The 46 references in paper I. Solovyeva A., E. Sobko A., A. Kraposhina Yu., I. Demko V., A. Salmina B., И. Соловьева А., Е. Собко А., А. Крапошина Ю., И. Демко В., А. Салмина Б. (2014) “Современные представления о роли CD38 в патогенезе бронхиальной астмы // Current view on a role of CD38 for pathogenesis of bronchial asthma” / spz:neicon:pulmonology:y:2013:i:5:p:81-84

1
Чучалин А.Г. (ред.). Глобальная стратегия лечения и профилактики бронхиальной астмы. М.: Атмосфера; 2007.
(check this in PDF content)
2
Федосеев Г.Б.(ред.). Многоликая бронхиальная астма, диагностика, лечение и профилактика. СПб: Нордмедиздат; 2011.
(check this in PDF content)
3
Global Initiative for Asthma. Global strategy for asthma management and prevention. 2011. Available on [www. ginasthma.org].
(check this in PDF content)
4
Караулов А.В.Новая концепция развития бронхиальной астмы: иммунологические и генетические аспекты. Практикующий врач 1998; 12: 3–4.
(check this in PDF content)
5
Deaglio S., Malavasi F.The CD38/CD157 mammalian gene family: an evolutionary paradigm for other leukocyte surface enzymes. Purinergic. Signalling 2006; 2: 431–441.
(check this in PDF content)
6
Салмина А.Б., Инжутова А.И., Моргун А.В. и др. НАД+конвертирующие ферменты в клетках нейрональной и глиальной природы: СD38 как новая молекула-мишень для нейропротекции. Вестник РАМН 2012; 10: 29–37.
(check this in PDF content)
7
Higashida H., Salmina A.B., Olovyannikova R.Y. et al. Cyclic ADP-ribose as a universal calcium signal molecule in the nervous system. Neurochem. Int. 2007; 51: 192–199.
(check this in PDF content)
8
Salmina A.B., Olovyannikova R.Ya., Mami N. et al.NAD+ metabolism and ADP-ribosyl cyclase as targets for central nervous system therapy. Curr. Med. Chem. 2006; 6 (3): 193–210.
(check this in PDF content)
9
Deshpande D.A., White T.A., Guedes A.G.P. et al. Altered airway responsiveness in CD38-deficient mice. Am. J. Respir. Cell Mol. Biol. 2005; 32: 149–156.
(check this in PDF content)
10
Malavasi F., Deaglio S., Ferrero E. et al.CD38 and CD157 as receptors of the immune system: a bridge between innate and adaptive immunity. Mol. Med. 2006; 12: 334–341.
(check this in PDF content)
11
Perraud A.L., Fleig A., Dunn C.A. et al. ADP-ribose gating of the calcium-permeable LTRPC2 channel revealed by Nudix motif homology. Nature 2001; 411: 595–599.
(check this in PDF content)
12
Prakash Y.S., Kannan M.S., Walseth T.F. et al. Role of cyclic ADPribose in the regulation of [Ca2+](i) in porcine tracheal smooth muscle. Am. J. Physiol. 1998; 274: 1653–1660.
(check this in PDF content)
13
Wills&Karp M., Chiaramonte Wills&Karp M.Interleukin-13 in asthma. Curr. Opin. Pulm. Med. 2003; 9 (1): 21–27.
(check this in PDF content)
14
Yamasaki M., Churchill G.C., Galione A.Calcium signalling by nicotinic acid adenine dinucleotidephosphate (NAADP). FEBS J. 2005; 272: 4598–4606.
(check this in PDF content)
15
Wang J., Peng Y., Sun Y.W. et al. All-trans retinoic acid induces xaf1 expression through an interferon regulatory factor-1 element in colon cancer. Gastroenterology 2006; 130: 747–758.
(check this in PDF content)
16
Zubiaur M., Fernandez O., Ferrero E. et al.CD38 is associated with lipid rafts and upon receptor stimulation leads to Akt/protein kinase B and Erk activation in the absence of the CD3-immune receptor tyrosine-based activation motifs. J. Biol. Chem. 2002; 277: 13–22.
(check this in PDF content)
17
Laporte J.C., Moore P.E., Baraldo S. et al.Direct effects of interleukin-13 on signaling pathways for physiological responses in cultured human airway smooth muscle cells. Am. J. Respir. Crit. Care Med. 2001; 164: 141–148.
(check this in PDF content)
18
Feske S. Calcium signalling in lymphocyte activation and disease. Nature Rev. Immunol. 2007; 7: 690–702.
(check this in PDF content)
19
Frasca L., Fedele G., Deaglio S. et al. CD38 orchestrates migration, survival, and Th1 immune response of human mature dendritic cells. Blood 2006; 107: 2392–2399.
(check this in PDF content)
20
Shore S.A., Moore P.E.Effects of cytokines on contractile and dilator responses of airway smooth muscle. Clin. Exp. Pharmacol. Physiol. 2002; 29 (10): 859–866.
(check this in PDF content)
21
Deterre P., Berthelier V., Bauvois B. et al.CD38 in T- and B-cell functions. Chem. Immunol. 2000; 75: 146–168.
(check this in PDF content)
22
Hoogsteden H.C., Verhoeven G.T., Lambrecht B.N. et al. Airway inflammation in asthma and chronic obstructive pulmonary disease with special emphasis on the antigenpresenting dendritic cell: influence of treatment with fluticasone propionate. Clin. Exp. Allergy 1999; 29 (2): 116–124.
(check this in PDF content)
23
Jahnsen F.L., Moloney E.D., Hogan T. et al.Rapid dendritic cell recruitment to the bronchial mucosa of patients with atopic asthma in response to local allergen challenge. Thorax 2001; 56: 823–826.
(check this in PDF content)
24
Partida&Sanchez S., Goodrich S., Kusser K. еt al. Regulation of dendritic cell trafficking by the ADP-ribosyl cyclase CD38: impact on the development of humoral immunity. Immunity 2004; 20 (3): 279–291.
(check this in PDF content)
25
Partida&Sanchez S., Cockayne D.A., Monard S. et al. Cyclic ADP-ribose production by CD38 regulates intracellular calcium release, extracellular calcium influx and chemotaxis in neutrophils and is required for bacterial clearance in vivo. Nature Med. 2001; 7: 1209–1216.
(check this in PDF content)
26
Thomas P.S. Tumour necrosis factor-alpha: the role of this multifunctional cytokine in asthma. Immunol. Cell Biol. 2001; 79 (2): 132–140.
(check this in PDF content)
27
Partida&Sanchez S., Rivero&Nava L., Shi G. et al. CD38: an ectoenzyme at the crossroads of innate and adaptive immune responses. Adv. Exp. Med. Biol. 2007; 590: 171–183.
(check this in PDF content)
28
Hirota S., Helli P.B., Catalli A. et al.Airway smooth muscle excitation-contraction coupling and airway hyperresponsiveness. Can. J. Physiol. Pharmacol. 2005; 83: 725–732.
(check this in PDF content)
29
Alonso D., Radomski M.W. The nitric oxide-endothelin-1 connection. Heart Fail. Rev. 2003; 8 (1): 107–115.
(check this in PDF content)
30
Gally F., Hartney J.M., Janssen W.J. et al.CD38 plays a dual role in allergen – induced airway hyperresponsiveness. Am. J. Respir. Cell Mol. Biol. 2009; 40: 433–442.
(check this in PDF content)
31
Любавина Н.А., Варварина, Г.Н., Караулов А.В.Влияние стандартной патогенетической терапии на сывороточный уровень на сывороточный уровень молекул SCD38, SCD25 И SCD95 у больных бронхиальной астмой смешанного типа. Иммунология 2011; 32 (5): 267–269.
(check this in PDF content)
32
Каптюк Л.И., Крапошина А.Ю., Собко Е.А. и др. Молекулярные механизмы стероидорезистентности при бронхиальной астме: р-гликопротеин и CD38 как новые мишени для фармакологической коррекции. Мол. мед. 2012; 2: 11–16.
(check this in PDF content)
33
Собко Е.А., Крапошина А.Ю., Демко И.В. и др. Уровень экспрессии CD38/АДФ-рибозилциклазы и цитокинов периферической крови при бронхиальной астме. Клинико-лабораторный консилиум: спец. вып. 2010; 2–3 (33–34): 61–66.
(check this in PDF content)
34
Собко Е.А., Крапошина А.Ю., Демко И.В. и др.Маркер эндотелиальной дисфункции CD38/АДФ-рибозилциклаза при бронхиальной астме. Клин. мед. 2013; 2: 34–38.
(check this in PDF content)
35
Scalzo&Inguanti K., Plebanski M. CD38 identifies a hypoproliferative IL-13-secreting CD4+T-cell subset that does not fit into existing naive and memory phenotype paradigms. Eur. J. Immunol. 2011; 41 (5): 1298–1308.
(check this in PDF content)
36
Amrani Y., Panettieri R.A. Jr. Modulation of calcium homeostasis as a mechanism for altering smooth muscle responsiveness in asthma. Curr. Opin. Allergy Clin. Immunol. 2002; 2 (1): 39–45.
(check this in PDF content)
37
Tliba O., Panettieri R.A. Jr, Tliba S. et al.Tumor necrosis factor-alpha differentially regulates the expression of proinflammatory genes in human airway smooth muscle cells by activation of interferon-beta-dependent cd38 pathway. Mol. Pharmacol. 2004; 66: 322–329.
(check this in PDF content)
38
Jude J.A., Wylam M.E., Walseth T.F. et al.Calcium signaling in airway smooth muscle. Proc. Am. Thorac. Soc. 2008; 5: 15–22.
(check this in PDF content)
39
Tenca C., Merlo A., Zarcone D. et al.Death of T cell precursors in the human thymus: a role for CD38. Int. Immunol. 2003; 15: 1105–1116.
(check this in PDF content)
40
Kim J., McKinley L., Natarajan S. et al.Anti-tumor necrosis factor-alpha antibody treatment reduces pulmonary inflammation and methacholine hyper-responsiveness in a murine asthma model induced by house dust. Clin. Exp. Allergy 2006; 36 (1): 122–132.
(check this in PDF content)
41
White T.A., Xue A., Chini E.N. et al.Role of Transient receptor potential C3 in TNF-α-enhanced calcium influx in human airway myocytes. Am. J. Respir. Cell Mol. Biol. 2006; 35: 243–251.
(check this in PDF content)
42
Chung F. Asthma. UK: Eur. Respir. Soc. Ltd; 2003.
(check this in PDF content)
43
Tliba O., Damera G., Banerjee A. et al. Cytokines induce an early steroid resistance in airway smooth muscle cells novel role of interferon regulatory factor-1. Am. J. Respir. Cell Mol. Biol. 2008; 38: 463–472.
(check this in PDF content)
44
Tirumurugaan K.G., Kang B.N., Panettieri R.A. et al. Regulation of the cd38 promoter in human airway smooth muscle cells by TNF-alpha and dexamethasone. Respir. Res. 2008; 9: 26.
(check this in PDF content)
45
Dagia N.M., Harii N., Meli A.E. et al.Phenyl methimazole inhibits tnf-alpha-induced vcam-1 expression in an ifn regulatory factor-1-dependent manner and reduces monocytic cell adhesion to endothelial cells. J. Immunol. 2004; 173: 2041–2049.
(check this in PDF content)
46
Yamada K., Elliott W.M., Hayashi S. et al.Latent adenoviral infection modifies the steroid response in allergic lung inflammation. J. Allergy Clin. Immunol. 2000; 106: 844–851. Информация об авторах
(check this in PDF content)