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Showing 1 to 12 of 12 entries
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Role of mesenchymal stem cells in neurogenesis and nervous system repair.

Neurochemistry international

Maltman DJ, Hardy SA, Przyborski SA.
PMID: 21718735
Neurochem Int. 2011 Sep;59(3):347-56. doi: 10.1016/j.neuint.2011.06.008. Epub 2011 Jun 21.

Bone marrow-derived mesenchymal stem cells (MSCs) are attractive candidates for use in regenerative medicine since they are easily accessible and can be readily expanded in vivo, and possess unique immunogenic properties. Moreover, these multipotent cells display intriguing environmental adaptability...

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Maltman DJ, Hardy SA, Przyborski SA. Role of mesenchymal stem cells in neurogenesis and nervous system repair. Neurochem Int. 2011;59(3):347-56doi: 10.1016/j.neuint.2011.06.008.
Maltman, D. J., Hardy, S. A., & Przyborski, S. A. (2011). Role of mesenchymal stem cells in neurogenesis and nervous system repair. Neurochemistry international, 59(3), 347-56. https://doi.org/10.1016/j.neuint.2011.06.008
Maltman, Daniel J, et al. "Role of mesenchymal stem cells in neurogenesis and nervous system repair." Neurochemistry international vol. 59,3 (2011): 347-56. doi: https://doi.org/10.1016/j.neuint.2011.06.008
Maltman DJ, Hardy SA, Przyborski SA. Role of mesenchymal stem cells in neurogenesis and nervous system repair. Neurochem Int. 2011 Sep;59(3):347-56. doi: 10.1016/j.neuint.2011.06.008. Epub 2011 Jun 21. PMID: 21718735.
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Tracing single-cell histories.

Science (New York, N.Y.)

Lee JH.
PMID: 29420280
Science. 2018 Feb 02;359(6375):521-522. doi: 10.1126/science.aar6335. Epub 2018 Feb 01.

No abstract available.

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Lee JH. Tracing single-cell histories. Science. 2018;359(6375):521-522doi: 10.1126/science.aar6335.
Lee, J. H. (2018). Tracing single-cell histories. Science (New York, N.Y.), 359(6375), 521-522. https://doi.org/10.1126/science.aar6335
Lee, Je H. "Tracing single-cell histories." Science (New York, N.Y.) vol. 359,6375 (2018): 521-522. doi: https://doi.org/10.1126/science.aar6335
Lee JH. Tracing single-cell histories. Science. 2018 Feb 02;359(6375):521-522. doi: 10.1126/science.aar6335. Epub 2018 Feb 01. PMID: 29420280; PMCID: PMC5812680.
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Cell-Derived Exosome Therapy: A Novel Approach to Treat Post-traumatic Brain Injury Mediated Neural Injury.

ACS chemical neuroscience

Ghosh S, Garg S, Ghosh S.
PMID: 32609493
ACS Chem Neurosci. 2020 Jul 15;11(14):2045-2047. doi: 10.1021/acschemneuro.0c00368. Epub 2020 Jul 01.

Traumatic brain injury (TBI) causes serious neuronal injury that often leads to death. To date there is no clinically successful treatment strategy that has been reported which offers repair of the brain injury or neural injury. Significant attempts have...

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Ghosh S, Garg S, Ghosh S. Cell-Derived Exosome Therapy: A Novel Approach to Treat Post-traumatic Brain Injury Mediated Neural Injury. ACS Chem Neurosci. 2020;11(14):2045-2047doi: 10.1021/acschemneuro.0c00368.
Ghosh, S., Garg, S., & Ghosh, S. (2020). Cell-Derived Exosome Therapy: A Novel Approach to Treat Post-traumatic Brain Injury Mediated Neural Injury. ACS chemical neuroscience, 11(14), 2045-2047. https://doi.org/10.1021/acschemneuro.0c00368
Ghosh, Satyajit, et al. "Cell-Derived Exosome Therapy: A Novel Approach to Treat Post-traumatic Brain Injury Mediated Neural Injury." ACS chemical neuroscience vol. 11,14 (2020): 2045-2047. doi: https://doi.org/10.1021/acschemneuro.0c00368
Ghosh S, Garg S, Ghosh S. Cell-Derived Exosome Therapy: A Novel Approach to Treat Post-traumatic Brain Injury Mediated Neural Injury. ACS Chem Neurosci. 2020 Jul 15;11(14):2045-2047. doi: 10.1021/acschemneuro.0c00368. Epub 2020 Jul 01. PMID: 32609493.
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Neural development: Keeping a lid on alternative fates.

Nature reviews. Neuroscience

Whalley K.
PMID: 28446787
Nat Rev Neurosci. 2017 Jun;18(6):323. doi: 10.1038/nrn.2017.54. Epub 2017 Apr 27.

No abstract available.

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Whalley K. Neural development: Keeping a lid on alternative fates. Nat Rev Neurosci. 2017;18(6):323doi: 10.1038/nrn.2017.54.
Whalley, K. (2017). Neural development: Keeping a lid on alternative fates. Nature reviews. Neuroscience, 18(6), 323. https://doi.org/10.1038/nrn.2017.54
Whalley, Katherine. "Neural development: Keeping a lid on alternative fates." Nature reviews. Neuroscience vol. 18,6 (2017): 323. doi: https://doi.org/10.1038/nrn.2017.54
Whalley K. Neural development: Keeping a lid on alternative fates. Nat Rev Neurosci. 2017 Jun;18(6):323. doi: 10.1038/nrn.2017.54. Epub 2017 Apr 27. PMID: 28446787.
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[Neonatal hypoxia-ischemia: cellular and molecular brain damage and therapeutic modulation of neurogenesis].

Revista de neurologia

Moral Y, Robertson NJ, Goni-de-Cerio F, Alonso-Alconada D.
PMID: 30560986
Rev Neurol. 2019 Jan 01;68(1):23-36.

INTRODUCTION: Perinatal asphyxia remains a major cause of both mortality and neurological morbidity. Neonatal encephalopathy affects to 1-3/1,000 newborns, leading to significant brain damage and childhood disability. The only standard therapy is moderate hypothermia, whose efficacy, despite proved, is...

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Moral Y, Robertson NJ, Goni-de-Cerio F, et al. Hipoxia-isquemia neonatal: bases celulares y moleculares del daño cerebral y modulacion terapeutica de la neurogenesis. [Neonatal hypoxia-ischemia: cellular and molecular brain damage and therapeutic modulation of neurogenesis]. Rev Neurol. 2019;68(1):23-36
Moral, Y., Robertson, N. J., Goni-de-Cerio, F., & Alonso-Alconada, D. (2019). Hipoxia-isquemia neonatal: bases celulares y moleculares del daño cerebral y modulacion terapeutica de la neurogenesis. [Neonatal hypoxia-ischemia: cellular and molecular brain damage and therapeutic modulation of neurogenesis]. Revista de neurologia, 68(1), 23-36.
Moral, Y, et al. "Hipoxia-isquemia neonatal: bases celulares y moleculares del daño cerebral y modulacion terapeutica de la neurogenesis." [Neonatal hypoxia-ischemia: cellular and molecular brain damage and therapeutic modulation of neurogenesis]. Revista de neurologia vol. 68,1 (2019): 23-36.
Moral Y, Robertson NJ, Goni-de-Cerio F, Alonso-Alconada D. Hipoxia-isquemia neonatal: bases celulares y moleculares del daño cerebral y modulacion terapeutica de la neurogenesis. [Neonatal hypoxia-ischemia: cellular and molecular brain damage and therapeutic modulation of neurogenesis]. Rev Neurol. 2019 Jan 01;68(1):23-36. Spanish. PMID: 30560986.
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Spatiotemporal Differences in the Regional Cortical Plate and Subplate Volume Growth during Fetal Development.

Cerebral cortex (New York, N.Y. : 1991)

Vasung L, Rollins CK, Velasco-Annis C, Yun HJ, Zhang J, Warfield SK, Feldman HA, Gholipour A, Grant PE.
PMID: 32147720
Cereb Cortex. 2020 Jun 30;30(8):4438-4453. doi: 10.1093/cercor/bhaa033.

The regional specification of the cerebral cortex can be described by protomap and protocortex hypotheses. The protomap hypothesis suggests that the regional destiny of cortical neurons and the relative size of the cortical area are genetically determined early during...

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Vasung L, Rollins CK, Velasco-Annis C, et al. Spatiotemporal Differences in the Regional Cortical Plate and Subplate Volume Growth during Fetal Development. Cereb Cortex. 2020;30(8):4438-4453doi: 10.1093/cercor/bhaa033.
Vasung, L., Rollins, C. K., Velasco-Annis, C., Yun, H. J., Zhang, J., Warfield, S. K., Feldman, H. A., Gholipour, A., & Grant, P. E. (2020). Spatiotemporal Differences in the Regional Cortical Plate and Subplate Volume Growth during Fetal Development. Cerebral cortex (New York, N.Y. : 1991), 30(8), 4438-4453. https://doi.org/10.1093/cercor/bhaa033
Vasung, Lana, et al. "Spatiotemporal Differences in the Regional Cortical Plate and Subplate Volume Growth during Fetal Development." Cerebral cortex (New York, N.Y. : 1991) vol. 30,8 (2020): 4438-4453. doi: https://doi.org/10.1093/cercor/bhaa033
Vasung L, Rollins CK, Velasco-Annis C, Yun HJ, Zhang J, Warfield SK, Feldman HA, Gholipour A, Grant PE. Spatiotemporal Differences in the Regional Cortical Plate and Subplate Volume Growth during Fetal Development. Cereb Cortex. 2020 Jun 30;30(8):4438-4453. doi: 10.1093/cercor/bhaa033. PMID: 32147720; PMCID: PMC7325717.
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Questioning human neurogenesis.

Nature

Snyder JS.
PMID: 29542697
Nature. 2018 Mar 15;555(7696):315-316. doi: 10.1038/d41586-018-02629-3.

No abstract available.

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Snyder JS. Questioning human neurogenesis. Nature. 2018;555(7696):315-316doi: 10.1038/d41586-018-02629-3.
Snyder, J. S. (2018). Questioning human neurogenesis. Nature, 555(7696), 315-316. https://doi.org/10.1038/d41586-018-02629-3
Snyder, Jason S. "Questioning human neurogenesis." Nature vol. 555,7696 (2018): 315-316. doi: https://doi.org/10.1038/d41586-018-02629-3
Snyder JS. Questioning human neurogenesis. Nature. 2018 Mar 15;555(7696):315-316. doi: 10.1038/d41586-018-02629-3. PMID: 29542697.
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CSF Makes Waves in the Neural Stem Cell Niche.

Cell stem cell

Dani N, Lehtinen MK.
PMID: 27814476
Cell Stem Cell. 2016 Nov 03;19(5):565-566. doi: 10.1016/j.stem.2016.10.008.

Adult neural stem cells reside in specialized niches that maintain neurogenesis, but the components of the niche and its secretome are only partially understood. In this issue of Cell Stem Cell, Silva-Vargas et al. (2016) show that choroid plexus,...

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Dani N, Lehtinen MK. CSF Makes Waves in the Neural Stem Cell Niche. Cell Stem Cell. 2016;19(5):565-566doi: 10.1016/j.stem.2016.10.008.
Dani, N., & Lehtinen, M. K. (2016). CSF Makes Waves in the Neural Stem Cell Niche. Cell stem cell, 19(5), 565-566. https://doi.org/10.1016/j.stem.2016.10.008
Dani, Neil, and Lehtinen, Maria K. "CSF Makes Waves in the Neural Stem Cell Niche." Cell stem cell vol. 19,5 (2016): 565-566. doi: https://doi.org/10.1016/j.stem.2016.10.008
Dani N, Lehtinen MK. CSF Makes Waves in the Neural Stem Cell Niche. Cell Stem Cell. 2016 Nov 03;19(5):565-566. doi: 10.1016/j.stem.2016.10.008. PMID: 27814476; PMCID: PMC5423542.
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Evaluation of Kjell et al.: Defining the Adult Neural Stem Cell Niche Proteome Identifies Key Regulators of Adult Neurogenesis.

Cell stem cell

Faissner A.
PMID: 32032519
Cell Stem Cell. 2020 Feb 06;26(2):127-128. doi: 10.1016/j.stem.2020.01.014.

An example of the peer review process for "Defining the Adult Neural Stem Cell Niche Proteome Identifies Key Regulators of Adult Neurogenesis" (Kjell et al., 2020) is presented here.

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Faissner A. Evaluation of Kjell et al.: Defining the Adult Neural Stem Cell Niche Proteome Identifies Key Regulators of Adult Neurogenesis. Cell Stem Cell. 2020;26(2):127-128doi: 10.1016/j.stem.2020.01.014.
Faissner, A. (2020). Evaluation of Kjell et al.: Defining the Adult Neural Stem Cell Niche Proteome Identifies Key Regulators of Adult Neurogenesis. Cell stem cell, 26(2), 127-128. https://doi.org/10.1016/j.stem.2020.01.014
Faissner, Andreas. "Evaluation of Kjell et al.: Defining the Adult Neural Stem Cell Niche Proteome Identifies Key Regulators of Adult Neurogenesis." Cell stem cell vol. 26,2 (2020): 127-128. doi: https://doi.org/10.1016/j.stem.2020.01.014
Faissner A. Evaluation of Kjell et al.: Defining the Adult Neural Stem Cell Niche Proteome Identifies Key Regulators of Adult Neurogenesis. Cell Stem Cell. 2020 Feb 06;26(2):127-128. doi: 10.1016/j.stem.2020.01.014. PMID: 32032519.
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Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders.

Cell

[No authors listed]
PMID: 31835028
Cell. 2019 Dec 12;179(7):1469-1482.e11. doi: 10.1016/j.cell.2019.11.020.

Genetic influences on psychiatric disorders transcend diagnostic boundaries, suggesting substantial pleiotropy of contributing loci. However, the nature and mechanisms of these pleiotropic effects remain unclear. We performed analyses of 232,964 cases and 494,162 controls from genome-wide studies of anorexia...

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Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. Cell. 2019;179(7):1469-1482.e11doi: 10.1016/j.cell.2019.11.020.
(2019). Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. Cell, 179(7), 1469-1482.e11. https://doi.org/10.1016/j.cell.2019.11.020
"Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders." Cell vol. 179,7 (2019): 1469-1482.e11. doi: https://doi.org/10.1016/j.cell.2019.11.020
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. Cell. 2019 Dec 12;179(7):1469-1482.e11. doi: 10.1016/j.cell.2019.11.020. PMID: 31835028; PMCID: PMC7077032.
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Update on forebrain evolution: From neurogenesis to thermogenesis.

Seminars in cell & developmental biology

Martínez-Cerdeño V, García-Moreno F, Tosches MA, Csillag A, Manger PR, Molnár Z.
PMID: 28964836
Semin Cell Dev Biol. 2018 Apr;76:15-22. doi: 10.1016/j.semcdb.2017.09.034. Epub 2017 Oct 21.

Comparative developmental studies provide growing understanding of vertebrate forebrain evolution. This short review directs the spotlight to some newly emerging aspects, including the evolutionary origin of the proliferative region known as the subventricular zone (SVZ) and of intermediate progenitor...

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Martínez-Cerdeño V, García-Moreno F, Tosches MA, et al. Update on forebrain evolution: From neurogenesis to thermogenesis. Semin Cell Dev Biol. 2017;76:15-22doi: 10.1016/j.semcdb.2017.09.034.
Martínez-Cerdeño, V., García-Moreno, F., Tosches, M. A., Csillag, A., Manger, P. R., & Molnár, Z. (2018). Update on forebrain evolution: From neurogenesis to thermogenesis. Seminars in cell & developmental biology, 7615-22. https://doi.org/10.1016/j.semcdb.2017.09.034
Martínez-Cerdeño, Verónica, et al. "Update on forebrain evolution: From neurogenesis to thermogenesis." Seminars in cell & developmental biology vol. 76 (2018): 15-22. doi: https://doi.org/10.1016/j.semcdb.2017.09.034
Martínez-Cerdeño V, García-Moreno F, Tosches MA, Csillag A, Manger PR, Molnár Z. Update on forebrain evolution: From neurogenesis to thermogenesis. Semin Cell Dev Biol. 2018 Apr;76:15-22. doi: 10.1016/j.semcdb.2017.09.034. Epub 2017 Oct 21. PMID: 28964836; PMCID: PMC5866743.
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Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders.

Cell

[No authors listed]
PMID: 31835028
Cell. 2019 Dec 12;179(7):1469-1482.e11. doi: 10.1016/j.cell.2019.11.020.

Genetic influences on psychiatric disorders transcend diagnostic boundaries, suggesting substantial pleiotropy of contributing loci. However, the nature and mechanisms of these pleiotropic effects remain unclear. We performed analyses of 232,964 cases and 494,162 controls from genome-wide studies of anorexia...

Cite
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. Cell. 2019;179(7):1469-1482.e11doi: 10.1016/j.cell.2019.11.020.
(2019). Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. Cell, 179(7), 1469-1482.e11. https://doi.org/10.1016/j.cell.2019.11.020
"Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders." Cell vol. 179,7 (2019): 1469-1482.e11. doi: https://doi.org/10.1016/j.cell.2019.11.020
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. Cell. 2019 Dec 12;179(7):1469-1482.e11. doi: 10.1016/j.cell.2019.11.020. PMID: 31835028; PMCID: PMC7077032.
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Showing 1 to 12 of 12 entries