Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 33 Records) |
Query Trace: Syndrome and MBL2[original query] |
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Mannose-binding lectin genotypes and pre-eclampsia: a case-control study. Human immunology 2007 Nov 68 (11): 888-93. van de Geijn Fleur E, Dolhain Radboud J E M, van Rijs Wouter, Hazes Johanna M W, de Groot Christianne J |
Detrimental effects of mannose-binding lectin (MBL2) promoter genotype XA/XA on HIV-1 vertical transmission and AIDS progression. The Journal of infectious diseases 2008 Sep 198 (5): 694-700. Mangano A, Rocco C, Marino S M, Mecikovsky D, Genre F, Aulicino P, Bologna R, Sen |
Mannose-binding lectin and mannose-binding lectin-associated serine protease 2 in susceptibility, severity, and outcome of pneumonia in adults. The Journal of allergy and clinical immunology 2008 Aug 122 (2): 368-74, 374.e1-2. Garcia-Laorden M Isabel, Sole-Violan Jordi, Rodriguez de Castro Felipe, Aspa Javier, Briones M Luisa, Garcia-Saavedra Ayoze, Rajas Olga, Blanquer Jose, Caballero-Hidalgo Araceli, Marcos-Ramos J Alberto, Hernandez-Lopez Javier, Rodriguez-Gallego Carl |
Association between donor MBL promoter haplotype and graft survival and the development of BOS after lung transplantation. Transplantation 2008 Dec 86 (12): 1857-63. Munster Janna M, van der Bij Wim, Breukink Myrte B, van der Steege Gerrit, Zuurman Mike W, Hepkema Bouke G, Verschuuren Erik A M, van Son Willem J, Seelen Marc A |
Mannose-binding lectin-2 genotypes and recurrent late pregnancy losses. Human reproduction (Oxford, England) 2009 Feb 24 (2): 291-9. Christiansen Ole B, Nielsen Henriette S, Lund Marie, Steffensen Rudi, Varming K |
Mannose-binding lectin gene polymorphism and early neonatal outcome in preterm infants. Neonatology 2010 98 (4): 305-12. Koroglu Ozge Altun, Onay Huseyin, Erdemir Gulin, Yalaz Mehmet, Cakmak Bilin, Akisu Mete, Ozkinay Ferda, Kultursay Nilg |
Genetic Polymorphisms of Molecules Associated with Innate Immune Responses, TRL2 and MBL2 Genes in Japanese Subjects with Functional Dyspepsia. Journal of clinical biochemistry and nutrition 2010 Nov 47 (3): 217-23. Tahara Tomomitsu, Shibata Tomoyuki, Wang Fangyu, Yamashita Hiromi, Hirata Ichiro, Arisawa Tomiya |
Genotypes coding for low serum levels of mannose-binding lectin are underrepresented among individuals suffering from noninfectious systemic inflammatory response syndrome. Clinical and vaccine immunology : CVI 2009 Dec . Smithson A, Perello R, Aibar J, Espinosa G, Tassies D, Freire C, Castro P, Suarez B, Lozano F, Nicolas JM |
Mannose binding lectin gene (MBL2) functional polymorphisms are associated with systemic lupus erythematosus in southern Brazilians. Human immunology 2011 Jun 72 (6): 516-21. Sandrin-Garcia Paula, Brandão Lucas André Cavalcanti, Coelho Antônio Victor Campos, Guimarães Rafael Lima, Pancoto João Alexandre Trés, Segat Ludovica, Donadi Eduardo Antônio, de Lima-Filho José Luiz, Crovella Serg |
High levels of mannose-binding lectin are associated with poor outcomes after lung transplantation. Transplantation 2011 May 91 (9): 1044-9. Carroll Katherine E, Dean Melinda M, Heatley Susan L, Meehan Aislin C, Mifsud Nicole A, Kotsimbos Tom C, Snell Greg I, Westall Glen |
The first report described as an important study: The association of mannose-binding lectin gene 2 polymorphisms in children with Down syndrome. Indian journal of human genetics 2011 May 17 (2): 59-64. Demirhan Osman, Ta?temir Deniz, Güne?açar Ramazan, Güzel Ali ?rfan, Alptekin Dav |
Inflammation and immune-related candidate gene associations with acute lung injury susceptibility and severity: a validation study. PloS one 2012 7 (12): 12. O'Mahony DS, Glavan BJ, Holden TD, Fong C, Black RA, Rona G, Tejera P, Christiani DC, Wurfel MM |
Risk of infection and sepsis in severely injured patients related to single nucleotide polymorphisms in the lectin pathway. The British journal of surgery 2013 Dec 100 (13): 1818-26. Bronkhorst M W G A, Lomax M A Z, Vossen R H A M, Bakker J, Patka P, van Lieshout E M |
Surfactant protein A genetic variants associate with severe respiratory insufficiency in pandemic influenza A virus infection. Critical care (London, England) 2014 18 (3): R127. Herrera-Ramos Estefanía, López-Rodríguez Marta, Ruíz-Hernández José Juan, Horcajada Juan Pablo, Borderías Luis, Lerma Elisabeth, Blanquer José, Pérez-González María Carmen, García-Laorden María Isabel, Florido Yanira, Mas-Bosch Virginia, Montero Milagro, Ferrer José María, Sorlí Luisa, Vilaplana Carlos, Rajas Olga, Briones Marisa, Aspa Javier, López-Granados Eduardo, Solé-Violán Jordi, de Castro Felipe Rodríguez, Rodríguez-Gallego Carl |
Mannose binding lectin and susceptibility to rheumatoid arthritis in Brazilian patients and their relatives. PloS one 2014 9 (4): e95519. Goeldner Isabela, Skare Thelma L, Utiyama Shirley R, Nisihara Renato M, Tong Hoang van, Messias-Reason Iara J T, Velavan Thirumalaisamy |
Mannose-binding lectin (MBL) insufficiency protects against the development of systemic inflammatory response after pediatric cardiac surgery. Immunobiology 2015 Sep . P?gowska-Klimek Izabela, ?wierzko Anna S, Michalski Mateusz, Moll Maciej, Szala-Po?dziej Agnieszka, Soko?owska Anna, Krajewski Wojciech R, Cedzy?ski Maci |
Multiple Infectious Complications in a Severely Injured Patient with Single Nucleotide Polymorphisms in Important Innate Immune Response Genes. The open orthopaedics journal 2015 9 367-71. Bronkhorst Maarten W G A, Patka Peter, Lieshout Esther M M V |
Candidate gene variants of the immune system and sudden infant death syndrome. International journal of legal medicine 2016 Mar . Fard Delnaz, Läer Katharina, Rothämel Thomas, Schürmann Peter, Arnold Matthias, Cohen Marta, Vennemann Mechtild, Pfeiffer Heidi, Bajanowski Thomas, Pfeufer Arne, Dörk Thilo, Klintschar Micha |
Whole-exome sequencing of sickle cell disease patients with hyperhemolysis syndrome suggests a role for rare variation in disease predisposition. Transfusion 2017 Dec . Mwesigwa Savannah, Moulds Joann M, Chen Alice, Flanagan Jonathan, Sheehan Vivien A, George Alex, Hanchard Neil |
CTLA-4 gene polymorphisms are associated with obesity in Turner Syndrome. Genetics and molecular biology 0 41 (4): 727-734. Santos Luana Oliveira Dos, Bispo Adriana Valéria Sales, Barros Juliana Vieira de, Laranjeira Raysa Samanta Moraes, Pinto Rafaella do Nascimento, Silva Jaqueline de Azevêdo, Duarte Andréa de Rezende, Araújo Jacqueline, Sandrin-Garcia Paula, Crovella Sergio, Bezerra Marcos André Cavalcanti, Belmont Taciana Furtado de Mendonça, Cavalcanti Maria do Socorro, Santos Nei |
Whole exome sequencing of patients who resolved Crohn's disease and complex regional pain syndrome following treatment for paratuberculosis. Gut pathogens 2019 6 11 34. Todd Kuenstner J, Kali Maher, Welch Christi |
Mannose-binding lectin gene polymorphism and its effect on short term outcomes in preterm infants. Jornal de pediatria 2019 Apr . Dogan Pelin, Ozkan Hilal, Koksal Nilgun, Oral Haluk Barbaros, Bagci Onur, Guney Varal Ip |
Genetic polymorphisms as multi-biomarkers in severe acute respiratory syndrome (SARS) by coronavirus infection: A systematic review of candidate gene association studies. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2021 5 93 104846. Dos Santos Ana Caroline Melo, Dos Santos Bárbara Rayssa Correia, Dos Santos Bruna Brandão, de Moura Edilson Leite, Ferreira Jean Moisés, Dos Santos Luana Karen Correia, Oliveira Susana Paiva, Dias Renise Bastos Farias, Pereira E Silva Aline Cristine, de Farias Karol Fireman, de Souza Figueiredo Elaine Virgínia Marti |
MBL deficiency-causing B allele (rs1800450) as a risk factor for severe COVID-19. Immunobiology 2021 10 226 (6): 152136. Speletas Matthaios, Dadouli Katerina, Syrakouli Argyro, Gatselis Nikolaos, Germanidis Georgios, Mouchtouri Varvara A, Koulas Ioannis, Samakidou Anna, Nikolaidou Anastasia, Stefos Aggelos, Mimtsoudis Iordanis, Hatzianastasiou Sophia, Koureas Michalis, Anagnostopoulos Lemonia, Tseroni Maria, Tsinti Gerasimina, Metallidis Symeon, Dalekos George, Hadjichristodoulou Christ |
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 |
Association of mannose-binding lectin 2 gene polymorphisms with Guillain-Barré syndrome. Scientific reports 2022 4 12 (1): 5791. Jahan Israt, Hayat Shoma, Khalid Mir M, Ahammad Rijwan U, Asad Asaduzzaman, Islam Badrul, Mohammad Quazi D, Jacobs Bart C, Islam Zhahir |
Role of MBL2 Polymorphisms in Sepsis and Survival: A Pilot Study and In Silico Analysis. Diagnostics (Basel, Switzerland) 2022 Feb 12 (2): . Behairy Mohammed Y, Abdelrahman Ali A, Abdallah Hoda Y, Ibrahim Emad El-Deen A, Hashem Hany R, Sayed Anwar A, Azab Marwa |
Recognition and inhibition of SARS-CoV-2 by humoral innate immunity pattern recognition molecules. Nature immunology 2022 2 23 (2): 275-286. Stravalaci Matteo, Pagani Isabel, Paraboschi Elvezia Maria, Pedotti Mattia, Doni Andrea, Scavello Francesco, Mapelli Sarah N, Sironi Marina, Perucchini Chiara, Varani Luca, Matkovic Milos, Cavalli Andrea, Cesana Daniela, Gallina Pierangela, Pedemonte Nicoletta, Capurro Valeria, Clementi Nicola, Mancini Nicasio, Invernizzi Pietro, Bayarri-Olmos Rafael, Garred Peter, Rappuoli Rino, Duga Stefano, Bottazzi Barbara, Uguccioni Mariagrazia, Asselta Rosanna, Vicenzi Elisa, Mantovani Alberto, Garlanda Cecil |
The effect of the MBL2 gene rs1800450 variant on COVID-19 development in Turkish patients. Nucleosides, nucleotides & nucleic acids 2024 8 1-11. Mustafa Capraz, Akin Tekcan, Mustafa Cihangiroglu, Ayse Feyda Nursal, Aylin Capraz, Elif Menekse, Hatice Dortok Demir, Nilufer Kuruca, Serbulent Yig |
Increased Complement Activation and Decreased ADAMTS13 Activity Are Associated with Genetic Susceptibility in Patients with Preeclampsia/HELLP Syndrome Compared to Healthy Pregnancies: An Observational Case-Controlled Study. Journal of personalized medicine 2024 4 14 (4): . Theodora-Maria Venou, Evangelia Vetsiou, Christos Varelas, Angelos Daniilidis, Kyriakos Psarras, Evaggelia-Evdoxia Koravou, Maria Koutra, Tasoula Touloumenidou, Vasilis Tsolakidis, Apostolia Papalexandri, Fani Minti, Evdokia Mandala, Konstantinos Dinas, Efthymia Vlachaki, Eleni Gavriila |
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