G. Guzman

发表

Familial Hypertrophic Cardiomyopathy Mutations in the Regulatory Light Chains of Myosin Affect Their Structure, Ca2+Binding, and Phosphorylation*

J. Stull, D. Szczesna, D. Ghosh, 2001, The Journal of Biological Chemistry.

Familial Hypertrophic Cardiomyopathy-linked Alterations in Ca2+ Binding of Human Cardiac Myosin Regulatory Light Chain Affect Cardiac Muscle Contraction*

G. Guzman, D. Szczesna‐Cordary, S. Ng, 2004, Journal of Biological Chemistry.

The role of the N-terminus of the myosin essential light chain in cardiac muscle contraction.

G. Guzman, D. Szczesna‐Cordary, W. Kerrick, 2009, Journal of molecular biology.

F110I and R278C Troponin T Mutations That Cause Familial Hypertrophic Cardiomyopathy Affect Muscle Contraction in Transgenic Mice and Reconstituted Human Cardiac Fibers*

G. Guzman, J. Potter, D. Szczesna‐Cordary, 2005, Journal of Biological Chemistry.

Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy.

D. Szczesna, G. Guzman, J. Potter, 2001, The Journal of biological chemistry.

The Role of the Four Ca Binding Sites of Troponin C in the Regulation of Skeletal Muscle Contraction (*)

D. Szczesna, G. Guzman, J. Potter, 1996, The Journal of Biological Chemistry.

Optical spectroscopic characterization of single tryptophan mutants of chicken skeletal troponin C: evidence for interdomain interaction.

G. Guzman, J. Potter, S. Venyaminov, 1999, Biochemistry.

Myosin essential light chain in health and disease.

G. Guzman, D. Szczesna‐Cordary, O. Hernandez, 2007, American journal of physiology. Heart and circulatory physiology.

Cardiac Troponin T Isoforms Affect the Ca2+Sensitivity and Inhibition of Force Development

A. Gomes, G. Guzman, J. Potter, 2002, The Journal of Biological Chemistry.

Altered Regulation of Cardiac Muscle Contraction by Troponin T Mutations That Cause Familial Hypertrophic Cardiomyopathy*

D. Szczesna, G. Guzman, J. Potter, 2000, The Journal of Biological Chemistry.

Investigation of a genetically engineered mutant of barnacle troponin C containing a central helix deletion

Q. Li, G. Guzman, J. Potter, 1999, Pflügers Archiv.

Investigating the role of Ca2+-binding site IV in barnacle troponin C

Q. Li, G. Guzman, J. Potter, 2000, Pflügers Archiv.

Prolonged Ca2+ and force transients in myosin RLC transgenic mouse fibers expressing malignant and benign FHC mutations.

G. Guzman, D. Szczesna‐Cordary, W. Kerrick, 2006, Journal of molecular biology.

The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice

G. Guzman, D. Szczesna‐Cordary, Jiaju Zhao, 2005, Journal of Cell Science.

Fast skeletal muscle regulatory light chain is required for fast and slow skeletal muscle development

G. Guzman, J. Potter, D. Szczesna‐Cordary, 2007, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Characterisation of a mutant of barnacle troponin C lacking Ca2+-binding sites at positions II and IV

Q. Li, G. Guzman, J. Potter, 1999, Pflügers Archiv.

E22K mutation of RLC that causes familial hypertrophic cardiomyopathy in heterozygous mouse myocardium: effect on cross-bridge kinetics.

G. Guzman, D. Szczesna‐Cordary, G. Guzman, 2006, American journal of physiology. Heart and circulatory physiology.