US National Institutes of Health (NIH)

Forschungs- / Wissenschaftsorganisation

Standort der Organisation:
Rockville Pike, Vereinigte Staaten von Amerika (USA)

Von dieser Organisation verliehene Preise / Auszeichnungen

Publikationen in Kooperation mit FAU-Wissenschaftern

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Wright, J.T., Fete, M., Schneider, H., Zinser, M., Koster, M.I., Clarke, A.J.,... Morasso, M.I. (2019). Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway. American Journal of Medical Genetics Part A, 179(3), 442-447.
Boeltz, S., Amini, P., Anders, H.-J., Andrade, F., Bilyy, R., Chatfield, S.,... Herrmann, M. (2019). To NET or not to NET: current opinions and state of the science regarding the formation of neutrophil extracellular traps. Cell Death and Differentiation, 26(3), 395-408.
Capdevila, J., Bodei, L., Davies, P., Gorbounova, V., Jensen, R.T., Knigge, U.P.,... Wiedenmann, B. (2019). Unmet medical needs in metastatic lung and digestive neuroendocrine neoplasms. Neuroendocrinology, 108(1), 18-25.
Serr, I., Scherm, M.G., Zahm, A.M., Schug, J., Flynn, V.K., Hippich, M.,... Daniel, C. (2018). A miRNA181a/NFAT5 axis links impaired T cell tolerance induction with autoimmune type 1 diabetes. Science Translational Medicine, 10(422).
Beziat, V., Li, J., Lin, J.-X., Ma, C.S., Li, P., Bousfiha, A.,... Casanova, J.-L. (2018). A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity. Science immunology, 3(24).
Johnston, J.J., Van Der Smagt, J.J., Rosenfeld, J.A., Pagnamenta, A.T., Alswaid, A., Baker, E.H.,... Biesecker, L.G. (2018). Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants. Genetics in Medicine.
Teumer, A., Chaker, L., Groeneweg, S., Li, Y., Di Munno, C., Barbieri, C.,... Medici, M. (2018). Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation. Nature Communications, 9(1).
Kraus, V.B., Collins, J.E., Charles, H.C., Pieper, C.F., Whitley, L., Losina, E.,... Hunter, D.J. (2018). Predictive Validity of Radiographic Trabecular Bone Texture in Knee Osteoarthritis: The Osteoarthritis Research Society International/Foundation for the National Institutes of Health Osteoarthritis Biomarkers Consortium. Arthritis and Rheumatology, 70(1), 80-87.
Frey-Jakobs, S., Hartberger, J.M., Fliegauf, M., Bossen, C., Wehmeyer, M.L., Neubauer, J.C.,... Grimbacher, B. (2018). ZNF341 controls STAT3 expression and thereby immunocompetence. Science immunology, 3(24).
Munoz, L.E., Kaplan, M.J., Radic, M., Herrmann, M., & Munoz Becerra, L.E. (2017). Editorial: NETosis 2: The Excitement Continues. Frontiers in Immunology, 8, 1318.
Wilck, N., Matus, M.G., Kearney, S.M., Olesen, S.W., Forslund, K., Bartolomaeus, H.,... Mueller, D.N. (2017). Salt-responsive gut commensal modulates TH17 axis and disease. Nature, 551(7682), 585-589.
Serr, I., Fuerst, R.W., Ott, V.B., Scherm, M.G., Nikolaev, A., Goekmen, F.,... Daniel, C. (2016). miRNA92a targets KLF2 and the phosphatase PTEN signaling to promote human T follicular helper precursors in T1D islet autoimmunity. Proceedings of the National Academy of Sciences of the United States of America, 113(43), E6659-E6668.
Meyer, E., Carss, K.J., Rankin, J., Nichols, J.M.E., Grozeva, D., Joseph, A.P.,... Kurian, M.A. (2016). Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia. Nature Genetics.
Maerkens, A., Olive, M., Schreiner, A., Feldkirchner, S., Schessl, J., Uszkoreit, J.,... Kley, R.A. (2016). New insights into the protein aggregation pathology in myotilinopathy by combined proteomic and immunolocalization analyses. Acta Neuropathologica Communications, 4, 8.
Grayson, P.C., Schauer, C., Herrmann, M., & Kaplan, M.J. (2016). Review: Neutrophils as Invigorated Targets in Rheumatic Diseases. Arthritis and Rheumatology, 68(9), 2071-82.
Kozlenkov, A., Wang, M., Roussos, P., Rudchenko, S., Barbu, M., Bibikova, M.,... Dracheva, S. (2016). Substantial DNA methylation differences between two major neuronal subtypes in human brain. Nucleic Acids Research, 44(6), 2593-612.
Kreins, A.Y., Ciancanelli, M.J., Okada, S., Kong, X.-F., Ramirez-Alejo, N., Kilic, S.S.,... Boisson-Dupuis, S. (2015). Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome. Journal of Experimental Medicine, 212(10), 1641-62.
Saleh, M.A., Mcmaster, W.G., Wu, J., Norlander, A.E., Funt, S.A., Thabet, S.R.,... Madhur, M.S. (2015). Lymphocyte adaptor protein LNK deficiency exacerbates hypertension and end-organ inflammation. Journal of Clinical Investigation, 125(3), 1189-202.
Haller, F., Moskalev, E., Faucz, F.R., Barthelmeß, S., Wiemann, S., Bieg, M.,... Agaimy, A. (2014). Aberrant DNA hypermethylation of SDHC: a novel mechanism of tumor development in Carney triad. Endocrine-Related Cancer, 21(4), 567-77.
Perry, J.R.B., Hsu, Y.-H., Chasman, D.I., Johnson, A.D., Elks, C., Albrecht, E.,... Murray, A. (2014). DNA mismatch repair gene MSH6 implicated in determining age at natural menopause. Human Molecular Genetics, 23(9), 2490-7.

Zuletzt aktualisiert 2013-02-07 um 12:11