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Solen Gokhan

Researcher at Albert Einstein College of Medicine

Publications -  37
Citations -  6870

Solen Gokhan is an academic researcher from Albert Einstein College of Medicine. The author has contributed to research in topics: Neural stem cell & Neurogenesis. The author has an hindex of 26, co-authored 37 publications receiving 5885 citations. Previous affiliations of Solen Gokhan include Yeshiva University.

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Fate Mapping Analysis Reveals That Adult Microglia Derive from Primitive Macrophages

TL;DR: Results identify microglia as an ontogenically distinct population in the mononuclear phagocyte system and have implications for the use of embryonically derived microglial progenitors for the treatment of various brain disorders.
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Long noncoding RNAs in neuronal-glial fate specification and oligodendrocyte lineage maturation

TL;DR: This is the first report of long ncRNAs expression in neuronal and glial cell differentiation and of the modulation of ncRNA expression by modification of chromatin architecture.
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The CSF-1 receptor ligands IL-34 and CSF-1 exhibit distinct developmental brain expression patterns and regulate neural progenitor cell maintenance and maturation

TL;DR: Compared to wild type mice, CSF-1R-deficient mice have smaller brains of greater mass and ablation of the Csf1r gene in Nestin-positive neural progenitors led to a smaller brain size, an expanded Neural progenitor pool and elevated cellular apoptosis in cortical forebrain, indicating novel roles for the CSF/IL-34 receptor in the regulation of corticogenesis.
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Developmental changes in progenitor cell responsiveness to bone morphogenetic proteins differentially modulate progressive CNS lineage fate.

TL;DR: Observations suggest that developmental changes in neural progenitor cell responsiveness to the BMPs may represent a novel mechanism for orchestrating context-specific cellular events such as lineage elaboration and cellular viability.
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Emerging Roles for CSF-1 Receptor and its Ligands in the Nervous System

TL;DR: The roles of the CSF-1R and its ligands in microglial and neural development and function, and their relevance to the understanding of neurodegenerative disease are reviewed.