Resultats de la cerca - Miguel Coca‐Prados
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The Blood-Aqueous Barrier in Health and Disease per Miguel Coca‐Prados
Publicat 2014Revisão -
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Cloning and characterization of subtracted cDNAs from a human ciliary body library encoding <i>TIGR</i>, a protein involved in juvenile open angle glaucoma with homology to myosin... per Javier Ortego, Julio Escribano, Miguel Coca‐Prados
Publicat 1997Artigo -
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Myocilin Mutations Causing Glaucoma Inhibit the Intracellular Endoproteolytic Cleavage of Myocilin between Amino Acids Arg226 and Ile227 per José‐Daniel Aroca‐Aguilar, Francisco Sánchez‐Sánchez, Sikha Ghosh, Miguel Coca‐Prados, Julio Escribano
Publicat 2005Artigo -
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The Zinc-Metallothionein Redox System Reduces Oxidative Stress in Retinal Pigment Epithelial Cells per Sara Rodríguez-Menéndez, Montserrat García, Beatriz Fernández, Lydia Álvarez, Andrés Fernández-Vega-Cueto, Miguel Coca‐Prados, Rosario Pereiro, Héctor González‐Iglesias
Publicat 2018Artigo -
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Identification ofPKD2L,a HumanPKD2-Related Gene: Tissue-Specific Expression and Mapping to Chromosome 10q25 per Guanqing Wu, Tomohito Hayashi, Jong-Hoon Park, Mehul Dixit, David M. Reynolds, Li Li, Yoshiko Maeda, Yiqiang Cai, Miguel Coca‐Prados, Stefan Somlo
Publicat 1998Artigo -
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Sequence Analysis and Homology Modeling Suggest That Primary Congenital Glaucoma on 2p21 Results from Mutations Disrupting Either the Hinge Region or the Conserved Core Structures... per Ivaylo Stoilov, Nurten Akarsu, Ihuoma Alozie, Anne Child, Magda Barsoum‐Homsy, M. Erol Turaçlı, Meral Or, Richard A. Lewis, Nusret Özdemir, Glen Brice, Sedat Aktan, Line Chevrette, Miguel Coca‐Prados, Mansoor Sarfarazi
Publicat 1998Artigo -
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CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix per Juan‐Manuel Bonet‐Fernández, José‐Daniel Aroca‐Aguilar, Marta Cortón, Ana-Isabel Ramírez, Susana Alexandre-Moreno, María-Teresa García-Antón, J. Gomez Ma de Salazar, Jesús‐José Ferre‐Fernández, Raquel Atienzar-Aroca, Cristina Villaverde, Ionut-Florin Iancu, Alejandra Tamayo, Carmen Méndez-Hernández, Laura Morales‐Fernández, Blanca Rojas, Carmen Ayuso, Miguel Coca‐Prados, J.M. Martínez-de-la-Casa, J. García–Sánchez, Julio Escribano
Publicat 2020Artigo -
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Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci per Tin Aung, Mineo Ozaki, Mei Lee, Ursula Schlötzer‐Schrehardt, Guðmar Þorleifsson, Takanori Mizoguchi, Robert P. Igo, Aravind Haripriya, Susan Williams, Yury S Astakhov, Andrew Orr, Kathryn P. Burdon, S Nakano, Kazuhiko Mori, Khaled K. Abu‐Amero, Michael A. Hauser, Zheng Li, Prakadeeswari Gopalakrishnan, Jessica N. Cooke Bailey, Alina Popa‐Cherecheanu, Jae H. Kang, Sarah C. Nelson, Ken Hayashi, Shin-ichi Manabe, Shigeyasu Kazama, Tomasz Żarnowski, Kenji Inoue, Murat İrkeç, Miguel Coca‐Prados, Kazuhisa Sugiyama, Irma Järvelä, Patricio G. Schlottmann, S. Lerner, Hasnaa Lamari, Nilgün Yıldırım, Mukharram M. Bikbov, Ki Ho Park, Soon Cheol, Kenji Yamashiro, Juan Carlos Zenteno, Jost B. Jonas, Rajesh S. Kumar, Shamira Perera, Anita Chan, Nino Kobakhidze, Ronnie George, Lingam Vijaya, Tan Do, Deepak P. Edward, Lourdes de Juan Marcos, Mohammad Pakravan, Sasan Moghimi, Ryuichi Ideta, Daniella Bach‐Holm, Per Kappelgaard, Barbara Wirostko, Samuel Thomas, Daniel Gaston, Karen Bedard, Wenda Greer, Zhenglin Yang, Xueyi Chen, Lulin Huang, Jinghong Sang, Hongyan Jia, Liyun Jia, Chunyan Qiao, Hui Zhang, Xuyang Liu, Bowen Zhao, Ya Xing Wang, Liang Xu, Stéphanie Leruez, Pascal Reynier, George Chichua, S Tabagari, Steffen Uebe, Matthias Zenkel, Daniel Berner, Georg Mossböck, Nicole Weisschuh, Ursula Hoja, Ulrich-Christoph Welge-Luessen, Christian Y. Mardin, Panayiota Founti, A. Chatzikyriakidou, Theofanis Pappas, Eleftherios Anastasopoulos, Alexandros Lambropoulos, Arkasubhra Ghosh, Rohit Shetty, Natalia Porporato, Saravanan Vijayan, Rengaraj Venkatesh, Chandrashekaran Shivkumar, Narendran Kalpana, Sripriya Sarangapani, Mozhgan R. Kanavi, Afsaneh Naderi Beni, Shahin Yazdani
Publicat 2017Revisão
Eines de cerca:
Matèries relacionades
Biology
Biochemistry
Genetics
Cell biology
Gene
Chemistry
Molecular biology
Medicine
Homology (biology)
Intracellular
Neuroscience
Anatomy
Enzyme
Gene expression
Glaucoma
Metallothionein
Organic chemistry
Oxidative stress
Pathology
Peptide sequence
Trabecular meshwork
Zinc
ATPase
Adherens junction
Alpha (finance)
Amino acid
Anterior Eye Segment
Antioxidant
Autosomal dominant polycystic kidney disease
CYP24A1