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232 related items for PubMed ID: 28340352
21. Interleukin-7 receptor-α gene mutations are not detected in adult T-cell acute lymphoblastic leukemia. Rozovski U, Li P, Harris D, Ohanian M, Kantarjian H, Estrov Z. Cancer Med; 2014 Jun; 3(3):550-4. PubMed ID: 24678068 [Abstract] [Full Text] [Related]
22. Genetic variants in interleukin 7 receptor α chain (IL-7Ra) are associated with multiple sclerosis risk and disability progression in Central European Slovak population. Čierny D, Hányšová S, Michalik J, Kantorová E, Kurča E, Škereňová M, Lehotský J. J Neuroimmunol; 2015 May 15; 282():80-4. PubMed ID: 25903732 [Abstract] [Full Text] [Related]
23. Association of interleukin 7 receptor gene polymorphism rs6897932 with multiple sclerosis patients in Khuzestan. Majdinasab N, Hosseini Behbahani M, Galehdari H, Mohaghegh M. Iran J Neurol; 2014 Jul 04; 13(3):168-71. PubMed ID: 25422737 [Abstract] [Full Text] [Related]
24. Genetic variants in IL2RA and IL7R affect multiple sclerosis disease risk and progression. Traboulsee AL, Bernales CQ, Ross JP, Lee JD, Sadovnick AD, Vilariño-Güell C. Neurogenetics; 2014 Aug 04; 15(3):165-9. PubMed ID: 24770783 [Abstract] [Full Text] [Related]
25. A functional variant that affects exon-skipping and protein expression of SP140 as genetic mechanism predisposing to multiple sclerosis. Matesanz F, Potenciano V, Fedetz M, Ramos-Mozo P, Abad-Grau Mdel M, Karaky M, Barrionuevo C, Izquierdo G, Ruiz-Peña JL, García-Sánchez MI, Lucas M, Fernández Ó, Leyva L, Otaegui D, Muñoz-Culla M, Olascoaga J, Vandenbroeck K, Alloza I, Astobiza I, Antigüedad A, Villar LM, Álvarez-Cermeño JC, Malhotra S, Comabella M, Montalban X, Saiz A, Blanco Y, Arroyo R, Varadé J, Urcelay E, Alcina A. Hum Mol Genet; 2015 Oct 01; 24(19):5619-27. PubMed ID: 26152201 [Abstract] [Full Text] [Related]
26. Interleukin 7 receptor alpha chain haplotypes vary in their influence on multiple sclerosis susceptibility and response to interferon Beta. Hoe E, McKay F, Schibeci S, Heard R, Stewart G, Booth D. J Interferon Cytokine Res; 2010 May 01; 30(5):291-8. PubMed ID: 20187771 [Abstract] [Full Text] [Related]
27. Aberrant expression of alternative splicing variants in multiple sclerosis - A systematic review. Hecker M, Rüge A, Putscher E, Boxberger N, Rommer PS, Fitzner B, Zettl UK. Autoimmun Rev; 2019 Jul 01; 18(7):721-732. PubMed ID: 31059848 [Abstract] [Full Text] [Related]
28. Systematic analysis of alternative exon-dependent interactome remodeling reveals multitasking functions of gene regulatory factors. Roth JF, Braunschweig U, Wu M, Li JD, Lin ZY, Larsen B, Weatheritt RJ, Gingras AC, Blencowe BJ. Mol Cell; 2023 Dec 07; 83(23):4222-4238.e10. PubMed ID: 38065061 [Abstract] [Full Text] [Related]
29. Alternative splicing of interleukin-7 (IL-7) and interleukin-7 receptor alpha (IL-7Ralpha) in peripheral blood from patients with multiple sclerosis (MS). Rane L, Vudattu N, Bourcier K, Graniar E, Hillert J, Seyfert V, Maeurer MJ. J Neuroimmunol; 2010 May 07; 222(1-2):82-6. PubMed ID: 20226540 [Abstract] [Full Text] [Related]
30. Expression and clinical significance of IL7R, NFATc2, and RNF213 in familial and sporadic multiple sclerosis. Imani SZH, Hojati Z, Khalilian S, Dehghanian F, Kheirollahi M, Khorrami M, Shaygannejad V, Mirmosayyeb O. Sci Rep; 2021 Sep 28; 11(1):19260. PubMed ID: 34584155 [Abstract] [Full Text] [Related]
31. Transcriptome-wide modulation of splicing by the exon junction complex. Wang Z, Murigneux V, Le Hir H. Genome Biol; 2014 Sep 28; 15(12):551. PubMed ID: 25476502 [Abstract] [Full Text] [Related]
32. Haplotype 4 of the multiple sclerosis-associated interleukin-7 receptor alpha gene influences the frequency of recent thymic emigrants. Broux B, Hellings N, Venken K, Rummens JL, Hensen K, Van Wijmeersch B, Stinissen P. Genes Immun; 2010 Jun 28; 11(4):326-33. PubMed ID: 20072142 [Abstract] [Full Text] [Related]
33. Association between the IL7R T244I polymorphism and multiple sclerosis risk: a meta analysis. Wu S, Liu Q, Zhu JM, Wang MR, Li J, Sun MG. Neurol Sci; 2016 Sep 28; 37(9):1467-74. PubMed ID: 27188999 [Abstract] [Full Text] [Related]
34. Dual role of the ddx5/ddx17 RNA helicases in the control of the pro-migratory NFAT5 transcription factor. Germann S, Gratadou L, Zonta E, Dardenne E, Gaudineau B, Fougère M, Samaan S, Dutertre M, Jauliac S, Auboeuf D. Oncogene; 2012 Oct 18; 31(42):4536-49. PubMed ID: 22266867 [Abstract] [Full Text] [Related]
35. Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. Paraboschi EM, Rimoldi V, Soldà G, Tabaglio T, Dall'Osso C, Saba E, Vigliano M, Salviati A, Leone M, Benedetti MD, Fornasari D, Saarela J, De Jager PL, Patsopoulos NA, D'Alfonso S, Gemmati D, Duga S, Asselta R. Hum Mol Genet; 2014 Dec 20; 23(25):6746-61. PubMed ID: 25080502 [Abstract] [Full Text] [Related]