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The Journal of Clinical Investigation
|
October 28, 1998
Transit time of leukocytes rolling through venules controls cytokine-induced inflammatory cell recruitment in vivo
U Jung, K E Norman, K Scharffetter-Kochanek, et al.
European Journal of Pediatrics
|
April 1, 1983
Lactic acidosis, neurological deterioration and compromised cellular pyruvate oxidation due to a defect in the reoxidation of cytoplasmically generated NADH
B H Robinson, J Taylor, B Francois, et al.
American Journal of Human Genetics
|
October 1, 1990
Benign missense variations in the cystic fibrosis gene
K Kobayashi, M R Knowles, R C Boucher, et al.
American Journal of Human Genetics
|
June 1, 1988
Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLA
H Y Zoghbi, S P Daiger, A McCall, et al.
The Journal of Biological Chemistry
|
July 5, 1990
Heterogeneity of mutations in argininosuccinate synthetase causing human citrullinemia
K Kobayashi, M J Jackson, D B Tick, et al.
Human Mutation
|
January 1, 1994
A robotics-assisted procedure for large scale cystic fibrosis mutation analysis
J M DeMarchi, C S Richards, R G Fenwick, et al.
The Journal of Pediatrics
|
March 1, 1975
Variation in the phenotypic expression of beta-glucuronidase deficiency
A L Beaudet, N M DiFerrante, G D Ferry, et al.
Human Molecular Genetics
|
September 25, 1997
X-linked glycerol kinase deficiency in the mouse leads to growth retardation, altered fat metabolism, autonomous glucocorticoid secretion and neonatal death
A H Huq, R S Lovell, C N Ou, et al.
Archives of Environmental Health
|
March 1, 1979
Collagen breakdown and ammonia inhalation
D V Hatton, C S Leach, A L Beaudet, et al.
Blood
|
October 15, 1996
Inhibition of delayed-type contact hypersensitivity in mice deficient in both E-selectin and P-selectin
N D Staite, J M Justen, L M Sly, et al.
Page
of 24
Search research articles
Search
Showing results (111-120 of 233) with videos related to
Sort By:
Page
of 24
The Journal of Clinical Investigation
|
October 28, 1998
Transit time of leukocytes rolling through venules controls cytokine-induced inflammatory cell recruitment in vivo
U Jung, K E Norman, K Scharffetter-Kochanek, et al.
European Journal of Pediatrics
|
April 1, 1983
Lactic acidosis, neurological deterioration and compromised cellular pyruvate oxidation due to a defect in the reoxidation of cytoplasmically generated NADH
B H Robinson, J Taylor, B Francois, et al.
American Journal of Human Genetics
|
October 1, 1990
Benign missense variations in the cystic fibrosis gene
K Kobayashi, M R Knowles, R C Boucher, et al.
American Journal of Human Genetics
|
June 1, 1988
Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLA
H Y Zoghbi, S P Daiger, A McCall, et al.
The Journal of Biological Chemistry
|
July 5, 1990
Heterogeneity of mutations in argininosuccinate synthetase causing human citrullinemia
K Kobayashi, M J Jackson, D B Tick, et al.
Human Mutation
|
January 1, 1994
A robotics-assisted procedure for large scale cystic fibrosis mutation analysis
J M DeMarchi, C S Richards, R G Fenwick, et al.
The Journal of Pediatrics
|
March 1, 1975
Variation in the phenotypic expression of beta-glucuronidase deficiency
A L Beaudet, N M DiFerrante, G D Ferry, et al.
Human Molecular Genetics
|
September 25, 1997
X-linked glycerol kinase deficiency in the mouse leads to growth retardation, altered fat metabolism, autonomous glucocorticoid secretion and neonatal death
A H Huq, R S Lovell, C N Ou, et al.
Archives of Environmental Health
|
March 1, 1979
Collagen breakdown and ammonia inhalation
D V Hatton, C S Leach, A L Beaudet, et al.
Blood
|
October 15, 1996
Inhibition of delayed-type contact hypersensitivity in mice deficient in both E-selectin and P-selectin
N D Staite, J M Justen, L M Sly, et al.
Page
of 24