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Folia Morphologica|December 16, 2006
The neuronal structure of the dorsal nucleus of the lateral geniculate body in the common shrew (Sorex araneus) and the bank vole (Clethrionomys glareolus): Golgi and Nissl studiesJ Najdzion, B Wasilewska, S Szteyn, et al.Anatomia, Histologia, Embryologia|September 5, 2014
Distribution of Galanin and Galanin Receptor 2 in the Pre-optic Area of the Female Guinea PigB Hermanowicz, K Bogus-Nowakowska, M Równiak, et al.Experimental Neurology|November 22, 2001
Cerebrospinal fluid contains biologically active bone morphogenetic protein-7B Dattatreyamurty, E Roux, C Horbinski, et al.Brain : a Journal of Neurology|November 16, 2017
Excessive burden of lysosomal storage disorder gene variants in Parkinson's diseaseLaurie A Robak, Iris E Jansen, Jeroen van Rooij, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 14, 2008
Synaptic function for the Nogo-66 receptor NgR1: regulation of dendritic spine morphology and activity-dependent synaptic strengthHakjoo Lee, Stephen J Raiker, Karthik Venkatesh, et al.Human Molecular Genetics|March 3, 2016
Missense variants in the middle domain of DNM1L in cases of infantile encephalopathy alter peroxisomes and mitochondria when assayed in DrosophilaYu-Hsin Chao, Laurie A Robak, Fan Xia, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 8, 2009
Molecular basis of the interactions of the Nogo-66 receptor and its homolog NgR2 with myelin-associated glycoprotein: development of NgROMNI-Fc, a novel antagonist of CNS myelin inhibitionLaurie A Robak, Karthik Venkatesh, Hakjoo Lee, et al.Cold Spring Harbor Molecular Case Studies|March 10, 2019
De novo missense variant in the GTPase effector domain (GED) of DNM1L leads to static encephalopathy and seizuresNurit Assia Batzir, Pranjali K Bhagwat, Tanya N Eble, et al.Human Mutation|July 10, 2020
The expanding clinical phenotype of germline ABL1-associated congenital heart defects and skeletal malformations syndromeChun-An Chen, Emeline Crutcher, Harinder Gill, et al.Journal of Genetics and Genomics = Yi Chuan Xue Bao|October 5, 2024
RFC2 may contribute to the pathogenicity of Williams syndrome revealed in a zebrafish modelJi-Won Park, Tae-Ik Choi, Tae-Yoon Kim, et al.Pageof 5