FAU.de
Deutsch
Login
Home
Publications
Research Grants
Inventions & Patents
Awards
Additional Research Activities
Faculties & Institutions
Research Areas
Japan (JP)
Overview
Projects
(15)
Publications
(2,072)
External partners
(603)
Types of publications
Toggle all
Journal article
Journal article
Book chapter / Article in edited volumes
Book chapter / Article in edited volumes
Authored book
Authored book
Translation
Translation
Thesis
Thesis
Edited Volume
Edited Volume
Conference contribution
Conference contribution
Other publication type
Other publication type
Unpublished / Preprint
Unpublished / Preprint
Publication year
From
To
Abstract
Journal
Filters (inactive)
Feasibility of cell-based therapy combined with descemetorhexis for treating Fuchs endothelial corneal dystrophy in rabbit model (2018)
Okumura N, Matsumoto D, Fukui Y, Teramoto M, Imai H, Kurosawa T, Shimada T, et al.
Journal article
Establishment of a drug screening system for Fuchs endothelial corneal dystrophy (2018)
Oshima T, Okumura N, Onishi T, Ueda E, Watanabe K, Tourtas T, Schlötzer-Schrehardt U, et al.
Conference contribution
Corrugated Bruch's membrane in high myopia (2018)
Jonas JB, Jonas RA, Ohno-Matsui K, Holbach L, Panda-Jonas S
Journal article
Association of rs613872 and trinucleotide repeat expansion in the TCF4 gene in Fuchs endothelial corneal dystrophy in Germany (2018)
Komori Y, Okumura N, Hayashi R, Nakano M, Tashiro K, Yoshii K, Aleff R, et al.
Conference contribution
Sellar Region Atypical Teratoid/Rhabdoid Tumors (ATRT) in Adults Display DNA Methylation Profiles of the ATRT-MYC Subgroup (2018)
Johann PD, Bens S, Oyen F, Wagener R, Giannini C, Perry A, Raisanen JM, et al.
Journal article
Dinuclear Iron(III) and Cobalt(III) Complexes Featuring a Biradical Bridge: Their Molecular Structures and Magnetic, Spectroscopic, and Redox Properties (2018)
Mondal D, Majee MC, Kundu S, Mörtel M, Abbas G, Endo A, Khusniyarov M, Chaudhury M
Journal article, Original article
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (2018)
Blok LS, Rousseau J, Twist J, Ehresmann S, Takaku M, Venselaar H, Rodan LH, et al.
Journal article
Pseudoexfoliation associated protective variant, rs7173049, reveals a novel regulatory region downstream of LOXL1 (2018)
Berner D, Pasutto F, Hoja U, Zenkel M, Ozaki M, Williams S, Ramsay M, et al.
Conference contribution
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation (2018)
Teumer A, Chaker L, Groeneweg S, Li Y, Di Munno C, Barbieri C, Schultheiss UT, et al.
Journal article
UTX-mediated enhancer and chromatin remodeling suppresses myeloid leukemogenesis through noncatalytic inverse regulation of ETS and GATA programs (2018)
Gozdecka M, Meduri E, Mazan M, Tzelepis K, Dudek M, Knights AJ, Pardo M, et al.
Journal article
‹
1
...
121
122
123
124
125
...
208
›