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FEBS Letters
|
September 17, 1990
The functional properties of full length and mutant chicken gizzard smooth muscle caldesmon expressed in Escherichia coli
C S Redwood, S B Marston, J Bryan, et al.
Molecular & General Genetics : MGG
|
August 27, 1996
Human DNA topoisomerases II alpha and II beta can functionally substitute for yeast TOP2 in chromosome segregation and recombination
S Jensen, C S Redwood, J R Jenkins, et al.
Heart (British Cardiac Society)
|
October 12, 2005
Does a well developed collateral circulation predispose to restenosis after percutaneous coronary intervention? An intravascular ultrasound study
D Perera, P Postema, R Rashid, et al.
Biochemical and Biophysical Research Communications
|
February 19, 2009
Dilated cardiomyopathy mutations in alpha-tropomyosin inhibit its movement during the ATPase cycle
Yurii S Borovikov, Olga E Karpicheva, Galina A Chudakova, et al.
Archives of Biochemistry and Biophysics
|
August 4, 2009
The effect of the dilated cardiomyopathy-causing mutation Glu54Lys of alpha-tropomyosin on actin-myosin interactions during the ATPase cycle
Yurii S Borovikov, Olga E Karpicheva, Stanislava V Avrova, et al.
Circulation
|
May 1, 1995
Angiographic stenosis progression and coronary events in patients with 'stabilized' unstable angina
L Chen, M R Chester, S Redwood, et al.
Environmental Science & Technology
|
May 6, 2005
Characterization of humic substances by environmental scanning electron microscopy
Paul S Redwood, Jamie R Lead, Roy M Harrison, et al.
The American Journal of Cardiology
|
January 15, 1996
Use of ventricular premature complexes for risk stratification after acute myocardial infarction in the thrombolytic era
D J Statters, M Malik, S Redwood, et al.
Biochimica Et Biophysica Acta
|
December 29, 2015
Myopathy-causing Q147P TPM2 mutation shifts tropomyosin strands further towards the open position and increases the proportion of strong-binding cross-bridges during the ATPase cycle
Olga E Karpicheva, Armen O Simonyan, Nadezhda V Kuleva, et al.
International Journal of Molecular Sciences
|
October 17, 2020
Looking for Targets to Restore the Contractile Function in Congenital Myopathy Caused by Gln<sup>147</sup>Pro Tropomyosin
Olga E Karpicheva, Armen O Simonyan, Nikita A Rysev, et al.
Page
of 9
Search research articles
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Showing results (31-40 of 85) with videos related to
Sort By:
Page
of 9
FEBS Letters
|
September 17, 1990
The functional properties of full length and mutant chicken gizzard smooth muscle caldesmon expressed in Escherichia coli
C S Redwood, S B Marston, J Bryan, et al.
Molecular & General Genetics : MGG
|
August 27, 1996
Human DNA topoisomerases II alpha and II beta can functionally substitute for yeast TOP2 in chromosome segregation and recombination
S Jensen, C S Redwood, J R Jenkins, et al.
Heart (British Cardiac Society)
|
October 12, 2005
Does a well developed collateral circulation predispose to restenosis after percutaneous coronary intervention? An intravascular ultrasound study
D Perera, P Postema, R Rashid, et al.
Biochemical and Biophysical Research Communications
|
February 19, 2009
Dilated cardiomyopathy mutations in alpha-tropomyosin inhibit its movement during the ATPase cycle
Yurii S Borovikov, Olga E Karpicheva, Galina A Chudakova, et al.
Archives of Biochemistry and Biophysics
|
August 4, 2009
The effect of the dilated cardiomyopathy-causing mutation Glu54Lys of alpha-tropomyosin on actin-myosin interactions during the ATPase cycle
Yurii S Borovikov, Olga E Karpicheva, Stanislava V Avrova, et al.
Circulation
|
May 1, 1995
Angiographic stenosis progression and coronary events in patients with 'stabilized' unstable angina
L Chen, M R Chester, S Redwood, et al.
Environmental Science & Technology
|
May 6, 2005
Characterization of humic substances by environmental scanning electron microscopy
Paul S Redwood, Jamie R Lead, Roy M Harrison, et al.
The American Journal of Cardiology
|
January 15, 1996
Use of ventricular premature complexes for risk stratification after acute myocardial infarction in the thrombolytic era
D J Statters, M Malik, S Redwood, et al.
Biochimica Et Biophysica Acta
|
December 29, 2015
Myopathy-causing Q147P TPM2 mutation shifts tropomyosin strands further towards the open position and increases the proportion of strong-binding cross-bridges during the ATPase cycle
Olga E Karpicheva, Armen O Simonyan, Nadezhda V Kuleva, et al.
International Journal of Molecular Sciences
|
October 17, 2020
Looking for Targets to Restore the Contractile Function in Congenital Myopathy Caused by Gln<sup>147</sup>Pro Tropomyosin
Olga E Karpicheva, Armen O Simonyan, Nikita A Rysev, et al.
Page
of 9