Taylor Lawson

Mr. Taylor Lawson


Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 May 2020 in Nature Communications
Verified
Journal Article
Open access
PDF file
PAParambath Anilkumar
Parambath Anilkumar
TLTaylor Lawson
Taylor Lawson
SASrinivas Abbina
Srinivas Abbina
JMJanne T.A. Mäkelä
Janne T.A. Mäkelä
RSRobert C. Sabatelle
Robert C. Sabatelle
JKJayachandran N. Kizhakkedathu
Jayachandran N. Kizhakkedathu
A longstanding goal in science and engineering is to mimic the size, structure, and functionality present in biology with synthetic analogs. Today, synthetic globular polymers of several million molecular weight are unknown, and, yet, these structures are expected to exhibit unanticipated properties due to their size, compactness, and low inter-chain interactions. Here we report the gram-scale synthesis of dendritic polymers, mega hyperbranched polyglycerols (mega HPGs), in million daltons. The mega HPGs are highly water soluble, soft, nanometer-scale single polymer particles that exhibit low intrinsic viscosities. Further, the mega HPGs are lubricants acting as interposed single molecule ball bearings to reduce the coefficient of friction between both hard and soft natural surfaces in a size dependent manner. We attribute this result to their globular and single particle nature together with its exceptional hydration. Collectively, these results set the stage for new opportunities in the design, synthesis, and evaluation of mega polymers.

1 January 2021 in Osteoarthritis and Cartilage
Verified
Journal Article
Closed access
KSK.M. Scott
K.M. Scott
David Joshua CohenDavid Joshua Cohen
David Joshua Cohen
MHM. Hays
M. Hays
DND.W. Nielson
D.W. Nielson
MGMark Grinstaff
Mark Grinstaff
Zvi SchwartzZvi Schwartz
Zvi Schwartz


29 August 2020 in Journal of Orthopaedic Research
Verified
Journal Article
Closed access
PDF file
TLTaylor Lawson
Taylor Lawson
JMJanne T.A. Mäkelä
Janne T.A. Mäkelä
TKTravis Klein
Travis Klein
BSBrian D. Snyder
Brian D. Snyder
MGMark Grinstaff
Mark Grinstaff

22 August 2020 in Journal of Orthopaedic Research
Verified
Journal Article
Closed access
PDF file
TLTaylor Lawson
Taylor Lawson
JMJanne T.A. Mäkelä
Janne T.A. Mäkelä
TKTravis Klein
Travis Klein
BSBrian D. Snyder
Brian D. Snyder
MGMark Grinstaff
Mark Grinstaff

Verified
Journal Article
Open access
PDF file
TLTaylor Lawson
Taylor Lawson
DSDevon E. Scott-Drechsel
Devon E. Scott-Drechsel
VCVenkat Keshav Chivukula
Venkat Keshav Chivukula
Sandra RugonyiSandra Rugonyi
Sandra Rugonyi
KTKent L. Thornburg
Kent L. Thornburg
MHMonica T. Hinds
Monica T. Hinds
Congenital heart defects (CHDs) represent the most common form of human birth defects; approximately one-third of heart defects involve malformations of the outflow tract (OFT). Maternal diabetes increases the risk of CHD by 3–5 fold. During heart organogenesis, little is known about the effects of hyperglycemia on hemodynamics, which are critical to normal heart development. Heart development prior to septation in the chick embryo was studied under hyperglycemic conditions. Sustained hyperglycemic conditions were induced, raising the average plasma glucose concentration from 70 mg/dL to 180 mg/dL, akin to the fasting plasma glucose of a patient with diabetes. The OFTs were assessed for structural and hemodynamic alterations using optical coherence tomography (OCT), confocal microscopy, and microcomputed tomography. In hyperglycemic embryos, the endocardial cushions of the proximal OFT were asymmetric, and the OFTs curvature and torsion were significantly altered. The blood flow velocity through the OFT of hyperglycemic embryos was significantly decreased, including flow reversal in 30% of the cardiac cycle. Thus, hyperglycemia at the onset of gestation results in asymmetric proximal endocardial cushions, abnormal OFT curvature, and altered hemodynamics in the developing heart. If present in humans, these results may identify early developmental alterations that contribute to the increased risk for cardiac malformations in babies from diabetic mothers.