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. https://dx.doi.org/10.1002/ajmg.a.61045
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. https://dx.doi.org/10.1038/s41418-018-0261-x
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. https://dx.doi.org/10.1159/000493319
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). https://dx.doi.org/10.1126/sciimmunol.aat4956
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. https://dx.doi.org/10.1038/gim.2017.249
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). https://dx.doi.org/10.1038/s41467-018-06356-1
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. https://dx.doi.org/10.1002/art.40348
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). https://dx.doi.org/10.1126/sciimmunol.aat4941
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. https://dx.doi.org/10.3389/fimmu.2017.01318
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. https://dx.doi.org/10.1038/nature24628
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. https://dx.doi.org/10.1073/pnas.1606646113
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. https://dx.doi.org/10.1038/ng.3740
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. https://dx.doi.org/10.1186/s40478-016-0280-0
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. https://dx.doi.org/10.1002/art.39745
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. https://dx.doi.org/10.1093/nar/gkv1304
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. https://dx.doi.org/10.1084/jem.20140280
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. https://dx.doi.org/10.1172/JCI76327
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. https://dx.doi.org/10.1530/ERC-14-0254
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. https://dx.doi.org/10.1093/hmg/ddt620

Zuletzt aktualisiert 2013-02-07 um 12:11