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Human Molecular Genetics
|
August 11, 1999
Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation
O I Buiakova, J Xu, S Lutsenko, et al.
Protein Science : a Publication of the Protein Society
|
December 29, 1998
Structural analysis of inhibitor binding to human carbonic anhydrase II
P A Boriack-Sjodin, S Zeitlin, H H Chen, et al.
Journal of Neuroscience Research
|
October 26, 1999
Enhanced sensitivity to N-methyl-D-aspartate receptor activation in transgenic and knockin mouse models of Huntington's disease
M S Levine, G J Klapstein, A Koppel, et al.
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of 4
Search research articles
Search
Showing results (31-40 of 33) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 33 results.
Human Molecular Genetics
|
August 11, 1999
Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation
O I Buiakova, J Xu, S Lutsenko, et al.
Protein Science : a Publication of the Protein Society
|
December 29, 1998
Structural analysis of inhibitor binding to human carbonic anhydrase II
P A Boriack-Sjodin, S Zeitlin, H H Chen, et al.
Journal of Neuroscience Research
|
October 26, 1999
Enhanced sensitivity to N-methyl-D-aspartate receptor activation in transgenic and knockin mouse models of Huntington's disease
M S Levine, G J Klapstein, A Koppel, et al.
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of 4