Volume 31, 2017
Table of Contents
Latest Issue:
Volume 31, Issue 4, 2017
Special Issue: Neurogenetics in Spain
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Special Issue Articles
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Editorial
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Original Research Articles
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Orb2 as modulator of Brat and their role at the neuromuscular junction
Elena Santana & Sergio Casas-Tintó
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Overexpression of Drosophila frataxin triggers cell death in an iron-dependent manner
Oliver Edenharter, Janik Clement, Stephan Schneuwly, & Juan A. Navarro
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Review Articles
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The pigmented epithelium, a bright partner against photoreceptor degeneration
Joaquín Letelier, Paola Bovolenta & Juan R. Martínez-Morales
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Aberrant Wnt signaling: a special focus in CNS diseases
Mercedes Arnés & Sergio Casas Tintó
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María Luz Montesinos
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Haritz Plazaola-Sasieta, Alejandra Fernández-Pineda, Qi Zhu & Marta Morey
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Neurogenetics of Drosophila circadian clock: expect the unexpected
Patricia Jarabo & Francisco A. Martin
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Germán Cuesto, Claude Everaerts, Leticia G. León, & Angel Acebes
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Novel genetic approaches to behavior in Drosophila
Fernando Martín & Esther Alcorta
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Maria Julia Cambiasso, Carla Daniela Cisternas, Isabel Ruiz-Palmero, Maria Julia Scerbo, Maria Angeles Arevalo, Iñigo Azcoitia & Luis M. Garcia-Segura
Alejandro Sánchez-Gracia, Sara Guirao-Rico, Silvia Hinojosa-Alvarez & Julio Rozas
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Regular Submissions
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Letters to the Editor
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RE: Six novel rare non-synonymous mutations for migraine without aura identified by exome sequencing
Cassie L. Albury, Zachary Gerring, Lyn R. Griffiths, Dale R. Nyhol & Astrid J. Rodriguez-Acevedo
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Xiao-Ping Wang, Zhi-Xiang Xu, Xiao-Jing Sun & Xingguang Luo
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Original Research Articles
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Hongyu Ruan, Atsushi Ueda, Xiaomin Xing, Xuxuan Wan, Benjamin Strub, Spencer Mukai, Kaan Certel, David Green, Kyle Belozerov, Wei-Dong Yao, Wayne Johnson, Jim Jung-Ching Lin, Arthur J. Hilliker & Chun-Fang Wu
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Zhi Cheng, Yingchun Shang, Shan Gao & Tao Zhang
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Fatemeh Alizadeh, Javad Tavakkoly-Bazzaz, Ali Bozorgmehr, Asa’ad Azarnezhad, Mina Tabrizi & Esmaeil Shahsavand Ananloo
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Corrigendum
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Volume 31, Issue 3, 2017
Special Issue: Zebrafish: From Genes and Neurons to Circuits, Behavior and Disease
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Special Issue Articles
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Editorial
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Zebrafish: from genes and neurons to circuits, behavior and disease
Guest Editors Anand Chandrasekhar, Su Guo, Ichiro Masai, & Teresa Nicolson; Editor-in-Chief Chun-Fang Wu
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Review Articles
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Estuardo Robles
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Genetic approaches to retinal research in zebrafish
Stephanie Niklaus & Stephan C. F. Neuhauss
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Maria Iribarne & Ichiro Masai
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The genetics of hair-cell function in zebrafish
Teresa Nicolson
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Light on a sensory interface linking the cerebrospinal fluid to motor circuits in vertebrate
Lydia Djenoune & Claire Wyart
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Original Research Articles
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Role of branchiomotor neurons in controlling food intake of zebrafish larvae
James R. Allen, Kiran D. Bhattacharyya, Emilia Asante, Badr Almadi, Kyle Schafer, Jeremy Davis, Jane Cox, Mark Voigt, John A. Viator,
& Anand Chandrasekhar
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Heritable natural variation of an anxiety-like behavior in larval zebrafish
Mahendra Wagle , Juliana Nguyen, Shinwoo Lee, Noah Zaitlen, & Su Guo
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Regular Submissions
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Short Communication
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Primary familial brain calcifications linked with a novel SLC20A2 gene mutation in a Chinese family
Tao-Mian Mi, Wei Mao, Yan-Ning Cai, Cai-Xia Yang, Chao-Dong Wang, Er-He Xu, Hui Zhang, & Piu Chan
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Original Articles
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Ali Bozorgmehr, Mohammad Ghadirivasfi, & Esmaeil Shahsavand Ananloo
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LGMD2E is the most common type of sarcoglycanopathies in the Iranian population
Afagh Alavi, Sara Esmaeili, Yalda Nilipour, Shahriar Nafissi, Seyed Hasan Tonekaboni, Gholamreza Zamani, Mahmoud Reza Ashrafi, Kimia Kahrizi, Hossein Najmabadi, & Fatemeh Jazayeri
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Carolina de Paiva Lima, Daniel Almeida da Silva e Silva, Samara Damasceno, Andrea Frozino Ribeiro, Cristiane S. Rocha, Alexandre H. Berenguer de Matos, Diego Correia, Roseli Boerngen-Lacerda, & Ana Lúcia Brunialti Godard
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Volume 31, Issue 1-2, 2017
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Review
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Gene polymorphisms associated with temperament
Xiaoyan Qiu, Graeme B. Martin, & Dominique Blache
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Short Communications
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Drift diffusion model of reward and punishment learning in rare alpha-synuclein gene carriers
Ahmed A. Moustafa, Szabolcs Kéri, Bertalan Polner, & Corey White
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Novel PNKP mutation in siblings with ataxia-oculomotor apraxia type 4
Nicoline Schiess, Davis S. Zee, Khurram A. Siddiqui, Miklos Szolics, & Ayman W. El-Hattab
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A novel mutation in ALS2 associated with severe and progressive infantile onset of spastic paralysis
Huma Tariq, Shahid Mukthar, & Sadaf Naz
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Original Research Articles
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Fanggeng Zou, Kirsty McWalter, Lindsay Schmidt, Amy Decker, Jonathan D. Picker, Sharyn Lincoln, David A. Sweetser, Lauren C. Briere, Chellamani Harini, Members of the Undiagnosed Diseases Network, Eric Marsh, Livija Medne, Raymond Y. Wang, Karen Leydiker, Andrew Mower, Gepke Visser, Inge Cuppen, Koen L. van Gassen, Jasper van der Smagt, Adeel Yousaf, Michael Tennison, Anita Shanmugham, Elizabeth Butler, Gabriele Richard & Dianalee McKnight
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Astroglial transcriptome dysregulation in early disease of an ALS mutant SOD1 mouse model
Sean J. Miller, Ping-wu Zhang, Jenna Glatzer, & Jeffrey D. Rothstein
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Quantitative analysis of visually induced courtship elements in Drosophila subobscura
Tomohiro Higuchi, Soh Kohatsu, & Daisuke Yamamoto