaroop Anand, Stambolian Dwight, Fauser Sascha, Hoyng Carel, Yu Yi, Atsuhiro Kanda, Branham Kari, Othman Mohammad, Chen Wei, Kortvely Elod, Chalmers Kevin, Hayward Caroline, Moore Anthony T, Dhillon Baljean, Ueffing Marius, Wright Alan |
Associating genetic variation at Perilipin 1, Complement Factor D and Adiponectin loci to the bone health status in North Indian population. Gene 2017 Feb . Sandhu Harkirat Singh, Puri Sanjeev, Sharma Rubina, Sokhi Jasmine, Singh Gagandeep, Matharoo Kawaljit, Bhanwer A |
Genetic risk factors for late age-related macular degeneration in India. The British journal of ophthalmology 2017 Dec . Rajendran Anand, Dhoble Pankaja, Sundaresan Periasamy, Saravanan Vijayan, Vashist Praveen, Nitsch Dorothea, Smeeth Liam, Chakravarthy Usha, Ravindran Ravilla D, Fletcher Astrid |
Mutational Epidemiology of Congenital Fibrinogen Disorders. Thrombosis and haemostasis 2018 10 118 (11): 1867-1874. Casini Alessandro, Blondon Marc, Tintillier Veronique, Goodyer Matthew, Sezgin Melike E, Gunes Adalet M, Hanss Michel, de Moerloose Philippe, Neerman-Arbez Margueri |
Association of Complement Factor D and H Polymorphisms with Recurrent Pregnancy Loss. International journal of molecular sciences 2019 12 21 (1): . Cho Hee Young, Park Han Sung, Ko Eun Ju, Ryu Chang Soo, Kim Jung Oh, Kim Young Ran, Ahn Eun Hee, Lee Woo Sik, Kim Nam Ke |
Properdin Modulates Complement Component Production in Stressed Human Primary Retinal Pigment Epithelium Cells. Antioxidants (Basel, Switzerland) 2020 8 9 (9): . Schäfer Nicole, Wolf Hannah N, Enzbrenner Anne, Schikora Juliane, Reichenthaler Maria, Enzmann Volker, Pauly Dia |
Effect of Gene-Based Warfarin Dosing on Anticoagulation Control and Clinical Events in a Real-World Setting. Frontiers in pharmacology 2020 2 10 1527. Zhang Jinhua, Wu Tingting, Chen Wenjun, Fu Jinglan, Xia Xiaotong, Chen Liangw |
Clinical and molecular characterization of Iranian patients with congenital fibrinogen disorders. Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis 2021 7 60 (6): 103203. Mohsenian Samin, Seidizadeh Omid, Mirakhorli Mojgan, Jazebi Mohammad, Azarkeivan Azi |
Whole Blood Thromboelastometry by ROTEM and Thrombin Generation by Genesia According to the Genotype and Clinical Phenotype in Congenital Fibrinogen Disorders. International journal of molecular sciences 2021 3 22 (5): . Szanto Timea, Lassila Riitta, Lemponen Marja, Lehtinen Elina, Neerman-Arbez Marguerite, Casini Alessand |
Targeted Genotyping of MIS-C Patients Reveals a Potential Alternative Pathway Mediated Complement Dysregulation during COVID-19 Infection. Current issues in molecular biology 2022 7 44 (7): 2811-2824. Gavriilaki Eleni, Tsiftsoglou Stefanos A, Touloumenidou Tasoula, Farmaki Evangelia, Panagopoulou Paraskevi, Michailidou Elissavet, Koravou Evaggelia-Evdoxia, Mavrikou Ioulia, Iosifidis Elias, Tsiatsiou Olga, Papadimitriou Eleni, Papadopoulou-Alataki Efimia, Papayanni Penelope Georgia, Varelas Christos, Kokkoris Styliani, Papalexandri Apostolia, Fotoulaki Maria, Galli-Tsinopoulou Assimina, Zafeiriou Dimitrios, Roilides Emmanuel, Sakellari Ioanna, Anagnostopoulos Achilles, Tragiannidis Athanasi |
Folic acid inhibits 5-methyltetrahydrofolate transport across the blood-cerebrospinal fluid barrier: Clinical biochemical data from two cases. JIMD reports 2022 11 63 (6): 529-535. Akiyama Tomoyuki, Kuki Ichiro, Kim Kiyohiro, Yamamoto Naohiro, Yamada Yumi, Igarashi Kazuya, Ishihara Tomohiko, Hatano Yuya, Kobayashi Katsuhi |
Targeted genotyping of COVID-19 patients reveals a signature of complement C3 and factor B coding SNPs associated with severe infection. Immunobiology 2023 2 228 (2): 152351. Tsiftsoglou Stefanos A, Gavriilaki Eleni, Touloumenidou Tasoula, Koravou Evaggelia-Evdoxia, Koutra Maria, Papayanni Penelope Georgia, Karali Vassiliki, Papalexandri Apostolia, Varelas Christos, Chatzopoulou Fani, Chatzidimitriou Maria, Chatzidimitriou Dimitrios, Veleni Anastasia, Rapti Evdoxia, Kioumis Ioannis, Kaimakamis Evaggelos, Bitzani Milly, Boumpas Dimitrios T, Tsantes Argyris, Sotiropoulos Damianos, Papadopoulou Anastasia, Sakellari Ioanna, Kokoris Styliani, Anagnostopoulos Achill |
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- Page last updated:Apr 16, 2024
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