de Vellis J - Search Results

1

Does ASPA gene mutation in Canavan disease alter oligodendrocyte development? A tissue culture study of ASPA KO mice brain.

Kumar S, Sowmyalakshmi R, Daniels SL, Chang R, Surendran S, Matalon R, de Vellis J. Kumar S, et al. Among authors: de vellis j. Adv Exp Med Biol. 2006;576:175-82; discussion 361-3. doi: 10.1007/0-387-30172-0_12. Adv Exp Med Biol. 2006. PMID: 16802712 No abstract available.

2

Lack of aspartoacylase activity disrupts survival and differentiation of neural progenitors and oligodendrocytes in a mouse model of Canavan disease.

Kumar S, Biancotti JC, Matalon R, de Vellis J. Kumar S, et al. Among authors: de vellis j. J Neurosci Res. 2009 Nov 15;87(15):3415-27. doi: 10.1002/jnr.22233. J Neurosci Res. 2009. PMID: 19739253

3

Canavan disease: a white matter disorder.

Kumar S, Mattan NS, de Vellis J. Kumar S, et al. Among authors: de vellis j. Ment Retard Dev Disabil Res Rev. 2006;12(2):157-65. doi: 10.1002/mrdd.20108. Ment Retard Dev Disabil Res Rev. 2006. PMID: 16807907 Review.

4

Aspartoacylase deficiency affects early postnatal development of oligodendrocytes and myelination.

Mattan NS, Ghiani CA, Lloyd M, Matalon R, Bok D, Casaccia P, de Vellis J. Mattan NS, et al. Among authors: de vellis j. Neurobiol Dis. 2010 Nov;40(2):432-43. doi: 10.1016/j.nbd.2010.07.003. Epub 2010 Jul 14. Neurobiol Dis. 2010. PMID: 20637282 Free PMC article.

5

Neurotrophin activates signal transduction in oligodendroglial cells: expression of functional TrkC receptor isoforms.

Kumar S, de Vellis J. Kumar S, et al. Among authors: de vellis j. J Neurosci Res. 1996 Jun 1;44(5):490-8. doi: 10.1002/(SICI)1097-4547(19960601)44:5<490::AID-JNR9>3.0.CO;2-A. J Neurosci Res. 1996. PMID: 8776670

6

Mice lacking NT-3, and its receptor TrkC, exhibit profound deficiencies in CNS glial cells.

Kahn MA, Kumar S, Liebl D, Chang R, Parada LF, De Vellis J. Kahn MA, et al. Among authors: de vellis j. Glia. 1999 Apr;26(2):153-65. Glia. 1999. PMID: 10384880

7

Transferrin regulates transcription of the MBP gene and its action synergizes with IGF-1 to enhance myelinogenesis in the md rat.

Espinosa-Jeffrey A, Kumar S, Zhao PM, Awosika O, Agbo C, Huang A, Chang R, De Vellis J. Espinosa-Jeffrey A, et al. Among authors: de vellis j. Dev Neurosci. 2002;24(2-3):227-41. doi: 10.1159/000065698. Dev Neurosci. 2002. PMID: 12401963

8

Transferrin gene expression and secretion by rat brain cells in vitro.

Espinosa de los Monteros A, Kumar S, Scully S, Cole R, de Vellis J. Espinosa de los Monteros A, et al. Among authors: de vellis j. J Neurosci Res. 1990 Apr;25(4):576-80. doi: 10.1002/jnr.490250416. J Neurosci Res. 1990. PMID: 2352292

9

Combination of growth factors enhances remyelination in a cuprizone-induced demyelination mouse model.

Kumar S, Biancotti JC, Yamaguchi M, de Vellis J. Kumar S, et al. Among authors: de vellis j. Neurochem Res. 2007 Apr-May;32(4-5):783-97. doi: 10.1007/s11064-006-9208-6. Epub 2006 Dec 21. Neurochem Res. 2007. PMID: 17186374

10

Activation of inflammatory response by a combination of growth factors in cuprizone-induced demyelinated brain leads to myelin repair.

Biancotti JC, Kumar S, de Vellis J. Biancotti JC, et al. Among authors: de vellis j. Neurochem Res. 2008 Dec;33(12):2615-28. doi: 10.1007/s11064-008-9792-8. Epub 2008 Jul 26. Neurochem Res. 2008. PMID: 18661234

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