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Human Molecular Genetics|May 6, 2006
Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteinsCorinne M Spencer, Ekaterina Serysheva, Lisa A Yuva-Paylor, et al.
American Journal of Human Genetics|December 31, 2005
Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier?Tohru Matsuura, Ping Fang, Christopher E Pearson, et al.
Human Molecular Genetics|April 21, 2009
Ectopic expression of CGG containing mRNA is neurotoxic in mammalsVera Hashem, Jocelyn N Galloway, Mayra Mori, et al.
European Journal of Haematology|November 21, 2008
Possible application of flow cytometry for evaluation of the structure and functional status of WASP in peripheral blood mononuclear cellsMasaru Nakajima, Masafumi Yamada, Koji Yamaguchi, et al.
Genetics and Molecular Research : GMR|February 14, 2004
Inheritance of acylsugar contents in tomatoes derived from an interspecific cross with the wild tomato Lycopersicon pennellii and their effect on spider mite repellenceJuliano T V Resende, Wilson Roberto Maluf, Maria das Graças Cardoso, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2012
AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndromeCarolyn M Yrigollen, Blythe Durbin-Johnson, Louise Gane, et al.
The American Journal of Occupational Therapy : Official Publication of the American Occupational Therapy Association|February 9, 2002
Interrater reliability, concurrent validity, responsiveness, and predictive validity of the Melville-Nelson Self-Care AssessmentDavid L Nelson, Lisa Link Melville, Julie D Wilkerson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 10, 2008
The Drosophila FMRP and LARK RNA-binding proteins function together to regulate eye development and circadian behaviorOyinkan Sofola, Vasudha Sundram, Fanny Ng, et al.
European Journal of Human Genetics : EJHG|October 2, 2014
MBD5 haploinsufficiency is associated with sleep disturbance and disrupts circadian pathways common to Smith-Magenis and fragile X syndromesSureni V Mullegama, Loren Pugliesi, Brooke Burns, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 8, 2016
Selective Deletion of Astroglial FMRP Dysregulates Glutamate Transporter GLT1 and Contributes to Fragile X Syndrome Phenotypes In VivoHaruki Higashimori, Christina S Schin, Ming Sum R Chiang, et al.
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