D
Denise Fabiano do Nascimento
Researcher
grad_student
1 h-index
3 pubs
10 cited
Research Areas
Links
Biography and Research Information
OverviewAI-generated summary
Denise Fabiano do Nascimento's research explores advancements in tissue engineering and cell culture techniques. Her recent publications focus on developing novel biomaterials for cell culture and investigating their application in disease modeling. One publication in 2024 details the use of a recombinant fragment E8 of laminin-511 as a xenofree alternative to Matrigel for human induced pluripotent stem cell (hiPSC) culture and differentiation into neurovascular cell types. Another 2024 publication describes a three-dimensional valve-on-chip microphysiological system designed to study the progression of calcific aortic valve disease, implicating cell cycle progression, cholesterol metabolism, and protein homeostasis. Nascimento collaborates with researchers at the University of Arkansas at Fayetteville, including Ishita Tandon and Kartik Balachandran, with whom she shares multiple publications. Her scholarship metrics include an h-index of 1 with 3 total publications and 9 total citations.
Metrics
- h-index: 1
- Publications: 3
- Citations: 10
Selected Publications
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The future is fully defined: recombinant fragment E8 of laminin-511 is a viable xenofree alternative to Matrigel for hiPSC culture and differentiation into neurovascular cell types (2024)
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A three-dimensional valve-on-chip microphysiological system implicates cell cycle progression, cholesterol metabolism and protein homeostasis in early calcific aortic valve disease progression (2024)
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The future is fully defined: recombinant fragment E8 of laminin-511 is a viable xenofree alternative to Matrigel for hiPSC culture and differentiation into neurovascular cell types (2024)
Collaboration Network
Top Collaborators
Ishita Tandon
University of Arkansas at Fayetteville
3 shared publications
In database
- A three-dimensional valve-on-chip microphysiological system implicates cell cycle progression, cholesterol metabolism and protein homeostasis in early calcific aortic valve disease progression
- The future is fully defined: recombinant fragment E8 of laminin-511 is a viable xenofree alternative to Matrigel for hiPSC culture and differentiation into neurovascular cell types
- The future is fully defined: recombinant fragment E8 of laminin-511 is a viable xenofree alternative to Matrigel for hiPSC culture and differentiation into neurovascular cell types
Kartik Balachandran
University of Arkansas at Fayetteville
3 shared publications
In database
- A three-dimensional valve-on-chip microphysiological system implicates cell cycle progression, cholesterol metabolism and protein homeostasis in early calcific aortic valve disease progression
- The future is fully defined: recombinant fragment E8 of laminin-511 is a viable xenofree alternative to Matrigel for hiPSC culture and differentiation into neurovascular cell types
- The future is fully defined: recombinant fragment E8 of laminin-511 is a viable xenofree alternative to Matrigel for hiPSC culture and differentiation into neurovascular cell types
Laís A. Ferreira
University of Arkansas at Fayetteville (US)
2 shared publications
- The future is fully defined: recombinant fragment E8 of laminin-511 is a viable xenofree alternative to Matrigel for hiPSC culture and differentiation into neurovascular cell types
- The future is fully defined: recombinant fragment E8 of laminin-511 is a viable xenofree alternative to Matrigel for hiPSC culture and differentiation into neurovascular cell types
Lance Cordes
University of Arkansas at Fayetteville
2 shared publications
In database
- The future is fully defined: recombinant fragment E8 of laminin-511 is a viable xenofree alternative to Matrigel for hiPSC culture and differentiation into neurovascular cell types
- The future is fully defined: recombinant fragment E8 of laminin-511 is a viable xenofree alternative to Matrigel for hiPSC culture and differentiation into neurovascular cell types
Alan E. Woessner
University of Arkansas at Fayetteville
1 shared publication
In database
- A three-dimensional valve-on-chip microphysiological system implicates cell cycle progression, cholesterol metabolism and protein homeostasis in early calcific aortic valve disease progression
Laís Ferreira
University of Arkansas at Fayetteville
1 shared publication
In database
- A three-dimensional valve-on-chip microphysiological system implicates cell cycle progression, cholesterol metabolism and protein homeostasis in early calcific aortic valve disease progression
Christine Shamblin
Scripps Research Institute (US)
1 shared publication
- A three-dimensional valve-on-chip microphysiological system implicates cell cycle progression, cholesterol metabolism and protein homeostasis in early calcific aortic valve disease progression
Gustavo Vaca-Diez
University of Arkansas at Fayetteville
1 shared publication
In database
- A three-dimensional valve-on-chip microphysiological system implicates cell cycle progression, cholesterol metabolism and protein homeostasis in early calcific aortic valve disease progression
Amanda Walls
University of Arkansas at Fayetteville
1 shared publication
In database
- A three-dimensional valve-on-chip microphysiological system implicates cell cycle progression, cholesterol metabolism and protein homeostasis in early calcific aortic valve disease progression
Patrick Kuczwara
University of Arkansas at Fayetteville
1 shared publication
In database
- A three-dimensional valve-on-chip microphysiological system implicates cell cycle progression, cholesterol metabolism and protein homeostasis in early calcific aortic valve disease progression
Alexis P. Applequist
University of Arkansas at Fayetteville
1 shared publication
In database
- A three-dimensional valve-on-chip microphysiological system implicates cell cycle progression, cholesterol metabolism and protein homeostasis in early calcific aortic valve disease progression
Swastika Tandon
University of Arkansas at Fayetteville
1 shared publication
In database
- A three-dimensional valve-on-chip microphysiological system implicates cell cycle progression, cholesterol metabolism and protein homeostasis in early calcific aortic valve disease progression
Jin-Woo Kim
University of Arkansas at Fayetteville
1 shared publication
In database
- A three-dimensional valve-on-chip microphysiological system implicates cell cycle progression, cholesterol metabolism and protein homeostasis in early calcific aortic valve disease progression
Manuel K. Rausch
The University of Texas at Austin (US)
1 shared publication
- A three-dimensional valve-on-chip microphysiological system implicates cell cycle progression, cholesterol metabolism and protein homeostasis in early calcific aortic valve disease progression
Tomasz A. Timek
Spectrum Health (US)
1 shared publication
- A three-dimensional valve-on-chip microphysiological system implicates cell cycle progression, cholesterol metabolism and protein homeostasis in early calcific aortic valve disease progression
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