-
1
-
-
40049093765
-
Systemic lupus erythematosus
-
Rahman A, Isenberg DA. Systemic lupus erythematosus. N Engl J Med 2008; 358:929-939.
-
(2008)
N Engl J Med
, vol.358
, pp. 929-939
-
-
Rahman, A.1
Isenberg, D.A.2
-
2
-
-
0020436689
-
The 1982 revised criteria for the classification of systemic lupus erythematosus
-
Tan EM, Cohen AS, Fries JF etal. The 1982 revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum 1982; 25:1271-1277.
-
(1982)
Arthritis Rheum
, vol.25
, pp. 1271-1277
-
-
Tan, E.M.1
Cohen, A.S.2
Fries, J.F.3
-
3
-
-
0031229830
-
Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus
-
Hochberg MC. Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum 1997; 40:1725.
-
(1997)
Arthritis Rheum
, vol.40
, pp. 1725
-
-
Hochberg, M.C.1
-
4
-
-
4043098932
-
Systemic lupus erythematosus in three ethnic groups. XIX. Natural history of the accrual of the American College of Rheumatology criteria prior to the occurrence of criteria diagnosis
-
Alarcon GS, McGwin G, Jr, Roseman JM etal. Systemic lupus erythematosus in three ethnic groups. XIX. Natural history of the accrual of the American College of Rheumatology criteria prior to the occurrence of criteria diagnosis. Arthritis Rheum 2004; 51:609-615.
-
(2004)
Arthritis Rheum
, vol.51
, pp. 609-615
-
-
Alarcon, G.S.1
McGwin Jr., G.2
Roseman, J.M.3
-
5
-
-
33744822178
-
Epidemiology of systemic lupus erythematosus: a comparison of worldwide disease burden
-
Danchenko N, Satia JA, Anthony MS. Epidemiology of systemic lupus erythematosus: a comparison of worldwide disease burden. Lupus 2006; 15:308-318.
-
(2006)
Lupus
, vol.15
, pp. 308-318
-
-
Danchenko, N.1
Satia, J.A.2
Anthony, M.S.3
-
6
-
-
77956294432
-
Prevalence and burden of pediatric-onset systemic lupus erythematosus
-
Kamphuis S, Silverman ED. Prevalence and burden of pediatric-onset systemic lupus erythematosus. Nat Rev Rheumatol 2010; 6:538-546.
-
(2010)
Nat Rev Rheumatol
, vol.6
, pp. 538-546
-
-
Kamphuis, S.1
Silverman, E.D.2
-
7
-
-
37349076340
-
General aspects of the genetics of SLE
-
Rhodes B, Vyse TJ. General aspects of the genetics of SLE. Autoimmunity 2007; 40:550-559.
-
(2007)
Autoimmunity
, vol.40
, pp. 550-559
-
-
Rhodes, B.1
Vyse, T.J.2
-
8
-
-
34250623606
-
Ultraviolet light and cutaneous lupus
-
Bijl M, Kallenberg CG. Ultraviolet light and cutaneous lupus. Lupus 2006; 15:724-727.
-
(2006)
Lupus
, vol.15
, pp. 724-727
-
-
Bijl, M.1
Kallenberg, C.G.2
-
9
-
-
34250662605
-
The curiously suspicious: a role for Epstein-Barr virus in lupus
-
Harley JB, Harley IT, Guthridge JM, James JA. The curiously suspicious: a role for Epstein-Barr virus in lupus. Lupus 2006; 15:768-777.
-
(2006)
Lupus
, vol.15
, pp. 768-777
-
-
Harley, J.B.1
Harley, I.T.2
Guthridge, J.M.3
James, J.A.4
-
10
-
-
77953552267
-
Genetics of SLE: evidence from mouse models
-
Morel L. Genetics of SLE: evidence from mouse models. Nat Rev Rheumatol 2010; 6:348-357.
-
(2010)
Nat Rev Rheumatol
, vol.6
, pp. 348-357
-
-
Morel, L.1
-
11
-
-
67349120686
-
Genetic susceptibility to SLE: new insights from fine mapping and genome-wide association studies
-
Harley IT, Kaufman KM, Langefeld CD, Harley JB, Kelly JA. Genetic susceptibility to SLE: new insights from fine mapping and genome-wide association studies. Nat Rev Genet 2009; 10:285-290.
-
(2009)
Nat Rev Genet
, vol.10
, pp. 285-290
-
-
Harley, I.T.1
Kaufman, K.M.2
Langefeld, C.D.3
Harley, J.B.4
Kelly, J.A.5
-
12
-
-
84868208900
-
CSK regulatory polymorphism is associated with systemic lupus erythematosus and influences B-cell signaling and activation
-
Manjarrez-Orduno N, Marasco E, Chung SA etal. CSK regulatory polymorphism is associated with systemic lupus erythematosus and influences B-cell signaling and activation. Nat Genet 2012; 44:1227-1230.
-
(2012)
Nat Genet
, vol.44
, pp. 1227-1230
-
-
Manjarrez-Orduno, N.1
Marasco, E.2
Chung, S.A.3
-
14
-
-
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
-
15
-
-
0023873028
-
Intrathecal synthesis of interferon-alpha in infants with progressive familial encephalopathy
-
Lebon P, Badoual J, Ponsot G, Goutieres F, Hemeury-Cukier F, Aicardi J. Intrathecal synthesis of interferon-alpha in infants with progressive familial encephalopathy. J Neurol Sci 1988; 84:201-208.
-
(1988)
J Neurol Sci
, vol.84
, pp. 201-208
-
-
Lebon, P.1
Badoual, J.2
Ponsot, G.3
Goutieres, F.4
Hemeury-Cukier, F.5
Aicardi, J.6
-
16
-
-
0028972864
-
The Aicardi-Goutieres syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis)
-
Tolmie JL, Shillito P, Hughes-Benzie R, Stephenson JB. The Aicardi-Goutieres syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis). J Med Genet 1995; 32:881-884.
-
(1995)
J Med Genet
, vol.32
, pp. 881-884
-
-
Tolmie, J.L.1
Shillito, P.2
Hughes-Benzie, R.3
Stephenson, J.B.4
-
17
-
-
77951737544
-
Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Goutieres syndrome
-
Ramantani G, Kohlhase J, Hertzberg C etal. Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Goutieres syndrome. Arthritis Rheum 2010; 62:1469-1477.
-
(2010)
Arthritis Rheum
, vol.62
, pp. 1469-1477
-
-
Ramantani, G.1
Kohlhase, J.2
Hertzberg, C.3
-
18
-
-
33746581694
-
Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus
-
Crow YJ, Hayward BE, Parmar R etal. Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus. Nat Genet 2006; 38:917-920.
-
(2006)
Nat Genet
, vol.38
, pp. 917-920
-
-
Crow, Y.J.1
Hayward, B.E.2
Parmar, R.3
-
19
-
-
33746522835
-
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection
-
Crow YJ, Leitch A, Hayward BE etal. Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection. Nat Genet 2006; 38:910-916.
-
(2006)
Nat Genet
, vol.38
, pp. 910-916
-
-
Crow, Y.J.1
Leitch, A.2
Hayward, B.E.3
-
20
-
-
67649861901
-
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response
-
Rice GI, Bond J, Asipu A etal. Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response. Nat Genet 2009; 41:829-832.
-
(2009)
Nat Genet
, vol.41
, pp. 829-832
-
-
Rice, G.I.1
Bond, J.2
Asipu, A.3
-
21
-
-
84868207785
-
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature
-
Rice GI, Kasher PR, Forte GM etal. Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature. Nat Genet 2012; 44:1243-1248.
-
(2012)
Nat Genet
, vol.44
, pp. 1243-1248
-
-
Rice, G.I.1
Kasher, P.R.2
Forte, G.M.3
-
22
-
-
33749006867
-
Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p
-
Lee-Kirsch MA, Gong M, Schulz H etal. Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p. Am J Hum Genet 2006; 79:731-737.
-
(2006)
Am J Hum Genet
, vol.79
, pp. 731-737
-
-
Lee-Kirsch, M.A.1
Gong, M.2
Schulz, H.3
-
23
-
-
34147185679
-
Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndrome
-
Rice G, Newman WG, Dean J etal. Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndrome. Am J Hum Genet 2007; 80:811-815.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 811-815
-
-
Rice, G.1
Newman, W.G.2
Dean, J.3
-
24
-
-
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 etal. A mutation in TREX1 that impairs susceptibility to granzyme A-mediated cell death underlies familial chilblain lupus. J Mol Med 2007; 85:531-537.
-
(2007)
J Mol Med
, vol.85
, pp. 531-537
-
-
Lee-Kirsch, M.A.1
Chowdhury, D.2
Harvey, S.3
-
25
-
-
34548334617
-
C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy
-
Richards A, Van Den Maagdenberg AM, Jen JC etal. C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy. Nat Genet 2007; 39:1068-1070.
-
(2007)
Nat Genet
, vol.39
, pp. 1068-1070
-
-
Richards, A.1
Van Den Maagdenberg, A.M.2
Jen, J.C.3
-
26
-
-
78349249767
-
A de novo p.Asp18Asn mutation in TREX1 in a patient with Aicardi-Goutières syndrome
-
Haaxma CA, Crow YJ, van Steensel MA etal. A de novo p.Asp18Asn mutation in TREX1 in a patient with Aicardi-Goutières syndrome. Am J Med Genet A 2010; 152A:2612-2617.
-
(2010)
Am J Med Genet A
, vol.152 A
, pp. 2612-2617
-
-
Haaxma, C.A.1
Crow, Y.J.2
van Steensel, M.A.3
-
27
-
-
84863326630
-
Inherited or de novo mutation affecting aspartate 18 of TREX1 results in either familial chilblain lupus or Aicardi-Goutières syndrome
-
Tungler V, Silver RM, Walkenhorst H, Gunther C, Lee-Kirsch MA. Inherited or de novo mutation affecting aspartate 18 of TREX1 results in either familial chilblain lupus or Aicardi-Goutières syndrome. Br J Dermatol 2012; 167:212-214.
-
(2012)
Br J Dermatol
, vol.167
, pp. 212-214
-
-
Tungler, V.1
Silver, R.M.2
Walkenhorst, H.3
Gunther, C.4
Lee-Kirsch, M.A.5
-
28
-
-
78650658122
-
Autosomal dominant inheritance of a heterozygous mutation in SAMHD1 causing familial chilblain lupus
-
Ravenscroft JC, Suri M, Rice GI, Szynkiewicz M, Crow YJ. Autosomal dominant inheritance of a heterozygous mutation in SAMHD1 causing familial chilblain lupus. Am J Med Genet A 2011; 155A:235-237.
-
(2011)
Am J Med Genet A
, vol.155 A
, pp. 235-237
-
-
Ravenscroft, J.C.1
Suri, M.2
Rice, G.I.3
Szynkiewicz, M.4
Crow, Y.J.5
-
29
-
-
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 etal. Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 are associated with systemic lupus erythematosus. Nat Genet 2007; 39:1065-1067.
-
(2007)
Nat Genet
, vol.39
, pp. 1065-1067
-
-
Lee-Kirsch, M.A.1
Gong, M.2
Chowdhury, D.3
-
30
-
-
77955626335
-
TREX1 gene variant in neuropsychiatric systemic lupus erythematosus
-
de Vries B, Steup-Beekman GM, Haan J etal. TREX1 gene variant in neuropsychiatric systemic lupus erythematosus. Ann Rheum Dis 2010; 69:1886-1887.
-
(2010)
Ann Rheum Dis
, vol.69
, pp. 1886-1887
-
-
de Vries, B.1
Steup-Beekman, G.M.2
Haan, J.3
-
31
-
-
79958015275
-
Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort
-
Namjou B, Kothari PH, Kelly JA etal. Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort. Genes Immun 2011; 12:270-279.
-
(2011)
Genes Immun
, vol.12
, pp. 270-279
-
-
Namjou, B.1
Kothari, P.H.2
Kelly, J.A.3
-
32
-
-
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; 274:19655-19660.
-
(1999)
J Biol Chem
, vol.274
, pp. 19655-19660
-
-
Mazur, D.J.1
Perrino, F.W.2
-
33
-
-
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 etal. 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; 23:133-142.
-
(2006)
Mol Cell
, vol.23
, pp. 133-142
-
-
Chowdhury, D.1
Beresford, P.J.2
Zhu, P.3
-
34
-
-
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; 131:873-886.
-
(2007)
Cell
, vol.131
, pp. 873-886
-
-
Yang, Y.G.1
Lindahl, T.2
Barnes, D.E.3
-
35
-
-
49549100511
-
Trex1 prevents cell-intrinsic initiation of autoimmunity
-
Stetson DB, Ko JS, Heidmann T, Medzhitov R. Trex1 prevents cell-intrinsic initiation of autoimmunity. Cell 2008; 134:587-598.
-
(2008)
Cell
, vol.134
, pp. 587-598
-
-
Stetson, D.B.1
Ko, J.S.2
Heidmann, T.3
Medzhitov, R.4
-
37
-
-
84862507347
-
Active human retrotransposons: variation and disease
-
Hancks DC, Kazazian HH Jr. Active human retrotransposons: variation and disease. Curr Opin Genet Dev 2012; 22:191-203.
-
(2012)
Curr Opin Genet Dev
, vol.22
, pp. 191-203
-
-
Hancks, D.C.1
Kazazian Jr., H.H.2
-
38
-
-
2442554169
-
Identification of autonomous IAP LTR retrotransposons mobile in mammalian cells
-
Dewannieux M, Dupressoir A, Harper F, Pierron G, Heidmann T. Identification of autonomous IAP LTR retrotransposons mobile in mammalian cells. Nat Genet 2004; 36:534-539.
-
(2004)
Nat Genet
, vol.36
, pp. 534-539
-
-
Dewannieux, M.1
Dupressoir, A.2
Harper, F.3
Pierron, G.4
Heidmann, T.5
-
39
-
-
84870294763
-
Resurrection of endogenous retroviruses in antibody-deficient mice
-
Young GR, Eksmond U, Salcedo R, Alexopoulou L, Stoye JP, Kassiotis G. Resurrection of endogenous retroviruses in antibody-deficient mice. Nature 2012; 491:774-778.
-
(2012)
Nature
, vol.491
, pp. 774-778
-
-
Young, G.R.1
Eksmond, U.2
Salcedo, R.3
Alexopoulou, L.4
Stoye, J.P.5
Kassiotis, G.6
-
40
-
-
84869169968
-
Nucleic acid-sensing Toll-like receptors are essential for the control of endogenous retrovirus viremia and ERV-induced tumors
-
Yu P, Lubben W, Slomka H etal. Nucleic acid-sensing Toll-like receptors are essential for the control of endogenous retrovirus viremia and ERV-induced tumors. Immunity 2012; 37:867-879.
-
(2012)
Immunity
, vol.37
, pp. 867-879
-
-
Yu, P.1
Lubben, W.2
Slomka, H.3
-
41
-
-
3242672339
-
Gene-targeted mice lacking the Trex1 (DNase III) 3′->5′ DNA exonuclease develop inflammatory myocarditis
-
Morita M, Stamp G, Robins P etal. Gene-targeted mice lacking the Trex1 (DNase III) 3′->5′ DNA exonuclease develop inflammatory myocarditis. Mol Cell Biol 2004; 24:6719-6727.
-
(2004)
Mol Cell Biol
, vol.24
, pp. 6719-6727
-
-
Morita, M.1
Stamp, G.2
Robins, P.3
-
42
-
-
84856301080
-
Autoimmunity initiates in nonhematopoietic cells and progresses via lymphocytes in an interferon-dependent autoimmune disease
-
Gall A, Treuting P, Elkon KB etal. Autoimmunity initiates in nonhematopoietic cells and progresses via lymphocytes in an interferon-dependent autoimmune disease. Immunity 2012; 36:120-131.
-
(2012)
Immunity
, vol.36
, pp. 120-131
-
-
Gall, A.1
Treuting, P.2
Elkon, K.B.3
-
43
-
-
80455174404
-
An autoimmune disease prevented by anti-retroviral drugs
-
Beck-Engeser GB, Eilat D, Wabl M. An autoimmune disease prevented by anti-retroviral drugs. Retrovirology 2011; 8:91.
-
(2011)
Retrovirology
, vol.8
, pp. 91
-
-
Beck-Engeser, G.B.1
Eilat, D.2
Wabl, M.3
-
44
-
-
58549086990
-
Contributions of the two accessory subunits, RNASEH2B and RNASEH2C, to the activity and properties of the human RNase H2 complex
-
Chon H, Vassilev A, DePamphilis ML etal. Contributions of the two accessory subunits, RNASEH2B and RNASEH2C, to the activity and properties of the human RNase H2 complex. Nucleic Acids Res 2009; 37:96-110.
-
(2009)
Nucleic Acids Res
, vol.37
, pp. 96-110
-
-
Chon, H.1
Vassilev, A.2
DePamphilis, M.L.3
-
45
-
-
79955993911
-
PCNA directs type 2 RNase H activity on DNA replication and repair substrates
-
Bubeck D, Reijns MA, Graham SC, Astell KR, Jones EY, Jackson AP. PCNA directs type 2 RNase H activity on DNA replication and repair substrates. Nucleic Acids Res 2011; 39:3652-3666.
-
(2011)
Nucleic Acids Res
, vol.39
, pp. 3652-3666
-
-
Bubeck, D.1
Reijns, M.A.2
Graham, S.C.3
Astell, K.R.4
Jones, E.Y.5
Jackson, A.P.6
-
46
-
-
77956921247
-
Genome instability due to ribonucleotide incorporation into DNA
-
Nick McElhinny SA, Kumar D, Clark AB etal. Genome instability due to ribonucleotide incorporation into DNA. Nat Chem Biol 2010; 6:774-781.
-
(2010)
Nat Chem Biol
, vol.6
, pp. 774-781
-
-
Nick McElhinny, S.A.1
Kumar, D.2
Clark, A.B.3
-
47
-
-
84861578543
-
Enzymatic removal of ribonucleotides from DNA is essential for mammalian genome integrity and development
-
Reijns MA, Rabe B, Rigby RE etal. Enzymatic removal of ribonucleotides from DNA is essential for mammalian genome integrity and development. Cell 2012; 149:1008-1022.
-
(2012)
Cell
, vol.149
, pp. 1008-1022
-
-
Reijns, M.A.1
Rabe, B.2
Rigby, R.E.3
-
48
-
-
84866462296
-
Mammalian RNase H2 removes ribonucleotides from DNA to maintain genome integrity
-
Hiller B, Achleitner M, Glage S, Naumann R, Behrendt R, Roers A. Mammalian RNase H2 removes ribonucleotides from DNA to maintain genome integrity. J Exp Med 2012; 209:1419-1426.
-
(2012)
J Exp Med
, vol.209
, pp. 1419-1426
-
-
Hiller, B.1
Achleitner, M.2
Glage, S.3
Naumann, R.4
Behrendt, R.5
Roers, A.6
-
49
-
-
84866851215
-
RNase H2-initiated ribonucleotide excision repair
-
Sparks JL, Chon H, Cerritelli SM etal. RNase H2-initiated ribonucleotide excision repair. Mol Cell 2012; 47:980-986.
-
(2012)
Mol Cell
, vol.47
, pp. 980-986
-
-
Sparks, J.L.1
Chon, H.2
Cerritelli, S.M.3
-
50
-
-
79959504063
-
Mutagenic processing of ribonucleotides in DNA by yeast topoisomerase I
-
Kim N, Huang SN, Williams JS etal. Mutagenic processing of ribonucleotides in DNA by yeast topoisomerase I. Science 2011; 332:1561-1564.
-
(2011)
Science
, vol.332
, pp. 1561-1564
-
-
Kim, N.1
Huang, S.N.2
Williams, J.S.3
-
51
-
-
83555164881
-
HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolase
-
Goldstone DC, Ennis-Adeniran V, Hedden JJ etal. HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolase. Nature 2011; 480:379-382.
-
(2011)
Nature
, vol.480
, pp. 379-382
-
-
Goldstone, D.C.1
Ennis-Adeniran, V.2
Hedden, J.J.3
-
52
-
-
79959858243
-
Vpx relieves inhibition of HIV-1 infection of macrophages mediated by the SAMHD1 protein
-
Hrecka K, Hao C, Gierszewska M etal. Vpx relieves inhibition of HIV-1 infection of macrophages mediated by the SAMHD1 protein. Nature 2011; 474:658-661.
-
(2011)
Nature
, vol.474
, pp. 658-661
-
-
Hrecka, K.1
Hao, C.2
Gierszewska, M.3
-
53
-
-
79959843617
-
SAMHD1 is the dendritic- and myeloid-cell-specific HIV-1 restriction factor counteracted by Vpx
-
Laguette N, Sobhian B, Casartelli N etal. SAMHD1 is the dendritic- and myeloid-cell-specific HIV-1 restriction factor counteracted by Vpx. Nature 2011; 474:654-657.
-
(2011)
Nature
, vol.474
, pp. 654-657
-
-
Laguette, N.1
Sobhian, B.2
Casartelli, N.3
-
54
-
-
84862777555
-
SAMHD1 restricts the replication of human immunodeficiency virus type 1 by depleting the intracellular pool of deoxynucleoside triphosphates
-
Lahouassa H, Daddacha W, Hofmann H etal. SAMHD1 restricts the replication of human immunodeficiency virus type 1 by depleting the intracellular pool of deoxynucleoside triphosphates. Nat Immunol 2012; 13:223-228.
-
(2012)
Nat Immunol
, vol.13
, pp. 223-228
-
-
Lahouassa, H.1
Daddacha, W.2
Hofmann, H.3
-
55
-
-
84876972365
-
Phosphorylation of SAMHD1 by cyclin A2/CDK1 regulates its restriction activity toward HIV-1
-
Cribier A, Descours B, Valadao AL, Laguette N, Benkirane M. Phosphorylation of SAMHD1 by cyclin A2/CDK1 regulates its restriction activity toward HIV-1. Cell Rep 2013; 3:1036-1043.
-
(2013)
Cell Rep
, vol.3
, pp. 1036-1043
-
-
Cribier, A.1
Descours, B.2
Valadao, A.L.3
Laguette, N.4
Benkirane, M.5
-
56
-
-
84876369203
-
The retroviral restriction ability of SAMHD1, but not its deoxynucleotide triphosphohydrolase activity, is regulated by phosphorylation
-
White TE, Brandariz-Nunez A, Valle-Casuso JC etal. The retroviral restriction ability of SAMHD1, but not its deoxynucleotide triphosphohydrolase activity, is regulated by phosphorylation. Cell Host Microbe 2013; 13:441-451.
-
(2013)
Cell Host Microbe
, vol.13
, pp. 441-451
-
-
White, T.E.1
Brandariz-Nunez, A.2
Valle-Casuso, J.C.3
-
57
-
-
77958114725
-
The cytosolic exonuclease TREX1 inhibits the innate immune response to human immunodeficiency virus type 1
-
Yan N, Regalado-Magdos AD, Stiggelbout B, Lee-Kirsch MA, Lieberman J. The cytosolic exonuclease TREX1 inhibits the innate immune response to human immunodeficiency virus type 1. Nat Immunol 2010; 11:1005-1013.
-
(2010)
Nat Immunol
, vol.11
, pp. 1005-1013
-
-
Yan, N.1
Regalado-Magdos, A.D.2
Stiggelbout, B.3
Lee-Kirsch, M.A.4
Lieberman, J.5
-
58
-
-
84861893309
-
SAMHD1 is a nucleic-acid binding protein that is mislocalized due to Aicardi-Goutières syndrome-associated mutations
-
Goncalves A, Karayel E, Rice GI etal. SAMHD1 is a nucleic-acid binding protein that is mislocalized due to Aicardi-Goutières syndrome-associated mutations. Hum Mutat 2012; 33:1116-1122.
-
(2012)
Hum Mutat
, vol.33
, pp. 1116-1122
-
-
Goncalves, A.1
Karayel, E.2
Rice, G.I.3
-
59
-
-
84878617993
-
Single-stranded nucleic acids promote SAMHD1 complex formation
-
Tungler V, Staroske W, Kind B etal. Single-stranded nucleic acids promote SAMHD1 complex formation. J Mol Med (Berl) 2013; 91:759-770.
-
(2013)
J Mol Med (Berl)
, vol.91
, pp. 759-770
-
-
Tungler, V.1
Staroske, W.2
Kind, B.3
-
60
-
-
84874959500
-
Nuclease activity of the human SAMHD1 protein implicated in the Aicardi-Goutières syndrome and HIV-1 restriction
-
Beloglazova N, Flick R, Tchigvintsev A etal. Nuclease activity of the human SAMHD1 protein implicated in the Aicardi-Goutières syndrome and HIV-1 restriction. J Biol Chem 2013; 288:8101-8110.
-
(2013)
J Biol Chem
, vol.288
, pp. 8101-8110
-
-
Beloglazova, N.1
Flick, R.2
Tchigvintsev, A.3
-
61
-
-
0028954270
-
Natural DNA precursor pool asymmetry and base sequence context as determinants of replication fidelity
-
Zhang X, Mathews CK. Natural DNA precursor pool asymmetry and base sequence context as determinants of replication fidelity. J Biol Chem 1995; 270:8401-8404.
-
(1995)
J Biol Chem
, vol.270
, pp. 8401-8404
-
-
Zhang, X.1
Mathews, C.K.2
-
62
-
-
80054119641
-
RNA editing catalyzed by ADAR1 and its function in mammalian cells
-
Wang Q. RNA editing catalyzed by ADAR1 and its function in mammalian cells. Biochemistry (Mosc) 2011; 76:900-911.
-
(2011)
Biochemistry (Mosc)
, vol.76
, pp. 900-911
-
-
Wang, Q.1
-
63
-
-
0034535312
-
Requirement of the RNA editing deaminase ADAR1 gene for embryonic erythropoiesis
-
Wang Q, Khillan J, Gadue P, Nishikura K. Requirement of the RNA editing deaminase ADAR1 gene for embryonic erythropoiesis. Science 2000; 290:1765-1768.
-
(2000)
Science
, vol.290
, pp. 1765-1768
-
-
Wang, Q.1
Khillan, J.2
Gadue, P.3
Nishikura, K.4
-
64
-
-
57849167057
-
A new function for the RNA-editing enzyme ADAR1
-
Iizasa H, Nishikura K. A new function for the RNA-editing enzyme ADAR1. Nat Immunol 2009; 10:16-18.
-
(2009)
Nat Immunol
, vol.10
, pp. 16-18
-
-
Iizasa, H.1
Nishikura, K.2
-
65
-
-
79952069367
-
Adenosine deaminases acting on RNA (ADARs) are both antiviral and proviral
-
Samuel CE. Adenosine deaminases acting on RNA (ADARs) are both antiviral and proviral. Virology 2011; 411:180-193.
-
(2011)
Virology
, vol.411
, pp. 180-193
-
-
Samuel, C.E.1
-
66
-
-
0344492212
-
Interferon-inducible gene expression signature in peripheral blood cells of patients with severe lupus
-
Baechler EC, Batliwalla FM, Karypis G etal. Interferon-inducible gene expression signature in peripheral blood cells of patients with severe lupus. Proc Natl Acad Sci USA 2003; 100:2610-2615.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 2610-2615
-
-
Baechler, E.C.1
Batliwalla, F.M.2
Karypis, G.3
-
68
-
-
0035525528
-
From T to B and back again: positive feedback in systemic autoimmune disease
-
Shlomchik MJ, Craft JE, Mamula MJ. From T to B and back again: positive feedback in systemic autoimmune disease. Nat Rev Immunol 2001; 1:147-153.
-
(2001)
Nat Rev Immunol
, vol.1
, pp. 147-153
-
-
Shlomchik, M.J.1
Craft, J.E.2
Mamula, M.J.3
-
69
-
-
0037061453
-
Chromatin-IgG complexes activate B cells by dual engagement of IgM and Toll-like receptors
-
Leadbetter EA, Rifkin IR, Hohlbaum AM, Beaudette BC, Shlomchik MJ, Marshak-Rothstein A. Chromatin-IgG complexes activate B cells by dual engagement of IgM and Toll-like receptors. Nature 2002; 416:603-607.
-
(2002)
Nature
, vol.416
, pp. 603-607
-
-
Leadbetter, E.A.1
Rifkin, I.R.2
Hohlbaum, A.M.3
Beaudette, B.C.4
Shlomchik, M.J.5
Marshak-Rothstein, A.6
-
70
-
-
2642528779
-
Induction of interferon-alpha production in plasmacytoid dendritic cells by immune complexes containing nucleic acid released by necrotic or late apoptotic cells and lupus IgG
-
Lovgren T, Eloranta ML, Bave U, Alm GV, Ronnblom L. Induction of interferon-alpha production in plasmacytoid dendritic cells by immune complexes containing nucleic acid released by necrotic or late apoptotic cells and lupus IgG. Arthritis Rheum 2004; 50:1861-1872.
-
(2004)
Arthritis Rheum
, vol.50
, pp. 1861-1872
-
-
Lovgren, T.1
Eloranta, M.L.2
Bave, U.3
Alm, G.V.4
Ronnblom, L.5
-
71
-
-
33750369226
-
Toll-like receptors in systemic autoimmune disease
-
Marshak-Rothstein A. Toll-like receptors in systemic autoimmune disease. Nat Rev Immunol 2006; 6:823-835.
-
(2006)
Nat Rev Immunol
, vol.6
, pp. 823-835
-
-
Marshak-Rothstein, A.1
-
72
-
-
33744945033
-
Mechanisms of Disease: the complement system and the pathogenesis of systemic lupus erythematosus
-
Cook HT, Botto M. Mechanisms of Disease: the complement system and the pathogenesis of systemic lupus erythematosus. Nat Clin Pract Rheumatol 2006; 2:330-337.
-
(2006)
Nat Clin Pract Rheumatol
, vol.2
, pp. 330-337
-
-
Cook, H.T.1
Botto, M.2
-
73
-
-
84874223452
-
Molecular basis of DNA recognition in the immune system
-
Atianand MK, Fitzgerald KA. Molecular basis of DNA recognition in the immune system. J Immunol 2013; 190:1911-1918.
-
(2013)
J Immunol
, vol.190
, pp. 1911-1918
-
-
Atianand, M.K.1
Fitzgerald, K.A.2
-
74
-
-
84873711885
-
Cyclic GMP-AMP synthase is a cytosolic DNA sensor that activates the type I interferon pathway
-
Sun L, Wu J, Du F, Chen X, Chen ZJ. Cyclic GMP-AMP synthase is a cytosolic DNA sensor that activates the type I interferon pathway. Science 2013; 339:786-791.
-
(2013)
Science
, vol.339
, pp. 786-791
-
-
Sun, L.1
Wu, J.2
Du, F.3
Chen, X.4
Chen, Z.J.5
-
75
-
-
75649106430
-
Intracellular DNA recognition
-
Hornung V, Latz E. Intracellular DNA recognition. Nat Rev Immunol 2010; 10:123-130.
-
(2010)
Nat Rev Immunol
, vol.10
, pp. 123-130
-
-
Hornung, V.1
Latz, E.2
-
76
-
-
0034114882
-
Features of systemic lupus erythematosus in Dnase1-deficient mice
-
Napirei M, Karsunky H, Zevnik B, Stephan H, Mannherz HG, Moroy T. Features of systemic lupus erythematosus in Dnase1-deficient mice. Nat Genet 2000; 25:177-181.
-
(2000)
Nat Genet
, vol.25
, pp. 177-181
-
-
Napirei, M.1
Karsunky, H.2
Zevnik, B.3
Stephan, H.4
Mannherz, H.G.5
Moroy, T.6
-
77
-
-
0034939627
-
Mutation of DNASE1 in people with systemic lupus erythematosus
-
Yasutomo K, Horiuchi T, Kagami S etal. Mutation of DNASE1 in people with systemic lupus erythematosus. Nat Genet 2001; 28:313-314.
-
(2001)
Nat Genet
, vol.28
, pp. 313-314
-
-
Yasutomo, K.1
Horiuchi, T.2
Kagami, S.3
-
78
-
-
35748949862
-
Autoimmune diseases caused by defects in clearing dead cells and nuclei expelled from erythroid precursors
-
Nagata S. Autoimmune diseases caused by defects in clearing dead cells and nuclei expelled from erythroid precursors. Immunol Rev 2007; 220:237-250.
-
(2007)
Immunol Rev
, vol.220
, pp. 237-250
-
-
Nagata, S.1
-
79
-
-
82255192363
-
Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus
-
Al-Mayouf SM, Sunker A, Abdwani R etal. Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus. Nat Genet 2011; 43:1186-1188.
-
(2011)
Nat Genet
, vol.43
, pp. 1186-1188
-
-
Al-Mayouf, S.M.1
Sunker, A.2
Abdwani, R.3
-
80
-
-
84871222424
-
Trex1 regulates lysosomal biogenesis and interferon-independent activation of antiviral genes
-
Hasan M, Koch J, Rakheja D etal. Trex1 regulates lysosomal biogenesis and interferon-independent activation of antiviral genes. Nat Immunol 2013; 14:61-71.
-
(2013)
Nat Immunol
, vol.14
, pp. 61-71
-
-
Hasan, M.1
Koch, J.2
Rakheja, D.3
-
81
-
-
67349258944
-
Why can't we find a new treatment for SLE?
-
Eisenberg R. Why can't we find a new treatment for SLE? J Autoimmun 2009; 32:223-230.
-
(2009)
J Autoimmun
, vol.32
, pp. 223-230
-
-
Eisenberg, R.1
-
82
-
-
78649363138
-
Advances in drug therapy for systemic lupus erythematosus
-
Wallace DJ. Advances in drug therapy for systemic lupus erythematosus. BMC Med 2010; 8:77.
-
(2010)
BMC Med
, vol.8
, pp. 77
-
-
Wallace, D.J.1
-
83
-
-
77951529848
-
Therapeutic antibodies for autoimmunity and inflammation
-
Chan AC, Carter PJ. Therapeutic antibodies for autoimmunity and inflammation. Nat Rev Immunol 2010; 10:301-316.
-
(2010)
Nat Rev Immunol
, vol.10
, pp. 301-316
-
-
Chan, A.C.1
Carter, P.J.2
-
84
-
-
84864863234
-
Belimumab is approved by the FDA: what more do we need to know to optimize decision making?
-
Horowitz DL, Furie R. Belimumab is approved by the FDA: what more do we need to know to optimize decision making? Curr Rheumatol Rep 2012; 14:318-323.
-
(2012)
Curr Rheumatol Rep
, vol.14
, pp. 318-323
-
-
Horowitz, D.L.1
Furie, R.2
-
85
-
-
77957768966
-
Activation of the type I interferon pathway in primary Sjogren's syndrome
-
Mavragani CP, Crow MK. Activation of the type I interferon pathway in primary Sjogren's syndrome. J Autoimmun 2010; 35:225-231.
-
(2010)
J Autoimmun
, vol.35
, pp. 225-231
-
-
Mavragani, C.P.1
Crow, M.K.2
-
86
-
-
77954965596
-
Type I interferon system activation and association with disease manifestations in systemic sclerosis
-
Eloranta ML, Franck-Larsson K, Lovgren T etal. Type I interferon system activation and association with disease manifestations in systemic sclerosis. Ann Rheum Dis 2010; 69:1396-1402.
-
(2010)
Ann Rheum Dis
, vol.69
, pp. 1396-1402
-
-
Eloranta, M.L.1
Franck-Larsson, K.2
Lovgren, T.3
|