Results 21 to 30 of about 66,104,498 (114)

Association of the AFF3 gene and IL2/IL21 gene region with juvenile idiopathic arthritis [PDF]

, 2010
Recent genetic studies have led to identification of numerous loci that are associated with susceptibility to autoimmune diseases. The strategy of using information from these studies has facilitated the identification of novel juvenile idiopathic ...
S Eyre, J Worthington, X Ke, P Martin, W Thomson, A Hinks, E Flynn, J Packham, A Barton, Martin, P., Barton, A., Gardner-Medwin, J. [CAPS and BSPAR study groups], UKRAG Consortium, Worthington, J., Thomson, W., Flynn, E., Packham, J., Hinks, A., British Society of Paediatric and Adolescent Rheumatology (BSPAR) Study Group, Eyre, S., Ke, X., Childhood Arthritis Prospective Study (CAPS)   +21 more
core   +2 more sources

소아청소년기에서 SLCO2A1 gene 연관 만성 장병증 (CEAS) 의 임상 양상 [PDF]

, 2022
학위논문(석사) -- 서울대학교대학원 : 의과대학 임상의과학과, 2022.2. 고재성.Background and Aims: The incidence of inflammatory bowel disease (IBD) is increasing worldwide, and many atypical IBDs are being discovered.
임진규
core  

A gene signature for post-infectious chronic fatigue syndrome [PDF]

, 2009
Background: At present, there are no clinically reliable disease markers for chronic fatigue syndrome. DNA chip microarray technology provides a method for examining the differential expression of mRNA from a large number of genes.
Gow John W, Herzyk, Pawel, Gow, J.W., Celia Cannon, Behan Peter O, Hagan Suzanne, Suzanne Hagan, Behan, Peter O., Hagan, S., Herzyk, P., Chaudhuri, A., John W Gow, Gow, John W., Chaudhuri, Abhijit, Peter O Behan, Cannon Celia, Cannon, Celia, Behan, P.O., Abhijit Chaudhuri, Pawel Herzyk, Cannon, C., Hagan, Suzanne; id_orcid, Herzyk Pawel, Chaudhuri Abhijit   +23 more
core   +2 more sources

SLCO2A1 mutation-mediated vascular endothelial cell dysfunction contributes to chronic enteropathy(CEAS) development and progression [PDF]

Jichu yixue yu linchuang
Objective To investigate the pathogenic mechanism of chronic enteropathy associated with SLCO2A1 with SLCO2A1 gene(CEAS), a hereditary disease caused by SLCO2A1 mutations, and to provide theoretical insight into potential therapeutic strategies.
ZHANG Yiyao, YUN Longxi, HUANG Jingyi, LI Xiaoyu, YUAN Jingyi, LI Yue, LIU Changzheng
doaj   +1 more source

High dose multiple micronutrient supplementation improves villous morphology in environmental enteropathy without HIV enteropathy: results from a double-blind randomised placebo controlled trial in Zambian adults [PDF]

, 2014
PMCID: PMC3897937This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided ...
Rose Banda, John Louis-Auguste, Greenwald, Stephen, Louis-Auguste, John, Banda, Rose, Simuyandi, M, Soko, Rose, Rose Soko, Paul Kelly, Stephen Greenwald, Greenwald, S, Soko, R, Louis-Auguste, J, Kelly, Paul, Simuyandi, Michelo, Banda, R, Kelly, P, Michelo Simuyandi   +17 more
core   +2 more sources

Abstracts

, 2022
JPGN Reports, Volume 3, Issue S1, September 2022.
wiley   +1 more source

Variants within the MMP3 gene are associated with achilles tendinopathy: possible interaction with the COL5A1 gene [PDF]

, 2009
Objectives: Sequence variation within the COL5A1 and TNC genes are known to associate with Achilles tendinopathy. The primary aim of this case-control genetic association study was to investigate whether variants within the matrix metalloproteinase 3 ...
Ribbans, William J, Raleigh, S M, Ribbans, W J, Smith, R K, Collins, M, Raleigh, Stuart M, Smith, R K W, Schwellnus, M P, van der Merwe, L, Ribbans, William J; id_orcid, Northampton   +10 more
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Assigning function to genome wide association study variants associated with complex gastrointestinal disease [PDF]

, 2009
PhDThe genome‐wide association study era has identified numerous loci associated with many common polygenic diseases. The next challenge is to identify the functional consequences of these variants and elicit how they impact on disease risk.
Heap, Graham Alastair Richard
core   +4 more sources

Mesalazine in the initial management of severely acutely malnourished children with environmental enteric dysfunction : a pilot randomized controlled trial [PDF]

, 2014
Background: Environmental enteric dysfunction (EED) is an acquired syndrome of impaired gastrointestinal mucosal barrier function that is thought to play a key role in the pathogenesis of stunting in early life. It has been conceptualized as an adaptive
Simon H Murch, Hünten-Kirsch, B, Mulongo, MM, Mulongo, Musa M., Berkley, James, Laving, AM, Sullivan, Peter, Odera, D, Ahmed MR Laving, Berkley, J, Barbara Hünten-Kirsch, Hünten-Kirsch, Barbara, Caroline W Munyi, James A Berkley, Murch, SH, Mikusa, Jenifer, Sullivan, PB, Owino, Moses, Ngari, M, Dennis Odera, John O Warner, Sullivan, P, Fegan, G, Timbwa, Molline, Moses Owino, Mikusa, J, Nassir, HS, Munyi, Caroline W., H Samira Nassir, Berkley, James A., Laving, Ahmed M. R., Peter B Sullivan, Odera, Dennis, Ngari, Moses, Owino, M, Warner, JO, Jones, Kelsey D. J., Warner, J. O. (John O.), Musa M Mulongo, Jones, KDJ, Berkley, JA, Kelsey DJ Jones, Greg Fegan, Laving, AMR, Nassir, H. Samira, Huenten-Kirsch, B, Munyi, CW, Molline Timbwa, Sullivan, Peter B., Moses Ngari, Jenifer Mikusa, Timbwa, M, Fegan, Greg, Murch, Simon, Jones, KD   +54 more
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Genetic variation in the interleukin-28B gene is associated with spontaneous clearance and progression of hepatitis C virus in Moroccan patients [PDF]

, 2013
Genetic variation in the IL28B gene has been strongly associated with treatment outcomes, spontaneous clearance and progression of the hepatitis C virus infection (HCV).
Alaoui, Rihmou, Diepolder H., Salwa Nadir, Helmut Diepolder, Thursz, Mark, Sayeh Ezzikouri (143566), Khakoo Salim I., Mark Thursz, Soumaya Benjelloun (143569), Alaoui R., Alaoui Rhimou, Khakoo, Salim I., Mark Thursz (276871), Helmut Diepolder (276870), Nadir S., Ezzikouri Sayeh, Rebbani K., Nadir Salwa, Fakhir Fatima-Zohra, Fakhir F.-Z., Benjelloun, Soumaya, Benjelloun S., Fatima-Zohra Fakhir, Salim I Khakoo, Diepolder, Helmut, Thursz Mark, Nadir, Salwa, Benjelloun Soumaya, Brahim Ikram, Rhimou Alaoui, Rhimou Alaoui (276865), Brahim I., Diepolder, Helmut M., Sayeh Ezzikouri, Rebbani Khadija, Ikram Brahim, Alaoui, Rhimou, Rebbani, Khadija, Fatima-Zohra Fakhir (276868), Soumaya Benjelloun, Khadija Rebbani, Ikram Brahim (276867), Ezzikouri S., Salwa Nadir (276869), Khakoo S.I., Thursz M., Diepolder Helmut, Khadija Rebbani (276866), Salim I. Khakoo (201172), Fakhir, Fatima-Zohra, Ezzikouri, Sayeh, Brahim, Ikram   +51 more
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