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Lehrstuhl für Arabistik und Semitistik
Friedrich-Alexander-Universität Erlangen-Nürnberg
Philosophische Fakultät und Fachbereich Theologie
Department Alte Welt und Asiatische Kulturen
Institut für Sprachen und Kulturen des Nahen Ostens und Ostasiens
Overview
Publications
(375)
Research Grants
(8)
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(2)
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Journal article
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Generation of two iPSC lines from patients with Aicardi-Goutières syndrome carrying either biallelic ADAR1 mutations (PC138) or a heterozygous IFIH1 mutation (PC139) (2025)
Zerad L, Didry-Barca B, Banal C, Onteniente B, Lefort N, Lepelley A, Seabra L, et al.
Journal article
Novel COL4A1 missense variant in a case of juvenile stroke (2025)
Kretz A, Arbeiter M, Strobel J, Blum K, Frischholz B, Rödiger A, Hackstein H, et al.
Journal article
Further Delineation of the AUTS2 HX Repeat Domain-Related Phenotype (2025)
Erdogan EN, Cheng CV, Caraffi SG, Ivanovski I, Piatelli G, Errichiello E, Papavasiliou AS, et al.
Journal article
Limited association between HRR gene alterations and HRD in molecular tumor board cancer samples: Who should be tested for HRD? (2025)
Schubart C, Tögel L, Carta MG, Hetzner P, Helbig L, Zaglas C, Ziegler M, et al.
Journal article
High-throughput differentiation of human blood vessel organoids reveals overlapping and distinct functions of the cerebral cavernous malformation proteins (2025)
Skowronek D, Pilz RA, Saenko VV, Mellinger L, Singer D, Ribback S, Weise A, et al.
Journal article
A homozygous TRIP13 pathogenic variant associated with familiar oocyte arrest and prematurely condensed sperm chromosomes (2025)
Schweiger M, Reis A, Gümüslü E, Krebsova A, Raab A, Lang C, Horn D, et al.
Journal article
A novel human organoid model system reveals requirement of TCF4 for oligodendroglial differentiation (2025)
Furlanetto F, Flegel N, Kremp M, Spear C, Fröb F, Alfonsetti M, Bohl B, et al.
Journal article
GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets (2025)
Dand N, Stuart PE, Bowes J, Ellinghaus D, Nititham J, Saklatvala JR, Teder-Laving M, et al.
Journal article
Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability (2025)
Sabeh P, Dumas SA, Maios C, Daghar H, Korzeniowski M, Rousseau J, Lines M, et al.
Journal article
Exploring Differentially Expressed Genes and Understanding the Underlying Mechanisms in Glioblastoma (2025)
Seven D, Ekici AB, Uebe S, Bilgiç B, Sencer A, Aydoseli A, Reis A, Buyru N
Journal article
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