Zobrazeno 1 - 10
of 39
pro vyhledávání: '"BFSP2"'
Autor:
Marc Kantorow, A. Sue Menko, Daniel Chauss, Joshua Disatham, Rifah Gheyas, Lisa A. Brennan, Lauren Daley, David Blanco
Publikováno v:
Developmental Biology. 453:86-104
Changes in chromatin accessibility regulate the expression of multiple genes by controlling transcription factor access to key gene regulatory sequences. Here, we sought to establish a potential function for altered chromatin accessibility in control
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::920392b32e2e40ab30a8fc795f750893
https://doi.org/10.1016/j.ydbio.2019.04.020
https://doi.org/10.1016/j.ydbio.2019.04.020
Publikováno v:
International Journal of Radiation Oncology*Biology*Physics. 111:e368
PURPOSE/OBJECTIVE(S) Intermediate filaments (IF) are a family of cytoskeletal proteins that play an integral role in critical cellular functions including cell migration, proliferation, and apoptosis. Previous studies have reported an association bet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3942dbc01c5e64c4ed150cbb6091bd89
https://doi.org/10.1016/j.ijrobp.2021.07.1090
https://doi.org/10.1016/j.ijrobp.2021.07.1090
Autor:
Raja Sekhar Nirujogi, Renu Goel, Pavithra Rajagopalan, Sneha M. Pinto, Mahashweta Dash, Bipin G. Nair, Abhijith K. Anil, Yashwanth Subbannayya, Subramanian Shankar, Krishna R Murthy, Gajanan Sathe, Harsha Gowda, B. L. Somani, Aditi Chatterjee, Gourav Dey, Dhanashree S. Kelkar, Akhilesh Pandey, Lavanya Balakrishnan, Shukti Chakravarti, Jayshree Advani, Nandini A. Sahasrabuddhe, T. S. Keshava Prasad, Praveen R Murthy, Srikanth S. Manda
Publikováno v:
OMICS: A Journal of Integrative Biology. 19:283-293
The aqueous humor is a colorless, transparent fluid that fills the anterior chamber of the eye. It plays an important role in maintaining the intraocular pressure and providing nourishment to the lens and cornea. The constitution of the aqueous humor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe29fd4600a0357c503e4213721f755c
https://doi.org/10.1089/omi.2015.0029
https://doi.org/10.1089/omi.2015.0029
Publikováno v:
Current Eye Research. 39:1013-1019
To identify the genetic defect in a Chinese family with bilateral pulverulent sutural cataract.A three-generation family with congenital cataract was recruited in the study. The study protocol followed the principles of the Declaration of Helsinki. D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a18acec9adb1394abbda8fd677b21481
https://doi.org/10.3109/02713683.2014.891749
https://doi.org/10.3109/02713683.2014.891749
The role of the eye lens is to focus light into the retina. To perform this unique function, the ocular lens must be transparent. Previous studies have demonstrated the expression of vimentin, BFSP1, and BFSP2 in the eye lens. These intermediate fila
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd78dbeab27a299e349b88e796cf3522
https://doi.org/10.1016/bs.mie.2015.09.010
https://doi.org/10.1016/bs.mie.2015.09.010
Autor:
Daljit Singh, Vanita Vanita
Publikováno v:
Molecular and Cellular Biochemistry. 368:167-172
To detect the underlying genetic defects in two autosomal dominant congenital cataract (ADCC) families, having respectively twenty and four members affected with bilateral congenital cataract. Detailed family history and clinical data were recorded.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c1aa157245a25727603e340f9f8eb6a
https://doi.org/10.1007/s11010-012-1355-2
https://doi.org/10.1007/s11010-012-1355-2
Publikováno v:
Journal of Huazhong University of Science and Technology [Medical Sciences]. 30:792-797
Congenital cataract is a highly heterogeneous disorder at both the genetic and the clinical-phenotypic levels. A unique cataract was observed in a 4-generation Chinese family, which was characterized by autosomal dominant inheritance and late-onset.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75a6ea934b51ceb4011ab37f96d6aeb7
https://doi.org/10.1007/s11596-010-0660-9
https://doi.org/10.1007/s11596-010-0660-9
Autor:
Christina Müller, Ottmar Distl
Publikováno v:
The Veterinary Journal. 182:342-345
Primary cataracts are breed-related eye diseases and are common in many dog breeds. In this study, 17 genes (BFSP2, EYA1, FOXE3, FTL, GCNT2, GJA3, GJA8, HSF4, MAF, MIP, PAX6, PITX3, SIX5, SORD, SOX1, SPARC, TRNT1) were evaluated as candidates for pri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c201a389a8f5f05ba506937bd28d1a86
https://doi.org/10.1016/j.tvjl.2008.06.006
https://doi.org/10.1016/j.tvjl.2008.06.006
Publikováno v:
Journal of Clinical Investigation. 119:1837-1848
Intermediate filaments (IFs) are a key component of the cytoskeleton in virtually all vertebrate cells, including those of the lens of the eye. IFs help integrate individual cells into their respective tissues. This Review focuses on the lens-specifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c25642d2e5e1815d53e45a1a0dee561
https://doi.org/10.1172/jci38277
https://doi.org/10.1172/jci38277
Publikováno v:
Journal of Biological Chemistry. 283:6607-6615
Lengsin is an eye lens-specific member of the glutamine synthetase (GS) superfamily. Lengsin has no GS activity, suggesting that it has a structural rather than catalytic role in lens. In situ hybridization and immunofluorescence showed that lengsin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd4f3bc664562b8abd2e67a67811d4a4
https://doi.org/10.1074/jbc.m709144200
https://doi.org/10.1074/jbc.m709144200