Resultados de búsqueda - Molecular Vision :: Descubridor de recursos de la Universidad Veracruzana

581

SOD2 gene polymorphisms in neovascular age-related macular degeneration and polypoidal choroidal vasculopathy

por Kondo, Naoshi, Bessho, Hiroaki, Honda, Shigeru, Negi, Akira
Publicado 2009

“…Molecular Vision…”

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SOD2 gene polymorphisms in neovascular age-related macular degeneration and polypoidal choroidal vasculopathy

582

Hypoxia reduces TGFβ1-induced corneal keratocyte myofibroblast transformation

por Xing, Dongmei, Bonanno, Joseph A.
Publicado 2009

“…Molecular Vision…”

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Hypoxia reduces TGFβ1-induced corneal keratocyte myofibroblast transformation

583

Muscarinic acetylcholine receptor 1 gene polymorphisms associated with high myopia

por Lin, Hui-Ju, Wan, Lei, Tsai, Yuhsin, Chen, Wen-Chi, Tsai, Shih-Wei, Tsai, Fuu-Jen
Publicado 2009

“…Molecular Vision…”

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Muscarinic acetylcholine receptor 1 gene polymorphisms associated with high myopia

584

Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in Southern India

por Sundaresan, Periasamy, Vijayalakshmi, P., Thompson, Stewart, Ko, Audrey C., Fingert, John H., Stone, Edwin M.
Publicado 2009

“…Molecular Vision…”

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Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in Southern India

585

Cis-urocanic acid suppresses UV-B-induced interleukin-6 and -8 secretion and cytotoxicity in human corneal and conjunctival epithelial cells in vitro

por Viiri, J., Jauhonen, H.M., Kauppinen, A., Ryhänen, T., Paimela, T., Hyttinen, J., Sorri, I., Laihia, J.K., Leino, L., Kaarniranta, K.
Publicado 2009

“…Molecular Vision…”

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Cis-urocanic acid suppresses UV-B-induced interleukin-6 and -8 secretion and cytotoxicity in human corneal and conjunctival epithelial cells in vitro

586

Compound heterozygosity for a novel and a recurrent MFRP gene mutation in a family with the nanophthalmos-retinitis pigmentosa complex

por Zenteno, Juan Carlos, Buentello-Volante, Beatriz, Quiroz-González, Miguel A., Quiroz-Reyes, Miguel A.
Publicado 2009

“…Molecular Vision…”

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Compound heterozygosity for a novel and a recurrent MFRP gene mutation in a family with the nanophthalmos-retinitis pigmentosa complex

587

Disease-causing mutations in the CLRN1 gene alter normal CLRN1 protein trafficking to the plasma membrane

por Isosomppi, Juha, Västinsalo, Hanna, Geller, Scott F., Heon, Elise, Flannery, John G., Sankila, Eeva-Marja
Publicado 2009

“…Molecular Vision…”

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Disease-causing mutations in the CLRN1 gene alter normal CLRN1 protein trafficking to the plasma membrane

588

A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family

por Azam, Maleeha, Collin, Rob W.J., Khan, Muhammad Imran, Shah, Syed Tahir Abbas, Qureshi, Nadeem, Ajmal, Muhammad, den Hollander, Anneke I., Qamar, Raheel, Cremers, Frans P.M.
Publicado 2009

“…Molecular Vision…”

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A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family

589

The GJA8 allele encoding CX50I247M is a rare polymorphism, not a cataract-causing mutation

por Graw, Jochen, Schmidt, Werner, Minogue, Peter J., Rodriguez, Jessica, Tong, Jun-Jie, Klopp, Norman, Illig, Thomas, Ebihara, Lisa, Berthoud, Viviana M., Beyer, Eric C.
Publicado 2009

“…Molecular Vision…”

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The GJA8 allele encoding CX50I247M is a rare polymorphism, not a cataract-causing mutation

590

Decursin inhibits retinal neovascularization via suppression of VEGFR-2 activation

por Kim, Jeong Hun, Kim, Jin Hyoung, Lee, You Mie, Ahn, Eun-Mi, Kim, Kyu-Won, Yu, Young Suk
Publicado 2009

“…Molecular Vision…”

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Decursin inhibits retinal neovascularization via suppression of VEGFR-2 activation

591

AAV retinal transduction in a large animal model species: Comparison of a self-complementary AAV2/5 with a single-stranded AAV2/5 vector

por Petersen-Jones, S.M., Bartoe, J.T., Fischer, A.J., Scott, M., Boye, S.L., Chiodo, V., Hauswirth, W.W.
Publicado 2009

“…Molecular Vision…”

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AAV retinal transduction in a large animal model species: Comparison of a self-complementary AAV2/5 with a single-stranded AAV2/5 vector

592

Expression of cadherin 23 isoforms is not conserved: implications for a mouse model of Usher syndrome type 1D

por Lagziel, Ayala, Overlack, Nora, Bernstein, Steven L., Morell, Robert J., Wolfrum, Uwe, Friedman, Thomas B.
Publicado 2009

“…Molecular Vision…”

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Expression of cadherin 23 isoforms is not conserved: implications for a mouse model of Usher syndrome type 1D

593

HLA-DRB1 among patients with Vogt-Koyanagi-Harada disease in Saudi Arabia

por Iqniebi, Alia, Gaafar, Ameera, Sheereen, Atia, Al-Suliman, Abdullah, Mohamed, Gamal, Al-Hussein, Khaled, Tabbara, Khalid F.
Publicado 2009

“…Molecular Vision…”

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HLA-DRB1 among patients with Vogt-Koyanagi-Harada disease in Saudi Arabia

594

Involvement of A(1) adenosine receptors in osmotic volume regulation of retinal glial cells in mice

por Wurm, Antje, Lipp, Stephan, Pannicke, Thomas, Linnertz, Regina, Färber, Katrin, Wiedemann, Peter, Reichenbach, Andreas, Bringmann, Andreas
Publicado 2009

“…Molecular Vision…”

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Involvement of A(1) adenosine receptors in osmotic volume regulation of retinal glial cells in mice

595

Müller cell activation, proliferation and migration following laser injury

por Tackenberg, Mark A., Tucker, Budd A., Swift, Jesse S., Jiang, Caihui, Redenti, Stephen, Greenberg, Kenneth P., Flannery, John G., Reichenbach, Andreas, Young, Michael J.
Publicado 2009

“…Molecular Vision…”

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