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Lancet (London, England)
|
April 11, 1992
Genetic diagnosis of Gaucher's disease
P K Mistry, S J Smith, M Ali, et al.
Conservation Biology : the Journal of the Society for Conservation Biology
|
September 22, 2007
Comparing effectiveness of experimental and implemented bycatch reduction measures: the ideal and the real
T M Cox, R L Lewison, R Zydelis, et al.
Journal of Inherited Metabolic Disease
|
September 17, 2010
Dietary modifications in patients receiving miglustat
H Champion, U Ramaswami, J Imrie, et al.
Blood
|
August 29, 2000
Pathologic gene expression in Gaucher disease: up-regulation of cysteine proteinases including osteoclastic cathepsin K
M T Moran, J P Schofield, A R Hayman, et al.
Clinical Chemistry
|
October 1, 1995
Generation and characterization of monoclonal antibodies to human type-5 tartrate-resistant acid phosphatase: development of a specific immunoassay of the isoenzyme in serum
P Chamberlain, J Compston, T M Cox, et al.
British Journal of Haematology
|
September 1, 1993
Hereditary ovalocytosis with compensated haemolysis
D M Reardon, C A Seymour, T M Cox, et al.
Genomics
|
December 1, 1991
Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22
D M Whitcombe, N P Carter, D G Albertson, et al.
Molecular Biology & Medicine
|
February 1, 1991
Regulation and expression of type V (tartrate-resistant) acid phosphatase in human mononuclear phagocytes
M A Bevilacqua, D K Lord, N C Cross, et al.
Brain Research
|
March 21, 1997
Transglutaminase activity is increased in Alzheimer's disease brain
G V Johnson, T M Cox, J P Lockhart, et al.
BMJ (Clinical Research Ed.)
|
February 3, 1990
Life threatening thrombocytopenia in sarcoidosis
A J Larner, C T Dollery, T M Cox, et al.
Page
of 15
Search research articles
Search
Showing results (111-120 of 146) with videos related to
Sort By:
Page
of 15
Lancet (London, England)
|
April 11, 1992
Genetic diagnosis of Gaucher's disease
P K Mistry, S J Smith, M Ali, et al.
Conservation Biology : the Journal of the Society for Conservation Biology
|
September 22, 2007
Comparing effectiveness of experimental and implemented bycatch reduction measures: the ideal and the real
T M Cox, R L Lewison, R Zydelis, et al.
Journal of Inherited Metabolic Disease
|
September 17, 2010
Dietary modifications in patients receiving miglustat
H Champion, U Ramaswami, J Imrie, et al.
Blood
|
August 29, 2000
Pathologic gene expression in Gaucher disease: up-regulation of cysteine proteinases including osteoclastic cathepsin K
M T Moran, J P Schofield, A R Hayman, et al.
Clinical Chemistry
|
October 1, 1995
Generation and characterization of monoclonal antibodies to human type-5 tartrate-resistant acid phosphatase: development of a specific immunoassay of the isoenzyme in serum
P Chamberlain, J Compston, T M Cox, et al.
British Journal of Haematology
|
September 1, 1993
Hereditary ovalocytosis with compensated haemolysis
D M Reardon, C A Seymour, T M Cox, et al.
Genomics
|
December 1, 1991
Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22
D M Whitcombe, N P Carter, D G Albertson, et al.
Molecular Biology & Medicine
|
February 1, 1991
Regulation and expression of type V (tartrate-resistant) acid phosphatase in human mononuclear phagocytes
M A Bevilacqua, D K Lord, N C Cross, et al.
Brain Research
|
March 21, 1997
Transglutaminase activity is increased in Alzheimer's disease brain
G V Johnson, T M Cox, J P Lockhart, et al.
BMJ (Clinical Research Ed.)
|
February 3, 1990
Life threatening thrombocytopenia in sarcoidosis
A J Larner, C T Dollery, T M Cox, et al.
Page
of 15