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    Results: 1 to 50 of 120

    1.

    Role of VEGF and tissue hypoxia in patterning of neural and vascular cells recruited to the embryonic heart.

    Liu H, Yang Q, Radhakrishnan K, Whitfield DE, Everhart CL, Parsons-Wingerter P, Fisher SA.

    Dev Dyn. 2009 Nov;238(11):2760-9.PMID: 19842184 [PubMed - in process]Related articles

    2.

    Altered hypoxia-inducible factor-1 alpha expression levels correlate with coronary vessel anomalies.

    Wikenheiser J, Wolfram JA, Gargesha M, Yang K, Karunamuni G, Wilson DL, Semenza GL, Agani F, Fisher SA, Ward N, Watanabe M.

    Dev Dyn. 2009 Oct;238(10):2688-700.PMID: 19777592 [PubMed - in process]Related articles

    3.

    Induction of PDE5 and de-sensitization to endogenous NO signaling in a systemic resistance artery under altered blood flow.

    Zhang H, Pakeerappa P, Lee HJ, Fisher SA.

    J Mol Cell Cardiol. 2009 Jul;47(1):57-65. Epub 2009 Apr 15.PMID: 19374906 [PubMed - in process]Related articles

    4.

    Searching for genotype-phenotype structure: using hierarchical log-linear models in Crohn disease.

    Chapman JM, Onnie CM, Prescott NJ, Fisher SA, Mansfield JC, Mathew CG, Lewis CM, Verzilli CJ, Whittaker JC.

    Am J Hum Genet. 2009 Feb;84(2):178-87. Epub 2009 Jan 29.PMID: 19185283 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.

    Anderson CA, Massey DC, Barrett JC, Prescott NJ, Tremelling M, Fisher SA, Gwilliam R, Jacob J, Nimmo ER, Drummond H, Lees CW, Onnie CM, Hanson C, Blaszczyk K, Ravindrarajah R, Hunt S, Varma D, Hammond N, Lewis G, Attlesey H, Watkins N, Ouwehand W, Strachan D, McArdle W, Lewis CM; Wellcome Trust Case Control Consortium, Lobo A, Sanderson J, Jewell DP, Deloukas P, Mansfield JC, Mathew CG, Satsangi J, Parkes M.

    Gastroenterology. 2009 Feb;136(2):523-9.e3. Epub 2008 Oct 25.PMID: 19068216 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Meta-analysis of genome-wide linkage studies across autoimmune diseases.

    Forabosco P, Bouzigon E, Ng MY, Hermanowski J, Fisher SA, Criswell LA, Lewis CM.

    Eur J Hum Genet. 2009 Feb;17(2):236-43. Epub 2008 Sep 10.PMID: 18781189 [PubMed - indexed for MEDLINE]Related articles

    7.

    Tra2beta as a novel mediator of vascular smooth muscle diversification.

    Shukla S, Fisher SA.

    Circ Res. 2008 Aug 29;103(5):485-92. Epub 2008 Jul 31.PMID: 18669920 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Power of genetic association studies in the presence of linkage disequilibrium and allelic heterogeneity.

    Fisher SA, Lewis CM.

    Hum Hered. 2008;66(4):210-22. Epub 2008 Jul 9.PMID: 18612206 [PubMed - indexed for MEDLINE]Related articles

    9.

    Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.

    Barrett JC, Hansoul S, Nicolae DL, Cho JH, Duerr RH, Rioux JD, Brant SR, Silverberg MS, Taylor KD, Barmada MM, Bitton A, Dassopoulos T, Datta LW, Green T, Griffiths AM, Kistner EO, Murtha MT, Regueiro MD, Rotter JI, Schumm LP, Steinhart AH, Targan SR, Xavier RJ; NIDDK IBD Genetics Consortium, Libioulle C, Sandor C, Lathrop M, Belaiche J, Dewit O, Gut I, Heath S, Laukens D, Mni M, Rutgeerts P, Van Gossum A, Zelenika D, Franchimont D, Hugot JP, de Vos M, Vermeire S, Louis E; Belgian-French IBD Consortium; Wellcome Trust Case Control Consortium, Cardon LR, Anderson CA, Drummond H, Nimmo E, Ahmad T, Prescott NJ, Onnie CM, Fisher SA, Marchini J, Ghori J, Bumpstead S, Gwilliam R, Tremelling M, Deloukas P, Mansfield J, Jewell D, Satsangi J, Mathew CG, Parkes M, Georges M, Daly MJ.

    Nat Genet. 2008 Aug;40(8):955-62. Epub 2008 Jun 29.PMID: 18587394 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA.

    Fritsche LG, Loenhardt T, Janssen A, Fisher SA, Rivera A, Keilhauer CN, Weber BH.

    Nat Genet. 2008 Jul;40(7):892-6. Epub 2008 May 30.PMID: 18511946 [PubMed - indexed for MEDLINE]Related articles

    11.

    Hypoxia-inducible transcription factor-1alpha triggers an autocrine survival pathway during embryonic cardiac outflow tract remodeling.

    Liu H, Fisher SA.

    Circ Res. 2008 Jun 6;102(11):1331-9. Epub 2008 May 8.PMID: 18467628 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease.

    Fisher SA, Tremelling M, Anderson CA, Gwilliam R, Bumpstead S, Prescott NJ, Nimmo ER, Massey D, Berzuini C, Johnson C, Barrett JC, Cummings FR, Drummond H, Lees CW, Onnie CM, Hanson CE, Blaszczyk K, Inouye M, Ewels P, Ravindrarajah R, Keniry A, Hunt S, Carter M, Watkins N, Ouwehand W, Lewis CM, Cardon L; Wellcome Trust Case Control Consortium, Lobo A, Forbes A, Sanderson J, Jewell DP, Mansfield JC, Deloukas P, Mathew CG, Parkes M, Satsangi J.

    Nat Genet. 2008 Jun;40(6):710-2. Epub 2008 Apr 27.PMID: 18438406 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    Uterine artery myosin phosphatase isoform switching and increased sensitivity to SNP in a rat L-NAME model of hypertension of pregnancy.

    Lu Y, Zhang H, Gokina N, Mandala M, Sato O, Ikebe M, Osol G, Fisher SA.

    Am J Physiol Cell Physiol. 2008 Feb;294(2):C564-71. Epub 2007 Dec 19.PMID: 18094148 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Diverse effects of the CARD15 and IBD5 loci on clinical phenotype in 630 patients with Crohn's disease.

    Onnie CM, Fisher SA, Prescott NJ, Mirza MM, Green P, Sanderson J, Forbes A, Lewis CM, Mathew CG.

    Eur J Gastroenterol Hepatol. 2008 Jan;20(1):37-45.PMID: 18090989 [PubMed - indexed for MEDLINE]Related articles

    15.

    The developing embryonic cardiac outflow tract is highly sensitive to oxidant stress.

    Fisher SA.

    Dev Dyn. 2007 Dec;236(12):3496-502.PMID: 17994543 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.

    Wellcome Trust Case Control Consortium; Australo-Anglo-American Spondylitis Consortium (TASC), Burton PR, Clayton DG, Cardon LR, Craddock N, Deloukas P, Duncanson A, Kwiatkowski DP, McCarthy MI, Ouwehand WH, Samani NJ, Todd JA, Donnelly P, Barrett JC, Davison D, Easton D, Evans DM, Leung HT, Marchini JL, Morris AP, Spencer CC, Tobin MD, Attwood AP, Boorman JP, Cant B, Everson U, Hussey JM, Jolley JD, Knight AS, Koch K, Meech E, Nutland S, Prowse CV, Stevens HE, Taylor NC, Walters GR, Walker NM, Watkins NA, Winzer T, Jones RW, McArdle WL, Ring SM, Strachan DP, Pembrey M, Breen G, St Clair D, Caesar S, Gordon-Smith K, Jones L, Fraser C, Green EK, Grozeva D, Hamshere ML, Holmans PA, Jones IR, Kirov G, Moskivina V, Nikolov I, O'Donovan MC, Owen MJ, Collier DA, Elkin A, Farmer A, Williamson R, McGuffin P, Young AH, Ferrier IN, Ball SG, Balmforth AJ, Barrett JH, Bishop TD, Iles MM, Maqbool A, Yuldasheva N, Hall AS, Braund PS, Dixon RJ, Mangino M, Stevens S, Thompson JR, Bredin F, Tremelling M, Parkes M, Drummond H, Lees CW, Nimmo ER, Satsangi J, Fisher SA, Forbes A, Lewis CM, Onnie CM, Prescott NJ, Sanderson J, Matthew CG, Barbour J, Mohiuddin MK, Todhunter CE, Mansfield JC, Ahmad T, Cummings FR, Jewell DP, Webster J, Brown MJ, Lathrop MG, Connell J, Dominiczak A, Marcano CA, Burke B, Dobson R, Gungadoo J, Lee KL, Munroe PB, Newhouse SJ, Onipinla A, Wallace C, Xue M, Caulfield M, Farrall M, Barton A; Biologics in RA Genetics and Genomics Study Syndicate (BRAGGS) Steering Committee, Bruce IN, Donovan H, Eyre S, Gilbert PD, Hilder SL, Hinks AM, John SL, Potter C, Silman AJ, Symmons DP, Thomson W, Worthington J, Dunger DB, Widmer B, Frayling TM, Freathy RM, Lango H, Perry JR, Shields BM, Weedon MN, Hattersley AT, Hitman GA, Walker M, Elliott KS, Groves CJ, Lindgren CM, Rayner NW, Timpson NJ, Zeggini E, Newport M, Sirugo G, Lyons E, Vannberg F, Hill AV, Bradbury LA, Farrar C, Pointon JJ, Wordsworth P, Brown MA, Franklyn JA, Heward JM, Simmonds MJ, Gough SC, Seal S; Breast Cancer Susceptibility Collaboration (UK), Stratton MR, Rahman N, Ban M, Goris A, Sawcer SJ, Compston A, Conway D, Jallow M, Newport M, Sirugo G, Rockett KA, Bumpstead SJ, Chaney A, Downes K, Ghori MJ, Gwilliam R, Hunt SE, Inouye M, Keniry A, King E, McGinnis R, Potter S, Ravindrarajah R, Whittaker P, Widden C, Withers D, Cardin NJ, Davison D, Ferreira T, Pereira-Gale J, Hallgrimsdo'ttir IB, Howie BN, Su Z, Teo YY, Vukcevic D, Bentley D, Brown MA, Compston A, Farrall M, Hall AS, Hattersley AT, Hill AV, Parkes M, Pembrey M, Stratton MR, Mitchell SL, Newby PR, Brand OJ, Carr-Smith J, Pearce SH, McGinnis R, Keniry A, Deloukas P, Reveille JD, Zhou X, Sims AM, Dowling A, Taylor J, Doan T, Davis JC, Savage L, Ward MM, Learch TL, Weisman MH, Brown M.

    Nat Genet. 2007 Nov;39(11):1329-37. Epub 2007 Oct 21.PMID: 17952073 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD15) gene.

    King K, Bagnall R, Fisher SA, Sheikh F, Cuthbert A, Tan S, Mundy NI, Rosenstiel P, Schreiber S, Mathew CG, Roberts RG.

    Genomics. 2007 Oct;90(4):493-501. Epub 2007 Aug 24.PMID: 17719742 [PubMed - indexed for MEDLINE]Related articles

    18.

    Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohorts.

    Browning BL, Annese V, Barclay ML, Bingham SA, Brand S, Büning C, Castro M, Cucchiara S, Dallapiccola B, Drummond H, Ferguson LR, Ferraris A, Fisher SA, Gearry RB, Glas J, Henckaerts L, Huebner C, Knafelz D, Lakatos L, Lakatos PL, Latiano A, Liu X, Mathew C, Müller-Myhsok B, Newman WG, Nimmo ER, Noble CL, Palmieri O, Parkes M, Petermann I, Rutgeerts P, Satsangi J, Shelling AN, Siminovitch KA, Török HP, Tremelling M, Vermeire S, Valvano MR, Witt H.

    J Med Genet. 2008 Jan;45(1):36-42. Epub 2007 Aug 10.PMID: 17693570 [PubMed - indexed for MEDLINE]Related articles

    19.

    Role of hypoxia in the evolution and development of the cardiovascular system.

    Fisher SA, Burggren WW.

    Antioxid Redox Signal. 2007 Sep;9(9):1339-52. Review.PMID: 17627471 [PubMed - indexed for MEDLINE]Related articles

    20.

    Workshop report on the extraction of foetal DNA from maternal plasma.

    Legler TJ, Liu Z, Mavrou A, Finning K, Hromadnikova I, Galbiati S, Meaney C, Hultén MA, Crea F, Olsson ML, Maddocks DG, Huang D, Fisher SA, Sprenger-Haussels M, Soussan AA, van der Schoot CE.

    Prenat Diagn. 2007 Sep;27(9):824-9.PMID: 17604339 [PubMed - indexed for MEDLINE]Related articles

    21.

    Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.

    Parkes M, Barrett JC, Prescott NJ, Tremelling M, Anderson CA, Fisher SA, Roberts RG, Nimmo ER, Cummings FR, Soars D, Drummond H, Lees CW, Khawaja SA, Bagnall R, Burke DA, Todhunter CE, Ahmad T, Onnie CM, McArdle W, Strachan D, Bethel G, Bryan C, Lewis CM, Deloukas P, Forbes A, Sanderson J, Jewell DP, Satsangi J, Mansfield JC; Wellcome Trust Case Control Consortium, Cardon L, Mathew CG.

    Nat Genet. 2007 Jul;39(7):830-2. Epub 2007 Jun 6.PMID: 17554261 [PubMed - indexed for MEDLINE]Related articlesFree article

    22.

    Combined evidence from three large British Association studies rejects TUCAN/CARD8 as an IBD susceptibility gene.

    Fisher SA, Mirza MM, Onnie CM, Soars D, Lewis CM, Prescott NJ, Mathew CG, Sanderson J, Forbes A, Todhunter C, Donaldson P, Mansfield J.

    Gastroenterology. 2007 May;132(5):2078-80. No abstract available. PMID: 17484911 [PubMed - indexed for MEDLINE]Related articles

    23.

    A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5.

    Prescott NJ, Fisher SA, Franke A, Hampe J, Onnie CM, Soars D, Bagnall R, Mirza MM, Sanderson J, Forbes A, Mansfield JC, Lewis CM, Schreiber S, Mathew CG.

    Gastroenterology. 2007 May;132(5):1665-71. Epub 2007 Mar 24.PMID: 17484864 [PubMed - indexed for MEDLINE]Related articles

    24.

    IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease.

    Tremelling M, Cummings F, Fisher SA, Mansfield J, Gwilliam R, Keniry A, Nimmo ER, Drummond H, Onnie CM, Prescott NJ, Sanderson J, Bredin F, Berzuini C, Forbes A, Lewis CM, Cardon L, Deloukas P, Jewell D, Mathew CG, Parkes M, Satsangi J.

    Gastroenterology. 2007 May;132(5):1657-64. Epub 2007 Feb 24.PMID: 17484863 [PubMed - indexed for MEDLINE]Related articlesFree article

    25.

    Data acquisition for meta-analysis of genome-wide linkage studies using the genome search meta-analysis method.

    Forabosco P, Ng MY, Bouzigon E, Fisher SA, Levinson DF, Lewis CM.

    Hum Hered. 2007;64(1):74-81. Epub 2007 Apr 27.PMID: 17483599 [PubMed - indexed for MEDLINE]Related articlesFree article

    26.

    Meta-analysis of genome-wide linkage studies for multiple sclerosis, using an extended GSMA method.

    Hermanowski J, Bouzigon E, Forabosco P, Ng MY, Fisher SA, Lewis CM.

    Eur J Hum Genet. 2007 Jun;15(6):703-10. Epub 2007 Mar 21.PMID: 17377519 [PubMed - indexed for MEDLINE]Related articlesFree article

    27.

    Conditioning effect of blood flow on resistance artery smooth muscle myosin phosphatase.

    Zhang H, Fisher SA.

    Circ Res. 2007 Mar 16;100(5):730-7. Epub 2007 Feb 9.PMID: 17293476 [PubMed - indexed for MEDLINE]Related articlesFree article

    28.

    Case-control genetic association study of fibulin-6 (FBLN6 or HMCN1) variants in age-related macular degeneration (AMD).

    Fisher SA, Rivera A, Fritsche LG, Keilhauer CN, Lichtner P, Meitinger T, Rudolph G, Weber BH.

    Hum Mutat. 2007 Apr;28(4):406-13.PMID: 17216616 [PubMed - indexed for MEDLINE]Related articles

    29.

    Genetic variation in myosin IXB is associated with ulcerative colitis.

    van Bodegraven AA, Curley CR, Hunt KA, Monsuur AJ, Linskens RK, Onnie CM, Crusius JB, Annese V, Latiano A, Silverberg MS, Bitton A, Fisher SA, Steinhart AH, Forbes A, Sanderson J, Prescott NJ, Strachan DP, Playford RJ, Mathew CG, Wijmenga C, Daly MJ, Rioux JD, van Heel DA.

    Gastroenterology. 2006 Dec;131(6):1768-74. Epub 2006 Sep 8.PMID: 17087940 [PubMed - indexed for MEDLINE]Related articles

    30.

    Assessment of the contribution of CFH and chromosome 10q26 AMD susceptibility loci in a Russian population isolate.

    Fisher SA, Rivera A, Fritsche LG, Babadjanova G, Petrov S, Weber BH.

    Br J Ophthalmol. 2007 May;91(5):576-8. Epub 2006 Oct 18.PMID: 17050575 [PubMed - indexed for MEDLINE]Related articles

    31.

    Meta-analysis of genome-wide linkage studies of systemic lupus erythematosus.

    Forabosco P, Gorman JD, Cleveland C, Kelly JA, Fisher SA, Ortmann WA, Johansson C, Johanneson B, Moser KL, Gaffney PM, Tsao BP, Cantor RM, Alarcón-Riquelme ME, Behrens TW, Harley JB, Lewis CM, Criswell LA.

    Genes Immun. 2006 Oct;7(7):609-14. Epub 2006 Sep 14.PMID: 16971955 [PubMed - indexed for MEDLINE]Related articles

    32.

    Investigation of association of the DLG5 gene with phenotypes of inflammatory bowel disease in the British population.

    Pearce AV, Fisher SA, Prescott NJ, Onnie CM, Pattni R, Green P, Forbes A, Mansfield J, Sanderson J, Schreiber S, Lewis CM, Mathew CG.

    Int J Colorectal Dis. 2007 Apr;22(4):419-24. Epub 2006 May 31.PMID: 16944184 [PubMed - indexed for MEDLINE]Related articles

    33.

    Cardiac myocyte cytokinesis: The contractile ring is the thing.

    Egelhoff TT, Fisher SA.

    J Mol Cell Cardiol. 2006 Oct;41(4):592-4. Epub 2006 Aug 24. No abstract available. PMID: 16934289 [PubMed - indexed for MEDLINE]Related articles

    34.

    Brood patches of American kestrels altered by experimental exposure to PCBs.

    Fisher SA, Bortolotti GR, Fernie KJ, Bird DM, Smits JE.

    J Toxicol Environ Health A. 2006 Sep;69(17):1603-12.PMID: 16854788 [PubMed - indexed for MEDLINE]Related articles

    35.

    Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease.

    Fisher SA, Hampe J, Onnie CM, Daly MJ, Curley C, Purcell S, Sanderson J, Mansfield J, Annese V, Forbes A, Lewis CM, Schreiber S, Rioux JD, Mathew CG.

    Hum Mutat. 2006 Aug;27(8):778-85.PMID: 16835882 [PubMed - indexed for MEDLINE]Related articles

    36.

    Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31.

    Onnie C, Fisher SA, King K, Mirza M, Roberts R, Forbes A, Sanderson J, Lewis CM, Mathew CG.

    Genes Immun. 2006 Jul;7(5):359-65. Epub 2006 May 18.PMID: 16724073 [PubMed - indexed for MEDLINE]Related articles

    37.

    Associations of allelic variants of the multidrug resistance gene (ABCB1 or MDR1) and inflammatory bowel disease and their effects on disease behavior: a case-control and meta-analysis study.

    Onnie CM, Fisher SA, Pattni R, Sanderson J, Forbes A, Lewis CM, Mathew CG.

    Inflamm Bowel Dis. 2006 Apr;12(4):263-71.PMID: 16633048 [PubMed - indexed for MEDLINE]Related articlesFree article

    38.

    Myosin phosphatase isoform switching in vascular smooth muscle development.

    Payne MC, Zhang HY, Prosdocimo T, Joyce KM, Koga Y, Ikebe M, Fisher SA.

    J Mol Cell Cardiol. 2006 Feb;40(2):274-82. Epub 2005 Dec 13.PMID: 16356512 [PubMed - indexed for MEDLINE]Related articles

    39.

    Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15.

    King K, Sheikh MF, Cuthbert AP, Fisher SA, Onnie CM, Mirza MM, Pattni RC, Sanderson J, Forbes A, Mansfield J, Lewis CM, Roberts RG, Mathew CG.

    Hum Mutat. 2006 Jan;27(1):44-54.PMID: 16278823 [PubMed - indexed for MEDLINE]Related articles

    40.

    A general autoimmunity gene (PTPN22) is not associated with inflammatory bowel disease in a British population.

    Prescott NJ, Fisher SA, Onnie C, Pattni R, Steer S, Sanderson J, Forbes A, Lewis CM, Mathew CG.

    Tissue Antigens. 2005 Oct;66(4):318-20.PMID: 16185328 [PubMed - indexed for MEDLINE]Related articles

    41.

    Competition of PTB with TIA proteins for binding to a U-rich cis-element determines tissue-specific splicing of the myosin phosphatase targeting subunit 1.

    Shukla S, Del Gatto-Konczak F, Breathnach R, Fisher SA.

    RNA. 2005 Nov;11(11):1725-36. Epub 2005 Sep 21.PMID: 16177139 [PubMed - indexed for MEDLINE]Related articlesFree article

    42.

    Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk.

    Rivera A, Fisher SA, Fritsche LG, Keilhauer CN, Lichtner P, Meitinger T, Weber BH.

    Hum Mol Genet. 2005 Nov 1;14(21):3227-36. Epub 2005 Sep 20.PMID: 16174643 [PubMed - indexed for MEDLINE]Related articlesFree article

    43.

    Behavioral variation and its consequences during incubation for American kestrels exposed to polychlorinated biphenyls.

    Fisher SA, Bortolotti GR, Fernie KJ, Bird DM, Smits JE.

    Ecotoxicol Environ Saf. 2006 Feb;63(2):226-35.PMID: 16169079 [PubMed - indexed for MEDLINE]Related articles

    44.

    Differential levels of tissue hypoxia in the developing chicken heart.

    Wikenheiser J, Doughman YQ, Fisher SA, Watanabe M.

    Dev Dyn. 2006 Jan;235(1):115-23.PMID: 16028272 [PubMed - indexed for MEDLINE]Related articlesFree article

    45.

    No association of the NFKB1 promoter polymorphism with ulcerative colitis in a British case control cohort.

    Mirza MM, Fisher SA, Onnie C, Lewis CM, Mathew CG, Sanderson J, Forbes A.

    Gut. 2005 Aug;54(8):1205-6. No abstract available. PMID: 16009698 [PubMed - indexed for MEDLINE]Related articlesFree article

    46.

    Meta-analysis of genome scans of age-related macular degeneration.

    Fisher SA, Abecasis GR, Yashar BM, Zareparsi S, Swaroop A, Iyengar SK, Klein BE, Klein R, Lee KE, Majewski J, Schultz DW, Klein ML, Seddon JM, Santangelo SL, Weeks DE, Conley YP, Mah TS, Schmidt S, Haines JL, Pericak-Vance MA, Gorin MB, Schulz HL, Pardi F, Lewis CM, Weber BH.

    Hum Mol Genet. 2005 Aug 1;14(15):2257-64. Epub 2005 Jun 29.PMID: 15987700 [PubMed - indexed for MEDLINE]Related articlesFree article

    47.

    Corneodesmosin (CDSN) gene association with psoriasis vulgaris in Caucasian but not in Japanese populations.

    Ameen M, Allen MH, Fisher SA, Lewis CM, Cuthbert A, Kondeatis E, Vaughan RW, Murakami H, Nakagawa H, Barker JN.

    Clin Exp Dermatol. 2005 Jul;30(4):414-8.PMID: 15953084 [PubMed - indexed for MEDLINE]Related articles

    48.

    Association of DLG5 R30Q variant with inflammatory bowel disease.

    Daly MJ, Pearce AV, Farwell L, Fisher SA, Latiano A, Prescott NJ, Forbes A, Mansfield J, Sanderson J, Langelier D, Cohen A, Bitton A, Wild G, Lewis CM, Annese V, Mathew CG, Rioux JD.

    Eur J Hum Genet. 2005 Jul;13(7):835-9.PMID: 15841097 [PubMed - indexed for MEDLINE]Related articlesFree article

    49.

    Association of R602W in a protein tyrosine phosphatase gene with a high risk of rheumatoid arthritis in a British population: evidence for an early onset/disease severity effect.

    Steer S, Lad B, Grumley JA, Kingsley GH, Fisher SA.

    Arthritis Rheum. 2005 Jan;52(1):358-60. No abstract available. PMID: 15641088 [PubMed - indexed for MEDLINE]Related articlesFree article

    50.

    The development of the embryonic outflow tract provides novel insights into cardiac differentiation and remodeling.

    Sugishita Y, Watanabe M, Fisher SA.

    Trends Cardiovasc Med. 2004 Aug;14(6):235-41. Review.PMID: 15451515 [PubMed - indexed for MEDLINE]Related articles

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