Will P. Walker, Ph.D. - Publications
Affiliations: | 2010 | Cornell University, Ithaca, NY, United States |
Area:
Genetics, Molecular Biology, Neuroscience BiologyYear | Citation | Score | |||
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2016 | Walker WP, Oehler A, Edinger AL, Wagner KU, Gunn TM. Oligodendroglial deletion of ESCRT-I component TSG101 causes spongiform encephalopathy. Biology of the Cell / Under the Auspices of the European Cell Biology Organization. PMID 27406702 DOI: 10.1111/Boc.201600014 | 0.665 | |||
2010 | Walker WP, Gunn TM. Shades of meaning: the pigment-type switching system as a tool for discovery. Pigment Cell & Melanoma Research. 23: 485-95. PMID 20465596 DOI: 10.1111/J.1755-148X.2010.00721.X | 0.606 | |||
2010 | Walker WP, Gunn TM. Piecing together the pigment-type switching puzzle. Pigment Cell & Melanoma Research. 23: 4-6. PMID 20042018 DOI: 10.1111/J.1755-148X.2009.00654.X | 0.555 | |||
2009 | Jiao J, Sun K, Walker WP, Bagher P, Cota CD, Gunn TM. Abnormal regulation of TSG101 in mice with spongiform neurodegeneration. Biochimica Et Biophysica Acta. 1792: 1027-35. PMID 19703557 DOI: 10.1016/J.Bbadis.2009.08.009 | 0.509 | |||
2007 | Walker WP, Aradhya S, Hu CL, Shen S, Zhang W, Azarani A, Lu X, Barsh GS, Gunn TM. Genetic analysis of attractin homologs. Genesis (New York, N.Y. : 2000). 45: 744-56. PMID 18064672 DOI: 10.1002/Dvg.20351 | 0.677 | |||
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