Showing results (11-20 of 25) with videos related to
Sort By:
Pageof 3
Glia|September 28, 2011
The QKI-PLP pathway controls SIRT2 abundance in CNS myelinH Zhu, L Zhao, E Wang, et al.Journal of Cellular Biochemistry|January 5, 2000
Cell cycle arrest induced by ectopic expression of p27 is not sufficient to promote oligodendrocyte differentiationX M Tang, J S Beesley, J B Grinspan, et al.American Journal of Medical Genetics|September 5, 2002
Further evidence for a fourth gene causing X-linked pure spastic paraplegiaA Starling, P Rocco, F Cambi, et al.Neurology|April 1, 1996
Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegiaF Cambi, X M Tang, P Cordray, et al.Journal of Neuroscience Research|August 10, 2000
Gtx, an oligodendrocyte-specific homeodomain protein, has repressor activityR Awatramani, J Beesley, H Yang, et al.Neurology|October 13, 2006
Skin biopsies demonstrate MPZ splicing abnormalities in Charcot-Marie-Tooth neuropathy 1BA Sabet, J Li, K Ghandour, et al.The Journal of Comparative Neurology|September 6, 2001
Differentiation of glial cells and motor neurons during the formation of neuromuscular junctions in cocultures of rat spinal cord explant and human muscleT Mars, K J Yu, X M Tang, et al.American Journal of Medical Genetics. Part A|February 19, 2015
17q12 microduplications: a challenge for cliniciansV Bertini, A Orsini, A Bonuccelli, et al.European Radiology|October 17, 2018
Prospective multimodal imaging assessment of locally advanced cervical cancer patients administered by chemoradiation followed by radical surgery-the "PRICE" study 2: role of conventional and DW-MRIB Gui, M Miccò, A L Valentini, et al.Annals of the New York Academy of Sciences|December 10, 1999
Peripheral neuropathy caused by proteolipid protein gene mutationsJ Y Garbern, F Cambi, R Lewis, et al.Pageof 3