Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Sabine Foja"'
Autor:
Sabine Foja, Joana Heinzelmann, Anja Viestenz, Christiane Rueger, Sabine Hecht, Arne Viestenz
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 2, p 588 (2024)
This study investigates the possible toxic effects of the preoperative antiseptic substances povidone iodine (PVI) and polyhexanide (PHMB; Serasept® 2) on wound healing in ophthalmology. To assess this impact, human telomerase-immortalized corneal e
Externí odkaz:
https://doaj.org/article/223b6f723dca4591858d693e6e60ee41
Autor:
Christiane Kesper, Joana Heinzelmann, Anja Viestenz, Thomas Hammer, Sabine Foja, Marlene Stein, Arne Viestenz
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 2, p 645 (2023)
Limbal stem cell deficiency (LSCD) severely impairs vision and can lead to blindness. LSCD causes include chemical burns, infections, multiple previous operations and congenital malformations. Allogeneic limbal transplantation is a procedure for trea
Externí odkaz:
https://doaj.org/article/943b076ecd2743cf9f1c54cb5c6cdbff
PurposeLimbal stem cell deficiency (LSCD) is a rare but extremely relevant disease of the eye. LSCD patients often require a variety of surgical procedures, including keratoplasty in some cases. However, the outcome of these surgeries, including opac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c117f9c7239c0d703c2f089f23886e3
https://doi.org/10.21203/rs.3.rs-1034919/v1
https://doi.org/10.21203/rs.3.rs-1034919/v1
Autor:
Anja Viestenz, Christiane Kesper, Thomas Hammer, Joana Heinzelmann, Sabine Foja, Arne Viestenz
Publikováno v:
International ophthalmology. 42(12)
Purpose Limbal stem cell deficiency (LSCD) is a rare but extremely relevant disease of the eye. LSCD patients often require a variety of surgical procedures, including keratoplasty in some cases. However, the outcome of these surgeries, including opa
Autor:
E. Passarge, A. Rupprecht, Sabine Foja, Katrin Hoffmann, E. Weidle, M. Luther, C. Grünauer-Kloevekorn
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 233:187-194
Hintergrund: Als molekulargenetische Ursache der Fuchs-Hornhautendotheldystrophie (FECD), eine der haufigsten Indikationen fur eine Keratoplastik, wurde sowohl eine TGC-Trinukleotid-Repeat-Expansion im Intron 2 des TCF4-Gens als auch das Allel G des
Publikováno v:
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie. 255(8)
It was the aim of this investigation to elucidate the functional effects of CTG18.1 trinucleotide repeat expansion and the polymorphism rs613872 in the transcription factor 4 (TCF4) in corneas of patients affected by Fuchs’ endothelial corneal dyst
Autor:
Claudia Auw-Haedrich, Thomas Reinhard, Andreas Rupprecht, Katrin Hoffmann, Claudia Gruenauer-Kloevekorn, Sabine Foja
Publikováno v:
International ophthalmology. 36(6)
The purpose of this study was to report on two novel missense mutations of the cornea-specific TGFBI gene in one single patient and in two generations of a family diagnosed with unique corneal dystrophy (CD) phenotypes. Ophthalmologic examination, in
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 229
Autor:
Insa S. Schroeder, Bernadette Harwardt, Matthias Jung, Sabine Foja, Dagmar Riemann, Oliver Pelz-Ackermann
Publikováno v:
Cellular reprogramming. 15(1)
Pluripotency is characterized by specific transcription factors such as OCT4, NANOG, and SOX2, but also by pluripotency-associated microRNAs (miRs). Somatic cells can be reprogrammed by forced expression of these factors leading to induced pluripoten
Autor:
Sabine Foja, Stefan Burdach, Christoph Hutter, Uwe Hattenhorst, Danny Afar, Martin S. Staege, Gesine Hansen, Ingo Neumann
Publikováno v:
Cancer research. 64(22)
Ewing family tumors (EFTs) are small round blue cell tumors that show features of neuroectodermal differentiation. However, the histogenetic origin of EFTs is still a matter of debate. We used high-density DNA microarrays for the identification of EF