-
2
-
-
0030752511
-
Complement deficiency and autoimmunity
-
Walport M.J., Davies K.A., Morley B.J., Botto M. Complement deficiency and autoimmunity. Ann. N. Y. Acad. Sci. 1997, 815:267-281.
-
(1997)
Ann. N. Y. Acad. Sci.
, vol.815
, pp. 267-281
-
-
Walport, M.J.1
Davies, K.A.2
Morley, B.J.3
Botto, M.4
-
3
-
-
0018286381
-
Clinical and immunological studies in a case of selective complete C1q deficiency
-
Berkel A.I., Loos M., Sanal O., Mauff G., Gungen Y., Ors U., et al. Clinical and immunological studies in a case of selective complete C1q deficiency. Clin. Exp. Immunol. 1979, 38:52-63.
-
(1979)
Clin. Exp. Immunol.
, vol.38
, pp. 52-63
-
-
Berkel, A.I.1
Loos, M.2
Sanal, O.3
Mauff, G.4
Gungen, Y.5
Ors, U.6
-
4
-
-
0023902375
-
Ahomozygous point mutation results in a stop codon in the C1q B-chain of a C1q-deficient individual
-
McAdam R.A., Goundis D., Reid K.B. Ahomozygous point mutation results in a stop codon in the C1q B-chain of a C1q-deficient individual. Immunogenetics 1988, 27:259-264.
-
(1988)
Immunogenetics
, vol.27
, pp. 259-264
-
-
McAdam, R.A.1
Goundis, D.2
Reid, K.B.3
-
5
-
-
82555194114
-
Molecular basis of hereditary C1q deficiency-revisited: identification of several novel disease-causing mutations
-
Schejbel L., Skattum L., Hagelberg S., Ahlin A., Schiller B., Berg S., et al. Molecular basis of hereditary C1q deficiency-revisited: identification of several novel disease-causing mutations. Genes. Immun. 2011, 12:626-634.
-
(2011)
Genes. Immun.
, vol.12
, pp. 626-634
-
-
Schejbel, L.1
Skattum, L.2
Hagelberg, S.3
Ahlin, A.4
Schiller, B.5
Berg, S.6
-
6
-
-
0033752720
-
Systemic lupus erythematosus, complement deficiency, and apoptosis
-
Pickering M.C., Botto M., Taylor P.R., Lachmann P.J., Walport M.J. Systemic lupus erythematosus, complement deficiency, and apoptosis. Adv. Immunol. 2000, 76:227-324.
-
(2000)
Adv. Immunol.
, vol.76
, pp. 227-324
-
-
Pickering, M.C.1
Botto, M.2
Taylor, P.R.3
Lachmann, P.J.4
Walport, M.J.5
-
7
-
-
84964227455
-
Identification of a novel non-coding mutation in C1qB in a Dutch child with C1q deficiency associated with recurrent infections
-
van Schaarenburg R.A., Daha N.A., Schonkeren J.J., Nivine Levarht E.W., van Gijlswijk-Janssen D.J., Kurreeman F.A., et al. Identification of a novel non-coding mutation in C1qB in a Dutch child with C1q deficiency associated with recurrent infections. Immunobiology 2015, 220(3):422-427.
-
(2015)
Immunobiology
, vol.220
, Issue.3
, pp. 422-427
-
-
van Schaarenburg, R.A.1
Daha, N.A.2
Schonkeren, J.J.3
Nivine Levarht, E.W.4
van Gijlswijk-Janssen, D.J.5
Kurreeman, F.A.6
-
8
-
-
84893695691
-
New C1q mutation in a Tunisian family
-
Jlajla H., Sellami M.K., Sfar I., Laadhar L., Zerzeri Y., Abdelmoula M.S., et al. New C1q mutation in a Tunisian family. Immunobiology 2014, 219:241-246.
-
(2014)
Immunobiology
, vol.219
, pp. 241-246
-
-
Jlajla, H.1
Sellami, M.K.2
Sfar, I.3
Laadhar, L.4
Zerzeri, Y.5
Abdelmoula, M.S.6
-
9
-
-
79960460140
-
Complement activation by (auto-) antibodies
-
Daha N.A., Banda N.K., Roos A., Beurskens F.J., Bakker J.M., Daha M.R., et al. Complement activation by (auto-) antibodies. Mol. Immunol. 2011, 48:1656-1665.
-
(2011)
Mol. Immunol.
, vol.48
, pp. 1656-1665
-
-
Daha, N.A.1
Banda, N.K.2
Roos, A.3
Beurskens, F.J.4
Bakker, J.M.5
Daha, M.R.6
-
11
-
-
0025907162
-
Binding and complement activation by C-reactive protein via the collagen-like region of C1q and inhibition of these reactions by monoclonal antibodies to C-reactive protein and C1q
-
Jiang H.X., Siegel J.N., Gewurz H. Binding and complement activation by C-reactive protein via the collagen-like region of C1q and inhibition of these reactions by monoclonal antibodies to C-reactive protein and C1q. J.Immunol. 1991, 146:2324-2330.
-
(1991)
J.Immunol.
, vol.146
, pp. 2324-2330
-
-
Jiang, H.X.1
Siegel, J.N.2
Gewurz, H.3
-
12
-
-
0031569975
-
C1q binds directly and specifically to surface blebs of apoptotic human keratinocytes: complement deficiency and systemic lupus erythematosus revisited
-
Korb L.C., Ahearn J.M. C1q binds directly and specifically to surface blebs of apoptotic human keratinocytes: complement deficiency and systemic lupus erythematosus revisited. J.Immunol. 1997, 158:4525-4528.
-
(1997)
J.Immunol.
, vol.158
, pp. 4525-4528
-
-
Korb, L.C.1
Ahearn, J.M.2
-
13
-
-
37349079469
-
Role of complement and complement regulators in the removal of apoptotic cells
-
Trouw L.A., Blom A.M., Gasque P. Role of complement and complement regulators in the removal of apoptotic cells. Mol. Immunol. 2008, 45:1199-1207.
-
(2008)
Mol. Immunol.
, vol.45
, pp. 1199-1207
-
-
Trouw, L.A.1
Blom, A.M.2
Gasque, P.3
-
14
-
-
0036083789
-
Direct binding of C1q to apoptotic cells and cell blebs induces complement activation
-
Nauta A.J., Trouw L.A., Daha M.R., Tijsma O., Nieuwland R., Schwaeble W.J., et al. Direct binding of C1q to apoptotic cells and cell blebs induces complement activation. Eur. J. Immunol. 2002, 32:1726-1736.
-
(2002)
Eur. J. Immunol.
, vol.32
, pp. 1726-1736
-
-
Nauta, A.J.1
Trouw, L.A.2
Daha, M.R.3
Tijsma, O.4
Nieuwland, R.5
Schwaeble, W.J.6
-
15
-
-
0035849176
-
Complement. Second of two parts
-
Walport M.J. Complement. Second of two parts. NEnglJMed 2001, 344:1140-1144.
-
(2001)
NEnglJMed
, vol.344
, pp. 1140-1144
-
-
Walport, M.J.1
-
16
-
-
0034618113
-
Ahierarchical role for classical pathway complement proteins in the clearance of apoptotic cells invivo
-
Taylor P.R., Carugati A., Fadok V.A., Cook H.T., Andrews M., Carroll M.C., et al. Ahierarchical role for classical pathway complement proteins in the clearance of apoptotic cells invivo. J.Exp. Med. 2000, 192:359-366.
-
(2000)
J.Exp. Med.
, vol.192
, pp. 359-366
-
-
Taylor, P.R.1
Carugati, A.2
Fadok, V.A.3
Cook, H.T.4
Andrews, M.5
Carroll, M.C.6
-
17
-
-
34848855068
-
C1q deficiency promotes the production of transgenic-derived IgM and IgG3 autoantibodies in anti-DNA knock-in transgenic mice
-
Fossati-Jimack L., Cortes-Hernandez J., Norsworthy P.J., Walport M.J., Cook H.T., Botto M. C1q deficiency promotes the production of transgenic-derived IgM and IgG3 autoantibodies in anti-DNA knock-in transgenic mice. Mol. Immunol. 2008, 45:787-795.
-
(2008)
Mol. Immunol.
, vol.45
, pp. 787-795
-
-
Fossati-Jimack, L.1
Cortes-Hernandez, J.2
Norsworthy, P.J.3
Walport, M.J.4
Cook, H.T.5
Botto, M.6
-
18
-
-
65349090158
-
C1q enhances IFN-gamma production by antigen-specific T cells via the CD40 costimulatory pathway on dendritic cells
-
Baruah P., Dumitriu I.E., Malik T.H., Cook H.T., Dyson J., Scott D., et al. C1q enhances IFN-gamma production by antigen-specific T cells via the CD40 costimulatory pathway on dendritic cells. Blood 2009, 113:3485-3493.
-
(2009)
Blood
, vol.113
, pp. 3485-3493
-
-
Baruah, P.1
Dumitriu, I.E.2
Malik, T.H.3
Cook, H.T.4
Dyson, J.5
Scott, D.6
-
19
-
-
0037232241
-
Tcell activation by soluble C1q-bearing immune complexes: implications for the pathogenesis of rheumatoid arthritis
-
Jiang K., Chen Y., Xu C.S., Jarvis J.N. Tcell activation by soluble C1q-bearing immune complexes: implications for the pathogenesis of rheumatoid arthritis. Clin. Exp. Immunol. 2003, 131:61-67.
-
(2003)
Clin. Exp. Immunol.
, vol.131
, pp. 61-67
-
-
Jiang, K.1
Chen, Y.2
Xu, C.S.3
Jarvis, J.N.4
-
20
-
-
78049496573
-
C1q deficiency leads to the defective suppression of IFN-alpha in response to nucleoprotein containing immune complexes
-
Santer D.M., Hall B.E., George T.C., Tangsombatvisit S., Liu C.L., Arkwright P.D., et al. C1q deficiency leads to the defective suppression of IFN-alpha in response to nucleoprotein containing immune complexes. J.Immunol. 2010, 185:4738-4749.
-
(2010)
J.Immunol.
, vol.185
, pp. 4738-4749
-
-
Santer, D.M.1
Hall, B.E.2
George, T.C.3
Tangsombatvisit, S.4
Liu, C.L.5
Arkwright, P.D.6
-
21
-
-
34848852711
-
Clinical variability and characteristic autoantibody profile in primary C1q complement deficiency
-
Vassallo G., Newton R.W., Chieng S.E., Haeney M.R., Shabani A., Arkwright P.D. Clinical variability and characteristic autoantibody profile in primary C1q complement deficiency. Rheumatol. 2007, 46:1612-1614.
-
(2007)
Rheumatol.
, vol.46
, pp. 1612-1614
-
-
Vassallo, G.1
Newton, R.W.2
Chieng, S.E.3
Haeney, M.R.4
Shabani, A.5
Arkwright, P.D.6
-
22
-
-
84886121183
-
The identification of a novel splicing mutation in C1qB in a Japanese family with C1q deficiency: a case report
-
Higuchi Y., Shimizu J., Hatanaka M., Kitano E., Kitamura H., Takada H., et al. The identification of a novel splicing mutation in C1qB in a Japanese family with C1q deficiency: a case report. Pediatr. Rheumatol. Online J. 2013, 11:41.
-
(2013)
Pediatr. Rheumatol. Online J.
, vol.11
, pp. 41
-
-
Higuchi, Y.1
Shimizu, J.2
Hatanaka, M.3
Kitano, E.4
Kitamura, H.5
Takada, H.6
-
23
-
-
84863728005
-
C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma
-
Topaloglu R., Taskiran E.Z., Tan C., Erman B., Ozaltin F., Sanal O. C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma. Clin. Rheumatol. 2012, 31:1123-1126.
-
(2012)
Clin. Rheumatol.
, vol.31
, pp. 1123-1126
-
-
Topaloglu, R.1
Taskiran, E.Z.2
Tan, C.3
Erman, B.4
Ozaltin, F.5
Sanal, O.6
-
24
-
-
84897879965
-
Rothmund-Thomson syndrome and glomerulonephritis in a homozygous C1q-deficient patient due to a Gly164Ser C1qC mutation
-
Lopez-Lera A., Torres-Canizales M., Garrido S., Morales A., Lopez-Trascasa M. Rothmund-Thomson syndrome and glomerulonephritis in a homozygous C1q-deficient patient due to a Gly164Ser C1qC mutation. J.Invest Dermatol 2014, 134:1152-1154.
-
(2014)
J.Invest Dermatol
, vol.134
, pp. 1152-1154
-
-
Lopez-Lera, A.1
Torres-Canizales, M.2
Garrido, S.3
Morales, A.4
Lopez-Trascasa, M.5
-
25
-
-
84878344482
-
Systemic lupus erythematosus due to C1q deficiency with progressive encephalopathy, intracranial calcification and acquired moyamoya cerebral vasculopathy
-
Troedson C., Wong M., Dalby-Payne J., Wilson M., Dexter M., Rice G.I., et al. Systemic lupus erythematosus due to C1q deficiency with progressive encephalopathy, intracranial calcification and acquired moyamoya cerebral vasculopathy. Lupus 2013, 22:639-643.
-
(2013)
Lupus
, vol.22
, pp. 639-643
-
-
Troedson, C.1
Wong, M.2
Dalby-Payne, J.3
Wilson, M.4
Dexter, M.5
Rice, G.I.6
-
26
-
-
79952475512
-
SLE with C1q deficiency treated with fresh frozen plasma: a 10-year experience
-
Mehta P., Norsworthy P.J., Hall A.E., Kelly S.J., Walport M.J., Botto M., et al. SLE with C1q deficiency treated with fresh frozen plasma: a 10-year experience. Rheumatol. 2010, 49:823-824.
-
(2010)
Rheumatol.
, vol.49
, pp. 823-824
-
-
Mehta, P.1
Norsworthy, P.J.2
Hall, A.E.3
Kelly, S.J.4
Walport, M.J.5
Botto, M.6
-
27
-
-
10944226539
-
Restoration of C1q levels by bone marrow transplantation attenuates autoimmune disease associated with C1q deficiency in mice
-
Cortes-Hernandez J., Fossati-Jimack L., Petry F., Loos M., Izui S., Walport M.J., et al. Restoration of C1q levels by bone marrow transplantation attenuates autoimmune disease associated with C1q deficiency in mice. Eur. J. Immunol. 2004, 34:3713-3722.
-
(2004)
Eur. J. Immunol.
, vol.34
, pp. 3713-3722
-
-
Cortes-Hernandez, J.1
Fossati-Jimack, L.2
Petry, F.3
Loos, M.4
Izui, S.5
Walport, M.J.6
-
28
-
-
0035477983
-
Reconstitution of the complement function in C1q-deficient (C1qa-/-) mice with wild-type bone marrow cells
-
Petry F., Botto M., Holtappels R., Walport M.J., Loos M. Reconstitution of the complement function in C1q-deficient (C1qa-/-) mice with wild-type bone marrow cells. J.Immunol. 2001, 167:4033-4037.
-
(2001)
J.Immunol.
, vol.167
, pp. 4033-4037
-
-
Petry, F.1
Botto, M.2
Holtappels, R.3
Walport, M.J.4
Loos, M.5
-
29
-
-
84939569276
-
Allogeneic haematopoietic stem cell transplantation restores complement function in human hereditary C1q deficiency
-
Olsson R., Hagelberg S., Ringden O., Truedsson L., Åhlin A. Allogeneic haematopoietic stem cell transplantation restores complement function in human hereditary C1q deficiency. Bone Marrow Transplant. 2013, 48. S338.
-
(2013)
Bone Marrow Transplant.
, vol.48
, pp. S338
-
-
Olsson, R.1
Hagelberg, S.2
Ringden, O.3
Truedsson, L.4
Åhlin, A.5
-
30
-
-
84891748872
-
Successful cure of C1q deficiency in human subjects treated with hematopoietic stem cell transplantation
-
Arkwright P.D., Riley P., Hughes S.M., Alachkar H., Wynn R.F. Successful cure of C1q deficiency in human subjects treated with hematopoietic stem cell transplantation. J.Allergy Clin. Immunol. 2014, 133:265-267.
-
(2014)
J.Allergy Clin. Immunol.
, vol.133
, pp. 265-267
-
-
Arkwright, P.D.1
Riley, P.2
Hughes, S.M.3
Alachkar, H.4
Wynn, R.F.5
-
31
-
-
84939561784
-
Allogeneic haematopoietic stem cell transplantation in the treatment for human C1q deficiency - the Karolinska experience
-
Olsson R., Hagelberg S., Schiller B., Ringden O., Truedsson L., Åhlin A. Allogeneic haematopoietic stem cell transplantation in the treatment for human C1q deficiency - the Karolinska experience. Bone Marrow Transpl. 2015, 50. S489.
-
(2015)
Bone Marrow Transpl.
, vol.50
, pp. S489
-
-
Olsson, R.1
Hagelberg, S.2
Schiller, B.3
Ringden, O.4
Truedsson, L.5
Åhlin, A.6
-
32
-
-
9444254614
-
Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish family
-
Topaloglu R., Bakkaloglu A., Slingsby J.H., Mihatsch M.J., Pascual M., Norsworthy P., et al. Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish family. Kidney Int. 1996, 50:635-642.
-
(1996)
Kidney Int.
, vol.50
, pp. 635-642
-
-
Topaloglu, R.1
Bakkaloglu, A.2
Slingsby, J.H.3
Mihatsch, M.J.4
Pascual, M.5
Norsworthy, P.6
-
33
-
-
0035189062
-
Physician response to surveys. A review of the literature
-
Kellerman S.E., Herold J. Physician response to surveys. A review of the literature. Am. J. Prev. Med. 2001, 20:61-67.
-
(2001)
Am. J. Prev. Med.
, vol.20
, pp. 61-67
-
-
Kellerman, S.E.1
Herold, J.2
-
34
-
-
0033954028
-
Molecular, genetic and epidemiologic studies on selective complete C1q deficiency in Turkey
-
Berkel A.I., Birben E., Oner C., Oner R., Loos M., Petry F. Molecular, genetic and epidemiologic studies on selective complete C1q deficiency in Turkey. Immunobiology 2000, 201:347-355.
-
(2000)
Immunobiology
, vol.201
, pp. 347-355
-
-
Berkel, A.I.1
Birben, E.2
Oner, C.3
Oner, R.4
Loos, M.5
Petry, F.6
-
35
-
-
0034235827
-
Twins: mirrors of the immune system
-
Salvetti M., Ristori G., Bomprezzi R., Pozzilli P., Leslie R.D. Twins: mirrors of the immune system. Immunol. Today 2000, 21:342-347.
-
(2000)
Immunol. Today
, vol.21
, pp. 342-347
-
-
Salvetti, M.1
Ristori, G.2
Bomprezzi, R.3
Pozzilli, P.4
Leslie, R.D.5
-
36
-
-
79955623575
-
Epigenetic alterations in autoimmune rheumatic diseases
-
Ballestar E. Epigenetic alterations in autoimmune rheumatic diseases. Nat. Rev. Rheumatol. 2011, 7:263-271.
-
(2011)
Nat. Rev. Rheumatol.
, vol.7
, pp. 263-271
-
-
Ballestar, E.1
-
37
-
-
84973431871
-
Allogeneic haematopoietic stem cell transplantation in the treatment for human C1q deficiency -- the Karolinska experience
-
in press
-
Olsson R., Hagelberg S., Schiller B., Ringden O., Truedsson L., Åhlin A. Allogeneic haematopoietic stem cell transplantation in the treatment for human C1q deficiency -- the Karolinska experience. Transplantation 2015, in press.
-
(2015)
Transplantation
-
-
Olsson, R.1
Hagelberg, S.2
Schiller, B.3
Ringden, O.4
Truedsson, L.5
Åhlin, A.6
|