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Carl Dobkin

Showing results (11-20 of 26) with videos related to

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Gene|December 26, 2012
A 5-methylcytosine hotspot responsible for the prevalent HSD17B10 mutationSong-Yu Yang, Carl Dobkin, Xue-Ying He, et al.
American Journal of Medical Genetics. Part A|December 13, 2007
Fragile X full mutation alleles composed of few alleles: implications for CGG repeat expansionSarah L Nolin, Xiao-hua Ding, George E Houck, et al.
The Journal of Steroid Biochemistry and Molecular Biology|July 11, 2014
Roles of 17β-hydroxysteroid dehydrogenase type 10 in neurodegenerative disordersSong-Yu Yang, Xue-Ying He, Charles Isaacs, et al.
Plos One|May 23, 2012
The therapeutic effect of memantine through the stimulation of synapse formation and dendritic spine maturation in autism and fragile X syndromeHongen Wei, Carl Dobkin, Ashfaq M Sheikh, et al.
Neuroscience Letters|March 10, 2005
Decreased GABA(A) receptor expression in the seizure-prone fragile X mouseAbdeslem El Idrissi, Xiao-Hua Ding, Jason Scalia, et al.
Genes|October 23, 2021
Development of a Quantitative FMRP Assay for Mouse Tissue ApplicationsTatyana Adayev, Giuseppe LaFauci, Weimin Xu, et al.
Journal of Neuroinflammation|May 21, 2011
IL-6 is increased in the cerebellum of autistic brain and alters neural cell adhesion, migration and synaptic formationHongen Wei, Hua Zou, Ashfaq M Sheikh, et al.
Prenatal Diagnosis|July 1, 2011
Fragile X analysis of 1112 prenatal samples from 1991 to 2010Sarah L Nolin, Anne Glicksman, Xiaohua Ding, et al.
The Journal of Molecular Diagnostics : JMD|May 11, 2013
Fragile X screening by quantification of FMRP in dried blood spots by a Luminex immunoassayGiuseppe LaFauci, Tatyana Adayev, Richard Kascsak, et al.
American Journal of Medical Genetics. Part A|May 20, 2011
Terminal deletions of the long arm of chromosome X that include the FMR1 gene in female patients: a case seriesNaomi Yachelevich, Julia Klein Gittler, Susan Klugman, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Gene|December 26, 2012
A 5-methylcytosine hotspot responsible for the prevalent HSD17B10 mutationSong-Yu Yang, Carl Dobkin, Xue-Ying He, et al.
American Journal of Medical Genetics. Part A|December 13, 2007
Fragile X full mutation alleles composed of few alleles: implications for CGG repeat expansionSarah L Nolin, Xiao-hua Ding, George E Houck, et al.
The Journal of Steroid Biochemistry and Molecular Biology|July 11, 2014
Roles of 17β-hydroxysteroid dehydrogenase type 10 in neurodegenerative disordersSong-Yu Yang, Xue-Ying He, Charles Isaacs, et al.
Plos One|May 23, 2012
The therapeutic effect of memantine through the stimulation of synapse formation and dendritic spine maturation in autism and fragile X syndromeHongen Wei, Carl Dobkin, Ashfaq M Sheikh, et al.
Neuroscience Letters|March 10, 2005
Decreased GABA(A) receptor expression in the seizure-prone fragile X mouseAbdeslem El Idrissi, Xiao-Hua Ding, Jason Scalia, et al.
Genes|October 23, 2021
Development of a Quantitative FMRP Assay for Mouse Tissue ApplicationsTatyana Adayev, Giuseppe LaFauci, Weimin Xu, et al.
Journal of Neuroinflammation|May 21, 2011
IL-6 is increased in the cerebellum of autistic brain and alters neural cell adhesion, migration and synaptic formationHongen Wei, Hua Zou, Ashfaq M Sheikh, et al.
Prenatal Diagnosis|July 1, 2011
Fragile X analysis of 1112 prenatal samples from 1991 to 2010Sarah L Nolin, Anne Glicksman, Xiaohua Ding, et al.
The Journal of Molecular Diagnostics : JMD|May 11, 2013
Fragile X screening by quantification of FMRP in dried blood spots by a Luminex immunoassayGiuseppe LaFauci, Tatyana Adayev, Richard Kascsak, et al.
American Journal of Medical Genetics. Part A|May 20, 2011
Terminal deletions of the long arm of chromosome X that include the FMR1 gene in female patients: a case seriesNaomi Yachelevich, Julia Klein Gittler, Susan Klugman, et al.
Pageof 3