Page 16 - 北京京煤集团总医院第十一届·2023学术年会论文集
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北京京煤集团总医院 第十一届·2023 学术年会论文集
Fitzpatrick AM, Chandler JD: Exacerbation-prone pediatric asthma is associated with arginine,
lysine, methionine pathway alterations. The Journal of allergy and clinical immunology 2022.
28. Wypych TP, Marzi R, Wu GF, Lanzavecchia A, Sallusto F: Role of B cells in T(H) cell responses
in a mouse model of asthma. The Journal of allergy and clinical immunology 2018, 141(4):1395-
1410.
29. Méndez-Enríquez E, Hallgren J: Mast Cells and Their Progenitors in Allergic Asthma. Frontiers
in immunology 2019, 10:821.
30. Cong J, Wei H: Natural Killer Cells in the Lungs. Frontiers in immunology 2019, 10:1416.
31. Barnig C, Cernadas M, Dutile S, Liu X, Perrella MA, Kazani S, Wechsler ME, Israel E, Levy
BD: Lipoxin A4 regulates natural killer cell and type 2 innate lymphoid cell activation in asthma.
Science translational medicine 2013, 5(174):174ra126.
32. Duvall MG, Barnig C: Natural killer cell-mediated inflammation resolution is disabled in severe
asthma. 2017, 2(9).
33. DelBove J, Rosson G, Strobeck M, Chen J, Archer TK, Wang W, Knudsen ES, Weissman BE:
Identification of a core member of the SWI/SNF complex, BAF155/SMARCC1, as a human tumor
suppressor gene. Epigenetics 2011, 6(12):1444-1453.
34. Kowalik K, Waniewska-Leczycka M, Sarnowska E, Rusetska N, Ligaj M, Chrzan A, Popko M:
The SWI/SNF complex in eosinophilic and non eosinophilic chronic rhinosinusitis. Acta
otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e
chirurgia cervico-facciale 2021, 41(2):159-167.
35. Li J, Duns G, Westers H, Sijmons R, van den Berg A, Kok K: SETD2: an epigenetic modifier
with tumor suppressor functionality. Oncotarget 2016, 7(31):50719-50734.
36. Santibáñez-Andrade M, Sánchez-Pérez Y, Chirino YI, Morales-Bárcenas R, Quintana-Belmares
R, García-Cuellar CM: Particulate matter (PM(10)) destabilizes mitotic spindle through
downregulation of SETD2 in A549 lung cancer cells. Chemosphere 2022, 295:133900.
37. Meyer E, Carss KJ, Rankin J, Nichols JM, Grozeva D, Joseph AP, Mencacci NE: Mutations in
the histone methyltransferase gene KMT2B cause complex early-onset dystonia. 2017, 49(2):223-
237.
38. Merner N, Forgeot d'Arc B, Bell SC, Maussion G, Peng H, Gauthier J, Crapper L, Hamdan FF,
Michaud JL, Mottron L et al: A de novo frameshift mutation in chromodomain helicase DNA-
binding domain 8 (CHD8): A case report and literature review. American journal of medical genetics
Part A 2016, 170a(5):1225-1235.
39. Goorsenberg AW, d’Hooghe JN, Srikanthan K, Ten Hacken NH, Weersink EJ, Roelofs JJ, Kemp
SV, Bel EH, Shah PL, Annema JT: Bronchial thermoplasty induced airway smooth muscle reduction
and clinical response in severe asthma. The TASMA randomized trial. American journal of
respiratory and critical care medicine 2021, 203(2):175-184.
40. Yon C, Thompson DA, Jude JA, Panettieri Jr RA, Rastogi D: Crosstalk between CD4+ T cells
and airway smooth muscle in pediatric obesity-related asthma. American journal of respiratory and
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