-
1
-
-
0034920305
-
-
Ophoff RA, DeYoung J, Service SK, et al. Hereditary vascular retinopathy, cerebroretinal vasculopathy and hereditary endotheliopathy with retinopathy, nephropathy and stroke map to a single locus on chromosome 3p21.1-p21.3. Am J Hum Genet 2001; 69:447-53.
-
Ophoff RA, DeYoung J, Service SK, et al. Hereditary vascular retinopathy, cerebroretinal vasculopathy and hereditary endotheliopathy with retinopathy, nephropathy and stroke map to a single locus on chromosome 3p21.1-p21.3. Am J Hum Genet 2001; 69:447-53.
-
-
-
-
2
-
-
34548334617
-
Truncations in the carboxyl-terminus of human 3′-5′ DNA exonuclear TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy
-
Richards A, van den Maagdenberg AM, Jen JC, et al. Truncations in the carboxyl-terminus of human 3′-5′ DNA exonuclear TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy. Nat Genet 2007; 39:1068-70.
-
(2007)
Nat Genet
, vol.39
, pp. 1068-1070
-
-
Richards, A.1
van den Maagdenberg, A.M.2
Jen, J.C.3
-
3
-
-
33746581694
-
Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutieres syndrome at the AGS1 locus
-
Crow YJ, Hayward BE, Parmar R, et al. Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutieres syndrome at the AGS1 locus. Nat Genet 2006; 38:917-20.
-
(2006)
Nat Genet
, vol.38
, pp. 917-920
-
-
Crow, Y.J.1
Hayward, B.E.2
Parmar, R.3
-
4
-
-
33749006867
-
Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p
-
Lee-Kirsch MA, Gong M, Schulz H, et al. Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p. Am J Hum Genet 2006; 79:731-7.
-
(2006)
Am J Hum Genet
, vol.79
, pp. 731-737
-
-
Lee-Kirsch, M.A.1
Gong, M.2
Schulz, H.3
-
5
-
-
34147185679
-
Heterozygous mutations in TREX1 cause familial Chilblain lupus and dominant Aicardi-Goutieres syndrome
-
Rice G, Newman WG, Dean J, et al. Heterozygous mutations in TREX1 cause familial Chilblain lupus and dominant Aicardi-Goutieres syndrome. Am J Hum Genet 2007; 80:811-5.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 811-815
-
-
Rice, G.1
Newman, W.G.2
Dean, J.3
-
6
-
-
34548327158
-
Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 are associated with systemic lupus erythematosus
-
Lee-Kirsch MA, Gong M, Chowdhury D, et al. Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 are associated with systemic lupus erythematosus. Nat Genet 2007; 39:1065-7.
-
(2007)
Nat Genet
, vol.39
, pp. 1065-1067
-
-
Lee-Kirsch, M.A.1
Gong, M.2
Chowdhury, D.3
-
8
-
-
0014690918
-
Properties of deoxyribonuclease 3 from mammalian tissues
-
Lindahl T, Gally JA, Edelman GM. Properties of deoxyribonuclease 3 from mammalian tissues. J Biol Chem 1969; 244:5014-9.
-
(1969)
J Biol Chem
, vol.244
, pp. 5014-5019
-
-
Lindahl, T.1
Gally, J.A.2
Edelman, G.M.3
-
11
-
-
0015013523
-
Excision of pyrimidine dimers from ultraviolet-irradiated DNA by exonucleases from mammalian cells
-
Lindahl T. Excision of pyrimidine dimers from ultraviolet-irradiated DNA by exonucleases from mammalian cells. Eur J Biochem 1971; 18:407-14.
-
(1971)
Eur J Biochem
, vol.18
, pp. 407-414
-
-
Lindahl, T.1
-
12
-
-
0037786682
-
A human DNA editing enzyme homologous to the Escherichia coli DnaQ/MutD protein
-
Hoss M, Robins P, Naven TJ, Pappin DJ, Sgouros J, Lindahl T. A human DNA editing enzyme homologous to the Escherichia coli DnaQ/MutD protein. EMBO J 1999; 18:3868-75.
-
(1999)
EMBO J
, vol.18
, pp. 3868-3875
-
-
Hoss, M.1
Robins, P.2
Naven, T.J.3
Pappin, D.J.4
Sgouros, J.5
Lindahl, T.6
-
13
-
-
0033538461
-
Identification and expression of the TREX1 and TREX2 cDNA sequences encoding mammalian 3′→5′ exonucleases
-
Mazur DJ, Perrino FW. Identification and expression of the TREX1 and TREX2 cDNA sequences encoding mammalian 3′→5′ exonucleases. J Biol Chem 1999; 274:19655-60.
-
(1999)
J Biol Chem
, vol.274
, pp. 19655-19660
-
-
Mazur, D.J.1
Perrino, F.W.2
-
14
-
-
0028862397
-
The 3′-5′ exonuclease site of DNA polymerase III from gram-positive bacteria: Definition of a novel motif structure
-
Barnes MH, Spacciapoli P, Li DH, Brown NC. The 3′-5′ exonuclease site of DNA polymerase III from gram-positive bacteria: definition of a novel motif structure. Gene 1995; 165:45-50.
-
(1995)
Gene
, vol.165
, pp. 45-50
-
-
Barnes, M.H.1
Spacciapoli, P.2
Li, D.H.3
Brown, N.C.4
-
15
-
-
0030841057
-
Role of proofreading and mismatch repair in maintaining the stability of nucleotide repeats in DNA
-
Strauss BS, Sagher D, Acharya S. Role of proofreading and mismatch repair in maintaining the stability of nucleotide repeats in DNA. Nucleic Acids Res 1997; 25:806-13.
-
(1997)
Nucleic Acids Res
, vol.25
, pp. 806-813
-
-
Strauss, B.S.1
Sagher, D.2
Acharya, S.3
-
16
-
-
0032167849
-
Mutational analysis of the 3′→5′ proofreading exonuclease of Escherichia coli DNA polymerase III
-
Taft-Benz SA, Schaaper RM. Mutational analysis of the 3′→5′ proofreading exonuclease of Escherichia coli DNA polymerase III. Nucleic Acids Res 1998; 26:4005-11.
-
(1998)
Nucleic Acids Res
, vol.26
, pp. 4005-4011
-
-
Taft-Benz, S.A.1
Schaaper, R.M.2
-
17
-
-
34249848019
-
The crystal structure of TREX1 explains the 3′ nucleotide specificity and reveals a polyproline II helix for protein partnering
-
de Silva U, Choudhury S, Bailey SL, Harvey S, Perrino FW, Hollis T. The crystal structure of TREX1 explains the 3′ nucleotide specificity and reveals a polyproline II helix for protein partnering. J Biol Chem 2007; 282:10537-43.
-
(2007)
J Biol Chem
, vol.282
, pp. 10537-10543
-
-
de Silva, U.1
Choudhury, S.2
Bailey, S.L.3
Harvey, S.4
Perrino, F.W.5
Hollis, T.6
-
18
-
-
34347265261
-
Structure of the dimeric exonuclease TREX1 in complex with DNA displays a proline-rich binding site for WW domains
-
Brucet M, Querol-Audi J, Serra M, et al. Structure of the dimeric exonuclease TREX1 in complex with DNA displays a proline-rich binding site for WW domains. J Biol Chem 2007.
-
(2007)
J Biol Chem
-
-
Brucet, M.1
Querol-Audi, J.2
Serra, M.3
-
20
-
-
0035951880
-
Proofreading of DNA polymerase eta-dependent replication errors
-
Bebenek K, Matsuda T, Masutani C, Hanaoka F, Kunkel TA. Proofreading of DNA polymerase eta-dependent replication errors. J Biol Chem 2001; 276:2317-20.
-
(2001)
J Biol Chem
, vol.276
, pp. 2317-2320
-
-
Bebenek, K.1
Matsuda, T.2
Masutani, C.3
Hanaoka, F.4
Kunkel, T.A.5
-
21
-
-
0035805548
-
Structure and expression of the TREX1 and TREX2 3′→5′ exonuclease genes
-
Mazur DJ, Perrino FW. Structure and expression of the TREX1 and TREX2 3′→5′ exonuclease genes. J Biol Chem 2001; 276:14718-27.
-
(2001)
J Biol Chem
, vol.276
, pp. 14718-14727
-
-
Mazur, D.J.1
Perrino, F.W.2
-
22
-
-
3242672339
-
Gene-targeted mice lacking the Trex1 (DNase III) 3′→5′ DNA exonuclease develop inflammatory myocarditis
-
Morita M, Stamp G, Robins P, et al. Gene-targeted mice lacking the Trex1 (DNase III) 3′→5′ DNA exonuclease develop inflammatory myocarditis. Mol Cell Biol 2004; 24:6719-27.
-
(2004)
Mol Cell Biol
, vol.24
, pp. 6719-6727
-
-
Morita, M.1
Stamp, G.2
Robins, P.3
-
23
-
-
33745501366
-
The exonuclease TREX1 is in the SET complex and acts in concert with NM23-H1 to degrade DNA during granzyme A-mediated cell death
-
Chowdhury D, Beresford PJ, Zhu P, et al. The exonuclease TREX1 is in the SET complex and acts in concert with NM23-H1 to degrade DNA during granzyme A-mediated cell death. Mol Cell 2006; 23:133-42.
-
(2006)
Mol Cell
, vol.23
, pp. 133-142
-
-
Chowdhury, D.1
Beresford, P.J.2
Zhu, P.3
-
24
-
-
36248988008
-
Trex1 Exonuclease Degrades ssDNA to Prevent Chronic Checkpoint Activation and Autoimmune Disease
-
Yang YG, Lindahl T, Barnes DE. Trex1 Exonuclease Degrades ssDNA to Prevent Chronic Checkpoint Activation and Autoimmune Disease. Cell 2007; 131:873-86.
-
(2007)
Cell
, vol.131
, pp. 873-886
-
-
Yang, Y.G.1
Lindahl, T.2
Barnes, D.E.3
-
25
-
-
36248943050
-
DNA mismanagement leads to immune system oversight
-
Coscoy L, Raulet DH. DNA mismanagement leads to immune system oversight. Cell 2007; 131:836-8.
-
(2007)
Cell
, vol.131
, pp. 836-838
-
-
Coscoy, L.1
Raulet, D.H.2
-
26
-
-
34250303902
-
Biochemical and cellular characteristics of the 3′→5′ exonuclease TREX2
-
Chen MJ, Ma SM, Dumitrache LC, Hasty P. Biochemical and cellular characteristics of the 3′→5′ exonuclease TREX2. Nucleic Acids Res 2007; 35:2682-94.
-
(2007)
Nucleic Acids Res
, vol.35
, pp. 2682-2694
-
-
Chen, M.J.1
Ma, S.M.2
Dumitrache, L.C.3
Hasty, P.4
-
27
-
-
0021336060
-
A progressive familial encephalopathy in infancy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis
-
Aicardi J, Goutieres F. A progressive familial encephalopathy in infancy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis. Ann Neurol 1984; 15:49-54.
-
(1984)
Ann Neurol
, vol.15
, pp. 49-54
-
-
Aicardi, J.1
Goutieres, F.2
-
28
-
-
14644400436
-
-
Goutieres F. Aicardi-Goutieres syndrome. Brain Dev 2005; 27:201-6.
-
Goutieres F. Aicardi-Goutieres syndrome. Brain Dev 2005; 27:201-6.
-
-
-
-
29
-
-
0031593632
-
Aicardi-Goutieres syndrome: An update and results of interferon-alpha studies
-
Goutieres F, Aicardi J, Barth PG, Lebon P. Aicardi-Goutieres syndrome: an update and results of interferon-alpha studies. Ann Neurol 1998; 44:900-7.
-
(1998)
Ann Neurol
, vol.44
, pp. 900-907
-
-
Goutieres, F.1
Aicardi, J.2
Barth, P.G.3
Lebon, P.4
-
30
-
-
0022875811
-
A syndrome with intracranial calcification and microcephaly in two sibs, resembling intrauterine infection
-
Burn J, Wickramasinghe HT, Harding B, Baraitser M. A syndrome with intracranial calcification and microcephaly in two sibs, resembling intrauterine infection. Clin Genet 1986; 30:112-6.
-
(1986)
Clin Genet
, vol.30
, pp. 112-116
-
-
Burn, J.1
Wickramasinghe, H.T.2
Harding, B.3
Baraitser, M.4
-
31
-
-
0028017854
-
Autosomal recessive congenital intrauterine infecction-like syndrome of microcephaly, intracranial calcification and CNS disease
-
Reardon W, Hockey A, Silberstein P, et al. Autosomal recessive congenital intrauterine infecction-like syndrome of microcephaly, intracranial calcification and CNS disease. American Journal Medical Genetics 1994; 52:58-65.
-
(1994)
American Journal Medical Genetics
, vol.52
, pp. 58-65
-
-
Reardon, W.1
Hockey, A.2
Silberstein, P.3
-
32
-
-
85011942048
-
Encephalitis among Cree children in northern Quebec
-
Black DN, Watters GV, Andermann E, et al. Encephalitis among Cree children in northern Quebec. J Med Genet 1988; 40:183-7.
-
(1988)
J Med Genet
, vol.40
, pp. 183-187
-
-
Black, D.N.1
Watters, G.V.2
Andermann, E.3
-
33
-
-
18144395424
-
Genetic syndromes mimic congenital infections
-
Sanchis A, Cervero L, Bataller A, et al. Genetic syndromes mimic congenital infections. J Pediatr 2005; 146:701-5.
-
(2005)
J Pediatr
, vol.146
, pp. 701-705
-
-
Sanchis, A.1
Cervero, L.2
Bataller, A.3
-
34
-
-
0037338578
-
Cree encephalitis is allelic with Aicardi-Goutieres syndrome: Implications for the pathogenesis of disorders of interferon alpha metabolism
-
Crow YJ, Black DN, Ali M, et al. Cree encephalitis is allelic with Aicardi-Goutieres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism. J Med Genet 2003; 40:183-7.
-
(2003)
J Med Genet
, vol.40
, pp. 183-187
-
-
Crow, Y.J.1
Black, D.N.2
Ali, M.3
-
35
-
-
0033915684
-
Familial systemic lupus erythematosus and congenital infection-like syndrome
-
Dale RC, Tang SP, Heckmatt JZ, Tatnall FM. Familial systemic lupus erythematosus and congenital infection-like syndrome. Neuropediatrics 2000; 31:155-8.
-
(2000)
Neuropediatrics
, vol.31
, pp. 155-158
-
-
Dale, R.C.1
Tang, S.P.2
Heckmatt, J.Z.3
Tatnall, F.M.4
-
36
-
-
18444387671
-
Cerebral thrombotic microangiopathy and antiphospholipid antibodies in Aicardi-Goutieres syndrome - report of two sisters
-
Rasmussen M, Skullerud K, Bakke SJ, Lebon P, Jahnsen FL. Cerebral thrombotic microangiopathy and antiphospholipid antibodies in Aicardi-Goutieres syndrome - report of two sisters. Neuropediatrics 2005; 36:40-4.
-
(2005)
Neuropediatrics
, vol.36
, pp. 40-44
-
-
Rasmussen, M.1
Skullerud, K.2
Bakke, S.J.3
Lebon, P.4
Jahnsen, F.L.5
-
37
-
-
31544481206
-
Phenotypic overlap between infantile systemic lupus erythematosus and Aicardi-Goutieres syndrome
-
De Laet C, Goyens P, Christophe C, Ferster A, Mascart F, Dan B. Phenotypic overlap between infantile systemic lupus erythematosus and Aicardi-Goutieres syndrome. Neuropediatrics 2005; 36:399-402.
-
(2005)
Neuropediatrics
, vol.36
, pp. 399-402
-
-
De Laet, C.1
Goyens, P.2
Christophe, C.3
Ferster, A.4
Mascart, F.5
Dan, B.6
-
38
-
-
0020511070
-
Synthesis of intrathecal interferon in systemic lupus erythematosus with neurological complications
-
Lebon P, Lenoir GR, Fischer A, Lagrue A. Synthesis of intrathecal interferon in systemic lupus erythematosus with neurological complications. Br Med J (Clin Res Ed) 1983; 287:1165-7.
-
(1983)
Br Med J (Clin Res Ed)
, vol.287
, pp. 1165-1167
-
-
Lebon, P.1
Lenoir, G.R.2
Fischer, A.3
Lagrue, A.4
-
39
-
-
33746522835
-
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection
-
Crow YJ, Leitch A, Hayward BE, et al. Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection. Nat Genet 2006; 38:910-6.
-
(2006)
Nat Genet
, vol.38
, pp. 910-916
-
-
Crow, Y.J.1
Leitch, A.2
Hayward, B.E.3
-
40
-
-
0032573155
-
Cloning of the cDNA encoding the large subunit of human RNase HI, a homologue of the prokaryotic RNase HII
-
Frank P, Braunshofer-Reiter C, Wintersberger U, Grimm R, Busen W. Cloning of the cDNA encoding the large subunit of human RNase HI, a homologue of the prokaryotic RNase HII. Proc Natl Acad Sci USA 1998; 95:12872-7.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 12872-12877
-
-
Frank, P.1
Braunshofer-Reiter, C.2
Wintersberger, U.3
Grimm, R.4
Busen, W.5
-
41
-
-
0025911370
-
Ribonuclease H from K562 human erythroleukemia cells. Purification, characterization and substrate specificity
-
Eder PS, Walder JA. Ribonuclease H from K562 human erythroleukemia cells. Purification, characterization and substrate specificity. J Biol Chem 1991; 266:6472-9.
-
(1991)
J Biol Chem
, vol.266
, pp. 6472-6479
-
-
Eder, P.S.1
Walder, J.A.2
-
43
-
-
34247842779
-
A mutation in TREX1 that impairs susceptibility to granzyme A-mediated cell death underlies familial chilblain lupus
-
Lee-Kirsch MA, Chowdhury D, Harvey S, et al. A mutation in TREX1 that impairs susceptibility to granzyme A-mediated cell death underlies familial chilblain lupus. J Mol Med 2007; 85:531-7.
-
(2007)
J Mol Med
, vol.85
, pp. 531-537
-
-
Lee-Kirsch, M.A.1
Chowdhury, D.2
Harvey, S.3
-
44
-
-
0018181190
-
Chilblain lupus erythematosus (Hutchinson). A clinical and laboratory study of 17 patients
-
Millard LG, Rowell NR. Chilblain lupus erythematosus (Hutchinson). A clinical and laboratory study of 17 patients. Br J Dermatol 1978; 98:497-506.
-
(1978)
Br J Dermatol
, vol.98
, pp. 497-506
-
-
Millard, L.G.1
Rowell, N.R.2
-
45
-
-
0023923348
-
Cerebroretinal vasculopathy: A new hereditary syndrome
-
Grand MG, Kaine J, Fulling K, et al. Cerebroretinal vasculopathy: A new hereditary syndrome. Ophthalmology 1988; 95:649-59.
-
(1988)
Ophthalmology
, vol.95
, pp. 649-659
-
-
Grand, M.G.1
Kaine, J.2
Fulling, K.3
-
46
-
-
0024465713
-
Hereditary retinal vasculopathy with cerebral white matter lesions
-
Gutmann DH, Fischbeck KH, Sergott RC. Hereditary retinal vasculopathy with cerebral white matter lesions. Am J Med Genet 1989; 34:217-20.
-
(1989)
Am J Med Genet
, vol.34
, pp. 217-220
-
-
Gutmann, D.H.1
Fischbeck, K.H.2
Sergott, R.C.3
-
47
-
-
0033546629
-
Cerebroretinal vasculopathy mimicking a brain tumor: A case of a rare hereditary syndrome
-
Weil S, Reifenberger G, Dudel C, Yousry TA, Schriever S, Noachtar S. Cerebroretinal vasculopathy mimicking a brain tumor: a case of a rare hereditary syndrome. Neurology 1999; 53:629-31.
-
(1999)
Neurology
, vol.53
, pp. 629-631
-
-
Weil, S.1
Reifenberger, G.2
Dudel, C.3
Yousry, T.A.4
Schriever, S.5
Noachtar, S.6
-
49
-
-
0025688878
-
Familial vascular retinopathy. A preliminary report
-
Storimans CW, Oosterhuis JA, van Schooneveld MJ, Bos PJ, Maaswinkel-Mooy PD. Familial vascular retinopathy. A preliminary report. Doc Ophthalmol 1990; 75:259-61.
-
(1990)
Doc Ophthalmol
, vol.75
, pp. 259-261
-
-
Storimans, C.W.1
Oosterhuis, J.A.2
van Schooneveld, M.J.3
Bos, P.J.4
Maaswinkel-Mooy, P.D.5
-
50
-
-
0031907348
-
Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon
-
Terwindt GM, Haan J, Ophoff RA, et al. Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon. Brain 1998; 121:303-16.
-
(1998)
Brain
, vol.121
, pp. 303-316
-
-
Terwindt, G.M.1
Haan, J.2
Ophoff, R.A.3
-
51
-
-
0030712287
-
Hereditary endotheliopathy with retinopathy, nephropathy and stroke (HERNS)
-
Jen J, Cohen AH, Yue Q, et al. Hereditary endotheliopathy with retinopathy, nephropathy and stroke (HERNS). Neurology 1997; 49:1322-30.
-
(1997)
Neurology
, vol.49
, pp. 1322-1330
-
-
Jen, J.1
Cohen, A.H.2
Yue, Q.3
-
52
-
-
18644369123
-
Novel ophthalmological features in hereditary endotheliopathy with retinopathy, nephropathy and stroke syndrome
-
Cohn AC, Kotschet K, Veitch A, Delatycki MB, McCombe MF. Novel ophthalmological features in hereditary endotheliopathy with retinopathy, nephropathy and stroke syndrome. Clinical & Experimental Ophthalmology 2005; 33:181-3.
-
(2005)
Clinical & Experimental Ophthalmology
, vol.33
, pp. 181-183
-
-
Cohn, A.C.1
Kotschet, K.2
Veitch, A.3
Delatycki, M.B.4
McCombe, M.F.5
-
53
-
-
38549110683
-
Hereditary Systemic Angiopathy (HSA) with cerebral calcifications, retinopathy, progressive nephropathy and hepatopathy
-
Winkler DT, Lyrer P, Probst A, et al. Hereditary Systemic Angiopathy (HSA) with cerebral calcifications, retinopathy, progressive nephropathy and hepatopathy. J Neurol 2008; 255:77-88.
-
(2008)
J Neurol
, vol.255
, pp. 77-88
-
-
Winkler, D.T.1
Lyrer, P.2
Probst, A.3
-
54
-
-
40049093765
-
Systemic lupus erythematosus
-
Rahman A, Isenberg DA. Systemic lupus erythematosus. N Engl J Med 2008; 358:929-39.
-
(2008)
N Engl J Med
, vol.358
, pp. 929-939
-
-
Rahman, A.1
Isenberg, D.A.2
-
55
-
-
40049099006
-
Collaborations, genetic associations and lupus erythematosus
-
Crow MK. Collaborations, genetic associations and lupus erythematosus. N Engl J Med 2008; 358:956-61.
-
(2008)
N Engl J Med
, vol.358
, pp. 956-961
-
-
Crow, M.K.1
-
56
-
-
45749097533
-
TREX1 polymorphisms associated with autoantibodies in patients with systemic lupus erythematosus
-
Hur JW, Sung YK, Shin HD, Park BL, Cheong HS, Bae SC. TREX1 polymorphisms associated with autoantibodies in patients with systemic lupus erythematosus. Rheumatol Int 2007.
-
(2007)
Rheumatol Int
-
-
Hur, J.W.1
Sung, Y.K.2
Shin, H.D.3
Park, B.L.4
Cheong, H.S.5
Bae, S.C.6
-
57
-
-
37849012459
-
The interplay between viruses and innate immune signaling: Recent insights and therapeutic opportunities
-
Unterholzner L, Bowie AG. The interplay between viruses and innate immune signaling: recent insights and therapeutic opportunities. Biochem Pharmacol 2008; 75:589-602.
-
(2008)
Biochem Pharmacol
, vol.75
, pp. 589-602
-
-
Unterholzner, L.1
Bowie, A.G.2
-
58
-
-
0018775078
-
Immune interferon in the circulation of patients with autoimmune disease
-
Hooks JJ, Moutsopoulos HM, Geis SA, Stahl NI, Decker JL, Notkins AL. Immune interferon in the circulation of patients with autoimmune disease. N Engl J Med 1979; 301:5-8.
-
(1979)
N Engl J Med
, vol.301
, pp. 5-8
-
-
Hooks, J.J.1
Moutsopoulos, H.M.2
Geis, S.A.3
Stahl, N.I.4
Decker, J.L.5
Notkins, A.L.6
-
59
-
-
0034533825
-
Activation of type I interferon system in systemic lupus erythematosus correlates with disease activity but not with antiretroviral antibodies
-
Bengtsson AA, Sturfelt G, Truedsson L, et al. Activation of type I interferon system in systemic lupus erythematosus correlates with disease activity but not with antiretroviral antibodies. Lupus 2000; 9:664-71.
-
(2000)
Lupus
, vol.9
, pp. 664-671
-
-
Bengtsson, A.A.1
Sturfelt, G.2
Truedsson, L.3
-
60
-
-
27944464836
-
Type I interferon correlates with serological and clinical manifestations of SLE
-
Dall'era MC, Cardarelli PM, Preston BT, Witte A, Davis JC Jr. Type I interferon correlates with serological and clinical manifestations of SLE. Ann Rheum Dis 2005; 64:1692-7.
-
(2005)
Ann Rheum Dis
, vol.64
, pp. 1692-1697
-
-
Dall'era, M.C.1
Cardarelli, P.M.2
Preston, B.T.3
Witte, A.4
Davis Jr, J.C.5
-
61
-
-
0345359586
-
Induction of clinical autoimmune disease by therapeutic interferonalpha
-
Gota C, Calabrese L. Induction of clinical autoimmune disease by therapeutic interferonalpha. Autoimmunity 2003; 36:511-8.
-
(2003)
Autoimmunity
, vol.36
, pp. 511-518
-
-
Gota, C.1
Calabrese, L.2
-
62
-
-
0025911863
-
Autoimmunity after alpha-interferon therapy for malignant carcinoid tumors
-
Ronnblom LE, Alm GV, Oberg KE. Autoimmunity after alpha-interferon therapy for malignant carcinoid tumors. Ann Intern Med 1991; 115:178-83.
-
(1991)
Ann Intern Med
, vol.115
, pp. 178-183
-
-
Ronnblom, L.E.1
Alm, G.V.2
Oberg, K.E.3
-
63
-
-
0018086341
-
Interferon treatment of NZB mice: Accelerated progression of autoimmune disease
-
Heremans H, Billiau A, Colombatti A, Hilgers J, de Somer P. Interferon treatment of NZB mice: accelerated progression of autoimmune disease. Infect Immun 1978; 21:925-30.
-
(1978)
Infect Immun
, vol.21
, pp. 925-930
-
-
Heremans, H.1
Billiau, A.2
Colombatti, A.3
Hilgers, J.4
de Somer, P.5
-
64
-
-
0018902074
-
The effect of exogenous interferon: Acceleration of autoimmune and renal diseases in (NZB/W) F1 mice
-
Adam C, Thoua Y, Ronco P, Verroust P, Tovey M, Morel-Maroger L. The effect of exogenous interferon: acceleration of autoimmune and renal diseases in (NZB/W) F1 mice. Clin Exp Immunol 1980; 40:373-82.
-
(1980)
Clin Exp Immunol
, vol.40
, pp. 373-382
-
-
Adam, C.1
Thoua, Y.2
Ronco, P.3
Verroust, P.4
Tovey, M.5
Morel-Maroger, L.6
-
65
-
-
14044278824
-
IFNalpha induces early lethal lupus in preautoimmune (New Zealand Black x New Zealand White) F1 but not in BALB/c mice
-
Mathian A, Weinberg A, Gallegos M, Banchereau J, Koutouzov S. IFNalpha induces early lethal lupus in preautoimmune (New Zealand Black x New Zealand White) F1 but not in BALB/c mice. J Immunol 2005; 174:2499-506.
-
(2005)
J Immunol
, vol.174
, pp. 2499-2506
-
-
Mathian, A.1
Weinberg, A.2
Gallegos, M.3
Banchereau, J.4
Koutouzov, S.5
-
66
-
-
0017687927
-
Accelerated mortality in young NZB/NZW mice treated with the interferon inducer tilorone hydrochloride
-
Walker SE. Accelerated mortality in young NZB/NZW mice treated with the interferon inducer tilorone hydrochloride. Clin Immunol Immunopathol 1977; 8:204-12.
-
(1977)
Clin Immunol Immunopathol
, vol.8
, pp. 204-212
-
-
Walker, S.E.1
-
67
-
-
0037451124
-
Type-I interferon receptor deficiency reduces lupus-like disease in NZB mice
-
Santiago-Raber ML, Baccala R, Haraldsson KM, et al. Type-I interferon receptor deficiency reduces lupus-like disease in NZB mice. J Exp Med 2003; 197:777-88.
-
(2003)
J Exp Med
, vol.197
, pp. 777-788
-
-
Santiago-Raber, M.L.1
Baccala, R.2
Haraldsson, K.M.3
-
68
-
-
0037320208
-
Type I Interferon controls the onset and severity of autoimmune manifestations in lpr mice
-
Braun D, Geraldes P, Demengeot J. Type I Interferon controls the onset and severity of autoimmune manifestations in lpr mice. J Autoimmun 2003; 20:15-25.
-
(2003)
J Autoimmun
, vol.20
, pp. 15-25
-
-
Braun, D.1
Geraldes, P.2
Demengeot, J.3
-
69
-
-
0032211097
-
Transgenic expression of IFNalpha in the central nervous system of mice protects against lethal neurotropic viral infection but induces inflammation and neurodegeneration
-
Akwa Y, Hassett DE, Eloranta ML, et al. Transgenic expression of IFNalpha in the central nervous system of mice protects against lethal neurotropic viral infection but induces inflammation and neurodegeneration. J Immunol 1998; 161:5016-26.
-
(1998)
J Immunol
, vol.161
, pp. 5016-5026
-
-
Akwa, Y.1
Hassett, D.E.2
Eloranta, M.L.3
-
71
-
-
0027939453
-
Retinal complications with elevated circulating plasma C5a associated with interferon-alpha therapy for chronic active hepatitis C
-
Sugano S, Yanagimoto M, Suzuki T, et al. Retinal complications with elevated circulating plasma C5a associated with interferon-alpha therapy for chronic active hepatitis C. Am J Gastroenterol 1994; 89:2054-6.
-
(1994)
Am J Gastroenterol
, vol.89
, pp. 2054-2056
-
-
Sugano, S.1
Yanagimoto, M.2
Suzuki, T.3
-
72
-
-
0028915147
-
Retinopathy and subconjunctival haemorrhage in patients with chronic viral hepatitis receiving interferon alfa
-
Hayasaka S, Fujii M, Yamamoto Y, Noda S, Kurome H, Sasaki M. Retinopathy and subconjunctival haemorrhage in patients with chronic viral hepatitis receiving interferon alfa. Br J Ophthalmol 1995; 79:150-2.
-
(1995)
Br J Ophthalmol
, vol.79
, pp. 150-152
-
-
Hayasaka, S.1
Fujii, M.2
Yamamoto, Y.3
Noda, S.4
Kurome, H.5
Sasaki, M.6
-
73
-
-
0030032871
-
Evaluation of risk factors of interferon-associated retinopathy in patients with type C chronic active hepatitis]
-
Soushi S, Kobayashi F, Obazawa H, et al. [Evaluation of risk factors of interferon-associated retinopathy in patients with type C chronic active hepatitis]. Nippon Ganka Gakkai Zasshi 1996; 100:69-76.
-
(1996)
Nippon Ganka Gakkai Zasshi
, vol.100
, pp. 69-76
-
-
Soushi, S.1
Kobayashi, F.2
Obazawa, H.3
-
74
-
-
0030064354
-
Retinal complications during interferon therapy for chronic hepatitis C
-
Kawano T, Shigehira M, Uto H, et al. Retinal complications during interferon therapy for chronic hepatitis C. Am J Gastroenterol 1996; 91:309-13.
-
(1996)
Am J Gastroenterol
, vol.91
, pp. 309-313
-
-
Kawano, T.1
Shigehira, M.2
Uto, H.3
-
75
-
-
0022398563
-
Inhibition of herpes simplex virus type 1-induced interferon synthesis by monoclonal antibodies against viral glycoprotein D and by lysosomotropic drugs
-
Lebon P. Inhibition of herpes simplex virus type 1-induced interferon synthesis by monoclonal antibodies against viral glycoprotein D and by lysosomotropic drugs. J Gen Virol 1985; 66:2781-6.
-
(1985)
J Gen Virol
, vol.66
, pp. 2781-2786
-
-
Lebon, P.1
-
76
-
-
0037451167
-
Interferon and granulopoiesis signatures in systemic lupus erythematosus blood
-
Bennett L, Palucka AK, Arce E, et al. Interferon and granulopoiesis signatures in systemic lupus erythematosus blood. J Exp Med 2003; 197:711-23.
-
(2003)
J Exp Med
, vol.197
, pp. 711-723
-
-
Bennett, L.1
Palucka, A.K.2
Arce, E.3
-
77
-
-
0035823645
-
Characterization and humanization of a monoclonal antibody that neutralizes human leukocyte interferon: A candidate therapeutic for IDDM and SLE
-
Chuntharapai A, Lai J, Huang X, et al. Characterization and humanization of a monoclonal antibody that neutralizes human leukocyte interferon: a candidate therapeutic for IDDM and SLE. Cytokine 2001; 15:250-60.
-
(2001)
Cytokine
, vol.15
, pp. 250-260
-
-
Chuntharapai, A.1
Lai, J.2
Huang, X.3
-
78
-
-
0035933041
-
Antiviral activities of the soluble extracellular domains of type I interferon receptors
-
Han CS, Chen Y, Ezashi T, Roberts RM. Antiviral activities of the soluble extracellular domains of type I interferon receptors. Proc Natl Acad Sci USA 2001; 98:6138-43.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 6138-6143
-
-
Han, C.S.1
Chen, Y.2
Ezashi, T.3
Roberts, R.M.4
|