Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Michio Niinobe"'
Autor:
Ruth Halaban, Gregory E. Hannigan, Kazuaki Yoshikawa, Michio Niinobe, Terence Wu, E. Sergio Trombetta, Elaine Cheng, Aaron J. Berger, Harriet M. Kluger, Aiping Lin, Stephan Ariyan, Hongyu Zhao, Kenneth R. Williams, David L. Rimm, Keith Hoek
Supplementary Table 1 from Expression Profiling Reveals Novel Pathways in the Transformation of Melanocytes to Melanomas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5c80823512110dac15802efaec0b085
https://doi.org/10.1158/0008-5472.22363580.v1
https://doi.org/10.1158/0008-5472.22363580.v1
Autor:
Ruth Halaban, Gregory E. Hannigan, Kazuaki Yoshikawa, Michio Niinobe, Terence Wu, E. Sergio Trombetta, Elaine Cheng, Aaron J. Berger, Harriet M. Kluger, Aiping Lin, Stephan Ariyan, Hongyu Zhao, Kenneth R. Williams, David L. Rimm, Keith Hoek
Affymetrix and spotted oligonucleotide microarrays were used to assess global differential gene expression comparing normal human melanocytes with six independent melanoma cell strains from advanced lesions. The data, validated at the protein level f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::310810d868b6792ede2c2b029597843d
https://doi.org/10.1158/0008-5472.c.6493784.v1
https://doi.org/10.1158/0008-5472.c.6493784.v1
Autor:
Ruth Halaban, Gregory E. Hannigan, Kazuaki Yoshikawa, Michio Niinobe, Terence Wu, E. Sergio Trombetta, Elaine Cheng, Aaron J. Berger, Harriet M. Kluger, Aiping Lin, Stephan Ariyan, Hongyu Zhao, Kenneth R. Williams, David L. Rimm, Keith Hoek
Supplementary Table 3 from Expression Profiling Reveals Novel Pathways in the Transformation of Melanocytes to Melanomas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b23246b0b74bfd37cc43101f7cc903a
https://doi.org/10.1158/0008-5472.22363574.v1
https://doi.org/10.1158/0008-5472.22363574.v1
Autor:
Xiao-Hui Xu, Michio Niinobe, Yonggang Wang, Cheng He, Chang-Lin Lu, Xiujie Liu, Kazuaki Yoshikawa, Yong Zhang, Wei Zhu
Publikováno v:
Molecular and Cellular Neuroscience. 41:51-61
Nogo-A has been identified in the central nervous system as an inhibitor for axonal regeneration. Previous works have mainly focused on Nogo-A in oligodendrocytes and the roles of neuronal intracellular Nogo-A remain elusive. To gain deep insight int
Publikováno v:
Developmental Neuroscience. 22:310-319
Necdin is a 325-amino-acid residue protein encoded by a cDNA clone isolated from neurally differentiated embryonal carcinoma cells. Ectopic expression of necdin induces growth arrest of proliferative cells. Necdin binds to major transcription factors
Publikováno v:
Experimental Cell Research. 251:442-451
Neurons withdraw from the cell cycle immediately after differentiation from their proliferative precursors. E2F1, a principal transcription factor that promotes cell cycle progression, must be silenced in neurons. We investigated the E2F1 system in p
Autor:
Michio Niinobe, Mariko Okamoto, Taichi Uetsuki, Kazuaki Yoshikawa, Kiwamu Takemoto, Isao Nishimura, Masayuki Miura, Takashi Momoi
Publikováno v:
The Journal of Neuroscience. 19:6955-6964
Forced overexpression of wild-type Alzheimer amyloid precursor protein (APP) causes postmitotic neurons to degenerate. Caspase-3 (CPP32) is a principal cell death protease involved in neuronal apoptosis during physiological development and under path
Publikováno v:
Neuroscience. 77:937-943
To determine the functional role of synaptotagmin (Syt) regulatory domains, affinity-purified antibodies specific for C2A or C2B domains were injected into presynaptic neurons of cholinergic synapses formed between rat sympathetic neurons in culture.
Publikováno v:
Journal of Biological Chemistry. 271:27838-27846
Myelin proteolipid protein (PLP) and its alternatively spliced isoform, DM-20, are the major integral membrane proteins of central nervous system myelin. It is known that PLP and DM-20 are delivered to myelin by a finely regulated vesicular transport
Publikováno v:
Journal of Biological Chemistry. 270:26523-26527
Synaptotagmins I and II are inositol high polyphosphate series (inositol 1,3,4,5-tetrakisphosphate (IP4), inositol 1,3,4,5,6-pentakisphosphate, and inositol 1,2,3,4,5,6-hexakisphosphate) binding proteins, which are thought to be essential for Ca(2+)-