Zobrazeno 1 - 10 of 18 pro vyhledávání: '"M. W. Seeliger"'
1
Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel–associated retinopathy
Autor: Richard G. Weleber, Robert Lukowski, M. W. Seeliger, Christina Brennenstuhl, Anne E. Bausch, Xiangang Zong, Sascha Venturelli, John R. Heckenlively, Vithiyanjali Sothilingam, Stylianos Michalakis, Susanne C. Beck, Günther Rudolph, Naoyuki Tanimoto, Ulrich Kellner, Peggy Reuter, Anja K. Mayer, Ditta Zobor, Susanne Kohl, Bernd Wissinger, Gesa Astrid Hahn, Britta Baumann, Paul A. Sieving, Xi-Qin Ding, Nicole Weisschuh, Christian P. Hamel, Martin Biel, Robert K. Koenekoop, Peter Ruth, Peter Charbel Issa, Timm Krätzig, Gesine Huber, Elvir Becirovic, Markus Burkard, Katrin Junger
Publikováno v: The Journal of clinical investigation, vol 128, iss 12
Journal of Clinical Investigation
Journal of Clinical Investigation, American Society for Clinical Investigation, 2018, 128 (12), pp.5663--5675. ⟨10.1172/JCI96098⟩
International audience; Mutations in CNGA3 and CNGB3, the genes encoding the subunits of the tetrameric cone photoreceptor cyclic nucleotide–gated ion channel, cause achromatopsia, a congenital retinal disorder characterized by loss of cone functio
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::470e7ba4f9a01dd349b61665c4c93838
https://doi.org/10.1172/jci96098
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2
Genersatztherapie bei hereditären Netzhauterkrankungen
Autor: Naoyuki Tanimoto, M. W. Seeliger, Regine Mühlfriedel, Vithiyanjali Sothilingam
Publikováno v: Klinische Monatsblätter für Augenheilkunde. 234:320-328
ZusammenfassungCharakteristisch für erblich bedingte Netzhauterkrankungen sind Funktionsausfälle in der Reizaufnahme und Reizweiterleitung innerhalb der Netzhaut, die zur Reduktion des Sehvermögens bis zur Blindheit führen. Dabei verursachen gene
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a8d34769655baf3fa8181493af9ea218
https://doi.org/10.1055/s-0043-101817
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3
PALS1 is essential for retinal pigment epithelium structure and neural retina stratification
Autor: B. Park, M. W. Seeliger, Celso H. Alves, Naoyuki Tanimoto, Jan Klooster, Till F. M. Andlauer, A. le Bivic, Eric C. Swindell, Susanne C. Beck, Fabrice Richard, Gesine Huber, Milan Jamrich, Ditte M. S. Lundvig, Jan Wijnholds
Publikováno v: Journal of Neuroscience
Journal of Neuroscience, Society for Neuroscience, 2011, 31 (47), pp.17230-41. ⟨10.1523/JNEUROSCI.4430-11.2011⟩
Journal of Neuroscience; Vol 31
Journal of Neuroscience, 2011, 31 (47), pp.17230-41. ⟨10.1523/JNEUROSCI.4430-11.2011⟩
The Journal of Neuroscience, 31, 17230-17241
The Journal of Neuroscience, 31, pp. 17230-17241
Journal of Neuroscience, 31, 17230-17241. Society for Neuroscience
The membrane-associated palmitoylated protein 5 (MPP5 or PALS1) is thought to organize intracellular PALS1-CRB-MUPP1 protein scaffolds in the retina that are involved in maintenance of photoreceptor–Müller glia cell adhesion. In humans, the Crumbs
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7f774d4c89692e7709ce636bd1a04d2
https://doi.org/10.1523/jneurosci.4430-11.2011
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4
Cone loss is delayed relative to rod loss during induced retinal degeneration in the diurnal cone-rich rodent Arvicanthis ansorgei
Autor: Gesine Huber, M. W. Seeliger, Naoyuki Tanimoto, Domitille L. Boudard, David Hicks, Susanne C. Beck
Publikováno v: Neuroscience. 169:1815-1830
Cone photoreceptor breakdown underlies functional vision loss in many blinding diseases. Cone loss is often secondary to that of rods, but little experimental data are available on the relationship between the two populations. Because of its high con
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acce3a0548e52517babbee100cbaafdb
https://doi.org/10.1016/j.neuroscience.2010.06.037
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5
Cooperative Phagocytes
Autor: Martin Zinkernagel, Christian Grimm, Sandrine Joly, Andreas Reichenbach, Elke Ulbricht, M. W. Seeliger, Marijana Samardzija, Bernhard Odermatt, Karl S. Lang, Johannes Hirrlinger, Petra G. Hirrlinger, Mike Francke, Charlotte E. Remé, Susanne C. Beck
Publikováno v: The American Journal of Pathology. 174:2310-2323
Phagocytosis is essential for the removal of photoreceptor debris following retinal injury. We used two mouse models, mice injected with green fluorescent protein-labeled bone marrow cells or green fluorescent protein-labeled microglia, to study the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0fa6fe728036acc0d66a870c9117fb7d
https://doi.org/10.2353/ajpath.2009.090023
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6
[Gene replacement therapy in achromatopsia type 2]
Autor: R, Mühlfriedel, N, Tanimoto, M W, Seeliger
Publikováno v: Klinische Monatsblatter fur Augenheilkunde. 231(3)
Achromatopsia is an autosomal recessive inherited retinal disease caused by a complete loss of cone photoreceptor function. About 80 % of achromatopsia patients show mutations in the alpha or beta subunit (A3 and B3) of the cGMP controlled cation cha
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::81c784555d0e29db4812ca305313521a
https://pubmed.ncbi.nlm.nih.gov/24658860
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8
Retinal degeneration modulates intracellular localization of CDC42 in photoreceptors
Autor: S R, Heynen, N, Tanimoto, S, Joly, M W, Seeliger, M, Samardzija, C, Grimm
Publikováno v: Molecular Vision
Purpose Rho GTPases such as RAS-related C3 botulinum substrate 1 (RAC1) and cell division cycle 42 homolog (S. cerevisiae; CDC42) have been linked to cellular processes including movement, development, and apoptosis. Recently, RAC1 has been shown to
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::48059923ae3a5d2e34a273cb20d047ce
https://pubmed.ncbi.nlm.nih.gov/22128240
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9
[Usher syndrome: clinical features, diagnostic options, and therapeutic prospects]
Autor: M W, Seeliger, M D, Fischer, M, Pfister
Publikováno v: Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft. 106(6)
Usher syndrome denotes a clinically and genetically heterogeneous combination of retinitis pigmentosa and sensorineural deafness. The division into subtypes I, II, and III is based on the degree of hearing loss: Type I is characterized by deafness fr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::625062e25a7ac23fad3a439b1204d1c0
https://pubmed.ncbi.nlm.nih.gov/19517115
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10
Funktionsprüfungen der Makula
Autor: E. Zrenner, M. W. Seeliger, J. Reinhard
Publikováno v: Altersabhängige Makuladegeneration ISBN: 9783662056820
Die menschliche Makula mit ihrem Zentrum, der Foveola, ist das leistungsfahigste sensorische Organ des Menschen fur die raumlich differenzierende Wahrnehmung. Dies grundet sich auf die hohe raumliche Dichte der Photorezeptoren von durchschnittlich me
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8a9807501db73e052be8f3796a93d1c7
https://doi.org/10.1007/978-3-662-05681-3_7
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