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Frontiers in Cellular Neuroscience
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August 22, 2012
Lipocalin 2 is present in the EAE brain and is modulated by natalizumab
Fernanda Marques, Sandro D Mesquita, João C Sousa, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
July 2, 2008
Targeting of VX2 rabbit liver tumor by selective delivery of 3-bromopyruvate: a biodistribution and survival study
Mustafa Vali, Josephina A Vossen, Manon Buijs, et al.
American Journal of Human Genetics
|
June 26, 2012
Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders
Rui Luo, Stephan J Sanders, Yuan Tian, et al.
Archives of Neurology
|
May 21, 2003
Novel tau polymorphisms, tau haplotypes, and splicing in familial and sporadic frontotemporal dementia
Maria-Jesús Sobrido, Bruce L Miller, Necat Havlioglu, et al.
Nature Medicine
|
November 29, 2011
Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome
Sergiu P Paşca, Thomas Portmann, Irina Voineagu, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 15, 2013
The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors
Joseph D Dougherty, Susan E Maloney, David F Wozniak, et al.
Biorxiv : the Preprint Server for Biology
|
November 26, 2025
Dysregulation of transcription networks regulating oligodendrogenesis in age-related decline in CNS remyelination
Penelope Dimas, Samuel Morabito, Khalil S Rawji, et al.
Journal of Neurology
|
April 14, 2009
Two novel CYP7B1 mutations in Italian families with SPG5: a clinical and genetic study
Chiara Criscuolo, Alessandro Filla, Giovanni Coppola, et al.
Science Translational Medicine
|
November 5, 2010
Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2
Ashley A Scott-Van Zeeland, Brett S Abrahams, Ana I Alvarez-Retuerto, et al.
Cell
|
October 4, 2011
Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits
Olga Peñagarikano, Brett S Abrahams, Edward I Herman, et al.
Page
of 81
Search research articles
Search
Showing results (531-540 of 809) with videos related to
Sort By:
Page
of 81
Frontiers in Cellular Neuroscience
|
August 22, 2012
Lipocalin 2 is present in the EAE brain and is modulated by natalizumab
Fernanda Marques, Sandro D Mesquita, João C Sousa, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
July 2, 2008
Targeting of VX2 rabbit liver tumor by selective delivery of 3-bromopyruvate: a biodistribution and survival study
Mustafa Vali, Josephina A Vossen, Manon Buijs, et al.
American Journal of Human Genetics
|
June 26, 2012
Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders
Rui Luo, Stephan J Sanders, Yuan Tian, et al.
Archives of Neurology
|
May 21, 2003
Novel tau polymorphisms, tau haplotypes, and splicing in familial and sporadic frontotemporal dementia
Maria-Jesús Sobrido, Bruce L Miller, Necat Havlioglu, et al.
Nature Medicine
|
November 29, 2011
Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome
Sergiu P Paşca, Thomas Portmann, Irina Voineagu, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 15, 2013
The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors
Joseph D Dougherty, Susan E Maloney, David F Wozniak, et al.
Biorxiv : the Preprint Server for Biology
|
November 26, 2025
Dysregulation of transcription networks regulating oligodendrogenesis in age-related decline in CNS remyelination
Penelope Dimas, Samuel Morabito, Khalil S Rawji, et al.
Journal of Neurology
|
April 14, 2009
Two novel CYP7B1 mutations in Italian families with SPG5: a clinical and genetic study
Chiara Criscuolo, Alessandro Filla, Giovanni Coppola, et al.
Science Translational Medicine
|
November 5, 2010
Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2
Ashley A Scott-Van Zeeland, Brett S Abrahams, Ana I Alvarez-Retuerto, et al.
Cell
|
October 4, 2011
Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits
Olga Peñagarikano, Brett S Abrahams, Edward I Herman, et al.
Page
of 81