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Journal of Neuroimmune Pharmacology : the Official Journal of the Society on Neuroimmune Pharmacology
|
April 18, 2016
B-Cell Depletion Reduces the Maturation of Cerebral Cavernous Malformations in Murine Models
Changbin Shi, Robert Shenkar, Hussein A Zeineddine, et al.
European Journal of Medical Genetics
|
September 16, 2014
NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathy
Ahmet Okay Caglayan, Sinan Comu, Jacob F Baranoski, et al.
Frontiers in Cellular Neuroscience
|
October 17, 2019
Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in <i>ATP1A3</i>
August A Allocco, Sheng Chih Jin, Phan Q Duy, et al.
Biorxiv : the Preprint Server for Biology
|
April 10, 2026
Human claustrum neurons encode uncertainty and prediction errors during aversive learning
Mingyue Hu, Rodrigo Dalvit, Mauricio Medina-Pizarro, et al.
Nature Neuroscience
|
August 15, 2017
AAV-mediated direct in vivo CRISPR screen identifies functional suppressors in glioblastoma
Ryan D Chow, Christopher D Guzman, Guangchuan Wang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 15, 2014
Exceptional aggressiveness of cerebral cavernous malformation disease associated with PDCD10 mutations
Robert Shenkar, Changbin Shi, Tania Rebeiz, et al.
Journal of the American Heart Association
|
August 29, 2025
Characterizing Stroke Clots Using Single-Cell Sequencing
Daniela Renedo, Tanyeri Barak, Jonathan DeLong, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 17, 2003
Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype
Matthew W State, John M Greally, Adam Cuker, et al.
Journal of Neurosurgery
|
December 4, 2020
Clinical and genomic factors associated with seizures in meningiomas
Trisha P Gupte, Chang Li, Lan Jin, et al.
Journal of Medical Genetics
|
November 30, 2018
MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive <i>c</i>erebellar, <i>o</i>cular, cranio<i>f</i>acial and <i>g</i>enital features (COFG syndrome)
Abolfazl Rad, Umut Altunoglu, Rebecca Miller, et al.
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of 12
Search research articles
Search
Showing results (61-70 of 118) with videos related to
Sort By:
Page
of 12
Journal of Neuroimmune Pharmacology : the Official Journal of the Society on Neuroimmune Pharmacology
|
April 18, 2016
B-Cell Depletion Reduces the Maturation of Cerebral Cavernous Malformations in Murine Models
Changbin Shi, Robert Shenkar, Hussein A Zeineddine, et al.
European Journal of Medical Genetics
|
September 16, 2014
NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathy
Ahmet Okay Caglayan, Sinan Comu, Jacob F Baranoski, et al.
Frontiers in Cellular Neuroscience
|
October 17, 2019
Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in <i>ATP1A3</i>
August A Allocco, Sheng Chih Jin, Phan Q Duy, et al.
Biorxiv : the Preprint Server for Biology
|
April 10, 2026
Human claustrum neurons encode uncertainty and prediction errors during aversive learning
Mingyue Hu, Rodrigo Dalvit, Mauricio Medina-Pizarro, et al.
Nature Neuroscience
|
August 15, 2017
AAV-mediated direct in vivo CRISPR screen identifies functional suppressors in glioblastoma
Ryan D Chow, Christopher D Guzman, Guangchuan Wang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 15, 2014
Exceptional aggressiveness of cerebral cavernous malformation disease associated with PDCD10 mutations
Robert Shenkar, Changbin Shi, Tania Rebeiz, et al.
Journal of the American Heart Association
|
August 29, 2025
Characterizing Stroke Clots Using Single-Cell Sequencing
Daniela Renedo, Tanyeri Barak, Jonathan DeLong, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 17, 2003
Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype
Matthew W State, John M Greally, Adam Cuker, et al.
Journal of Neurosurgery
|
December 4, 2020
Clinical and genomic factors associated with seizures in meningiomas
Trisha P Gupte, Chang Li, Lan Jin, et al.
Journal of Medical Genetics
|
November 30, 2018
MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive <i>c</i>erebellar, <i>o</i>cular, cranio<i>f</i>acial and <i>g</i>enital features (COFG syndrome)
Abolfazl Rad, Umut Altunoglu, Rebecca Miller, et al.
Page
of 12