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41.
Ho, J.E.* et al.: Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling. J. Clin. Invest. 123, 4208-4218 (2013)
42.
Müller, T.D. et al.: P62 links β-adrenergic input to mitochondrial function and thermogenesis. J. Clin. Invest. 123, 469-478 (2013)
43.
Neff, F. et al.: Rapamycin extends murine lifespan but has limited effects on aging. J. Clin. Invest. 123, 3272-3291 (2013)
44.
Pesic, M.* et al.: 2-photon imaging of phagocyte-mediated T cell activation in the CNS. J. Clin. Invest. 123, 1192-1201 (2013)
45.
Brüstle, A.* et al.: The NF-κB regulator MALT1 determines the encephalitogenic potential of Th17 cells. J. Clin. Invest. 122, 4698-4709 (2012)
46.
Boldt, K. et al.: Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice. J. Clin. Invest. 121, 2169-2180 (2011)
47.
Clauss, M.* et al.: Lung endothelial monocyte-activating protein 2 is a mediator of cigarette smoke-induced emphysema in mice. J. Clin. Invest. 121, 2470-2479 (2011)
48.
Hammerschmidt, S.I.* et al.: Retinoic acid induces homing of protective T and B cells to the gut after subcutaneous immunization in mice. J. Clin. Invest. 121, 3051-3061 (2011)
49.
Heeringa, S.F.* et al.: COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness. J. Clin. Invest. 121, 2013-2024 (2011)
50.
Zischka, H. et al.: Liver mitochondrial membrane crosslinking and destruction in a rat model of Wilson disease. J. Clin. Invest. 121, 1508-1518 (2011)
51.
Leisegang, M.* et al.: MHC-restricted fratricide of human lymphocytes expressing survivin-specific transgenic T cell receptors. J. Clin. Invest. 120, 3869-3877 (2010)
52.
O'Toole, J.F.* et al.: Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy. J. Clin. Invest. 120, 791-802 (2010)
53.
Eyerich, S.* et al.: Th22 cells represent a distinct human T cell subset involved in epidermal immunity and remodeling. J. Clin. Invest. 119, 3573-3585 (2009)
54.
Koegel, H.* et al.: Loss of serum response factor in keratinocytes results in hyperproliferative skin disease in mice. J. Clin. Invest. 119, 899-910 (2009)
55.
Königshoff, M. et al.: WNT1-inducible signaling protein-1 mediates pulmonary fibrosis in mice and is upregulated in humans with idiopathic pulmonary fibrosis. J. Clin. Invest. 119, 772-787 (2009)
56.
Paquet, D.* et al.: A zebrafish model of tauopathy allows in vivo imaging of neuronal cell death and drug evaluation. J. Clin. Invest. 119, 1382-1395 (2009)
57.
Kessenbrock, K.* et al.: Proteinase 3 and neutrophil elastase enhance inflammation in mice by inactivating antiinflammatory progranulin. J. Clin. Invest. 118, 2438-2447 (2008)
58.
Watanabe, H.* et al.: Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans. J. Clin. Invest. 118, 2260-2268 (2008)
59.
Schessl, C. et al.: The AML1-ETO fusion gene and the FLT3 lenght mutation collaborate in inducing acute leukemia in mice. J. Clin. Invest. 115, 2159-2186 (2005)
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