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Journal Abstract Search

231 related items for PubMed ID: 17661910

  • 1. Analysis of BTNL2 genetic polymorphisms in British and Dutch patients with sarcoidosis.
    Spagnolo P, Sato H, Grutters JC, Renzoni EA, Marshall SE, Ruven HJ, Wells AU, Tzouvelekis A, van Moorsel CH, van den Bosch JM, du Bois RM, Welsh KI.
    Tissue Antigens; 2007 Sep; 70(3):219-27. PubMed ID: 17661910
    [Abstract] [Full Text] [Related]

  • 2. Genetic characterization and susceptibility for sarcoidosis in Japanese patients: risk factors of BTNL2 gene polymorphisms and HLA class II alleles.
    Suzuki H, Ota M, Meguro A, Katsuyama Y, Kawagoe T, Ishihara M, Asukata Y, Takeuchi M, Ito N, Shibuya E, Nomura E, Uemoto R, Nishide T, Namba K, Kitaichi N, Morimoto S, Kaburaki T, Ando Y, Takenaka S, Nakamura J, Saeki K, Ohno S, Inoko H, Mizuki N.
    Invest Ophthalmol Vis Sci; 2012 Oct 11; 53(11):7109-15. PubMed ID: 22991420
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  • 3. BTNL2 gene polymorphism associations with susceptibility and phenotype expression in sarcoidosis.
    Morais A, Lima B, Peixoto MJ, Alves H, Marques A, Delgado L.
    Respir Med; 2012 Dec 11; 106(12):1771-7. PubMed ID: 23017494
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  • 4. Butyrophilin-like 2 gene is associated with ulcerative colitis in the Japanese under strong linkage disequilibrium with HLA-DRB1*1502.
    Mochida A, Kinouchi Y, Negoro K, Takahashi S, Takagi S, Nomura E, Kakuta Y, Tosa M, Shimosegawa T.
    Tissue Antigens; 2007 Aug 11; 70(2):128-35. PubMed ID: 17610417
    [Abstract] [Full Text] [Related]

  • 5. Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves' disease appears to be secondary to DRB1 exon 2 position beta74.
    Simmonds MJ, Heward JM, Barrett JC, Franklyn JA, Gough SC.
    Clin Endocrinol (Oxf); 2006 Oct 11; 65(4):429-32. PubMed ID: 16984233
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  • 6. A common haplotype of the C-C chemokine receptor 2 gene and HLA-DRB1*0301 are independent genetic risk factors for Löfgren's syndrome.
    Spagnolo P, Sato H, Grunewald J, Brynedal B, Hillert J, Mañá J, Wells AU, Eklund A, Welsh KI, du Bois RM.
    J Intern Med; 2008 Nov 11; 264(5):433-41. PubMed ID: 18513341
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  • 7. SNP Variants in Major Histocompatibility Complex Are Associated with Sarcoidosis Susceptibility-A Joint Analysis in Four European Populations.
    Wolin A, Lahtela EL, Anttila V, Petrek M, Grunewald J, van Moorsel CHM, Eklund A, Grutters JC, Kolek V, Mrazek F, Kishore A, Padyukov L, Pietinalho A, Ronninger M, Seppänen M, Selroos O, Lokki ML.
    Front Immunol; 2017 Nov 11; 8():422. PubMed ID: 28469621
    [Abstract] [Full Text] [Related]

  • 8. Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15.
    Traherne JA, Barcellos LF, Sawcer SJ, Compston A, Ramsay PP, Hauser SL, Oksenberg JR, Trowsdale J.
    Hum Mol Genet; 2006 Jan 01; 15(1):155-61. PubMed ID: 16321988
    [Abstract] [Full Text] [Related]

  • 9. Associations between sarcoidosis clinical course and ANXA11 rs1049550 C/T, BTNL2 rs2076530 G/A, and HLA class I and II alleles.
    Morais A, Lima B, Alves H, Melo N, Mota PC, Marques A, Delgado L.
    Clin Respir J; 2018 Feb 01; 12(2):532-537. PubMed ID: 27662826
    [Abstract] [Full Text] [Related]

  • 10. Sarcoidosis is associated with a truncating splice site mutation in BTNL2.
    Valentonyte R, Hampe J, Huse K, Rosenstiel P, Albrecht M, Stenzel A, Nagy M, Gaede KI, Franke A, Haesler R, Koch A, Lengauer T, Seegert D, Reiling N, Ehlers S, Schwinger E, Platzer M, Krawczak M, Müller-Quernheim J, Schürmann M, Schreiber S.
    Nat Genet; 2005 Apr 01; 37(4):357-64. PubMed ID: 15735647
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  • 13. C-C chemokine receptor 2 and sarcoidosis: association with Lofgren's syndrome.
    Spagnolo P, Renzoni EA, Wells AU, Sato H, Grutters JC, Sestini P, Abdallah A, Gramiccioni E, Ruven HJ, du Bois RM, Welsh KI.
    Am J Respir Crit Care Med; 2003 Nov 15; 168(10):1162-6. PubMed ID: 12882757
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  • 14. Association of tumour necrosis factor-alpha, lymphotoxin-alpha and HLA-DRB1 gene polymorphisms with Löfgren's syndrome in Czech patients with sarcoidosis.
    Mrazek F, Holla LI, Hutyrova B, Znojil V, Vasku A, Kolek V, Welsh KI, Vacha J, du Bois RM, Petrek M.
    Tissue Antigens; 2005 Feb 15; 65(2):163-71. PubMed ID: 15713215
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  • 17. Confirmation of the novel association at the BTNL2 locus with ulcerative colitis.
    Pathan S, Gowdy RE, Cooney R, Beckly JB, Hancock L, Guo C, Barrett JC, Morris A, Jewell DP.
    Tissue Antigens; 2009 Oct 15; 74(4):322-9. PubMed ID: 19659809
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  • 18. Exome sequencing identifies novel rheumatoid arthritis-susceptible variants in the BTNL2.
    Mitsunaga S, Hosomichi K, Okudaira Y, Nakaoka H, Kunii N, Suzuki Y, Kuwana M, Sato S, Kaneko Y, Homma Y, Kashiwase K, Azuma F, Kulski JK, Inoue I, Inoko H.
    J Hum Genet; 2013 Apr 15; 58(4):210-5. PubMed ID: 23364395
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  • 19. Novel 6p21.3 Risk Haplotype Predisposes to Acute Coronary Syndrome.
    Sinisalo J, Vlachopoulou E, Marchesani M, Nokelainen J, Mäyränpää MI, Lappalainen J, Paakkanen R, Wennerström A, Salli K, Niemi HJ, Männistö S, Salo P, Junttila J, Eskola M, Nikus K, Arstila TP, Perola M, Huikuri H, Karhunen PJ, Kovanen PT, Palotie A, Havulinna AS, Lluis-Ganella C, Marrugat J, Elosua R, Salomaa V, Nieminen MS, Lokki ML.
    Circ Cardiovasc Genet; 2016 Feb 15; 9(1):55-63. PubMed ID: 26679868
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