Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: Syndrome and C4B[original query] |
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Low complement C4B gene copy number predicts short-term mortality after acute myocardial infarction. International immunology 2008 Jan 20 (1): 31-7. Blaskó Bernadett, Kolka Ragnhildur, Thorbjornsdottir Perla, Sigurdarson Sigurdur Thór, Sigurdsson Gardar, Rónai Zsolt, Sasvári-Székely Mária, Bödvarsson Sigurdur, Thorgeirsson Gudmundur, Prohászka Zoltán, Kovács Margit, Füst George, Arason Gudmundur Jóha |
Human MHC region harbors both susceptibility and protective haplotypes for coronary artery disease. Tissue antigens 2007 Jan 69 (1): 47-55. Palikhe A, Sinisalo J, Seppänen M, Valtonen V, Nieminen M S, Lokki M |
Autoimmune-associated HLA-B8-DR3 haplotypes in Asian Indians are unique in C4 complement gene copy numbers and HSP-2 1267A/G. Human immunology 2008 Sep 69 (9): 580-7. Kaur Gurvinder, Kumar Neeraj, Szilagyi Agnes, Blasko Bernadett, Fust George, Rajczy Katalin, Pozsonyi Eva, Hosso Adrienn, Petranyi Gyozo, Tandon Nikhil, Mehra Narind |
A novel non-synonymous polymorphism (p.Arg240His) in C4b-binding protein is associated with atypical hemolytic uremic syndrome and leads to impaired alternative pathway cofactor activity. Journal of immunology (Baltimore, Md. : 1950) 2008 May 180 (9): 6385-91. Blom Anna M, Bergström Frida, Edey Matthew, Diaz-Torres Martha, Kavanagh David, Lampe Anne, Goodship Judith A, Strain Lisa, Moghal Nadeem, McHugh Mary, Inward Carol, Tomson Charles, Frémeaux-Bacchi Véronique, Villoutreix Bruno O, Goodship Timothy H |
Lack of association between polymorphisms in C4b-binding protein and atypical haemolytic uraemic syndrome in the Spanish population. Clinical and experimental immunology 2009 Jan 155 (1): 59-64. Martínez-Barricarte R, Goicoechea de Jorge E, Montes T, Layana A G, Rodríguez de Córdoba |
Thrombomodulin mutations in atypical hemolytic-uremic syndrome. The New England journal of medicine 2009 Jul 361 (4): 345-57. Delvaeye Mieke, Noris Marina, De Vriese Astrid, Esmon Charles T, Esmon Naomi L, Ferrell Gary, Del-Favero Jurgen, Plaisance Stephane, Claes Bart, Lambrechts Diether, Zoja Carla, Remuzzi Giuseppe, Conway Edward |
Mutations in complement regulatory proteins predispose to preeclampsia: a genetic analysis of the PROMISSE cohort. PLoS medicine 2011 Mar 8 (3): e1001013. Salmon Jane E, Heuser Cara, Triebwasser Michael, Liszewski M Kathryn, Kavanagh David, Roumenina Lubka, Branch D Ware, Goodship Tim, Fremeaux-Bacchi Veronique, Atkinson John |
Factor H autoantibodies and deletion of Complement Factor H-Related protein-1 in rheumatic diseases in comparison to atypical hemolytic uremic syndrome. Arthritis research & therapy 2012 14 (4): R185. Foltyn Zadura Anna, Zipfel Peter F, Bokarewa Maria I, Sturfelt Gunnar, Jönsen Andreas, Nilsson Sara C, Hillarp Andreas, Saxne Tore, Trouw Leendert A, Blom Anna |
Complement genes contribute sex-biased vulnerability in diverse disorders. Nature 2020 6 582 (7813): 577-581. Kamitaki Nolan, Sekar Aswin, Handsaker Robert E, de Rivera Heather, Tooley Katherine, Morris David L, Taylor Kimberly E, Whelan Christopher W, Tombleson Philip, Loohuis Loes M Olde, , Boehnke Michael, Kimberly Robert P, Kaufman Kenneth M, Harley John B, Langefeld Carl D, Seidman Christine E, Pato Michele T, Pato Carlos N, Ophoff Roel A, Graham Robert R, Criswell Lindsey A, Vyse Timothy J, McCarroll Steven |
Complement C4 Copy Number Variation is Linked to SSA/Ro and SSB/La Autoantibodies in Systemic Inflammatory Autoimmune Diseases. Arthritis & rheumatology (Hoboken, N.J.) 2022 3 74 (8): 1440-1450. Lundtoft Christian, Pucholt Pascal, Martin Myriam, Bianchi Matteo, Lundström Emeli, Eloranta Maija-Leena, Sandling Johanna K, Sjöwall Christopher, Jönsen Andreas, Gunnarsson Iva, Rantapää-Dahlqvist Solbritt, Bengtsson Anders A, Leonard Dag, Baecklund Eva, Jonsson Roland, Hammenfors Daniel, Forsblad-d'Elia Helena, Eriksson Per, Mandl Thomas, Magnusson Bucher Sara, Norheim Katrine B, Auglaend Johnsen Svein Joar, Omdal Roald, Kvarnström Marika, Wahren-Herlenius Marie, Notarnicola Antonella, Andersson Helena, Molberg Øyvind, Diederichsen Louise Pyndt, Almlöf Jonas, Syvänen Ann-Christine, Kozyrev Sergey V, Lindblad-Toh Kerstin, , , Nilsson Bo, Blom Anna M, Lundberg Ingrid E, Nordmark Gunnel, Diaz-Gallo Lina Marcela, Svenungsson Elisabet, Rönnblom La |
Evaluation of C4 gene copy number in Pediatric Acute Neuropsychiatric Syndrome. Developmental neuroscience 2023 6 . Agnieszka Kalinowski, Lu Tian, Reenal Pattni, Hanna Ollila, Maroof Khan, Cindy Manko, Melissa Silverman, Meiqian Ma, Laurie Columbo, Bahare Farhadian, Susan Swedo, Tanya Murphy, Mats Johnson, Elisabeth Fernell, Christopher Gillberg, Margo Thienemann, Elizabeth D Mellins, Douglas F Levinson, Alexander E Urban, Jennifer Frankovi |
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- Page last updated:Apr 16, 2024
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