

Volume 31, 2017
Table of Contents


Latest Issue:
Volume 31, Issue 4, 2017
Special Issue: Neurogenetics in Spain
Special Issue Articles
Editorial
Original Research Articles
Orb2 as modulator of Brat and their role at the neuromuscular junction
Elena Santana & Sergio Casas-Tintó
Overexpression of Drosophila frataxin triggers cell death in an iron-dependent manner
Oliver Edenharter, Janik Clement, Stephan Schneuwly, & Juan A. Navarro
Review Articles
The pigmented epithelium, a bright partner against photoreceptor degeneration
Joaquín Letelier, Paola Bovolenta & Juan R. Martínez-Morales
Aberrant Wnt signaling: a special focus in CNS diseases
Mercedes Arnés & Sergio Casas Tintó
María Luz Montesinos
Haritz Plazaola-Sasieta, Alejandra Fernández-Pineda, Qi Zhu & Marta Morey
Neurogenetics of Drosophila circadian clock: expect the unexpected
Patricia Jarabo & Francisco A. Martin
Germán Cuesto, Claude Everaerts, Leticia G. León, & Angel Acebes
Novel genetic approaches to behavior in Drosophila
Fernando Martín & Esther Alcorta
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
Regular Submissions
Letters to the Editor
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
Xiao-Ping Wang, Zhi-Xiang Xu, Xiao-Jing Sun & Xingguang Luo
Original Research Articles
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
Zhi Cheng, Yingchun Shang, Shan Gao & Tao Zhang
Fatemeh Alizadeh, Javad Tavakkoly-Bazzaz, Ali Bozorgmehr, Asa’ad Azarnezhad, Mina Tabrizi & Esmaeil Shahsavand Ananloo
Corrigendum
Volume 31, Issue 3, 2017
Special Issue: Zebrafish: From Genes and Neurons to Circuits, Behavior and Disease
Special Issue Articles
Editorial
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
Review Articles
Estuardo Robles
Genetic approaches to retinal research in zebrafish
Stephanie Niklaus & Stephan C. F. Neuhauss
Maria Iribarne & Ichiro Masai
The genetics of hair-cell function in zebrafish
Teresa Nicolson
Light on a sensory interface linking the cerebrospinal fluid to motor circuits in vertebrate
Lydia Djenoune & Claire Wyart
Original Research Articles
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
Heritable natural variation of an anxiety-like behavior in larval zebrafish
Mahendra Wagle , Juliana Nguyen, Shinwoo Lee, Noah Zaitlen, & Su Guo
Regular Submissions
Short Communication
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
Original Articles
Ali Bozorgmehr, Mohammad Ghadirivasfi, & Esmaeil Shahsavand Ananloo
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
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
Volume 31, Issue 1-2, 2017
Review
Gene polymorphisms associated with temperament
Xiaoyan Qiu, Graeme B. Martin, & Dominique Blache
Short Communications
Drift diffusion model of reward and punishment learning in rare alpha-synuclein gene carriers
Ahmed A. Moustafa, Szabolcs Kéri, Bertalan Polner, & Corey White
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
A novel mutation in ALS2 associated with severe and progressive infantile onset of spastic paralysis
Huma Tariq, Shahid Mukthar, & Sadaf Naz
Original Research Articles
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
Astroglial transcriptome dysregulation in early disease of an ALS mutant SOD1 mouse model
Sean J. Miller, Ping-wu Zhang, Jenna Glatzer, & Jeffrey D. Rothstein
Quantitative analysis of visually induced courtship elements in Drosophila subobscura
Tomohiro Higuchi, Soh Kohatsu, & Daisuke Yamamoto