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Journal of Hypertension
|
February 1, 1996
Nerve growth factor gene and hypertension in spontaneously hypertensive rats
M Kapuscinski, F Charchar, B Innes, et al.
Human Mutation
|
May 29, 1998
Molecular pathology of galactosialidosis in a patient affected with two new frameshift mutations in the cathepsin A/protective protein gene
C Richard, J Tranchemontagne, M A Elsliger, et al.
Thrombosis Research
|
November 1, 1985
Novel rhodamine tripeptide substrate for manual and automated colorimetric prothrombin time test
G A Mitchell, M M Solorzano, M I Riesgo, et al.
Microscopy Research and Technique
|
March 1, 1994
Variations in mitochondrial ultrastructure and dynamics observed by high resolution scanning electron microscopy (HRSEM)
P J Lea, R J Temkin, K B Freeman, et al.
Pediatric Nephrology (Berlin, Germany)
|
April 1, 1999
Cerebral vascular complication and hyperhomocysteinemia in a cystinotic uremic child
A Merouani, J Genest, R Rozen, et al.
Pediatric Research
|
October 6, 1997
Enzymes of ketone body utilization in human tissues: protein and messenger RNA levels of succinyl-coenzyme A (CoA):3-ketoacid CoA transferase and mitochondrial and cytosolic acetoacetyl-CoA thiolases
T Fukao, X Q Song, G A Mitchell, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
February 1, 1997
Hormone-sensitive lipase (Lipe): sequence analysis of the 129Sv mouse Lipe gene
R Sztrolovics, S P Wang, P Lapierre, et al.
Clinical Genetics
|
September 7, 2005
Population history and its impact on medical genetics in Quebec
A-M Laberge, J Michaud, A Richter, et al.
Human Molecular Genetics
|
November 1, 1994
Nonsense and missense mutations of the muscle chloride channel gene in patients with myotonia congenita
A L George, K Sloan-Brown, G M Fenichel, et al.
Archives of Pathology & Laboratory Medicine
|
November 1, 1988
Glutaric acidemia type II. Comparison of pathologic features in two infants
A D Colevas, J L Edwards, R H Hruban, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 110) with videos related to
Sort By:
Page
of 11
Journal of Hypertension
|
February 1, 1996
Nerve growth factor gene and hypertension in spontaneously hypertensive rats
M Kapuscinski, F Charchar, B Innes, et al.
Human Mutation
|
May 29, 1998
Molecular pathology of galactosialidosis in a patient affected with two new frameshift mutations in the cathepsin A/protective protein gene
C Richard, J Tranchemontagne, M A Elsliger, et al.
Thrombosis Research
|
November 1, 1985
Novel rhodamine tripeptide substrate for manual and automated colorimetric prothrombin time test
G A Mitchell, M M Solorzano, M I Riesgo, et al.
Microscopy Research and Technique
|
March 1, 1994
Variations in mitochondrial ultrastructure and dynamics observed by high resolution scanning electron microscopy (HRSEM)
P J Lea, R J Temkin, K B Freeman, et al.
Pediatric Nephrology (Berlin, Germany)
|
April 1, 1999
Cerebral vascular complication and hyperhomocysteinemia in a cystinotic uremic child
A Merouani, J Genest, R Rozen, et al.
Pediatric Research
|
October 6, 1997
Enzymes of ketone body utilization in human tissues: protein and messenger RNA levels of succinyl-coenzyme A (CoA):3-ketoacid CoA transferase and mitochondrial and cytosolic acetoacetyl-CoA thiolases
T Fukao, X Q Song, G A Mitchell, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
February 1, 1997
Hormone-sensitive lipase (Lipe): sequence analysis of the 129Sv mouse Lipe gene
R Sztrolovics, S P Wang, P Lapierre, et al.
Clinical Genetics
|
September 7, 2005
Population history and its impact on medical genetics in Quebec
A-M Laberge, J Michaud, A Richter, et al.
Human Molecular Genetics
|
November 1, 1994
Nonsense and missense mutations of the muscle chloride channel gene in patients with myotonia congenita
A L George, K Sloan-Brown, G M Fenichel, et al.
Archives of Pathology & Laboratory Medicine
|
November 1, 1988
Glutaric acidemia type II. Comparison of pathologic features in two infants
A D Colevas, J L Edwards, R H Hruban, et al.
Page
of 11