Zobrazeno 1 - 10
of 177
pro vyhledávání: '"Arthur A, Bergen"'
Autor:
Sara Risseeuw, MD, PhD, Matthew G. Pilgrim, PhD, Sergio Bertazzo, PhD, Connor N. Brown, PhD, Lajos Csincsik, PhD, Sarah Fearn, PhD, Richard B. Thompson, PhD, Arthur A. Bergen, PhD, Jacoline B. ten Brink, BAS, Elod Kortvely, PhD, Wilko Spiering, MD, PhD, Jeannette Ossewaarde–van Norel, MD, PhD, Redmer van Leeuwen, MD, PhD, Imre Lengyel, PhD
Publikováno v:
Ophthalmology Science, Vol 4, Iss 2, Pp 100416- (2024)
Purpose: To investigate the histology of Bruch’s membrane (BM) calcification in pseudoxanthoma elasticum (PXE) and correlate this to clinical retinal imaging. Design: Experimental study with clinicopathological correlation. Subjects and Controls: S
Externí odkaz:
https://doaj.org/article/65e33ea1989f44e58acf0137600ec7ab
Autor:
Andrea Heredero Berzal, Ellie L. Wagstaff, Anneloor L. M. A. ten Asbroek, Jacoline B. ten Brink, Arthur A. Bergen, Camiel J. F. Boon
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 3, p 1444 (2024)
Within the last decade, a wide variety of protocols have emerged for the generation of retinal organoids. A subset of studies have compared protocols based on stem cell source, the physical features of the microenvironment, and both internal and exte
Externí odkaz:
https://doaj.org/article/8296fe8aacce410a89954f9c2957da30
Autor:
Isa van der Veen, Andrea Heredero Berzal, Céline Koster, Anneloor L. M. A. ten Asbroek, Arthur A. Bergen, Camiel J. F. Boon
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 2, p 1267 (2024)
X-linked juvenile retinoschisis (XLRS) is an early-onset progressive inherited retinopathy affecting males. It is characterized by abnormalities in the macula, with formation of cystoid retinal cavities, frequently accompanied by splitting of the ret
Externí odkaz:
https://doaj.org/article/cdbed5334dc946c6a399cb0ffc4bb456
Autor:
Janine Reurink, Nicole Weisschuh, Alejandro Garanto, Adrian Dockery, L. Ingeborgh van den Born, Isabelle Fajardy, Lonneke Haer-Wigman, Susanne Kohl, Bernd Wissinger, G. Jane Farrar, Tamar Ben-Yosef, Fatma Kivrak Pfiffner, Wolfgang Berger, Marianna E. Weener, Lubica Dudakova, Petra Liskova, Dror Sharon, Manar Salameh, Ashley Offenheim, Elise Heon, Giorgia Girotto, Paolo Gasparini, Anna Morgan, Arthur A. Bergen, Jacoline B. ten Brink, Caroline C.W. Klaver, Lisbeth Tranebjærg, Nanna D. Rendtorff, Sascha Vermeer, Jeroen J. Smits, Ronald J.E. Pennings, Marco Aben, Jaap Oostrik, Galuh D.N. Astuti, Jordi Corominas Galbany, Hester Y. Kroes, Milan Phan, Wendy A.G. van Zelst-Stams, Alberta A.H.J. Thiadens, Joke B.G.M. Verheij, Mary J. van Schooneveld, Suzanne E. de Bruijn, Catherina H.Z. Li, Carel B. Hoyng, Christian Gilissen, Lisenka E.L.M. Vissers, Frans P.M. Cremers, Hannie Kremer, Erwin van Wijk, Susanne Roosing
Publikováno v:
HGG Advances, Vol 4, Iss 2, Pp 100181- (2023)
Summary: A significant number of individuals with a rare disorder such as Usher syndrome (USH) and (non-)syndromic autosomal recessive retinitis pigmentosa (arRP) remain genetically unexplained. Therefore, we assessed subjects suspected of USH2A-asso
Externí odkaz:
https://doaj.org/article/3a1d6bbbc0b84a3f9409fc1710e756ce
Publikováno v:
BMC Genomics, Vol 22, Iss 1, Pp 1-20 (2021)
Abstract Background To investigate whether copy number variations (CNVs) are implicated in molecular mechanisms underlying primary open-angle glaucoma (POAG), we used genotype data of POAG individuals and healthy controls from two case-control studie
Externí odkaz:
https://doaj.org/article/89db732c786f4bda997d42f26f1da698
Autor:
Xuan-Thanh-An Nguyen, Lude Moekotte, Astrid S. Plomp, Arthur A. Bergen, Maria M. van Genderen, Camiel J. F. Boon
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 8, p 7481 (2023)
Retinitis pigmentosa (RP) comprises a group of inherited retinal dystrophies characterized by the degeneration of rod photoreceptors, followed by the degeneration of cone photoreceptors. As a result of photoreceptor degeneration, affected individuals
Externí odkaz:
https://doaj.org/article/3c202c0264d3402cad9de3a43252f384
Autor:
Eszter Emri, Oisin Cappa, Caoimhe Kelly, Elod Kortvely, John Paul SanGiovanni, Brian S. McKay, Arthur A. Bergen, David A. Simpson, Imre Lengyel
Publikováno v:
Cells, Vol 12, Iss 5, p 773 (2023)
Zinc supplementation has been shown to be beneficial to slow the progression of age-related macular degeneration (AMD). However, the molecular mechanism underpinning this benefit is not well understood. This study used single-cell RNA sequencing to i
Externí odkaz:
https://doaj.org/article/3ed1ecb4cff647cbad6eee0dd785ff03
Autor:
Valeria Lo Faro, Ilja M. Nolte, Jacoline B. Ten Brink, Harold Snieder, Nomdo M. Jansonius, Arthur A. Bergen, Lifelines Cohort Study
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Background and purpose: Primary open-angle glaucoma (POAG) is an optic neuropathy characterized by death of retinal ganglion cells and atrophy of the optic nerve head. The susceptibility of the optic nerve to damage has been shown to be mediated by m
Externí odkaz:
https://doaj.org/article/a2d49cc5d6ec4e3e9fa4524d5b2c9765
Autor:
Cansu de Muijnck, Jacoline B. ten Brink, Arthur A. Bergen, Camiel J.F. Boon, Maria M. van Genderen
Publikováno v:
Survey of ophthalmology. 68(4):641-654
Wolfram-like syndrome (WFLS) is a recently described autosomal dominant disorder with phenotypic similarities to autosomal recessive Wolfram syndrome (WS), including optic atrophy, hearing impairment, and diabetes mellitus. We summarize current liter
Autor:
Céline Koster, Koen T. van den Hurk, Jacoline B. ten Brink, Colby F. Lewallen, Boris V. Stanzel, Kapil Bharti, Arthur A. Bergen
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 6, p 2918 (2022)
Purpose: The lack of suitable animal models for (dry) age-related macular degeneration (AMD) has hampered therapeutic research into the disease, so far. In this study, pigmented rats and mice were systematically injected with various doses of sodium
Externí odkaz:
https://doaj.org/article/6dbb73f8bfe9474a82b1249c21ab2f56