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Microbial Ecology
|
May 2, 2002
Specific 16S rDNA sequences associated with naphthalene degradation under sulfate-reducing conditions in harbor sediments
L A Hayes, Derek R Lovley
Child Development
|
December 1, 1979
Bidimensional sorting in preschoolers with an instrumental learning task
J S Watson, L A Hayes, P Vietze
Journal of Neuroimmunology
|
July 9, 1998
Selective reduction in CD2 expression on CD2bright/CD8+ lymphocytes from cynomolgus monkeys (Macaca fascicularis) in response to acute stress
C J Rogers, C S Brissette-Storkus, L A Hayes, et al.
Natural Immunity
|
January 1, 1995
Characterization and comparison of the lytic function of NKR-P1+ and NKR-P1-rat natural killer cell clones established from NKR-P1bright/TCR alpha beta-cell lines
C Brissette-Storkus, P M Appasamy, L A Hayes, et al.
Cancer Genetics and Cytogenetics
|
January 12, 2005
Isochromosome of a deleted 20q: a rare but recurrent chromosome abnormality in myelodysplastic syndromes
K Saunders, B Czepulkowski, R Sivalingam, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Microbial Ecology
|
May 2, 2002
Specific 16S rDNA sequences associated with naphthalene degradation under sulfate-reducing conditions in harbor sediments
L A Hayes, Derek R Lovley
Child Development
|
December 1, 1979
Bidimensional sorting in preschoolers with an instrumental learning task
J S Watson, L A Hayes, P Vietze
Journal of Neuroimmunology
|
July 9, 1998
Selective reduction in CD2 expression on CD2bright/CD8+ lymphocytes from cynomolgus monkeys (Macaca fascicularis) in response to acute stress
C J Rogers, C S Brissette-Storkus, L A Hayes, et al.
Natural Immunity
|
January 1, 1995
Characterization and comparison of the lytic function of NKR-P1+ and NKR-P1-rat natural killer cell clones established from NKR-P1bright/TCR alpha beta-cell lines
C Brissette-Storkus, P M Appasamy, L A Hayes, et al.
Cancer Genetics and Cytogenetics
|
January 12, 2005
Isochromosome of a deleted 20q: a rare but recurrent chromosome abnormality in myelodysplastic syndromes
K Saunders, B Czepulkowski, R Sivalingam, et al.
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of 1