Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sabrina Schreiber"'
Autor:
Sabrina Schreiber, Elisabeth Petrasch-Parwez, Elke Porrmann-Kelterbaum, Eckart Förster, Jörg T. Epplen, Wanda M. Gerding
Publikováno v:
IBRO Reports, Vol 5, Iss , Pp 43-53 (2018)
The Ccdc66-deficient (Ccdc66 -/-) mouse model exhibits slow progressive retinal degeneration. It is unclear whether CCDC66 protein also plays a role in the wildtype (WT; Ccdc66 +/+) mouse brain and whether the lack of Ccdc66 gene expression in the Cc
Externí odkaz:
https://doaj.org/article/0e4e456e3f9f4e44bd71f5d1dfce6f86
Autor:
Leonardo dos Santos Hochmuller, Augusto Mathias de Freitas, Sabrina Schreiber Jesus, Tarcisio Dorn de Oliveira
Publikováno v:
RECIMA21 - Revista Científica Multidisciplinar - ISSN 2675-6218. 2:e26387
A acessibilidade assegura aos sujeitos, portadores de deficiências ou não, o livre acesso e o uso de ambientes públicos com segurança e universalização. Por isso, sua aplicação e implementação deve ser instituída e assegurada em todos os a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80c3c74f09cf5b04e6b0e129f99e55f7
https://doi.org/10.47820/recima21.v2i6.387
https://doi.org/10.47820/recima21.v2i6.387
Publikováno v:
Nucleic Acids Research
Autonomously replicating vectors represent a simple and versatile model system for genetic modifications, but their localization in the nucleus and effect on endogenous gene expression is largely unknown. Using circular chromosome conformation captur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b273517e5e70b2dea742592a6e47799c
http://europepmc.org/articles/PMC5570033
http://europepmc.org/articles/PMC5570033
Autor:
Dale Green, Roberto Petroccia, Joao Alves, Petrika Gjanci, Sabrina Schreiber, Vincenzo Manzari, B. Cardeira, Carlo Vassale, Oleksiy Kebkal, Giovanni Zappa, Jean-Michel Passerieux, Ken Scussel, Davide Buselli, Fausto Ferreira
Underwater acoustic communications is a global domain in which different manufacturers produce different devices and implement different (and usually incompatible) communication protocols. The myriad of vendor-specific protocols is not conducive to c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7399c975f9450caa7ab90dbc1a09a3d
https://doi.org/10.23919/oceans40490.2019.8962607
https://doi.org/10.23919/oceans40490.2019.8962607
Publikováno v:
Journal of Animal Breeding and Genetics. 128:153-160
Weimaraner dogs are defined by light brown coat colour termed grey including several shadings ranging from silver and deer to mouse grey. In contrast, the so-called blue Weimaraners (BW) with lightened black-pigmented coat have been proposed to repre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39583a684d4aceb2e616868993c9e027
https://doi.org/10.1111/j.1439-0388.2010.00888.x
https://doi.org/10.1111/j.1439-0388.2010.00888.x
Autor:
Jörg T. Epplen, Gabriele Dekomien, Andreas Gal, Jan Kremers, Elisabeth Petrasch-Parwez, Thomas Rülicke, Wanda M. Gerding, Denis A. Akkad, Saleh M. Ibrahim, Sabrina Schreiber, Tobias Schulte-Middelmann, Rolf Dermietzel, Jenny Atorf, Andreia de Castro Marques
Publikováno v:
Human molecular genetics. 20(18)
Retinitis pigmentosa (RP) is a group of human retinal disorders, with more than 100 genes involved in retinal degeneration. Canine and murine models are useful for investigating human RP based on known, naturally occurring mutations. In Schapendoes d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ea69677669ea2a676ba2a4c20011189
https://pubmed.ncbi.nlm.nih.gov/21680557
https://pubmed.ncbi.nlm.nih.gov/21680557
Autor:
Jörg T. Epplen, Gabriele Dekomien, Sabine Hoffjan, Hasan Bagci, Simone Kastner, Selçuk Güneş, Sezgin Gunes, Elisabeth Petrasch-Parwez, Sabrina Schreiber, Wanda M. Gerding, Denis A. Akkad, Ina-Janine Thiemann
Publikováno v:
Investigative Opthalmology & Visual Science. 56:8045
Epplen, Joerg T./0000-0002-6087-3327 WOS: 000368243800055 PubMed: 26720455 PURPOSE. Retinitis pigmentosa (RP) is the most common inherited retinal disease with high genetic heterogeneity and variable phenotypes. Characteristic symptoms include night
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2d95e94028f327223ec5008c1a98818
https://doi.org/10.1167/iovs.15-17473
https://doi.org/10.1167/iovs.15-17473