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Page 1
SMN deficiency in severe models of spinal muscular atrophy causes widespread intron retention and DNA damage.
Jangi M, Fleet C, Cullen P, Gupta SV, Mekhoubad S, Chiao E, Allaire N, Bennett CF, Rigo F, Krainer AR, Hurt JA, Carulli JP, Staropoli JF. Jangi M, et al. Among authors: cullen p. Proc Natl Acad Sci U S A. 2017 Mar 21;114(12):E2347-E2356. doi: 10.1073/pnas.1613181114. Epub 2017 Mar 7. Proc Natl Acad Sci U S A. 2017. PMID: 28270613 Free PMC article.
Rescue of gene-expression changes in an induced mouse model of spinal muscular atrophy by an antisense oligonucleotide that promotes inclusion of SMN2 exon 7.
Staropoli JF, Li H, Chun SJ, Allaire N, Cullen P, Thai A, Fleet CM, Hua Y, Bennett CF, Krainer AR, Kerr D, McCampbell A, Rigo F, Carulli JP. Staropoli JF, et al. Among authors: cullen p. Genomics. 2015 Apr;105(4):220-8. doi: 10.1016/j.ygeno.2015.01.007. Epub 2015 Jan 31. Genomics. 2015. PMID: 25645699 Free article.
Identification of Novel CD4+ T Cell Subsets in the Target Tissue of Sjögren's Syndrome and Their Differential Regulation by the Lymphotoxin/LIGHT Signaling Axis.
Haskett S, Ding J, Zhang W, Thai A, Cullen P, Xu S, Petersen B, Kuznetsov G, Jandreski L, Hamann S, Reynolds TL, Allaire N, Zheng TS, Mingueneau M. Haskett S, et al. Among authors: cullen p. J Immunol. 2016 Nov 15;197(10):3806-3819. doi: 10.4049/jimmunol.1600407. Epub 2016 Oct 7. J Immunol. 2016. PMID: 27815440
Cx3cr1-deficient microglia exhibit a premature aging transcriptome.
Gyoneva S, Hosur R, Gosselin D, Zhang B, Ouyang Z, Cotleur AC, Peterson M, Allaire N, Challa R, Cullen P, Roberts C, Miao K, Reynolds TL, Glass CK, Burkly L, Ransohoff RM. Gyoneva S, et al. Among authors: cullen p. Life Sci Alliance. 2019 Dec 2;2(6):e201900453. doi: 10.26508/lsa.201900453. Print 2019 Dec. Life Sci Alliance. 2019. PMID: 31792059 Free PMC article.
Increased systemic HSP70B levels in spinal muscular atrophy infants.
Eichelberger EJ, Alves CRR, Zhang R, Petrillo M, Cullen P, Farwell W, Hurt JA, Staropoli JF, Swoboda KJ. Eichelberger EJ, et al. Among authors: cullen p. Ann Clin Transl Neurol. 2021 Jul;8(7):1495-1501. doi: 10.1002/acn3.51377. Epub 2021 May 15. Ann Clin Transl Neurol. 2021. PMID: 33991176 Free PMC article.
Identification of regulators of the myofibroblast phenotype of primary dermal fibroblasts from early diffuse systemic sclerosis patients.
Chadli L, Sotthewes B, Li K, Andersen SN, Cahir-McFarland E, Cheung M, Cullen P, Dorjée A, de Vries-Bouwstra JK, Huizinga TWJ, Fischer DF, DeGroot J, Viney JL, Zheng TS, Aarbiou J, Gardet A. Chadli L, et al. Among authors: cullen p. Sci Rep. 2019 Mar 14;9(1):4521. doi: 10.1038/s41598-019-41153-w. Sci Rep. 2019. PMID: 30872777 Free PMC article.
764 results