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Seung-Yun Yoo

Showing results (1-10 of 7) with videos related to

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Human Molecular Genetics|January 22, 2005
Neuronal dysfunction in a polyglutamine disease model occurs in the absence of ubiquitin-proteasome system impairment and inversely correlates with the degree of nuclear inclusion formationAaron B Bowman, Seung-Yun Yoo, Nico P Dantuma, et al.
Neuron|January 3, 2006
Genetic interactions between doublecortin and doublecortin-like kinase in neuronal migration and axon outgrowthThomas A S Deuel, Judy S Liu, Joseph C Corbo, et al.
American Journal of Medical Genetics. Part A|June 9, 2006
An autosomal recessive form of spastic cerebral palsy (CP) with microcephaly and mental retardationAnna Rajab, Seung-Yun Yoo, Aiman Abdulgalil, et al.
Neuron|February 11, 2003
SCA7 knockin mice model human SCA7 and reveal gradual accumulation of mutant ataxin-7 in neurons and abnormalities in short-term plasticitySeung Yun Yoo, Mark E Pennesi, Edwin J Weeber, et al.
Science (New York, N.Y.)|July 16, 2008
Identifying autism loci and genes by tracing recent shared ancestryEric M Morrow, Seung-Yun Yoo, Steven W Flavell, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 8, 2016
Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive featuresQing Ouyang, Tojo Nakayama, Ozan Baytas, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 15, 2010
Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disordersMichael S L Ching, Yiping Shen, Wen-Hann Tan, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Human Molecular Genetics|January 22, 2005
Neuronal dysfunction in a polyglutamine disease model occurs in the absence of ubiquitin-proteasome system impairment and inversely correlates with the degree of nuclear inclusion formationAaron B Bowman, Seung-Yun Yoo, Nico P Dantuma, et al.
Neuron|January 3, 2006
Genetic interactions between doublecortin and doublecortin-like kinase in neuronal migration and axon outgrowthThomas A S Deuel, Judy S Liu, Joseph C Corbo, et al.
American Journal of Medical Genetics. Part A|June 9, 2006
An autosomal recessive form of spastic cerebral palsy (CP) with microcephaly and mental retardationAnna Rajab, Seung-Yun Yoo, Aiman Abdulgalil, et al.
Neuron|February 11, 2003
SCA7 knockin mice model human SCA7 and reveal gradual accumulation of mutant ataxin-7 in neurons and abnormalities in short-term plasticitySeung Yun Yoo, Mark E Pennesi, Edwin J Weeber, et al.
Science (New York, N.Y.)|July 16, 2008
Identifying autism loci and genes by tracing recent shared ancestryEric M Morrow, Seung-Yun Yoo, Steven W Flavell, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 8, 2016
Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive featuresQing Ouyang, Tojo Nakayama, Ozan Baytas, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 15, 2010
Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disordersMichael S L Ching, Yiping Shen, Wen-Hann Tan, et al.
Pageof 1