An Update on Autoinflammatory Diseases: Interferonopathies

[1] Pestka S(2004)Interferons, interferon-like cytokines, and their receptors Immunol Rev 202 8-32

[2] Krause CD(2015)Type I interferons in infectious disease Nat Rev Immunol 15 87-103

[3] Walter MR(2014)Interferon-stimulated genes: a complex web of host defenses Annu Rev Immunol 32 513-545

[4] McNab F(2003)Cree encephalitis is allelic with Aicardi-Goutieres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism J Med Genet 40 183-187

[5] Mayer-Barber K(2016)Type I interferon-mediated monogenic autoinflammation: the type I interferonopathies, a conceptual overview J Exp Med 213 2527-2538

[6] Sher A(2017)Type I interferon-mediated autoinflammation and autoimmunity Curr Opin Immunol 49 96-102

[7] Wack A(2013)Singleton-Merten syndrome: an autosomal dominant disorder with variable expression Am J Med Genet A 161A 360-370

[8] O'Garra A(2014)Pattern recognition and signaling mechanisms of RIG-I and MDA5 Front Immunol 5 342-282

[9] Schneider WM(2015)A specific IFIH1 gain-of-function mutation causes Singleton-Merten syndrome Am J Hum Genet 96 275-125

[10] Chevillotte MD(2014)Aicardi-Goutieres syndrome is caused by IFIH1 mutations Am J Hum Genet 95 121-509

[1] Pestka S(2004)Interferons, interferon-like cytokines, and their receptors Immunol Rev 202 8-32

[2] Krause CD(2015)Type I interferons in infectious disease Nat Rev Immunol 15 87-103

[3] Walter MR(2014)Interferon-stimulated genes: a complex web of host defenses Annu Rev Immunol 32 513-545

[4] McNab F(2003)Cree encephalitis is allelic with Aicardi-Goutieres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism J Med Genet 40 183-187

[5] Mayer-Barber K(2016)Type I interferon-mediated monogenic autoinflammation: the type I interferonopathies, a conceptual overview J Exp Med 213 2527-2538

[6] Sher A(2017)Type I interferon-mediated autoinflammation and autoimmunity Curr Opin Immunol 49 96-102

[7] Wack A(2013)Singleton-Merten syndrome: an autosomal dominant disorder with variable expression Am J Med Genet A 161A 360-370

[8] O'Garra A(2014)Pattern recognition and signaling mechanisms of RIG-I and MDA5 Front Immunol 5 342-282

[9] Schneider WM(2015)A specific IFIH1 gain-of-function mutation causes Singleton-Merten syndrome Am J Hum Genet 96 275-125

[10] Chevillotte MD(2014)Aicardi-Goutieres syndrome is caused by IFIH1 mutations Am J Hum Genet 95 121-509