Alyssa Panitch

Dr. Alyssa Panitch

University of California - Davis
orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

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

Representative Publications

View All Publications
30 July 2021 in Materials Science and Engineering: R: Reports
Verified
Journal Article
Closed access
QXQinghua Xu
Qinghua Xu
JTJessica E. Torres
Jessica E. Torres
MHMazin Hakim
Mazin Hakim
PBPaulina M. Babiak
Paulina M. Babiak
PPPallabi Pal
Pallabi Pal
JLJulie C. Liu
Julie C. Liu

1 January 2011 in Journal of Surgical Research
Verified
Journal Article
Closed access
BWBRIAN WARD
BRIAN WARD
Alyssa PanitchAlyssa Panitch
Alyssa Panitch

29 December 2020 in Biomolecules
Verified
Journal Article
Open access
PDF file
Harkanwalpreet SodhiHarkanwalpreet Sodhi
Harkanwalpreet Sodhi
Alyssa PanitchAlyssa Panitch
Alyssa Panitch
Glycosaminoglycans are native components of the extracellular matrix that drive cell behavior and control the microenvironment surrounding cells, making them promising therapeutic targets for a myriad of diseases. Recent studies have shown that recapitulation of cell interactions with the extracellular matrix are key in tissue engineering, where the aim is to mimic and regenerate endogenous tissues. Because of this, incorporation of glycosaminoglycans to drive stem cell fate and promote cell proliferation in engineered tissues has gained increasing attention. This review summarizes the role glycosaminoglycans can play in tissue engineering and the recent advances in their use in these constructs. We also evaluate the general trend of research in this niche and provide insight into its future directions.


7 March 2020 in Acta Biomaterialia
Verified
Journal Article
Closed access
Dake HaoDake Hao
Dake Hao
YFYahan Fan
Yahan Fan
WXWenwu Xiao
Wenwu Xiao
RLRuiwu Liu
Ruiwu Liu
CPChristopher Pivetti
Christopher Pivetti
Aijun WangAijun Wang
Aijun Wang

1 October 2020 in Open Biology
Verified
Journal Article
Open access
TDTima Dehghani
Tima Dehghani
Alyssa PanitchAlyssa Panitch
Alyssa Panitch
Severe fibrotic and thrombotic events permeate the healthcare system, causing suffering for millions of patients with inflammatory disorders. As late-state consequences of chronic inflammation, fibrosis and thrombosis are the culmination of pathological interactions of activated endothelium, neutrophils and platelets after vessel injury. Coupling of these three cell types ensures a pro-coagulant, cytokine-rich environment that promotes the capture, activation and proliferation of circulating immune cells and recruitment of key pro-fibrotic cell types such as myofibroblasts. As the first responders to sterile inflammatory injury, it is important to understand how endothelial cells, neutrophils and platelets help create this environment. There has been a growing interest in this intersection over the past decade that has helped shape the development of therapeutics to target these processes. Here, we review recent insights into how neutrophils, platelets and endothelial cells guide the development of pathological vessel repair that can also result in underlying tissue fibrosis. We further discuss recent efforts that have been made to translate this knowledge into therapeutics and provide perspective as to how a compound or combination therapeutics may be most efficacious when tackling fibrosis and thrombosis that is brought upon by chronic inflammation.