Human Genome Epidemiology Literature Finder
Records 1 - 17 (of 17 Records) |
Query Trace: LAMB1[original query] |
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Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.
Nature genetics 2009 Dec 41 (12): 1330-4. , Barrett Jeffrey C, Lee James C, Lees Charles W, Prescott Natalie J, Anderson Carl A, Phillips Anne, Wesley Emma, Parnell Kirstie, Zhang Hu, Drummond Hazel, Nimmo Elaine R, Massey Dunecan, Blaszczyk Kasia, Elliott Timothy, Cotterill Lynn, Dallal Helen, Lobo Alan J, Mowat Craig, Sanderson Jeremy D, Jewell Derek P, Newman William G, Edwards Cathryn, Ahmad Tariq, Mansfield John C, Satsangi Jack, Parkes Miles, Mathew Christopher G, , Donnelly Peter, Peltonen Leena, Blackwell Jenefer M, Bramon Elvira, Brown Matthew A, Casas Juan P, Corvin Aiden, Craddock Nicholas, Deloukas Panos, Duncanson Audrey, Jankowski Janusz, Markus Hugh S, Mathew Christopher G, McCarthy Mark I, Palmer Colin N A, Plomin Robert, Rautanen Anna, Sawcer Stephen J, Samani Nilesh, Trembath Richard C, Viswanathan Anath C, Wood Nicholas, Spencer Chris C A, Barrett Jeffrey C, Bellenguez Céline, Davison Daniel, Freeman Colin, Strange Amy, Donnelly Peter, Langford Cordelia, Hunt Sarah E, Edkins Sarah, Gwilliam Rhian, Blackburn Hannah, Bumpstead Suzannah J, Dronov Serge, Gillman Matthew, Gray Emma, Hammond Naomi, Jayakumar Alagurevathi, McCann Owen T, Liddle Jennifer, Perez Marc L, Potter Simon C, Ravindrarajah Radhi, Ricketts Michelle, Waller Matthew, Weston Paul, Widaa Sara, Whittaker Pamela, Deloukas Panos, Peltonen Leena, Mathew Christopher G, Blackwell Jenefer M, Brown Matthew A, Corvin Aiden, McCarthy Mark I, Spencer Chris C A, Attwood Antony P, Stephens Jonathan, Sambrook Jennifer, Ouwehand Willem H, McArdle Wendy L, Ring Susan M, Strachan David |
HNF4a and CDH1 are associated with ulcerative colitis in a Dutch cohort. Inflammatory bowel diseases 2011 Aug 17 (8): 1714-8. van Sommeren Suzanne, Visschedijk Marijn C, Festen Eleonora A M, de Jong Dirk J, Ponsioen Cyriel Y, Wijmenga Cisca, Weersma Rinse |
Laminin gene LAMB4 is somatically mutated and expressionally altered in gastric and colorectal cancers. APMIS : acta pathologica, microbiologica, et immunologica Scandinavica 2015 Jan 123 (1): 65-71. Choi Mi Ryoung, An Chang Hyeok, Yoo Nam Jin, Lee Sug Hyu |
LAMB1 polymorphism is associated with autism symptom severity in Korean autism spectrum disorder patients. Nordic journal of psychiatry 2015 Nov 69 (8): 594-8. Kim Young Jong, Park Jin Kyung, Kang Won Sub, Kim Su Kang, Park Hae Jeong, Nam Min, Kim Jong W |
Wingless-type MMTV integration site family member 2 (WNT2) gene is associated with resistance to MAP in faecal culture and antibody response in Holstein cattle. Animal genetics 2015 Apr 46 (2): 122-32. Pauciullo A, Küpper J, Brandt H, Donat K, Iannuzzi L, Erhardt |
Variation in extracellular matrix genes is associated with weight regain after weight loss in a sex-specific manner. Genes & nutrition 2015 Nov 10 (6): 56. Roumans Nadia J T, Vink Roel G, Gielen Marij, Zeegers Maurice P, Holst Claus, Wang Ping, Astrup Arne, Saris Wim H, Valsesia Armand, Hager Jörg, van Baak Marleen A, Mariman Edwin C |
Genes involved in the regulation of intestinal permeability and their role in ulcerative colitis. Journal of digestive diseases 2015 Oct . Prager Matthias, Buettner Janine, Buening Carst |
The association of LAMB1 polymorphism and expression changes with the risk of coal workers' pneumoconiosis. Environmental toxicology 2017 Apr . Ji Xiaoming, Wu Baiqun, Han Ruhui, Yang Jingjin, Ayaaba Esther, Wang Ting, Han Lei, Ni Chunh |
Genetic associations of inflammatory bowel disease in a South Asian population. World journal of clinical cases 2018 Dec 6 (15): 908-915. Niriella Madunil Anuk, Liyanage Isurujith Kongala, Kodisinghe Senerath Kuleesha, Silva Arjuna Priyadarsin De, Rajapakshe Nimna, Nanayakkara Sunali D, Luke Dunya, Silva Thilakshi, Nawarathne Metthananda, Peiris Ranjith K, Kalubovila Udaya P, Kumarasena Sujeewa R, Dissanayake Vajira Harshadeva Weerabaddana, Jayasekara Rohan W, de Silva Hithanadura Jana |
HIF2? supports pro-metastatic behavior in pheochromocytomas/paragangliomas. Endocrine-related cancer 2020 10 27 (11): 625-640. Bechmann Nicole, Moskopp Mats Leif, Ullrich Martin, Calsina Bruna, Wallace Pål William, Richter Susan, Friedemann Markus, Langton Katharina, Fliedner Stephanie M J, Timmers Henri J L M, Nölting Svenja, Beuschlein Felix, Fassnacht Martin, Prejbisz Aleksander, Pacak Karel, Ghayee Hans K, Bornstein Stefan R, Dieterich Peter, Pietzsch Jens, Wielockx Ben, Robledo Mercedes, Qin Nan, Eisenhofer Grae |
End-Truncated LAMB1 Causes a Hippocampal Memory Defect and a Leukoencephalopathy. Annals of neurology 2021 10 90 (6): 962-975. Aloui Chaker, Hervé Dominique, Marenne Gaelle, Savenier Florian, Le Guennec Kilan, Bergametti Francoise, Verdura Edgard, Ludwig Thomas E, Lebenberg Jessica, Jabeur Waliyde, Morel Hélène, Coste Thibault, Demarquay Geneviève, Bachoumas Panagiotis, Cogez Julien, Mathey Guillaume, Bernard Emilien, , Chabriat Hugues, Génin Emmanuelle, Tournier-Lasserve Elisabe |
Compound variants of FKTN, POMGNT1, and LAMB1 gene identified by prenatal whole-exome sequencing in three fetuses with congenital hydrocephalus. The journal of obstetrics and gynaecology research 2022 7 48 (10): 2624-2629. Li Meng, Fu Huayu, Li Jiao, Meng Dahua, Zhang Qiang, Fei Dongm |
Evaluation of JUN, FN1 and LAMB1 polymorphisms in pterygium in a Chinese Han population. Ophthalmic genetics 2022 4 43 (4): 488-495. Wu Xiying, Dong Shiqi, Xu Yuting, Zhu Ge, Yan Mi |
FOXO3 Expression in Macrophages Is Lowered by a High-Fat Diet and Regulates Colonic Inflammation and Tumorigenesis. Metabolites 2022 3 12 (3): . Iftikhar Rida, Penrose Harrison M, King Angelle N, Kim Yunah, Ruiz Emmanuelle, Kandil Emad, Machado Heather L, Savkovic Suzana |
NLRP3 rs1539019 is significantly associated with chronic obstructive pulmonary disease in a Chinese Han population: a case-control study. European review for medical and pharmacological sciences 2022 Aug 26 (16): 5821-5828. Hou Z-F, Yuan Z-H, Chang K, Cao Y-H, Guan F-X, Gao |
Multi-ancestry GWAS of Fuchs corneal dystrophy highlights roles of laminins, collagen, and endothelial cell regulation. Research square 2023 5 . Neal Peachey, Bryan Gorman, Michael Francis, Cari Nealon, Christopher Halladay, Nalvi Duro, Kyriacos Markianos, Giulio Genovese, Pirro Hysi, Hélène Choquet, Natalie Afshari, Yi-Ju Li, J Michael Gaziano, Adriana Hung, Wen-Chih Wu, Paul Greenberg, Saiju Pyarajan, Jonathan Lass, Sudha Iyeng |
A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation. Communications biology 2024 4 7 (1): 418. Bryan R Gorman, Michael Francis, Cari L Nealon, Christopher W Halladay, Nalvi Duro, Kyriacos Markianos, Giulio Genovese, Pirro G Hysi, Hélène Choquet, Natalie A Afshari, Yi-Ju Li, , J Michael Gaziano, Adriana M Hung, Wen-Chih Wu, Paul B Greenberg, Saiju Pyarajan, Jonathan H Lass, Neal S Peachey, Sudha K Iyeng |
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