☰

Wenbo Xu, Ph.D. - Publications

Affiliations: 
2000 Wayne State University, Detroit, MI, United States 
Area:
Molecular Biology
Tree Info Grants Similar researchers PubMed Report error

8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2007 Gaboreanu AM, Hrstka R, Xu W, Shy M, Kamholz J, Lilien J, Balsamo J. Myelin protein zero/P0 phosphorylation and function require an adaptor protein linking it to RACK1 and PKC alpha. The Journal of Cell Biology. 177: 707-16. PMID 17502419 DOI: 10.1083/Jcb.200608060  0.599
2001 Xu W, Shy M, Kamholz J, Elferink L, Xu G, Lilien J, Balsamo J. Mutations in the cytoplasmic domain of P0 reveal a role for PKC-mediated phosphorylation in adhesion and myelination. The Journal of Cell Biology. 155: 439-46. PMID 11673479 DOI: 10.1083/Jcb.200107114  0.595
2000 Xu W, Manichella D, Jiang H, Vallat JM, Lilien J, Baron P, Scarlato G, Kamholz J, Shy ME. Absence of P0 leads to the dysregulation of myelin gene expression and myelin morphogenesis. Journal of Neuroscience Research. 60: 714-24. PMID 10861783 DOI: 10.1002/1097-4547(20000615)60:6<714::Aid-Jnr3>3.0.Co;2-1  0.631
1999 Kamholz J, Awatramani R, Menichella D, Jiang H, Xu W, Shy M. Regulation of Myelin-Specific Gene Expression: Relevance to CMT1. Annals of the New York Academy of Sciences. 883: 91-108. PMID 29086995 DOI: 10.1111/J.1749-6632.1999.Tb08572.X  0.612
1999 Menichella DM, Xu W, Jiang H, Sohi J, Vallat JM, Baron P, Kamholz J, Shy M. The Absence of Myelin P0 Protein Produces a Novel Molecular Phenotype in Schwann Cell. Annals of the New York Academy of Sciences. 883: 281-293. PMID 29086945 DOI: 10.1111/J.1749-6632.1999.Tb08590.X  0.637
1999 Menichella DM, Xu W, Jiang H, Sohi J, Vallat JM, Baron P, Kamholz J, Shy M. The absence of myelin P0 protein produces a novel molecular phenotype in Schwann cells. Annals of the New York Academy of Sciences. 883: 281-93. PMID 10586253  0.618
1999 Kamholz J, Awatramani R, Menichella D, Jiang H, Xu W, Shy M. Regulation of myelin-specific gene expression. Relevance to CMT1. Annals of the New York Academy of Sciences. 883: 91-108. PMID 10586235  0.597
1997 Shy ME, Arroyo E, Sladky J, Menichella D, Jiang H, Xu W, Kamholz J, Scherer SS. Heterozygous P0 knockout mice develop a peripheral neuropathy that resembles chronic inflammatory demyelinating polyneuropathy (CIDP). Journal of Neuropathology and Experimental Neurology. 56: 811-21. PMID 9210878 DOI: 10.1097/00005072-199756070-00008  0.603
Show low-probability matches.