Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: IKBKAP[original query] |
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Familial dysautonomia: detection of the IKBKAP IVS20(+6T --> C) and R696P mutations and frequencies among Ashkenazi Jews. American journal of medical genetics 2002 Jul 110 (3): 253-7. Dong Jianli, Edelmann Lisa, Bajwa Asghar M, Kornreich Ruth, Desnick Robert |
Association of sixty-one non-synonymous polymorphisms in forty-one hypertension candidate genes with blood pressure variation and hypertension. Hypertension research : official journal of the Japanese Society of Hypertension 2006 Aug 29 (8): 611-9. Kokubo Yoshihiro, Tomoike Hitonobu, Tanaka Chihiro, Banno Mariko, Okuda Tomohiko, Inamoto Nozomu, Kamide Kei, Kawano Yuhei, Miyata Toshiyu |
Genetic variation in the nuclear factor kappaB pathway in relation to susceptibility to rheumatoid arthritis. Annals of the rheumatic diseases 2009 Apr 68 (4): 579-83. Dieguez-Gonzalez R, Akar S, Calaza M, Perez-Pampin E, Costas J, Torres M, Vicario J L, Velloso M L, Navarro F, Narvaez J, Joven B, Herrero-Beaumont G, Gonzalez-Alvaro I, Fernandez-Gutierrez B, de la Serna A R, Carreño L, Lopez-Longo J, Caliz R, Collado-Escobar M D, Blanco F J, Fernandez-Lopez C, Balsa A, Pascual-Salcedo D, Gomez-Reino J J, Gonzalez |
Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation. Brain : a journal of neurology 2009 Oct 132 (Pt 10): 2699-711. Rotthier Annelies, Baets Jonathan, De Vriendt Els, Jacobs An, Auer-Grumbach Michaela, Lévy Nicolas, Bonello-Palot Nathalie, Kilic Sara Sebnem, Weis Joachim, Nascimento Andrés, Swinkels Marielle, Kruyt Moyo C, Jordanova Albena, De Jonghe Peter, Timmerman Vince |
Investigation of genetic variants within candidate genes of the TNFRSF1B signalling pathway on the response to anti-TNF agents in a UK cohort of rheumatoid arthritis patients. Pharmacogenetics and genomics 2009 Apr 19 (4): 319-23. Bowes John D, Potter Catherine, Gibbons Laura J, Hyrich Kimme, Plant Darren, Morgan Ann W, Wilson Anthony G, Isaacs John D, Worthington Jane, Barton Anne, |
Fine mapping of the 9q31 Hirschsprung's disease locus. Human genetics 2010 Apr . Tang CS, Sribudiani Y, Miao XP, de Vries AR, Burzynski G, So MT, Leon YY, Yip BH, Osinga J, Hui KJ, Verheij JB, Cherny SS, Tam PK, Sham PC, Hofstra RM, Garcia-Barceló MM |
Resequencing candidate genes implicates rare variants in asthma susceptibility. American journal of human genetics 2012 Feb 90 (2): 2. Torgerson DG, Capurso D, Mathias RA, Graves PE, Hernandez RD, Beaty TH, Bleecker ER, Raby BA, Meyers DA, Barnes KC, Weiss ST, Martinez FD, Nicolae DL, Ober C |
Female-Specific Association Between Variants on Chromosome 9 and Self-Reported Diagnosis of Irritable Bowel Syndrome.
Gastroenterology 2018 Apr . Bonfiglio Ferdinando, Zheng Tenghao, Garcia-Etxebarria Koldo, Hadizadeh Fatemeh, Bujanda Luis, Bresso Francesca, Agreus Lars, Andreasson Anna, Dlugosz Aldona, Lindberg Greger, Schmidt Peter T, Karling Pontus, Ohlsson Bodil, Simren Magnus, Walter Susanna, Nardone Gerardo, Cuomo Rosario, Usai-Satta Paolo, Galeazzi Francesca, Neri Matteo, Portincasa Piero, Bellini Massimo, Barbara Giovanni, Latiano Anna, Hübenthal Matthias, Thijs Vincent, Netea Mihai G, Jonkers Daisy, Chang Lin, Mayer Emeran A, Wouters Mira M, Boeckxstaens Guy, Camilleri Michael, Franke Andre, Zhernakova Alexandra, D'Amato Mau |
Founder mutation in IKBKAP gene causes vestibular impairment in familial dysautonomia. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology 2018 1 129 (2): 390-396. Gutiérrez Joel V, Kaufmann Horacio, Palma Jose-Alberto, Mendoza-Santiesteban Carlos, Macefield Vaughan G, Norcliffe-Kaufmann Lu |
Potentially functional genetic variants in the TNF/TNFR signaling pathway genes predict survival of patients with non-small cell lung cancer in the PLCO cancer screening trial. Molecular carcinogenesis 2019 Apr . Guo Yi, Feng Yun, Liu Hongliang, Luo Sheng, Clarke Jeffrey W, Moorman Patricia G, Su Li, Shen Sipeng, Christiani David C, Wei Qing |
Association between IKBKAP polymorphisms and Hirschsprung's disease susceptibility in Chinese children. Translational pediatrics 2022 Jun 11 (6): 789-796. Wang Ning, Xi Jiaojiao, Lan Chaoting, Wu Yuxin, Zhu Yun, Zuo Xiaoyu, Zhang Y |
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- Page last updated:Apr 22, 2024
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