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Neuro-Oncology Advances
|
February 27, 2023
Novel genetically engineered H3.3G34R model reveals cooperation with ATRX loss in upregulation of <i>Hoxa</i> cluster genes and promotion of neuronal lineage
Aalaa S Abdallah, Herminio J Cardona, Samantha L Gadd, et al.
Cell Reports
|
October 13, 2016
Voluntary Running Triggers VGF-Mediated Oligodendrogenesis to Prolong the Lifespan of Snf2h-Null Ataxic Mice
Matías Alvarez-Saavedra, Yves De Repentigny, Doo Yang, et al.
Human Molecular Genetics
|
May 12, 2023
A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defects
Rebekah Tillotson, Keqin Yan, Julie Ruston, et al.
EMBO Reports
|
March 1, 2024
PHF6-mediated transcriptional control of NSC via Ephrin receptors is impaired in the intellectual disability syndrome BFLS
Dilan Rasool, Audrey Burban, Ahmad Sharanek, et al.
Biorxiv : the Preprint Server for Biology
|
April 1, 2024
Conditional c-MYC activation in catecholaminergic cells drives distinct neuroendocrine tumors: neuroblastoma vs somatostatinoma
Tingting Wang, Lingling Liu, Jie Fang, et al.
Cancer Research
|
November 12, 2024
Conditional Activation of c-MYC in Distinct Catecholaminergic Cells Drives Development of Neuroblastoma or Somatostatinoma
Tingting Wang, Lingling Liu, Jie Fang, et al.
Theranostics
|
October 21, 2024
Single-cell profiling of brain pericyte heterogeneity following ischemic stroke unveils distinct pericyte subtype-targeted neural reprogramming potential and its underlying mechanisms
Allison Loan, Nidaa Awaja, Margarita Lui, et al.
Nature Communications
|
March 15, 2018
Atrx inactivation drives disease-defining phenotypes in glioma cells of origin through global epigenomic remodeling
Carla Danussi, Promita Bose, Prasanna T Parthasarathy, et al.
Nature Communications
|
June 21, 2014
Snf2h-mediated chromatin organization and histone H1 dynamics govern cerebellar morphogenesis and neural maturation
Matías Alvarez-Saavedra, Yves De Repentigny, Pamela S Lagali, et al.
Nature Communications
|
November 10, 2025
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition
Ghayda M Mirzaa, Keqin Yan, Raissa Relator, et al.
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Search research articles
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Showing results (51-60 of 60) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 60 results.
Neuro-Oncology Advances
|
February 27, 2023
Novel genetically engineered H3.3G34R model reveals cooperation with ATRX loss in upregulation of <i>Hoxa</i> cluster genes and promotion of neuronal lineage
Aalaa S Abdallah, Herminio J Cardona, Samantha L Gadd, et al.
Cell Reports
|
October 13, 2016
Voluntary Running Triggers VGF-Mediated Oligodendrogenesis to Prolong the Lifespan of Snf2h-Null Ataxic Mice
Matías Alvarez-Saavedra, Yves De Repentigny, Doo Yang, et al.
Human Molecular Genetics
|
May 12, 2023
A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defects
Rebekah Tillotson, Keqin Yan, Julie Ruston, et al.
EMBO Reports
|
March 1, 2024
PHF6-mediated transcriptional control of NSC via Ephrin receptors is impaired in the intellectual disability syndrome BFLS
Dilan Rasool, Audrey Burban, Ahmad Sharanek, et al.
Biorxiv : the Preprint Server for Biology
|
April 1, 2024
Conditional c-MYC activation in catecholaminergic cells drives distinct neuroendocrine tumors: neuroblastoma vs somatostatinoma
Tingting Wang, Lingling Liu, Jie Fang, et al.
Cancer Research
|
November 12, 2024
Conditional Activation of c-MYC in Distinct Catecholaminergic Cells Drives Development of Neuroblastoma or Somatostatinoma
Tingting Wang, Lingling Liu, Jie Fang, et al.
Theranostics
|
October 21, 2024
Single-cell profiling of brain pericyte heterogeneity following ischemic stroke unveils distinct pericyte subtype-targeted neural reprogramming potential and its underlying mechanisms
Allison Loan, Nidaa Awaja, Margarita Lui, et al.
Nature Communications
|
March 15, 2018
Atrx inactivation drives disease-defining phenotypes in glioma cells of origin through global epigenomic remodeling
Carla Danussi, Promita Bose, Prasanna T Parthasarathy, et al.
Nature Communications
|
June 21, 2014
Snf2h-mediated chromatin organization and histone H1 dynamics govern cerebellar morphogenesis and neural maturation
Matías Alvarez-Saavedra, Yves De Repentigny, Pamela S Lagali, et al.
Nature Communications
|
November 10, 2025
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition
Ghayda M Mirzaa, Keqin Yan, Raissa Relator, et al.
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of 6