-
1
-
-
33646061085
-
The Wiskott-Aldrich syndrome
-
1:CAS:528:DC%2BD28Xjslels7w%3D 16630926 10.1016/j.jaci.2006.02.005
-
Ochs HD, Thrasher AJ. The Wiskott-Aldrich syndrome. J Allergy Clin Immunol. 2006;117:725-38.
-
(2006)
J Allergy Clin Immunol
, vol.117
, pp. 725-738
-
-
Ochs, H.D.1
Thrasher, A.J.2
-
2
-
-
0028937177
-
X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP gene
-
1:CAS:528:DyaK2MXkvV2ju78%3D 7795648 10.1038/ng0495-414
-
Villa A, Notarangelo L, Macchi P, Mantuano E, Cavagni G, Brugnoni D, et al. X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP gene. Nat Genet. 1995;9:414-7.
-
(1995)
Nat Genet
, vol.9
, pp. 414-417
-
-
Villa, A.1
Notarangelo, L.2
Macchi, P.3
Mantuano, E.4
Cavagni, G.5
Brugnoni, D.6
-
3
-
-
9144241005
-
Clinicalcourse of patients with WASP gene mutations
-
1:CAS:528:DC%2BD2cXmsFequg%3D%3D 12969986 10.1182/blood-2003-05-1480
-
Imai K, Morio T, Zhu Y, Jin Y, Itoh S, Kajiwara M, et al. Clinicalcourse of patients with WASP gene mutations. Blood. 2004;103:456-64.
-
(2004)
Blood
, vol.103
, pp. 456-464
-
-
Imai, K.1
Morio, T.2
Zhu, Y.3
Jin, Y.4
Itoh, S.5
Kajiwara, M.6
-
4
-
-
77951460081
-
X-linked thrombocytopenia (XLT) due to WAS mutations: Clinical characteristics, long-term outcome, and treatment options
-
1:CAS:528:DC%2BC3cXlvVags7s%3D 20173115 10.1182/blood-2009-09-239087
-
Albert MH, Bittner TC, Nonoyama S, Notarangelo LD, Burns S, Imai K, et al. X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options. Blood. 2010;115:3231-8.
-
(2010)
Blood
, vol.115
, pp. 3231-3238
-
-
Albert, M.H.1
Bittner, T.C.2
Nonoyama, S.3
Notarangelo, L.D.4
Burns, S.5
Imai, K.6
-
5
-
-
0037736679
-
Autoimmunity in Wiskott-Aldrich syndrome: Risk factors, clinical features, and outcome in a single-center cohort of 55 patients
-
12728121 10.1542/peds.111.5.e622
-
Dupuis-Girod S, Medioni J, Haddad E, Quartier P, Cavazzana-Calvo M, Le Deist F, et al. Autoimmunity in Wiskott-Aldrich syndrome: risk factors, clinical features, and outcome in a single-center cohort of 55 patients. Pediatrics. 2003;111:e622-7.
-
(2003)
Pediatrics
, vol.111
, pp. 622-627
-
-
Dupuis-Girod, S.1
Medioni, J.2
Haddad, E.3
Quartier, P.4
Cavazzana-Calvo, M.5
Le Deist, F.6
-
6
-
-
84859783352
-
An update on the pathogenesis and treatment of IgA nephropathy
-
1:CAS:528:DC%2BC38Xls1Shtb0%3D 22318424 10.1038/ki.2011.501
-
Boyd JK, Cheung CK, Molyneux K, Feehally J, Barratt J. An update on the pathogenesis and treatment of IgA nephropathy. Kidney Int. 2012;81:833-43.
-
(2012)
Kidney Int
, vol.81
, pp. 833-843
-
-
Boyd, J.K.1
Cheung, C.K.2
Molyneux, K.3
Feehally, J.4
Barratt, J.5
-
7
-
-
84255172704
-
Mechanism of onset and exacerbation of chronic glomerulonephritis and its treatment
-
1:CAS:528:DC%2BC3sXlvVegsw%3D%3D 21902765 10.1111/j.1442-200X.2011.03469. x
-
Kawasaki Y. Mechanism of onset and exacerbation of chronic glomerulonephritis and its treatment. Pediatr Int. 2011;53:795-806.
-
(2011)
Pediatr Int
, vol.53
, pp. 795-806
-
-
Kawasaki, Y.1
-
8
-
-
34249289769
-
Patients with IgA nephropathy have increased serum galactose-deficient IgA1 levels
-
1:CAS:528:DC%2BD2sXls1GqurY%3D 17342176 10.1038/sj.ki.5002185
-
Moldoveanu Z, Wyatt RJ, Lee JY, Tomana M, Julian BA, Mestecky J, et al. Patients with IgA nephropathy have increased serum galactose-deficient IgA1 levels. Kidney Int. 2007;71:1148-54.
-
(2007)
Kidney Int
, vol.71
, pp. 1148-1154
-
-
Moldoveanu, Z.1
Wyatt, R.J.2
Lee, J.Y.3
Tomana, M.4
Julian, B.A.5
Mestecky, J.6
-
9
-
-
84856527556
-
Development of IgA nephropathy-like glomerulonephritis associated with Wiskott-Aldrich syndrome protein deficiency
-
1:CAS:528:DC%2BC38XhvVGntrk%3D 3273668 22079330 10.1016/j.clim.2011.10. 001
-
Shimizu M, Nikolov NP, Ueno K, Ohta K, Siegel RM, Yachie A, et al. Development of IgA nephropathy-like glomerulonephritis associated with Wiskott-Aldrich syndrome protein deficiency. Clin Immunol. 2012;142:160-6.
-
(2012)
Clin Immunol
, vol.142
, pp. 160-166
-
-
Shimizu, M.1
Nikolov, N.P.2
Ueno, K.3
Ohta, K.4
Siegel, R.M.5
Yachie, A.6
-
10
-
-
33846850600
-
Wiskott-Aldrich syndrome protein is required for regulatory T cell homeostasis
-
1:CAS:528:DC%2BD2sXhs1Oqtr0%3D 1764857 17218989 10.1172/JCI29539
-
Humblet-Baron S, Sather B, Anover S, Becker-Herman S, Kasprowicz DJ, Khim S, et al. Wiskott-Aldrich syndrome protein is required for regulatory T cell homeostasis. J Clin Invest. 2007;117:407-18.
-
(2007)
J Clin Invest
, vol.117
, pp. 407-418
-
-
Humblet-Baron, S.1
Sather, B.2
Anover, S.3
Becker-Herman, S.4
Kasprowicz, D.J.5
Khim, S.6
-
13
-
-
2342533795
-
IgA nephropathy associated with X-linked thrombocytopenia
-
14981635 10.1053/j.ajkd.2003.11.016
-
Matsukura H, Kanegane H, Miya K, Ohtsubo K, Higuchi A, Tanizawa T, et al. IgA nephropathy associated with X-linked thrombocytopenia. Am J Kidney Dis. 2004;43:e7-12.
-
(2004)
Am J Kidney Dis
, vol.43
, pp. 7-12
-
-
Matsukura, H.1
Kanegane, H.2
Miya, K.3
Ohtsubo, K.4
Higuchi, A.5
Tanizawa, T.6
-
14
-
-
84873410333
-
Aberrant glycosylation of IgA in Wiskott-Aldrich syndrome and X-linked thrombocytopenia
-
1:CAS:528:DC%2BC38XhsF2hsLrN 3563712 23107152 10.1016/j.jaci.2012.08.040
-
Shimizu M, Kanegane H, Wada T, Motoyoshi Y, Morio T, Candotti F, et al. Aberrant glycosylation of IgA in Wiskott-Aldrich syndrome and X-linked thrombocytopenia. J Allergy Clin Immunol. 2013;131:587-90.
-
(2013)
J Allergy Clin Immunol
, vol.131
, pp. 587-590
-
-
Shimizu, M.1
Kanegane, H.2
Wada, T.3
Motoyoshi, Y.4
Morio, T.5
Candotti, F.6
-
15
-
-
0002354663
-
IgA nephropathy: Current concepts and future trends
-
Sakai O. IgA nephropathy: current concepts and future trends. Nephrology 1997;3: 2-3.
-
(1997)
Nephrology
, vol.3
, pp. 2-3
-
-
Sakai, O.1
-
16
-
-
33744765798
-
Bone marrow transplantation attenuates murine IgA nephropathy: Role of a stem cell disorder
-
1:CAS:528:DyaK1MXnslajsr4%3D 10571789 10.1046/j.1523-1755.1999.00750.x
-
Imasawa T, Nagasawa R, Utsunomiya Y, Kawamura T, Zhong Y, Makita N, et al. Bone marrow transplantation attenuates murine IgA nephropathy: role of a stem cell disorder. Kidney Int. 1999;56:1809-17.
-
(1999)
Kidney Int
, vol.56
, pp. 1809-1817
-
-
Imasawa, T.1
Nagasawa, R.2
Utsunomiya, Y.3
Kawamura, T.4
Zhong, Y.5
Makita, N.6
-
17
-
-
34547480308
-
Th1 polarization in murine IgA nephropathy directed by bone marrow-derived cells
-
1:CAS:528:DC%2BD2sXot1Cmtrw%3D 17495863 10.1038/sj.ki.5002300
-
Suzuki H, Suzuki Y, Aizawa M, Yamanaka T, Kihara M, Pang H, et al. Th1 polarization in murine IgA nephropathy directed by bone marrow-derived cells. Kidney Int. 2007;72:319-27.
-
(2007)
Kidney Int
, vol.72
, pp. 319-327
-
-
Suzuki, H.1
Suzuki, Y.2
Aizawa, M.3
Yamanaka, T.4
Kihara, M.5
Pang, H.6
-
18
-
-
34249048273
-
Downregulation of the beta1, 3- galactosyl transferasegene in tonsillar B lymphocytes and aberrant lectin bindings to tonsillar IgA as a pathogenesis of IgA nephropathy
-
1:CAS:528:DC%2BD1cXhsFaru7nL 17495448
-
Inoue T, Sugiyama H, Kikumoto Y, Fukuoka N, Maeshima Y, Hattori H, et al. Downregulation of the beta1, 3- galactosyl transferasegene in tonsillar B lymphocytes and aberrant lectin bindings to tonsillar IgA as a pathogenesis of IgA nephropathy. Contrib Nephrol. 2007;157:120-4.
-
(2007)
Contrib Nephrol
, vol.157
, pp. 120-124
-
-
Inoue, T.1
Sugiyama, H.2
Kikumoto, Y.3
Fukuoka, N.4
Maeshima, Y.5
Hattori, H.6
-
19
-
-
78649499628
-
Down-regulation of core 1 beta1, 3-galactosyl transferase and Cosmc by Th2 cytokine alters O-glycosylation of IgA1
-
1:CAS:528:DC%2BC3cXhsFSgtr%2FE 20551088 10.1093/ndt/gfq325
-
Yamada K, Kobayashi N, Ikeda T, Suzuki Y, Tsuge T, Horikoshi S, et al. Down-regulation of core 1 beta1, 3-galactosyl transferase and Cosmc by Th2 cytokine alters O-glycosylation of IgA1. Nephrol Dial Transplant. 2010;25:3890-7.
-
(2010)
Nephrol Dial Transplant
, vol.25
, pp. 3890-3897
-
-
Yamada, K.1
Kobayashi, N.2
Ikeda, T.3
Suzuki, Y.4
Tsuge, T.5
Horikoshi, S.6
-
20
-
-
38849191296
-
IgA1-secreting cell lines from patients with IgA nephropathy produce aberrantly glycosylated IgA1
-
1:CAS:528:DC%2BD1cXhsFOmsrc%3D 2157566 18172551
-
Suzuki H, Moldoveanu Z, Hall S, Brown R, Vu HL, Novak L, et al. IgA1-secreting cell lines from patients with IgA nephropathy produce aberrantly glycosylated IgA1. J Clin Invest. 2008;118:629-39.
-
(2008)
J Clin Invest
, vol.118
, pp. 629-639
-
-
Suzuki, H.1
Moldoveanu, Z.2
Hall, S.3
Brown, R.4
Vu, H.L.5
Novak, L.6
-
21
-
-
57149101578
-
Toll-like receptor 9 affects severity of IgA nephropathy
-
1:CAS:528:DC%2BD1MXlvF2gtg%3D%3D 18776126 10.1681/ASN.2007121311
-
Suzuki H, Suzuki Y, Narita I, Aizawa M, Kihara M, Yamanaka T, et al. Toll-like receptor 9 affects severity of IgA nephropathy. J Am Soc Nephrol. 2008;19:2384-95.
-
(2008)
J Am Soc Nephrol
, vol.19
, pp. 2384-2395
-
-
Suzuki, H.1
Suzuki, Y.2
Narita, I.3
Aizawa, M.4
Kihara, M.5
Yamanaka, T.6
-
22
-
-
79954425766
-
Association between toll-like receptor 10 (TLR10) gene polymorphisms and childhood IgA nephropathy
-
1:CAS:528:DC%2BC3MXjt1Gntbc%3D 20953797 10.1007/s00431-010-1325-1
-
Park HJ, Hahn WH, Suh JS, Kim MJ, Kang SW, Lee JS, et al. Association between toll-like receptor 10 (TLR10) gene polymorphisms and childhood IgA nephropathy. Eur J Pediatr. 2011;170:503-9.
-
(2011)
Eur J Pediatr
, vol.170
, pp. 503-509
-
-
Park, H.J.1
Hahn, W.H.2
Suh, J.S.3
Kim, M.J.4
Kang, S.W.5
Lee, J.S.6
-
23
-
-
0036900202
-
Interleukin-12 alters the physicochemical characteristics of serum and glomerular IgA and modifies glycosylation in a ddY mouse strain having high IgA levels
-
1:CAS:528:DC%2BD38XptlOhsLo%3D 12454220 10.1093/ndt/17.12.2108
-
Kobayashi I, Nogaki F, Kusano H, Ono T, Miyawaki S, Yoshida H, et al. Interleukin-12 alters the physicochemical characteristics of serum and glomerular IgA and modifies glycosylation in a ddY mouse strain having high IgA levels. Nephrol Dial Transplant. 2002;17:2108-16.
-
(2002)
Nephrol Dial Transplant
, vol.17
, pp. 2108-2116
-
-
Kobayashi, I.1
Nogaki, F.2
Kusano, H.3
Ono, T.4
Miyawaki, S.5
Yoshida, H.6
-
24
-
-
0023281389
-
Disappearance of mesangial IgA deposits from the kidneys of two donors after transplantation
-
1:STN:280:DyaK3c3ovV2ksQ%3D%3D 3274493
-
Cuevas X, Lloveras J, Mir M, Aubia J, Masramon J. Disappearance of mesangial IgA deposits from the kidneys of two donors after transplantation. Transplant Proc. 1987;19:2208-9.
-
(1987)
Transplant Proc
, vol.19
, pp. 2208-2209
-
-
Cuevas, X.1
Lloveras, J.2
Mir, M.3
Aubia, J.4
Masramon, J.5
-
25
-
-
0031442159
-
Donor-transmitted IgA nephropathy: Long-term follow-up of kidney donors and recipients
-
1:STN:280:DyaK1c%2Fns1CntQ%3D%3D 9414767 10.1016/S0041-1345(97)00957-3
-
Koselj M, Rott T, Kandus A, Vizjak A, Malovrh M. Donor-transmitted IgA nephropathy: long-term follow-up of kidney donors and recipients. Transplant Proc. 1997;29:3406-7.
-
(1997)
Transplant Proc
, vol.29
, pp. 3406-3407
-
-
Koselj, M.1
Rott, T.2
Kandus, A.3
Vizjak, A.4
Malovrh, M.5
-
26
-
-
38049139182
-
Long-term outcome following hematopoietic stem-cell transplantation in Wiskott-Aldrich syndrome: Collaborative study of the European Society for Immunodeficiencies and European Group for Blood and Marrow Transplantation
-
1:CAS:528:DC%2BD1cXjtVKksQ%3D%3D 17901250 10.1182/blood-2007-03-076679
-
Ozsahin H, Cavazzana-Calvo M, Notarangelo LD, Schulz A, Thrasher AJ, Mazzolari E, et al. Long-term outcome following hematopoietic stem-cell transplantation in Wiskott-Aldrich syndrome: collaborative study of the European Society for Immunodeficiencies and European Group for Blood and Marrow Transplantation. Blood. 2008;111:439-45.
-
(2008)
Blood
, vol.111
, pp. 439-445
-
-
Ozsahin, H.1
Cavazzana-Calvo, M.2
Notarangelo, L.D.3
Schulz, A.4
Thrasher, A.J.5
Mazzolari, E.6
|