Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Karita Antunes Costa"'
Autor:
Fabiana Louise Motta, Mariana Vallim Salles, Karita Antunes Costa, Rafael Filippelli-Silva, Renan Paulo Martin, Juliana Maria Ferraz Sallum
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
Abstract Inherited retinal dystrophies are characterized by progressive retina degeneration and mutations in at least 250 genes have been associated as disease-causing. CRB1 is one of many genes analyzed in molecular diagnosis for inherited retinal d
Externí odkaz:
https://doaj.org/article/48f921f6bd6e4d558b8221a9c9f34ce4
Autor:
Chikara Inoue, José Álvaro Pereira Gomes, Tais Hitomi Wakamatsu, Shigeru Kinoshita, Juliana Maria Ferraz Sallum, Mayumi Ueta, Karita Antunes Costa, Laís Yumi Sakano
Publikováno v:
The Ocular Surface. 20:173-175
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fc474344330e29406c359ab7be0b0de
https://doi.org/10.1016/j.jtos.2021.02.008
https://doi.org/10.1016/j.jtos.2021.02.008
Autor:
Chris Whitebirch, Karita Antunes Costa, John Chiang, Mariana Vallim Salles, Juliana Maria Ferraz Sallum
Publikováno v:
International Journal of Retina and Vitreous, Vol 3, Iss 1, Pp 1-11 (2017)
International Journal of Retina and Vitreous
International Journal of Retina and Vitreous
Background Retinal dystrophies constitute a group of diseases characterized by clinical variability and pronounced genetic heterogeneity. Retinitis pigmentosa is the most common subtype of hereditary retinal dystrophy and is characterized by a progre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7696ab87d8e854be56ff99e1fce12b4
http://link.springer.com/article/10.1186/s40942-017-0087-6
http://link.springer.com/article/10.1186/s40942-017-0087-6
Autor:
Juliana Maria Ferraz Sallum, Renan Paulo Martin, Karita Antunes Costa, Fabiana Louise Motta, Rafael Filippelli-Silva, Mariana Vallim Salles
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
Scientific Reports
Scientific Reports
Inherited retinal dystrophies are characterized by progressive retina degeneration and mutations in at least 250 genes have been associated as disease-causing. CRB1 is one of many genes analyzed in molecular diagnosis for inherited retinal dystrophy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f42f0954b53a8f5d382f15179134f2cf
https://doaj.org/article/48f921f6bd6e4d558b8221a9c9f34ce4
https://doaj.org/article/48f921f6bd6e4d558b8221a9c9f34ce4
Autor:
Patricia Varela Lima Teixeira, Renan Paulo Martin, Fabiana Louise Motta, Rafael Filippelli-Silva, Elton Dias da Silva, Mariana Vallim Salles, Juliana Maria Ferraz Sallum, Karita Antunes Costa, João Bosco Pesquero
Publikováno v:
Ophthalmic genetics. 38(1)
Although the pathogenicity of the prominin-1 (PROM1) gene has already been described as associated with autosomal dominant Stargardt disease, little is known about sequence variations in this gene.The aim of this study was to evaluate PROM1 gene sequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::260eccf48033b5fa703007b4b19ef065
https://pubmed.ncbi.nlm.nih.gov/28095140
https://pubmed.ncbi.nlm.nih.gov/28095140
Autor:
Chie Sotozono, José Arthur Milhomens, José Álvaro Pereira Gomes, Karita Antunes Costa, Renata Ruoco Loureiro, Mayumi Ueta, Tais Hitomi Wakamatsu, Chikara Inoue, Yukinori Okada, Katsushi Tokunaga, Shigeru Kinoshita, Juliana Maria Ferraz Sallum
Publikováno v:
Repositório Institucional da UNIFESP
Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
Ministry of Education, Culture, Sports, Science and Technology of the Japanese government Japan Society for the Promotion of Science Core-to-Core Program Advanced Research Networks Japanese Ministry of Health, Labor and Welfare Kyoto Foundation for t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70b7d52dd614f055f094ccdd2aa8e643
https://repositorio.unifesp.br/handle/11600/54823
https://repositorio.unifesp.br/handle/11600/54823
Autor:
Rafael Filippelli-Silva, João Bosco Pesquero, Elton Dias da Silva, Mariana Vallim Salles, Renan Paulo Martin, Juliana Maria Ferraz Sallum, Karita Antunes Costa, Fabiana Louise Motta, John Chiang, Patrícia Siqueira Varela
Publikováno v:
Repositório Institucional da UNIFESP
Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) PURPOSE. To analyze the presence of complex alleles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34d2043102c47daf6ebb90f80d72e3d4
https://repositorio.unifesp.br/handle/11600/58184
https://repositorio.unifesp.br/handle/11600/58184
Autor:
Christiane Rolim de Moura, Mansoor Sarfarazi, Anil K Mandal, Inderjeet Kaur, Simone Finzi, Alberto Jorge Betinjane, Ivan Maynart Tavares, Mônica Barbosa de Melo, Victor Evangelista de Faria Ferraz, Karita Antunes Costa, Juliana Maria Ferraz Sallum, Maurício Della Paolera, Subhabrata Chakrabarti, Meha Kabra, José Paulo Cabral de Vasconcellos, Jayter Silva Paula, Mohammed Hasnat Ali, Sirisha Senthil, Rubens Belfort, Vital Paulino Costa
Publikováno v:
PLoS ONE, Vol 10, Iss 5, p e0127147 (2015)
PLoS ONE
PLoS ONE
BackgroundPrimary congenital glaucoma (PCG), occurs due to the developmental defects in the trabecular meshwork and anterior chamber angle in children. PCG exhibits genetic heterogeneity and the CYP1B1 gene has been widely implicated worldwide. Despi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a872cad0535dd3386416a735bd506809
https://doi.org/10.1371/journal.pone.0127147
https://doi.org/10.1371/journal.pone.0127147
Autor:
Kárita Antunes Costa, Mariana Vallim Salles, Chris Whitebirch, John Chiang, Juliana Maria Ferraz Sallum
Publikováno v:
International Journal of Retina and Vitreous, Vol 3, Iss 1, Pp 1-11 (2017)
Abstract Background Retinal dystrophies constitute a group of diseases characterized by clinical variability and pronounced genetic heterogeneity. Retinitis pigmentosa is the most common subtype of hereditary retinal dystrophy and is characterized by
Externí odkaz:
https://doaj.org/article/b04efcb315cd4c5ba5fe05ba979b6ba4