Publications by authors named "Suzanne Mudd"

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The serine protease TMPRSS6 is required to sense iron deficiency.
Xin Du, Ellen She, Terri Gelbart, Jaroslav Truksa, Pauline Lee, Suzanne Mudd

Science· May 2008

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Jinx, an MCMV susceptibility phenotype caused by disruption of Unc13d: a mouse model of type 3 familial hemophagocytic lymphohistiocytosis.
Karine Crozat, Kasper Hoebe, Sophie Ugolini, Nancy A Hong, Edith Janssen, Suzanne Mudd

J Exp Med· April 2007

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Details of Toll-like receptor:adapter interaction revealed by germ-line mutagenesis.
Zhengfan Jiang, Philippe Georgel, Chenglong Li, Jungwoo Choe, Karine Crozat, Suzanne Mudd

Proc Natl Acad Sci U S A· July 2006

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R-form LPS, the master key to the activation ofTLR4/MD-2-positive cells.
Michael Huber, Christoph Kalis, Simone Keck, Zhengfan Jiang, Philippe Georgel, Suzanne Mudd

Eur J Immunol· March 2006

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The Unc93b1 mutation 3d disrupts exogenous antigen presentation and signaling via Toll-like receptors 3, 7 and 9.
Koichi Tabeta, Kasper Hoebe, Edith M Janssen, Xin Du, Philippe Georgel, Suzanne Mudd

Nat Immunol· February 2006

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An essential role for Rxr alpha in the development of Th2 responses.
Xin Du, Koichi Tabeta, Navjiwan Mann, Karine Crozat, Suzanne Mudd

Eur J Immunol· December 2005

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CD14 is required for MyD88-independent LPS signaling.
Zhengfan Jiang, Philippe Georgel, Xin Du, Louis Shamel, Sosathya Sovath, Suzanne Mudd

Nat Immunol· June 2005

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CD36 is a sensor of diacylglycerides.
Kasper Hoebe, Philippe Georgel, Sophie Rutschmann, Xin Du, Suzanne Mudd

Nature· February 2005

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Toll-like receptors 9 and 3 as essential components of innate immune defense against mouse cytomegalovirus infection.
Koichi Tabeta, Philippe Georgel, Edith Janssen, Xin Du, Kasper Hoebe, Suzanne Mudd

Proc Natl Acad Sci U S A· March 2004

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Velvet, a dominant Egfr mutation that causes wavy hair and defective eyelid development in mice.
Xin Du, Koichi Tabeta, Kasper Hoebe, Haiquan Liu, Navjiwan Mann, Suzanne Mudd

Genetics· January 2004

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