Krishna Deo Sharma
Assistant Professor
faculty
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Biography and Research Information
OverviewAI-generated summary
Krishna Deo Sharma investigates the differentiation of neural stem cells and their potential applications in treating neurological conditions. His work includes studying the use of functionalized nanocellulose and gold nanorod substrates to guide rat fetal neural stem cells toward neuronal and oligodendrocyte differentiation, respectively. Sharma has also explored the role of TEMPO cellulose in supporting neural stem cell survival and differentiation. Beyond stem cell research, his publications address advancements in spinal cord injury treatment and potential therapeutic targets for neuropathic pain associated with diabetic peripheral neuropathy. He has also contributed to studies on anatomical variations, such as the absence of the fourth slip of the flexor digitorum brevis in the Nepalese population. Sharma's research network includes collaborators from Arkansas State University, with whom he has co-authored multiple publications.
Metrics
- h-index: 7
- Publications: 14
- Citations: 178
Selected Publications
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CAP1 (cyclase-associated protein 1) mediates the cyclic AMP signals that activate Rap1 in stimulating matrix adhesion of colon cancer cells (2023)
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Letters to the editor: Nicotinic acetylcholine receptor ligands as potential targets for managing neuropathic pain induced by diabetic peripheral neuropathy (2022)
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Gold Nanorod Substrate for Rat Fetal Neural Stem Cell Differentiation into Oligodendrocytes (2022)
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Functionalized Nanocellulose Drives Neural Stem Cells toward Neuronal Differentiation (2021)
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Absence of Fourth Slip of Flexor Digitorum Brevis in Nepalese Population (2021)
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Delving into the recent advancements of spinal cord injury treatment: a review of recent progress (2021)
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TEMPO Cellulose Supports Survival and <i>in vitro</i> Differentiation of Rat Neural Stem Cell (2021)
Collaboration Network
Top Collaborators
- CAP1 (cyclase-associated protein 1) mediates the cyclic AMP signals that activate Rap1 in stimulating matrix adhesion of colon cancer cells
- Functionalized Nanocellulose Drives Neural Stem Cells toward Neuronal Differentiation
- Gold Nanorod Substrate for Rat Fetal Neural Stem Cell Differentiation into Oligodendrocytes
- Letters to the editor: Nicotinic acetylcholine receptor ligands as potential targets for managing neuropathic pain induced by diabetic peripheral neuropathy
- TEMPO Cellulose Supports Survival and <i>in vitro</i> Differentiation of Rat Neural Stem Cell
- Functionalized Nanocellulose Drives Neural Stem Cells toward Neuronal Differentiation
- Gold Nanorod Substrate for Rat Fetal Neural Stem Cell Differentiation into Oligodendrocytes
- TEMPO Cellulose Supports Survival and <i>in vitro</i> Differentiation of Rat Neural Stem Cell
- CAP1 (cyclase-associated protein 1) mediates the cyclic AMP signals that activate Rap1 in stimulating matrix adhesion of colon cancer cells
- Gold Nanorod Substrate for Rat Fetal Neural Stem Cell Differentiation into Oligodendrocytes
- TEMPO Cellulose Supports Survival and <i>in vitro</i> Differentiation of Rat Neural Stem Cell
- TEMPO Cellulose Supports Survival and <i>in vitro</i> Differentiation of Rat Neural Stem Cell
- Delving into the recent advancements of spinal cord injury treatment: a review of recent progress
- Delving into the recent advancements of spinal cord injury treatment: a review of recent progress
- Absence of Fourth Slip of Flexor Digitorum Brevis in Nepalese Population
- Absence of Fourth Slip of Flexor Digitorum Brevis in Nepalese Population
- Functionalized Nanocellulose Drives Neural Stem Cells toward Neuronal Differentiation
- Functionalized Nanocellulose Drives Neural Stem Cells toward Neuronal Differentiation
- Functionalized Nanocellulose Drives Neural Stem Cells toward Neuronal Differentiation
- Functionalized Nanocellulose Drives Neural Stem Cells toward Neuronal Differentiation
- Functionalized Nanocellulose Drives Neural Stem Cells toward Neuronal Differentiation
- Gold Nanorod Substrate for Rat Fetal Neural Stem Cell Differentiation into Oligodendrocytes
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