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Australian Journal of Biological Sciences
|
June 1, 1977
The regulation of gluconeogenesis in pouch young of the tammar wallaby, Macropus eugenii (Desmarest)
P A Janssens, L A Jenkinson, B C Paton, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
December 1, 1972
Usefulness of echocardiography in patients undergoing mitral valve surgery
M L Johnson, J H Holmes, R D Spangler, et al.
Archives of Surgery (Chicago, Ill. : 1960)
|
December 1, 1970
Influence of preparation and immunosuppression upon longevity of grafted aortic valves
J L Sweatt, C F Allen, K H Kwong, et al.
The Biochemical Journal
|
July 15, 1992
Additional biochemical findings in a patient and fetal sibling with a genetic defect in the sphingolipid activator protein (SAP) precursor, prosaposin. Evidence for a deficiency in SAP-1 and for a normal lysosomal neuraminidase
B C Paton, B Schmid, B Kustermann-Kuhn, et al.
The Annals of Thoracic Surgery
|
August 1, 1976
Patent ductus arteriosus ligation and respiratory distress syndrome in premature infants
D R Clarke, B C Paton, G L Way, et al.
The Journal of Trauma
|
January 1, 1971
Acute treatment of traumatic aortic rupture
B C Paton, D P Elliott, J O Taubman, et al.
Archives of Surgery (Chicago, Ill. : 1960)
|
March 1, 1973
A nonionic surfactant and blood viscosity. Experimental observations
F L Grover, R S Kahn, M W Heron, et al.
Biochemical and Biophysical Research Communications
|
April 30, 1981
12-O-Tetradecanoylphorbol-13-acetate induced alterations in mouse epidermal 3-hydroxy-3-methylglutaryl CoA reductase
G S Kishore, B C Paton, R K Boutwell, et al.
American Journal of Human Genetics
|
June 1, 1997
Absence of mutations raises doubts about the role of the 70-kD peroxisomal membrane protein in Zellweger syndrome
B C Paton, S E Heron, P V Nelson, et al.
American Journal of Human Genetics
|
August 26, 2000
Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G
A C Muntau, P U Mayerhofer, B C Paton, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 70) with videos related to
Sort By:
Page
of 7
Australian Journal of Biological Sciences
|
June 1, 1977
The regulation of gluconeogenesis in pouch young of the tammar wallaby, Macropus eugenii (Desmarest)
P A Janssens, L A Jenkinson, B C Paton, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
December 1, 1972
Usefulness of echocardiography in patients undergoing mitral valve surgery
M L Johnson, J H Holmes, R D Spangler, et al.
Archives of Surgery (Chicago, Ill. : 1960)
|
December 1, 1970
Influence of preparation and immunosuppression upon longevity of grafted aortic valves
J L Sweatt, C F Allen, K H Kwong, et al.
The Biochemical Journal
|
July 15, 1992
Additional biochemical findings in a patient and fetal sibling with a genetic defect in the sphingolipid activator protein (SAP) precursor, prosaposin. Evidence for a deficiency in SAP-1 and for a normal lysosomal neuraminidase
B C Paton, B Schmid, B Kustermann-Kuhn, et al.
The Annals of Thoracic Surgery
|
August 1, 1976
Patent ductus arteriosus ligation and respiratory distress syndrome in premature infants
D R Clarke, B C Paton, G L Way, et al.
The Journal of Trauma
|
January 1, 1971
Acute treatment of traumatic aortic rupture
B C Paton, D P Elliott, J O Taubman, et al.
Archives of Surgery (Chicago, Ill. : 1960)
|
March 1, 1973
A nonionic surfactant and blood viscosity. Experimental observations
F L Grover, R S Kahn, M W Heron, et al.
Biochemical and Biophysical Research Communications
|
April 30, 1981
12-O-Tetradecanoylphorbol-13-acetate induced alterations in mouse epidermal 3-hydroxy-3-methylglutaryl CoA reductase
G S Kishore, B C Paton, R K Boutwell, et al.
American Journal of Human Genetics
|
June 1, 1997
Absence of mutations raises doubts about the role of the 70-kD peroxisomal membrane protein in Zellweger syndrome
B C Paton, S E Heron, P V Nelson, et al.
American Journal of Human Genetics
|
August 26, 2000
Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G
A C Muntau, P U Mayerhofer, B C Paton, et al.
Page
of 7