-
1
-
-
0033522220
-
Hyper-IgE syndrome with recurrent infections-an autosomal dominant multisystemic disorder
-
Grimbacher B, Holland SM, Gallin JI et al. Hyper-IgE syndrome with recurrent infections-an autosomal dominant multisystemic disorder. N Engl J Med 1999;340:692-702.
-
(1999)
N Engl J Med
, vol.340
, pp. 692-702
-
-
Grimbacher, B.1
Holland, S.M.2
Gallin, J.I.3
-
5
-
-
41449110468
-
Impaired T(H)17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome
-
Milner JD, Brenchley JM, Laurence A et al. Impaired T(H)17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome. Nature 2008;452:773-6.
-
(2008)
Nature
, vol.452
, pp. 773-776
-
-
Milner, J.D.1
Brenchley, J.M.2
Laurence, A.3
-
6
-
-
59349113185
-
Signal transducer and activator of transcription 3 (STAT3) gene mutations in two patients with Hyperimmunoglobulin E syndrome
-
Tang IMS, Lee TL, Chan KW et al. Signal transducer and activator of transcription 3 (STAT3) gene mutations in two patients with Hyperimmunoglobulin E syndrome. HK J Paediatr (New Series) 2009;14:4-10.
-
(2009)
HK J Paediatr (New Series)
, vol.14
, pp. 4-10
-
-
Tang, I.M.S.1
Lee, T.L.2
Chan, K.W.3
-
7
-
-
79959522179
-
Clinical, immunological and genetic features in Taiwanese patients with the phenotype of hyper-immunoglobulin E recurrent infection syndromes (HIES)
-
Lee WI, Huang JL, Lin SJ et al. Clinical, immunological and genetic features in Taiwanese patients with the phenotype of hyper-immunoglobulin E recurrent infection syndromes (HIES). Immunobiology 2011;216:909-17.
-
(2011)
Immunobiology
, vol.216
, pp. 909-917
-
-
Lee, W.I.1
Huang, J.L.2
Lin, S.J.3
-
8
-
-
77953519151
-
Hyper-IgE syndrome with STAT3 mutation: a case report in Mainland China
-
Xie L, Hu X, Li Y, Zhang W, Chen L. Hyper-IgE syndrome with STAT3 mutation: a case report in Mainland China. Clin Dev Immunol 2010; 2010: 289873.
-
(2010)
Clin Dev Immunol
, vol.2010
, pp. 289873
-
-
Xie, L.1
Hu, X.2
Li, Y.3
Zhang, W.4
Chen, L.5
-
9
-
-
79955572359
-
Destructive pulmonary staphylococcal infection in a boy with hyper-IgE syndrome: a novel mutation in the signal transducer and activator of transcription 3 (STAT3) gene (p.Y657S)
-
Liu JY, Li Q, Chen TT, Guo X, Ge J, Yuan LX. Destructive pulmonary staphylococcal infection in a boy with hyper-IgE syndrome: a novel mutation in the signal transducer and activator of transcription 3 (STAT3) gene (p.Y657S). Eur J Pediatr 2011;170:661-6.
-
(2011)
Eur J Pediatr
, vol.170
, pp. 661-666
-
-
Liu, J.Y.1
Li, Q.2
Chen, T.T.3
Guo, X.4
Ge, J.5
Yuan, L.X.6
-
10
-
-
0036796632
-
Cutaneous manifestations of hyper-IgE syndrome in infants and children
-
Chamlin SL, McCalmont TH, Cunningham BB et al. Cutaneous manifestations of hyper-IgE syndrome in infants and children. J Pediatr 2002;141:572-5.
-
(2002)
J Pediatr
, vol.141
, pp. 572-575
-
-
Chamlin, S.L.1
McCalmont, T.H.2
Cunningham, B.B.3
-
11
-
-
0033865435
-
Hyperimmunoglobulin-E syndrome with recurrent infection: a review of current opinion and treatment
-
Erlewyn-Lajeunesse MD. Hyperimmunoglobulin-E syndrome with recurrent infection: a review of current opinion and treatment. Pediatr Allergy Immunol 2000;11:133-41.
-
(2000)
Pediatr Allergy Immunol
, vol.11
, pp. 133-141
-
-
Erlewyn-Lajeunesse, M.D.1
-
12
-
-
46049106939
-
Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome
-
Renner ED, Rylaarsdam S, Anover-Sombke S et al. Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome. J Allergy Clin Immunol 2008;122:181-7.
-
(2008)
J Allergy Clin Immunol
, vol.122
, pp. 181-187
-
-
Renner, E.D.1
Rylaarsdam, S.2
Anover-Sombke, S.3
-
13
-
-
76049116822
-
Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome
-
Woellner C, Gertz EM, Schäffer AA et al. Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome. J Allergy Clin Immunol 2010;125:424-32.
-
(2010)
J Allergy Clin Immunol
, vol.125
, pp. 424-432
-
-
Woellner, C.1
Gertz, E.M.2
Schäffer, A.A.3
-
14
-
-
77956368467
-
Diagnostic approach to the hyper-IgE syndromes: immunologic and clinical key findings to differentiate hyper-IgE syndromes from atopic dermatitis
-
Schimke LF, Sawalle-Belohradsky J, Roesler J et al. Diagnostic approach to the hyper-IgE syndromes: immunologic and clinical key findings to differentiate hyper-IgE syndromes from atopic dermatitis. J Allergy Clin Immunol 2010;126:611-7.
-
(2010)
J Allergy Clin Immunol
, vol.126
, pp. 611-617
-
-
Schimke, L.F.1
Sawalle-Belohradsky, J.2
Roesler, J.3
-
15
-
-
84863722197
-
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey
-
Chandesris MO, Melki I, Natividad A et al. Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey. Medicine (Baltimore) 2012;91:e1-19.
-
(2012)
Medicine (Baltimore)
, vol.91
-
-
Chandesris, M.O.1
Melki, I.2
Natividad, A.3
-
16
-
-
79953028378
-
Paucity of genotype-phenotype correlations in STAT3 mutation positive Hyper IgE Syndrome (HIES)
-
Heimall J, Davis J, Shaw PA et al. Paucity of genotype-phenotype correlations in STAT3 mutation positive Hyper IgE Syndrome (HIES). Clin Immunol 2011;139:75-84.
-
(2011)
Clin Immunol
, vol.139
, pp. 75-84
-
-
Heimall, J.1
Davis, J.2
Shaw, P.A.3
-
17
-
-
70949098060
-
Combined immunodeficiency associated with DOCK8 mutations
-
Zhang Q, Davis JC, Lamborn IT et al. Combined immunodeficiency associated with DOCK8 mutations. N Engl J Med 2009;361:2046-55.
-
(2009)
N Engl J Med
, vol.361
, pp. 2046-2055
-
-
Zhang, Q.1
Davis, J.C.2
Lamborn, I.T.3
-
18
-
-
71149115670
-
Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome
-
e4.
-
Engelhardt KR, McGhee S, Winkler S et al. Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome. J Allergy Clin Immunol 2009;124:1289-302. e4.
-
(2009)
J Allergy Clin Immunol
, vol.124
, pp. 1289-1302
-
-
Engelhardt, K.R.1
McGhee, S.2
Winkler, S.3
-
19
-
-
0028349735
-
Stat3: a STAT family member activated by tyrosine phosphorylation in response to epidermal growth factor and interleukin-6
-
Zhong Z, Wen Z, Darnell JE Jr. Stat3: a STAT family member activated by tyrosine phosphorylation in response to epidermal growth factor and interleukin-6. Science 1994;264:95-8.
-
(1994)
Science
, vol.264
, pp. 95-98
-
-
Zhong, Z.1
Wen, Z.2
Darnell Jr., J.E.3
-
20
-
-
34548317417
-
Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome
-
Minegishi Y, Saito M, Tsuchiya S et al. Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome. Nature 2007;448:1058-62.
-
(2007)
Nature
, vol.448
, pp. 1058-1062
-
-
Minegishi, Y.1
Saito, M.2
Tsuchiya, S.3
-
21
-
-
44849139210
-
GP130-STAT3 regulates epithelial cell migration and is required for repair of the bronchiolar epithelium
-
Kida H, Mucenski ML, Thitoff AR et al. GP130-STAT3 regulates epithelial cell migration and is required for repair of the bronchiolar epithelium. Am J Pathol 2008;172:1542-54.
-
(2008)
Am J Pathol
, vol.172
, pp. 1542-1554
-
-
Kida, H.1
Mucenski, M.L.2
Thitoff, A.R.3
-
22
-
-
67449149963
-
Molecular explanation for the contradiction between systemic Th17 defect and localized bacterial infection in hyper-IgE syndrome
-
Minegishi Y, Saito M, Nagasawa M et al. Molecular explanation for the contradiction between systemic Th17 defect and localized bacterial infection in hyper-IgE syndrome. J Exp Med 2009; 206: 1291-301.
-
(2009)
J Exp Med
, vol.206
, pp. 1291-1301
-
-
Minegishi, Y.1
Saito, M.2
Nagasawa, M.3
-
23
-
-
80055079540
-
Plasma metalloproteinase levels are dysregulated in signal transducer and activator of transcription 3 mutated hyper-IgE syndrome
-
Sekhsaria V, Dodd LE, Hsu AP et al. Plasma metalloproteinase levels are dysregulated in signal transducer and activator of transcription 3 mutated hyper-IgE syndrome. J Allergy Clin Immunol 2011;128:1124-7.
-
(2011)
J Allergy Clin Immunol
, vol.128
, pp. 1124-1127
-
-
Sekhsaria, V.1
Dodd, L.E.2
Hsu, A.P.3
-
24
-
-
82055163110
-
A critical role for STAT3 transcription factor signaling in the development and maintenance of human T cell memory
-
Siegel AM, Heimall J, Freeman AF et al. A critical role for STAT3 transcription factor signaling in the development and maintenance of human T cell memory. Immunity 2011;35:806-18.
-
(2011)
Immunity
, vol.35
, pp. 806-818
-
-
Siegel, A.M.1
Heimall, J.2
Freeman, A.F.3
-
25
-
-
76149139419
-
B cell-intrinsic signaling through IL-21 receptor and STAT3 is required for establishing long-lived antibody responses in humans
-
Avery DT, Deenick EK, Ma CS et al. B cell-intrinsic signaling through IL-21 receptor and STAT3 is required for establishing long-lived antibody responses in humans. J Exp Med 2011;207:155-71.
-
(2011)
J Exp Med
, vol.207
, pp. 155-171
-
-
Avery, D.T.1
Deenick, E.K.2
Ma, C.S.3
-
26
-
-
55549117115
-
Reduced memory B cells in patients with hyper IgE syndrome
-
Speckmann C, Enders A, Woellner C et al. Reduced memory B cells in patients with hyper IgE syndrome. Clin Immunol 2008;129: 448-54.
-
(2008)
Clin Immunol
, vol.129
-
-
Speckmann, C.1
Enders, A.2
Woellner, C.3
-
27
-
-
84856448923
-
Heterozygous signal transducer and activator of transcription 3 mutations in hyper-IgE syndrome result in altered B-cell maturation
-
562, e1-e2.
-
Meyer-Bahlburg A, Renner ED, Rylaarsdam S et al. Heterozygous signal transducer and activator of transcription 3 mutations in hyper-IgE syndrome result in altered B-cell maturation. J Allergy Clin Immunol 2012;129:559-62, 562, e1-e2.
-
(2012)
J Allergy Clin Immunol
, vol.129
, pp. 559-562
-
-
Meyer-Bahlburg, A.1
Renner, E.D.2
Rylaarsdam, S.3
-
28
-
-
84862909005
-
Immature B cells preferentially switch to IgE with increased direct Sμ to Sε recombination
-
Wesemann DR, Magee JM, Boboila C et al. Immature B cells preferentially switch to IgE with increased direct Sμ to Sε recombination. J Exp Med 2011;208:2733-46.
-
(2011)
J Exp Med
, vol.208
, pp. 2733-2746
-
-
Wesemann, D.R.1
Magee, J.M.2
Boboila, C.3
-
29
-
-
27544490377
-
+ effector T cells develop via a lineage distinct from the T helper type 1 and 2 lineages
-
+ effector T cells develop via a lineage distinct from the T helper type 1 and 2 lineages. Nat Immunol 2005;6:1123-32.
-
(2005)
Nat Immunol
, vol.6
, pp. 1123-1132
-
-
Harrington, L.E.1
Hatton, R.D.2
Mangan, P.R.3
-
30
-
-
41549135632
-
The biological functions of T helper 17 cell effector cytokines in inflammation
-
Ouyang W, Kolls JK, Zheng Y. The biological functions of T helper 17 cell effector cytokines in inflammation. Immunity 2008;28:454-67.
-
(2008)
Immunity
, vol.28
, pp. 454-467
-
-
Ouyang, W.1
Kolls, J.K.2
Zheng, Y.3
-
31
-
-
34548125305
-
Interleukins 1beta and 6 but not transforming growth factor-beta are essential for the differentiation of interleukin 17-producing human T helper cells
-
Acosta-Rodriguez EV, Napolitani G, Lanzavecchia A, Sallusto F. Interleukins 1beta and 6 but not transforming growth factor-beta are essential for the differentiation of interleukin 17-producing human T helper cells. Nat Immunol 2007;8:942-9.
-
(2007)
Nat Immunol
, vol.8
, pp. 942-949
-
-
Acosta-Rodriguez, E.V.1
Napolitani, G.2
Lanzavecchia, A.3
Sallusto, F.4
-
32
-
-
34249079176
-
Surface phenotype and antigenic specificity of human interleukin 17-producing T helper memory cells
-
Acosta-Rodriguez EV, Rivino L, Geginat J et al. Surface phenotype and antigenic specificity of human interleukin 17-producing T helper memory cells. Nat Immunol 2007;8:639-46.
-
(2007)
Nat Immunol
, vol.8
, pp. 639-646
-
-
Acosta-Rodriguez, E.V.1
Rivino, L.2
Geginat, J.3
-
33
-
-
46949089128
-
Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3
-
Ma CS, Chew GY, Simpson N et al. Deficiency of Th17 cells in hyper IgE syndrome due to mutations in STAT3. J Exp Med 2008;205: 1551-7.
-
(2008)
J Exp Med
, vol.205
-
-
Ma, C.S.1
Chew, G.Y.2
Simpson, N.3
-
34
-
-
79953284685
-
Chronic mucocutaneous candidiasis in humans with inborn errors of interleukin-17 immunity
-
Puel A, Cypowyj S, Bustamante J et al. Chronic mucocutaneous candidiasis in humans with inborn errors of interleukin-17 immunity. Science 2011;332:65-8.
-
(2011)
Science
, vol.332
, pp. 65-68
-
-
Puel, A.1
Cypowyj, S.2
Bustamante, J.3
-
35
-
-
80955148980
-
Hyperimmunoglobulin E syndromes in pediatrics: hyperimmunoglobulin E syndromes in pediatrics
-
Zhang Q, Su HC. Hyperimmunoglobulin E syndromes in pediatrics: hyperimmunoglobulin E syndromes in pediatrics. Curr Opin Pediatr 2011;23:653-8.
-
(2011)
Curr Opin Pediatr
, vol.23
, pp. 653-658
-
-
Zhang, Q.1
Su, H.C.2
|