Publications
Found 8 results
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“Analysis of prognostic factors for infantile rotavirus infection”, vol. 14, pp. 790-796, 2015.
, “Anti-prostate cancer effects of CTL cell induction in vitro by recombinant adenovirus mediated PSMA/4-1BBL dendritic cells: an immunotherapy study”, vol. 14, pp. 7208-7217, 2015.
, “Identification and evaluation of endogenous control genes for use in quantitative RT-PCR during wheat (Triticum aestivum L.) grain filling”, vol. 14, pp. 10530-10542, 2015.
, “New compound heterozygous mutations of p. Thr101Ilefs*2 and p. Thr306Ale in a child from a Chinese family with 17α-hydroxylase/17, 20-lyase deficiency”, vol. 14, pp. 9318-9324, 2015.
, “Retrospective analysis of pathologic nipple discharge”, vol. 14, pp. 1443-1449, 2015.
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“Genetic variants on 17q21 are associated with asthma in a Han Chinese population”, vol. 11, pp. 340-347, 2012.
, Bisgaard H, Bonnelykke K, Sleiman PM, Brasholt M, et al. (2009). Chromosome 17q21 gene variants are associated with asthma and exacerbations but not atopy in early childhood. Am. J. Respir. Crit. Care Med. 179: 179-185.
http://dx.doi.org/10.1164/rccm.200809-1436OC
PMid:19029000
Bouzigon E, Corda E, Aschard H, Dizier MH, et al. (2008). Effect of 17q21 variants and smoking exposure in early-onset asthma. N. Engl. J. Med. 359: 1985-1994.
http://dx.doi.org/10.1056/NEJMoa0806604
PMid:18923164
Eder W, Ege MJ and von Mutius E (2006). The asthma epidemic. N. Engl. J. Med. 355: 2226-2235.
http://dx.doi.org/10.1056/NEJMra054308
PMid:17124020
Flory JH, Sleiman PM, Christie JD, Annaiah K, et al. (2009). 17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of European ancestry. J. Allergy Clin. Immunol. 124: 605-607.
http://dx.doi.org/10.1016/j.jaci.2009.05.047
PMid:19660801
Galanter J, Choudhry S, Eng C, Nazario S, et al. (2008). ORMDL3 gene is associated with asthma in three ethnically diverse populations. Am. J. Respir. Crit. Care Med. 177: 1194-1200.
http://dx.doi.org/10.1164/rccm.200711-1644OC
PMid:18310477 PMCid:2408437
Halapi E, Gudbjartsson DF, Jonsdottir GM, Bjornsdottir US, et al. (2010). A sequence variant on 17q21 is associated with age at onset and severity of asthma. Eur. J. Hum. Genet. 18: 902-908.
http://dx.doi.org/10.1038/ejhg.2010.38
PMid:20372189 PMCid:2987388
Hirota T, Harada M, Sakashita M, Doi S, et al. (2008). Genetic polymorphism regulating ORM1-like 3 (Saccharomyces cerevisiae) expression is associated with childhood atopic asthma in a Japanese population. J. Allergy Clin. Immunol. 121: 769-770.
http://dx.doi.org/10.1016/j.jaci.2007.09.038
PMid:18155279
Hjelmqvist L, Tuson M, Marfany G, Herrero E, et al. (2002). ORMDL proteins are a conserved new family of endoplasmic reticulum membrane proteins. Genome Biol. 3: RESEARCH0027.
Leung TF, Sy HY, Ng MC, Chan IH, et al. (2009). Asthma and atopy are associated with chromosome 17q21 markers in Chinese children. Allergy 64: 621-628.
http://dx.doi.org/10.1111/j.1398-9995.2008.01873.x
PMid:19175592
Li X, Yang XX, Hu NY, Sun JZ, et al. (2011). A risk-associated single nucleotide polymorphism of SMAD7 is common to colorectal, gastric, and lung cancers in a Han Chinese population. Mol. Biol. Rep. 38: 5093-5097.
http://dx.doi.org/10.1007/s11033-010-0656-3
PMid:21221812
Madore AM, Tremblay K, Hudson TJ and Laprise C (2008). Replication of an association between 17q21 SNPs and asthma in a French-Canadian familial collection. Hum. Genet. 123: 93-95.
http://dx.doi.org/10.1007/s00439-007-0444-x
PMid:17992541
Moffatt MF, Kabesch M, Liang L, Dixon AL, et al. (2007). Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. Nature 448: 470-473.
http://dx.doi.org/10.1038/nature06014
PMid:17611496
Ober C and Hoffjan S (2006). Asthma genetics 2006: the long and winding road to gene discovery. Genes Immun. 7: 95-100.
http://dx.doi.org/10.1038/sj.gene.6364284
PMid:16395390
Sleiman PM, Annaiah K, Imielinski M, Bradfield JP, et al. (2008). ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry. J. Allergy Clin. Immunol. 122: 1225-1227.
http://dx.doi.org/10.1016/j.jaci.2008.06.041
PMid:18760456
Tavendale R, MacGregor DF, Mukhopadhyay S and Palmer CN (2008). A polymorphism controlling ORMDL3 expression is associated with asthma that is poorly controlled by current medications. J. Allergy Clin. Immunol. 121: 860-863.
http://dx.doi.org/10.1016/j.jaci.2008.01.015
PMid:18395550
Wjst M (2008). ORMDL3 - guilt by association? Clin. Exp. Allergy 38: 1579-1581.
http://dx.doi.org/10.1111/j.1365-2222.2008.03086.x
Wu H, Romieu I, Sienra-Monge JJ, Li H, et al. (2009). Genetic variation in ORM1-like 3 (ORMDL3) and gasdermin-like (GSDML) and childhood asthma. Allergy 64: 629-635.
http://dx.doi.org/10.1111/j.1398-9995.2008.01912.x
PMid:19133921 PMCid:2697826
“Association between HLA-Cw*0602 polymorphism and psoriasis risk: a meta-analysis”, vol. 10, pp. 3109-3120, 2011.
, Asumalahti K, Laitinen T, Itkonen-Vatjus R, Lokki ML, et al. (2000). A candidate gene for psoriasis near HLA-C, HCR (Pg8), is highly polymorphic with a disease-associated susceptibility allele. Hum. Mol. Genet. 9: 1533-1542.
http://dx.doi.org/10.1093/hmg/9.10.1533
PMid:10888604
Attia J, Thakkinstian A and D’Este C (2003). Meta-analyses of molecular association studies: methodologic lessons for genetic epidemiology. J. Clin. Epidemiol. 56: 297-303.
http://dx.doi.org/10.1016/S0895-4356(03)00011-8
Brandrup F, Holm N, Grunnet N, Henningsen K, et al. (1982). Psoriasis in monozygotic twins: variations in expression in individuals with identical genetic constitution. Acta Derm. Venereol. 62: 229-236.
PMid:6179364
Brazzelli V, Quaglini M, Martinetti M, Nolli G, et al. (2000). A peculiar sequence motif in the alpha-1-domain of the HLA-C molecule in psoriasis. Dermatology 200: 99-103.
http://dx.doi.org/10.1159/000018338
PMid:10773694
Chandran V and Raychaudhuri SP (2010). Geoepidemiology and environmental factors of psoriasis and psoriatic arthritis. J. Autoimmun. 34: J314-J321.
http://dx.doi.org/10.1016/j.jaut.2009.12.001
PMid:20034760
Chang YT, Shiao YM, Chin PJ, Liu YL, et al. (2004). Genetic polymorphisms of the HCR gene and a genomic segment in close proximity to HLA-C are associated with patients with psoriasis in Taiwan. Br. J. Dermatol. 150: 1104-1111.
http://dx.doi.org/10.1111/j.1365-2133.2004.05972.x
PMid:15214895
Chang YT, Liu HN, Shiao YM, Lin MW, et al. (2005). A study of PSORS1C1 gene polymorphisms in Chinese patients with psoriasis. Br. J. Dermatol. 153: 90-96.
http://dx.doi.org/10.1111/j.1365-2133.2005.06570.x
PMid:16029332
Chang YT, Chou CT, Shiao YM, Lin MW, et al. (2006). Psoriasis vulgaris in Chinese individuals is associated with PSORS1C3 and CDSN genes. Br. J. Dermatol. 155: 663-669.
http://dx.doi.org/10.1111/j.1365-2133.2006.07420.x
PMid:16965413
Duffin KC, Chandran V, Gladman DD, Krueger GG, et al. (2008). Genetics of psoriasis and psoriatic arthritis: update and future direction. J. Rheumatol. 35: 1449-1453.
PMid:18609743 PMCid:2724000
Fan X, Yang S, Sun LD, Liang YH, et al. (2007). Comparison of clinical features of HLA-Cw*0602-positive and -negative psoriasis patients in a Han Chinese population. Acta Derm. Venereol. 87: 335-340.
http://dx.doi.org/10.2340/00015555-0253
PMid:17598037
Farber EM, Nall ML and Watson W (1974). Natural history of psoriasis in 61 twin pairs. Arch Dermatol. 109: 207-211.
http://dx.doi.org/10.1001/archderm.1974.01630020023005
PMid:4814926
Fojtíková M, Stolfa J, Novota P, Cejkova P, et al. (2009). HLA-Cw*06 class I region rather than MICA is associated with psoriatic arthritis in Czech population. Rheumatol. Int. 29: 1293-1299.
http://dx.doi.org/10.1007/s00296-009-0847-1
PMid:19184033
Gonzalez S, Martinez-Borra J, Torre-Alonso JC, Gonzalez-Roces S, et al. (1999). The MICA-A9 triplet repeat polymorphism in the transmembrane region confers additional susceptibility to the development of psoriatic arthritis and is independent of the association of Cw*0602 in psoriasis. Arthritis Rheum. 42: 1010-1016.
http://dx.doi.org/10.1002/1529-0131(199905)42:5<1010::AID-ANR21>3.0.CO;2-H
Griffiths CE and Barker JN (2007). Pathogenesis and clinical features of psoriasis. Lancet 370: 263-271.
http://dx.doi.org/10.1016/S0140-6736(07)61128-3
Gudjonsson JE, Karason A, Antonsdottir A, Runarsdottir EH, et al. (2003). Psoriasis patients who are homozygous for the HLA-Cw*0602 allele have a 2.5-fold increased risk of developing psoriasis compared with Cw6 heterozygotes. Br. J. Dermatol. 148: 233-235.
http://dx.doi.org/10.1046/j.1365-2133.2003.05115.x
PMid:12588373
Gudjonsson JE, Johnston A, Sigmundsdottir H and Valdimarsson H (2004). Immunopathogenic mechanisms in psoriasis. Clin. Exp. Immunol. 135: 1-8.
http://dx.doi.org/10.1111/j.1365-2249.2004.02310.x
PMid:14678257 PMCid:1808928
Higgins JP and Thompson SG (2002). Quantifying heterogeneity in a meta-analysis. Stat. Med. 21: 1539-1558.
http://dx.doi.org/10.1002/sim.1186
PMid:12111919
Holm SJ, Sanchez F, Carlen LM, Mallbris L, et al. (2005a). HLA-Cw*0602 associates more strongly to psoriasis in the Swedish population than variants of the novel 6p21.3 gene PSORS1C3. Acta Derm. Venereol. 85: 2-8.
http://dx.doi.org/10.1080/00015550410023527
Holm SJ, Sakuraba K, Mallbris L, Wolk K, et al. (2005b). Distinct HLA-C/KIR genotype profile associates with guttate psoriasis. J. Invest. Dermatol. 125: 721-730.
http://dx.doi.org/10.1111/j.0022-202X.2005.23879.x
PMid:16185272
Jobim M, Jobim LF, Salim PH, Cestari TF, et al. (2008). A study of the killer cell immunoglobulin-like receptor gene KIR2DS1 in a Caucasoid Brazilian population with Psoriasis vulgaris. Tissue Antigens 72: 392-396.
http://dx.doi.org/10.1111/j.1399-0039.2008.01096.x
PMid:18643961
Liu Y, Helms C, Liao W, Zaba LC, et al. (2008). A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. PLoS Genet. 4: e1000041.
http://dx.doi.org/10.1371/journal.pgen.1000041
PMid:18369459 PMCid:2274885
Lowes MA, Bowcock AM and Krueger JG (2007). Pathogenesis and therapy of psoriasis. Nature 445: 866-873.
http://dx.doi.org/10.1038/nature05663
PMid:17314973
Luft FC (2005). Light shed on the common skin scourge, psoriasis. J. Mol. Med. 83: 933-934.
http://dx.doi.org/10.1007/s00109-005-0724-7
PMid:16323032
Luszczek W, Kubicka W, Cislo M, Nockowski P, et al. (2003). Strong association of HLA-Cw6 allele with juvenile psoriasis in Polish patients. Immunol. Lett. 85: 59-64.
http://dx.doi.org/10.1016/S0165-2478(02)00212-2
Mallbris L, Wolk K, Sanchez F and Stahle M (2009). HLA-Cw*0602 associates with a twofold higher prevalence of positive streptococcal throat swab at the onset of psoriasis: a case control study. BMC Dermatol. 9: 5.
http://dx.doi.org/10.1186/1471-5945-9-5
PMid:19480679 PMCid:2696405
Martínez-Borra J, Gonzalez S, Santos-Juanes J, Sanchez del RJ, et al. (2003). Psoriasis vulgaris and psoriatic arthritis share a 100 kb susceptibility region telomeric to HLA-C. Rheumatology 42: 1089-1092.
http://dx.doi.org/10.1093/rheumatology/keg304
PMid:12730526
Martínez-Borra J, Brautbar C, Gonzalez S, Enk CD, et al. (2005). The region of 150 kb telometic to HLA-C is associated with psoriasis in the Jewish population. J. Invest. Dermatol. 125: 928-932.
PMid:16297191
Nair RP, Stuart PE, Nistor I, Hiremagalore R, et al. (2006). Sequence and haplotype analysis supports HLA-C as the psoriasis susceptibility 1 gene. Am. J. Hum. Genet. 78: 827-851.
http://dx.doi.org/10.1086/503821
PMid:16642438
Naldi L and Mercuri SR (2010). Epidemiology of comorbidities in psoriasis. Dermatol. Ther. 23: 114-118.
http://dx.doi.org/10.1111/j.1529-8019.2010.01304.x
PMid:20415817
Nestle FO, Kaplan DH and Barker J (2009). Psoriasis. N. Engl. J. Med. 361: 496-509.
http://dx.doi.org/10.1056/NEJMra0804595
PMid:19641206
Peters JL, Sutton AJ, Jones DR, Abrams KR, et al. (2006). Comparison of two methods to detect publication bias in meta-analysis. JAMA 295: 676-680.
http://dx.doi.org/10.1001/jama.295.6.676
PMid:16467236
Płoski R, Luszczek W, Kuśnierczyk P, Nockowski P, et al. (2006). A role for KIR gene variants other than KIR2DS1 in conferring susceptibility to psoriasis. Hum. Immunol. 67: 521-526.
http://dx.doi.org/10.1016/j.humimm.2006.04.001
PMid:16829306
Rani R, Narayan R, Fernandez-Vina MA and Stastny P (1998). Role of HLA-B and C alleles in development of psoriasis in patients from North India. Tissue Antigens 51: 618-622.
http://dx.doi.org/10.1111/j.1399-0039.1998.tb03004.x
PMid:9694354
Raychaudhuri SP and Gross J (2000a). A comparative study of pediatric onset psoriasis with adult onset psoriasis. Pediatr. Dermatol. 17: 174-178.
http://dx.doi.org/10.1046/j.1525-1470.2000.01746.x
PMid:10886746
Raychaudhuri SP and Gross J (2000b). Psoriasis risk factors: role of lifestyle practices. Cutis 66: 348-352.
PMid:11107520
Raychaudhuri SP and Farber EM (2001). The prevalence of psoriasis in the world. J. Eur. Acad. Dermatol. Venereol. 15: 16-17.
http://dx.doi.org/10.1046/j.1468-3083.2001.00192.x
PMid:11451313
Reveille JD and Williams FM (2006). Infection and musculoskeletal conditions: Rheumatologic complications of HIV infection. Best Pract. Res. Clin. Rheumatol. 20: 1159-1179.
http://dx.doi.org/10.1016/j.berh.2006.08.015
Sánchez F, Holm SJ, Mallbris L, O’Brien KP, et al. (2004). STG does not associate with psoriasis in the Swedish population. Exp. Dermatol. 13: 413-418.
http://dx.doi.org/10.1111/j.0906-6705.2004.00170.x
PMid:15217361
Schon MP and Boehncke WH (2005). Psoriasis. N. Engl. J. Med. 352: 1899-1912.
http://dx.doi.org/10.1056/NEJMra041320
PMid:15872205
Szczerkowska-Dobosz A (2005). Human leukocyte antigens as psoriasis inheritance and susceptibility markers. Arch. Immunol. Ther. Exp. 53: 428-433.
Valdimarsson H (2007). The genetic basis of psoriasis. Clin. Dermatol. 25: 563-567.
http://dx.doi.org/10.1016/j.clindermatol.2007.08.010
PMid:18021893
Vandenbroucke JP, von Elm E, Altman DG, Gotzsche PC, et al. (2007). Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): explanation and elaboration. Epidemiology 18: 805-835.
http://dx.doi.org/10.1097/EDE.0b013e3181577511
PMid:18049195
Watson W, Cann HM, Farber EM and Nall ML (1972). The genetics of psoriasis. Arch. Dermatol. 105: 197-207.
http://dx.doi.org/10.1001/archderm.1972.01620050011002
PMid:5060862
Zhang XJ, Zhang AP, Yang S, Gao M, et al. (2003). Association of HLA class I alleles with Psoriasis vulgaris in southeastern Chinese Hans. J. Dermatol. Sci. 33: 1-6.
http://dx.doi.org/10.1016/S0923-1811(03)00157-9
Zintzaras E and Ioannidis JP (2005). Heterogeneity testing in meta-analysis of genome searches. Genet. Epidemiol. 28: 123-137.
http://dx.doi.org/10.1002/gepi.20048
PMid:15593093