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Dr. rer. nat. Steffen Uebe
List of publications:
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Institute of Human Genetics
Publications
(82)
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Journal article
Journal article
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Book chapter / Article in edited volumes
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Tumor microenvironment-dependent epigenetic imprinting in the vasculature predicts colon cancer outcome (2023)
Naschberger E, Fuchs M, Dickel N, Kunz M, Popp B, Anchang CG, Demmler R, et al.
Journal article
Prevalence of hereditary tubulointerstitial kidney diseases in the German Chronic Kidney Disease study (2022)
Popp B, Ekici AB, Knaup K, Schneider K, Uebe S, Park J, Bafna V, et al.
Journal article
SRD5A3-CDG: Twins with an intragenic tandem duplication (2022)
Rieger M, Türk M, Kraus C, Uebe S, Ekici AB, Krumbiegel M, Huchzermeyer C, et al.
Journal article
Interspecies Single-Cell RNA-Seq Analysis Reveals the Novel Trajectory of Osteoclast Differentiation and Therapeutic Targets (2022)
Omata Y, Okada H, Uebe S, Izawa N, Ekici AB, Sarter-Zaiss K, Saito T, et al.
Journal article
EIF3F-related neurodevelopmental disorder: refining the phenotypic and expanding the molecular spectrum (2022)
Hüffmeier U, Kraus C, Reuter M, Uebe S, Abbott MA, Ahmed SA, Rawson KL, et al.
Conference contribution
Common RUNX3 missense variant contributes to psoriatic arthritis by modifying differentiation of CD8(+) T-cells (2022)
Kerker I, Löhr S, Uebe S, Popp B, Vasileiou G, Bowes J, Kirchner P, et al.
Conference contribution
Diverse molecular causes of unsolved autosomal dominant tubulointerstitial kidney diseases (2022)
Wopperer F, Knaup K, Stanzick KJ, Schneider K, Jobst-Schwan T, Ekici AB, Uebe S, et al.
Journal article
Transcriptomes of MPO-Deficient Patients with Generalized Pustular Psoriasis Reveals Expansion of CD4+ Cytotoxic T Cells and an Involvement of the Complement System (2022)
Haskamp S, Frey B, Becker I, Schulz-Kuhnt A, Atreya I, Berking C, Pauli D, et al.
Journal article
BDV Syndrome: An Emerging Syndrome with Profound Obesity and Neurodevelopmental Delay Resembling Prader-Willi Syndrome (2021)
Bosch E, Hebebrand M, Popp B, Penger T, Behring B, Cox H, Towner S, et al.
Journal article
EIF3F-related neurodevelopmental disorder: refining the phenotypic and expanding the molecular spectrum (2021)
Hüffmeier U, Kraus C, Reuter M, Uebe S, Abbott MA, Ahmed SA, Rawson KL, et al.
Journal article
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