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IEEE Transactions on Rehabilitation Engineering : a Publication of the IEEE Engineering in Medicine and Biology Society
|
July 15, 2000
A virtual reality testbed for brain-computer interface research
J D Bayliss, D H Ballard
Human Genetics
|
March 1, 1993
Characterization of genetic markers in the 5'flanking region of the apo A1 gene
C C Shoulders, T M Narcisi, A Jarmuz, et al.
The Journal of Biological Chemistry
|
September 2, 1994
Microsomal triglyceride transfer protein, the abetalipoproteinemia gene product, mediates the secretion of apolipoprotein B-containing lipoproteins from heterologous cells
J M Leiper, J D Bayliss, R J Pease, et al.
Nature
|
January 10, 1991
Familial combined hyperlipidaemia linked to the apolipoprotein AI-CII-AIV gene cluster on chromosome 11q23-q24
A P Wojciechowski, M Farrall, P Cullen, et al.
Human Molecular Genetics
|
December 1, 1993
Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein
C C Shoulders, D J Brett, J D Bayliss, et al.
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of 1
Search research articles
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Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
IEEE Transactions on Rehabilitation Engineering : a Publication of the IEEE Engineering in Medicine and Biology Society
|
July 15, 2000
A virtual reality testbed for brain-computer interface research
J D Bayliss, D H Ballard
Human Genetics
|
March 1, 1993
Characterization of genetic markers in the 5'flanking region of the apo A1 gene
C C Shoulders, T M Narcisi, A Jarmuz, et al.
The Journal of Biological Chemistry
|
September 2, 1994
Microsomal triglyceride transfer protein, the abetalipoproteinemia gene product, mediates the secretion of apolipoprotein B-containing lipoproteins from heterologous cells
J M Leiper, J D Bayliss, R J Pease, et al.
Nature
|
January 10, 1991
Familial combined hyperlipidaemia linked to the apolipoprotein AI-CII-AIV gene cluster on chromosome 11q23-q24
A P Wojciechowski, M Farrall, P Cullen, et al.
Human Molecular Genetics
|
December 1, 1993
Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein
C C Shoulders, D J Brett, J D Bayliss, et al.
Page
of 1