-
1
-
-
0002871590
-
Bacteria and complement
-
VOLANAKIS, J. E., and M. M. FRANK, editors. Marcel Dekker, Inc. New York
-
PETRY, F., and M. LOOS. (1998). Bacteria and complement. VOLANAKIS, J. E., and M. M. FRANK, editors. The human complement system in health and disease. Marcel Dekker, Inc. New York 17: 375 pp.
-
(1998)
The Human Complement System in Health and Disease
, vol.17
-
-
Petry, F.1
Loos, M.2
-
2
-
-
0026544128
-
Localization of the gene cluster encoding the A, B, and C chains of human C1q to 1p34.1-1p36.3
-
SELLAR, G. C., D. COCKBURN, and K. B. M. REID. 1992. Localization of the gene cluster encoding the A, B, and C chains of human C1q to 1p34.1-1p36.3. Immunogenetics 35: 214.
-
(1992)
Immunogenetics
, vol.35
, pp. 214
-
-
Sellar, G.C.1
Cockburn, D.2
Reid, K.B.M.3
-
3
-
-
0026019308
-
Characterisation and organisation of the genes encoding the A, B and C chain of human C1q. The complete derived amino acid sequence of human C1q
-
SELLAR, G. C., D. J. BLAKE, and K. B. M. REID. 1981. Characterisation and organisation of the genes encoding the A, B and C chain of human C1q. The complete derived amino acid sequence of human C1q. Biochem. J. 274: 481.
-
(1981)
Biochem. J.
, vol.274
, pp. 481
-
-
Sellar, G.C.1
Blake, D.J.2
Reid, K.B.M.3
-
4
-
-
0024341918
-
Chemistry and molecular genetics of C1q
-
REID, K. B. M. 1989. Chemistry and molecular genetics of C1q. Behring Inst. Mitt. 84: 8.
-
(1989)
Behring Inst. Mitt.
, vol.84
, pp. 8
-
-
Reid, K.B.M.1
-
5
-
-
0024308036
-
Deficiency of the first component of human complement
-
REID, K. B. M. 1989. Deficiency of the first component of human complement. Immunodeficiency Reviews 1: 247.
-
(1989)
Immunodeficiency Reviews
, vol.1
, pp. 247
-
-
Reid, K.B.M.1
-
6
-
-
0021858437
-
Low molecular weight C1q in systemic lupus erythematosus
-
HOEKZEMA, R., A. J. HANNEMA, T. J. G. SWAAK, J. PAARDEKOOPER, and C. E. HACK. 1985. Low molecular weight C1q in systemic lupus erythematosus. J. Immunol. 135: 265.
-
(1985)
J. Immunol.
, vol.135
, pp. 265
-
-
Hoekzema, R.1
Hannema, A.J.2
Swaak, T.J.G.3
Paardekooper, J.4
Hack, C.E.5
-
7
-
-
0028093373
-
Hereditary C1q deficiency and systemic lupus erythematosus
-
BOWNESS, P., K. A. DAVIES, P. J. NORSWORTHY, P. ATHANASSIOU, J. TAYLOR WIEDEMANN, L. K. BORYSIEWICZ, P. A. MEYER, and M. J. WALPORT. 1994. Hereditary C1q deficiency and systemic lupus erythematosus. QJM 87: 455.
-
(1994)
QJM
, vol.87
, pp. 455
-
-
Bowness, P.1
Davies, K.A.2
Norsworthy, P.J.3
Athanassiou, P.4
Taylor Wiedemann, J.5
Borysiewicz, L.K.6
Meyer, P.A.7
Walport, M.J.8
-
8
-
-
0030857510
-
Multiple identification of a particular type of hereditary C1q deficiency in the Turkish population: Review of the cases and additional genetic and functional analysis
-
PETRY, F., A. I. BERKEL, and M. LOOS. 1997. Multiple identification of a particular type of hereditary C1q deficiency in the Turkish population: review of the cases and additional genetic and functional analysis. Hum. Genet. 100: 51.
-
(1997)
Hum. Genet.
, vol.100
, pp. 51
-
-
Petry, F.1
Berkel, A.I.2
Loos, M.3
-
9
-
-
0028791743
-
Non-sense and missense mutations in the structural genes of complement component C1q A and C chains are linked with two different types of complete selective C1q deficiencies
-
PETRY, F., D. T. LE, M. KIRSCHFINK, and M. LOOS. 1995. Non-sense and missense mutations in the structural genes of complement component C1q A and C chains are linked with two different types of complete selective C1q deficiencies. J. Immunol. 155: 4734.
-
(1995)
J. Immunol.
, vol.155
, pp. 4734
-
-
Petry, F.1
Le, D.T.2
Kirschfink, M.3
Loos, M.4
-
10
-
-
0017624218
-
A case of selective C1q deficiency
-
BERKEL, A. I., O. SANAL, R. THESEN, and M. LOOS. 1977. A case of selective C1q deficiency. Turk. J. Pediatr. 19: 101.
-
(1977)
Turk. J. Pediatr.
, vol.19
, pp. 101
-
-
Berkel, A.I.1
Sanal, O.2
Thesen, R.3
Loos, M.4
-
11
-
-
0018908838
-
Immunochemical and functional analyses of a complete C1q deficiency in man: Evidence that C1r and C1s are in the native form, and that they reassociate with purified C1q to form macromolecular C1
-
LOOS, M., A. B. LAURELL, A. G. SJÖRHOLM, U. MARTENSSON, and A. I. BERKEL. 1980. Immunochemical and functional analyses of a complete C1q deficiency in man: evidence that C1r and C1s are in the native form, and that they reassociate with purified C1q to form macromolecular C1. J. Immunol. 124: 59.
-
(1980)
J. Immunol.
, vol.124
, pp. 59
-
-
Loos, M.1
Laurell, A.B.2
Sjörholm, A.G.3
Martensson, U.4
Berkel, A.I.5
-
12
-
-
0019519472
-
Selective complete C1q deficiency - Report of two new cases
-
BERKEL, A. I., M. LOOS, O. SANAL, F. ERSOY, and O. YEGIN. 1981. Selective complete C1q deficiency - report of two new cases. Immunology Letters 2: 263.
-
(1981)
Immunology Letters
, vol.2
, pp. 263
-
-
Berkel, A.I.1
Loos, M.2
Sanal, O.3
Ersoy, F.4
Yegin, O.5
-
13
-
-
0031033380
-
Development of systemic lupus erythematosus in a patient with complete C1q deficiency
-
BERKEL, A. I., F. PETRY, O. SANAL, K. TINAZTEPE, F. ERSOY, A. BAKKALOGLU, and M. LOOS. 1998. Development of systemic lupus erythematosus in a patient with complete C1q deficiency. European Journal of Pediatrics 156: 113.
-
(1998)
European Journal of Pediatrics
, vol.156
, pp. 113
-
-
Berkel, A.I.1
Petry, F.2
Sanal, O.3
Tinaztepe, K.4
Ersoy, F.5
Bakkaloglu, A.6
Loos, M.7
-
14
-
-
9444254614
-
Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a turkish family
-
TOPALOGLU, R., A. BAKKALOGLU, J. H. SLINGSBY, M. J. MIHATSCH, M. PASCUAL, P. NORSWORTHY, B. J. MORLEY, U. SAATCI, J. A. SCHIFFERLI, and M. J. WALPORT. 1996. Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a turkish family. Kidney International 50: 635.
-
(1996)
Kidney International
, vol.50
, pp. 635
-
-
Topaloglu, R.1
Bakkaloglu, A.2
Slingsby, J.H.3
Mihatsch, M.J.4
Pascual, M.5
Norsworthy, P.6
Morley, B.J.7
Saatci, U.8
Schifferli, J.A.9
Walport, M.J.10
-
15
-
-
0023902375
-
A homozygous point mutation results in a stop codon in the C1qB-chain of a C1q-deficient individual
-
MCADAM, R. A., D. GOUNDIS, and K. B. M. REID. 1988. A homozygous point mutation results in a stop codon in the C1qB-chain of a C1q-deficient individual. Immunogenetics 27: 259.
-
(1988)
Immunogenetics
, vol.27
, pp. 259
-
-
McAdam, R.A.1
Goundis, D.2
Reid, K.B.M.3
-
16
-
-
0029984710
-
Homozygous hereditary C1q deficiency and systemic lupus erythematosus. A new family and the molecular basis of C1q deficiency in three families
-
SLINGSBY, J. H., P. NORSWORTHY, G. PEARCE, A. K. VAISHNAW, H. ISSLER, B. J. MORLEY, and M. J. WALPORT. 1996. Homozygous hereditary C1q deficiency and systemic lupus erythematosus. A new family and the molecular basis of C1q deficiency in three families. Arthritis Rheum. 39: 663.
-
(1996)
Arthritis Rheum.
, vol.39
, pp. 663
-
-
Slingsby, J.H.1
Norsworthy, P.2
Pearce, G.3
Vaishnaw, A.K.4
Issler, H.5
Morley, B.J.6
Walport, M.J.7
-
17
-
-
0019953247
-
Structural and functional studies in C1q deficiency
-
CHAPUIS, R. M., G. HAUPTMANN, E. GROSSHANS, and H. ISLIKER. 1998. Structural and functional studies in C1q deficiency. J. Immunol. 129: 1509.
-
(1998)
J. Immunol.
, vol.129
, pp. 1509
-
-
Chapuis, R.M.1
Hauptmann, G.2
Grosshans, E.3
Isliker, H.4
-
18
-
-
0031442782
-
Molecular basis of a new type of C1q-deficiency associated with a non-functional low molecular weight (LMW) C1q - Parallels and differences to other known genetic C1q-defects
-
PETRY, F., G. HAUPTMANN, J. GOETZ, E. GROSSHANS, and M. LOOS. 1997. Molecular basis of a new type of C1q-deficiency associated with a non-functional low molecular weight (LMW) C1q - parallels and differences to other known genetic C1q-defects. Immunopharmacol. 38: 189.
-
(1997)
Immunopharmacol.
, vol.38
, pp. 189
-
-
Petry, F.1
Hauptmann, G.2
Goetz, J.3
Grosshans, E.4
Loos, M.5
-
19
-
-
0027379543
-
Complete functional C1q deficiency associated with systemic lupus erythematosus (SLE)
-
KIRSCHFINK, M., F. PETRY, K. KHIRWADKAR, R. WIGAND, J. P. KALTWASSER, and M. LOOS. 1993. Complete functional C1q deficiency associated with systemic lupus erythematosus (SLE). Clin. Exp. Immunol. 94: 267.
-
(1993)
Clin. Exp. Immunol.
, vol.94
, pp. 267
-
-
Kirschfink, M.1
Petry, F.2
Khirwadkar, K.3
Wigand, R.4
Kaltwasser, J.P.5
Loos, M.6
-
20
-
-
0007285284
-
Dysfunctional and antigenetically abnormal C1q resulting from a point mutation in codon 6 of the C chain
-
abstr.
-
SUWAIRI, W., S. BAHABRI, D. BEVING, J. WISNIESKI, and M. WARMAN. 1997. Dysfunctional and antigenetically abnormal C1q resulting from a point mutation in codon 6 of the C chain. Arth. Rheum. 40: S308 (abstr.).
-
(1997)
Arth. Rheum.
, vol.40
-
-
Suwairi, W.1
Bahabri, S.2
Beving, D.3
Wisnieski, J.4
Warman, M.5
|