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David L Nelson

Showing results (71-80 of 153) with videos related to

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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.
Neuron|August 19, 2007
RNA-binding proteins hnRNP A2/B1 and CUGBP1 suppress fragile X CGG premutation repeat-induced neurodegeneration in a Drosophila model of FXTASOyinkan A Sofola, Peng Jin, Yunlong Qin, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 30, 2011
FXR1P but not FMRP regulates the levels of mammalian brain-specific microRNA-9 and microRNA-124Xia-Lian Xu, Ruiting Zong, Zhaodong Li, et al.
Human Molecular Genetics|November 27, 2018
Metabolic pathways modulate the neuronal toxicity associated with fragile X-associated tremor/ataxia syndromeHa Eun Kong, Junghwa Lim, Feiran Zhang, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 14, 2006
Pharmacologic characterization of the cloned human trace amine-associated receptor1 (TAAR1) and evidence for species differences with the rat TAAR1David B Wainscott, Sheila P Little, Tinggui Yin, et al.
The Journal of Clinical Investigation|May 3, 2003
Second-site mutation in the Wiskott-Aldrich syndrome (WAS) protein gene causes somatic mosaicism in two WAS siblingsTaizo Wada, Akihiro Konno, Shepherd H Schurman, et al.
Human Molecular Genetics|October 11, 2013
Genome-wide alteration of 5-hydroxymethylcytosine in a mouse model of fragile X-associated tremor/ataxia syndromeBing Yao, Li Lin, R Craig Street, et al.
Pageof 16

Showing results (71-80 of 153) with videos related to

Sort By:
Pageof 16
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.
Neuron|August 19, 2007
RNA-binding proteins hnRNP A2/B1 and CUGBP1 suppress fragile X CGG premutation repeat-induced neurodegeneration in a Drosophila model of FXTASOyinkan A Sofola, Peng Jin, Yunlong Qin, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 30, 2011
FXR1P but not FMRP regulates the levels of mammalian brain-specific microRNA-9 and microRNA-124Xia-Lian Xu, Ruiting Zong, Zhaodong Li, et al.
Human Molecular Genetics|November 27, 2018
Metabolic pathways modulate the neuronal toxicity associated with fragile X-associated tremor/ataxia syndromeHa Eun Kong, Junghwa Lim, Feiran Zhang, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 14, 2006
Pharmacologic characterization of the cloned human trace amine-associated receptor1 (TAAR1) and evidence for species differences with the rat TAAR1David B Wainscott, Sheila P Little, Tinggui Yin, et al.
The Journal of Clinical Investigation|May 3, 2003
Second-site mutation in the Wiskott-Aldrich syndrome (WAS) protein gene causes somatic mosaicism in two WAS siblingsTaizo Wada, Akihiro Konno, Shepherd H Schurman, et al.
Human Molecular Genetics|October 11, 2013
Genome-wide alteration of 5-hydroxymethylcytosine in a mouse model of fragile X-associated tremor/ataxia syndromeBing Yao, Li Lin, R Craig Street, et al.
Pageof 16