Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response
暂无分享,去创建一个
Jonathan C. Fuller | D. Bonthron | E. Bertini | L. Lagae | A. Vanderver | C. Bodemer | R. Jackson | B. Gener | Y. Crow | J. Bond | M. Shinawi | M. Knaap | D. Stetson | B. Hamel | S. Orcesi | A. Aeby | M. McDermott | I. Carr | P. Lebon | G. Rice | T. Briggs | I. Desguerre | L. Brueton | E. Wassmer | P. Landrieu | E. Fazzi | K. Brockmann | E. Wakeling | Manir Ali | R. Spiegel | S. Shalev | I. Manfield | P. Corry | H. Gornall | A. Heiberg | Ram Kumar | T. Tan | M. Hunter | S. Attard-Montalto | E. Whittaker | Daniel B. Stetson | A. Asipu | Charles M Lourenço | Daphna Marom | M. Rasmussen | J. Prendiville | D. Soler | W. V. D. Merwe | Rebecca L. Brunette | T. Lamb | Lydia R Couthard | Á. G. Cazorla | Teresa Lamb | S. Attard‐Montalto | T. Tan
[1] Dongchi Zhao,et al. Inhibition of G1P3 expression found in the differential display study on respiratory syncytial virus infection , 2008, Virology Journal.
[2] T. Heidmann,et al. Trex1 Prevents Cell-Intrinsic Initiation of Autoimmunity , 2008, Cell.
[3] Zhijian J. Chen,et al. Linking Retroelements to Autoimmunity , 2008, Cell.
[4] Y. Mok,et al. Dendritic cell‐derived interferon‐γ‐induced protein mediates tumor necrosis factor‐α stimulation of human lung fibroblasts , 2008, Proteomics.
[5] Y. Crow,et al. Aicardi‐Goutières syndrome: an important Mendelian mimic of congenital infection , 2008, Developmental medicine and child neurology.
[6] W. Minor,et al. Structural insight into the mechanism of substrate specificity and catalytic activity of an HD-domain phosphohydrolase: the 5'-deoxyribonucleotidase YfbR from Escherichia coli. , 2008, Journal of molecular biology.
[7] L. Coscoy,et al. DNA Mismanagement Leads to Immune System Oversight , 2007, Cell.
[8] D. Barnes,et al. Trex1 Exonuclease Degrades ssDNA to Prevent Chronic Checkpoint Activation and Autoimmune Disease , 2007, Cell.
[9] A. Green,et al. Clinical and molecular phenotype of Aicardi-Goutieres syndrome. , 2007, American journal of human genetics.
[10] J. Lieberman,et al. Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 are associated with systemic lupus erythematosus , 2007, Nature Genetics.
[11] D. Barnes,et al. Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndrome. , 2007, American journal of human genetics.
[12] A. Felice,et al. Molecular genetics of tetrahydrobiopterin (BH4) deficiency in the Maltese population. , 2007, Molecular genetics and metabolism.
[13] A. Kiang,et al. Adenovirus Infection Triggers a Rapid, MyD88-Regulated Transcriptome Response Critical to Acute-Phase and Adaptive Immune Responses In Vivo , 2006, Journal of Virology.
[14] M. Alarcón-Riquelme. Nucleic acid by-products and chronic inflammation , 2006, Nature Genetics.
[15] C. Ponting,et al. Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection , 2006, Nature Genetics.
[16] D. Barnes,et al. Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus , 2006, Nature Genetics.
[17] Florian C. Oberstrass,et al. Shape-specific recognition in the structure of the Vts1p SAM domain with RNA , 2006, Nature Structural &Molecular Biology.
[18] B. Dan,et al. Phenotypic Overlap between Infantile Systemic Lupus Erythematosus and Aicardi-Goutières Syndrome , 2005, Neuropediatrics.
[19] F. Mégret,et al. Monique Lafon Producers of Beta Interferon Human Neurons to Become Strong Virus Infection Switches Tlr-3-positive , 2005 .
[20] J. Bowie,et al. The Many Faces of SAM , 2005, Science's STKE.
[21] P. Lebon,et al. Cerebral thrombotic microangiopathy and antiphospholipid antibodies in Aicardi-Goutieres syndrome--report of two sisters. , 2005, Neuropediatrics.
[22] M. Crow,et al. Microarray Analysis of Interferon-regulated Genes in SLE , 2003, Autoimmunity.
[23] C. Woods,et al. Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism , 2003, Journal of medical genetics.
[24] D. Bechhofer,et al. Bacillus subtilis YhaM, a Member of a New Family of 3′-to-5′ Exonucleases in Gram-Positive Bacteria , 2002, Journal of bacteriology.
[25] Nan Li,et al. Identification of human homologue of mouse IFN-γ induced protein from human dendritic cells , 2000 .
[26] J. Heckmatt,et al. Familial Systemic Lupus Erythematosus and Congenital Infection-Like Syndrome , 2000, Neuropediatrics.
[27] J. Aicardi,et al. Systemic Lupus Erythematosus or Aicardi-Goutières Syndrome? , 2000, Neuropediatrics.
[28] E V Koonin,et al. The HD domain defines a new superfamily of metal-dependent phosphohydrolases. , 1998, Trends in biochemical sciences.
[29] G. Ponsot,et al. Intrathecal synthesis of different alpha‐interferons in patients with various neurological diseases , 1985, Acta neurologica Scandinavica.
[30] M. Crow. Type I interferon in systemic lupus erythematosus. , 2007, Current topics in microbiology and immunology.
[31] X. Cao,et al. Identification of human homologue of mouse IFN-gamma induced protein from human dendritic cells. , 2000, Immunology letters.