A. Tu

发表

Myosin S2 is not required for effects of myosin binding protein‐C on motility

M. Regnier, J. Shaffer, S. Harris, 2007, FEBS letters.

Neutralization and Transfer of Lipopolysaccharide by Phospholipid Transfer Protein (*)

S. Wright, J. Albers, G. Wolfbauer, 1996, The Journal of Biological Chemistry.

Relationship between phospholipid transfer protein activity and HDL level and size among inbred mouse strains.

B. Paigen, S. Marcovina, H. Kennedy, 1999, Journal of lipid research.

Molecular biology of phospholipid transfer protein

S. Marcovina, J. Albers, M. Cheung, 1996, Current opinion in lipidology.

High density lipoprotein conversion mediated by human plasma phospholipid transfer protein.

T. Nishida, A. Tu, H. Nishida, 1993, The Journal of biological chemistry.

Organization of human phospholipid transfer protein gene.

S. Deeb, J. Albers, J. R. Day, 1995, Biochemical and biophysical research communications.

DNA sequences essential for transcription of human phospholipid transfer protein gene in HepG2 cells.

J. Albers, G. Wolfbauer, A. Tu, 1997, Biochemical and biophysical research communications.

Characterization of the mouse gene encoding phospholipid transfer protein.

B. Paigen, J. Albers, K. Johnson, 1997, Gene.

Functional analysis of the transcriptional activity of the mouse phospholipid transfer protein gene.

J. Albers, A. Tu, 2001, Biochemical and biophysical research communications.

Introduction of the human PLTP transgene suppresses the atherogenic diet-induced increase in plasma phospholipid transfer activity in C57BL/6 mice

B. Paigen, H. Kennedy, J. Albers, 1999, International journal of clinical & laboratory research.

DNA sequences responsible for reduced promoter activity of human phospholipid transfer protein by fibrate.

J. Albers, A. Tu, 1999, Biochemical and biophysical research communications.

Functional expression of human and mouse plasma phospholipid transfer protein: effect of recombinant and plasma PLTP on HDL subspecies.

J. Albers, M. Cheung, G. Wolfbauer, 1995, Biochimica et biophysica acta.

Cell‐Associated and Extracellular Phospholipid Transfer Protein in Human Coronary Atherosclerosis

A. Chait, T. McDonald, S. Marcovina, 2003, Circulation.

Transgenic mice expressing human phospholipid transfer protein have increased HDL/non-HDL cholesterol ratio

B. Paigen, S. Marcovina, J. Albers, 1996, International journal of clinical & laboratory research.

Low-Density Lipoprotein Inhibits Secretion of Phospholipid Transfer Protein in Human Trophoblastic BeWo Cells

J. Albers, R. Knopp, M. Cheung, 2004, Experimental biology and medicine.

Structural Basis of Type 2A von Willebrand Disease Investigated by Molecular Dynamics Simulations and Experiments

W. Thomas, M. Ling, D. Chung, 2012, PloS one.

Contribution of the Myosin Binding Protein C Motif to Functional Effects in Permeabilized Rat Trabeculae

M. Regnier, S. Harris, M. Razumova, 2008, The Journal of general physiology.

dATP Elevation Induces Myocardial Metabolic Remodeling to Support Improved Cardiac Function

R. Tian, D. Raftery, Sonette Steczina, 2022, bioRxiv.

Structural and functional consequences of the cardiac troponin C L48Q Ca(2+)-sensitizing mutation.

I. M. Robertson, V. Daggett, B. Sykes, 2012, Biochemistry.

dATP Elevation Induces Myocardial Metabolic Remodeling to Support Improved Cardiac Function

R. Tian, D. Raftery, Sonette Steczina, 2022, bioRxiv.

Structural and functional consequences of the cardiac troponin C L48Q Ca2+-sensitizing mutation

Dan Wang, Valerie Daggett, Brian D. Sykes, 2012 .

Structural and functional consequences of cardiac troponin C L57Q and I61Q Ca(2+)-desensitizing variants.

V. Daggett, M. Regnier, Dan D. Wang, 2013, Archives of biochemistry and biophysics.

Thin filament incorporation of an engineered cardiac troponin C variant (L48Q) enhances contractility in intact cardiomyocytes from healthy and infarcted hearts.

C. Murry, Erik R. Feest, Michael Regnier, 2014, Journal of molecular and cellular cardiology.

Enhanced Ca2+ binding of cardiac troponin reduces sarcomere length dependence of contractile activation independently of strong crossbridges.

Michael Regnier, M. Regnier, Maria V Razumova, 2012, American journal of physiology. Heart and circulatory physiology.

sliding , G203S, K206Q) enhance filament Δ troponin I (K183 Familial hypertrophic cardiomyopathy mutations in

A. M. Gordon, D. Martyn, M. Regnier, 2015 .

Effects of the N-terminal Domains of Myosin Binding Protein-C in an in Vitro Motility Assay

M. Regnier, J. Shaffer, S. Harris, 2006, Journal of Biological Chemistry.

Quantitative Trait Locus Mapping of Genes That Regulate Phospholipid Transfer Activity in SM/J and NZB/BlNJ Inbred Mice

G. Churchill, R. Korstanje, Renhua Li, 2004, Arteriosclerosis, thrombosis, and vascular biology.

Effects of Cardiac Troponin I Mutation P83S on Contractile Properties and the Modulation by PKA-Mediated Phosphorylation.

A. McCulloch, S. Lindert, M. Regnier, 2016, The journal of physical chemistry. B.

Troponin I Mutations R146G and R21C Alter Cardiac Troponin Function, Contractile Properties, and Modulation by Protein Kinase A (PKA)-mediated Phosphorylation*

A. McCulloch, J. Mccammon, S. Lindert, 2015, The Journal of Biological Chemistry.

Specific electrostatic interactions between charged amino acid residues regulate binding of von Willebrand factor to blood platelets

Junmei Chen, José A López, W. Thomas, 2017, The Journal of Biological Chemistry.

Glucose regulates the transcription of human genes relevant to HDL metabolism: responsive elements for peroxisome proliferator-activated receptor are involved in the regulation of phospholipid transfer protein.

J. Albers, A. Tu, 2001, Diabetes.

Functional characterization of the promoter region of the human phospholipid transfer protein gene.

J. Albers, G. Wolfbauer, A. Tu, 1995, Biochemical and biophysical research communications.

Phosphorylation of Ser283 enhances the stiffness of the tropomyosin head-to-tail overlap domain.

Stefan Fischer, M. Regnier, Jeffrey R. Moore, 2015, Archives of biochemistry and biophysics.

Phospholipid transfer protein maps to distal mouse chromosome 2.

R. Leboeuf, J. Albers, A. Tu, 1996, Genomics.

Specific electrostatic interactions between charged amino acid residues regulate binding of von Willebrand factor to blood platelets

Junmei Chen, José A López, W. Thomas, 2017, The Journal of Biological Chemistry.