Charge-based separation of proteins and peptides by electrically induced dynamic pH profiles von Brod, E., S. Ben-Yosef, V., Bandhakavi, S., Sivan, U.

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Fragile-X Syndrome: Methods and Protocols von Ben-Yosef, Dalit, Mayshar, Yoav

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Induced Neurons for the Study of Neurodegenerative and Neurodevelopmental Disorders von Sauter, Evelyn J., Kutsche, Lisa K., Klapper, Simon D., Busskamp, Volker

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Pathophysiology Mechanisms in Fragile-X Primary Ovarian Insufficiency von Elizur, Shai E., Friedman Gohas, Moran, Dratviman-Storobinsky, Olga, Cohen, Yoram

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Assays for Determining Repeat Number, Methylation Status, and AGG Interruptions in the Fragile X-Related Disorders von Hayward, Bruce E., Usdin, Karen

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One-Step Generation of Seamless Luciferase Gene Knockin Using CRISPR/Cas9 Genome Editing in Human Pluripotent Stem Cells von Li, Meng, Hunt, Jack Faro Vander Stoep, Bhattacharyya, Anita, Zhao, Xinyu

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Using Human Neural Progenitor Cell Models to Conduct Large-Scale Drug Screens for Neurological and Psychiatric Diseases von Hunt, Jack Faro Vander Stoep, Li, Meng, Zhao, Xinyu, Bhattacharyya, Anita

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Modeling FXS: Human Pluripotent Stem Cells and In Vitro Neural Differentiation von Kuznitsov-Yanovsky, Liron, Mayshar, Yoav, Ben-Yosef, Dalit

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Fragile X Syndrome: Introduction von Reches, Adi

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Fragile X Syndrome Pre-Clinical Research: Comparing Mouse- and Human-Based Models von Telias, Michael

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Monitoring for Epigenetic Modifications at the FMR1 Locus von Epsztejn-Litman, Silvina, Eiges, Rachel

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Patch-Clamp Recordings from Human Embryonic Stem Cells-Derived Fragile X Neurons von Telias, Michael, Segal, Menahem

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Clinical Genetic Testing for Fragile X Syndrome by Polymerase Chain Reaction Amplification and Southern Blot Analyses von Cai, Xiaoqiang, Arif, Mohammad, Wan, Haolei, Kornreich, Ruth, Edelmann, Lisa J.

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Application of Drosophila Model Toward Understanding the Molecular Basis of Fragile X Syndrome von Kong, Ha Eun, Lim, Junghwa, Jin, Peng

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Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) von Zafarullah, Marwa, Tassone, Flora

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Modeling FXS with Mouse Neural Progenitors von Peteri, Ulla-Kaisa, Castrén, Maija L.

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Imaging of Somatic Ca2+ Transients in Differentiated Human Neurons von Vertkin, Irena, Ben-Yosef, Dalit

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A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia von Kohl, Susanne, Coppieters, Frauke, Meire, Françoise, Schaich, Simone, Roosing, Susanne, Brennenstuhl, Christina, Bolz, Sylvia, van Genderen, Maria M., Riemslag, Frans C.C., Lukowski, Robert, den Hollander, Anneke I., Cremers, Frans P.M., De Baere, Elfride, Hoyng, Carel B., Wissinger, Bernd

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Exome Sequencing and cis-Regulatory Mapping Identify Mutations in MAK, a Gene Encoding a Regulator of Ciliary Length, as a Cause of Retinitis Pigmentosa von Özgül, Rıza Köksal, Siemiatkowska, Anna M., Yücel, Didem, Myers, Connie A., Collin, Rob W.J., Zonneveld, Marijke N., Beryozkin, Avigail, Banin, Eyal, Hoyng, Carel B., van den Born, L. Ingeborgh, Bose, Ron, Shen, Wei, Sharon, Dror, Cremers, Frans P.M., Klevering, B. Jeroen, den Hollander, Anneke I., Corbo, Joseph C.

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Association of Sex With Frequent and Mild ABCA4 Alleles in Stargardt Disease von Runhart, Esmee H, Khan, Mubeen, Cornelis, Stéphanie S, Roosing, Susanne, Del Pozo-Valero, Marta, Lamey, Tina M, Liskova, Petra, Roberts, Lisa, Stöhr, Heidi, Klaver, Caroline C. W, Hoyng, Carel B, Cremers, Frans P. M, Dhaenens, Claire-Marie

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