Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Quantifying the relation between bond number and myoblast proliferation.

Faraday discussions - 1 Jan 2008

Boontheekul Tanyarut, Kong Hyun-Joon, Hsiong Susan X, Huang Yen-Chen, Mahadevan L, Vandenburgh Herman, Mooney David J

Abstract excerpt

Many functions of the extracellular matrix can be mimicked by small peptide fragments (e.g., arginine-glycine-aspartic acid (RGD) sequence) of the entire molecule, but the presentation of the peptides is critical to their effects on cells. It is likely that some effects of peptide presentation from biomaterials simply relate to the number of bonds formed between cell receptors and the adhesion ligands, but a lack...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Receptors, Peptide
Share to Cell Adhesion

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Cell Proliferation

Share to Fluorescence Resonance Energy Transfer

Share to Myoblasts

Share to Oligopeptides

Share to Receptors, Immunologic

Source

Identifiers

PMID: 19048990
DOI: 10.1039/b719928g

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Quantifying the relation between bond number and myoblast proliferation.PMID 19048990Read ↗

Quantifying the relation between adhesion ligand-receptor bond formation and cell phenotype.Semantic proximity Read ↗

Changing the Fate of Dystrophin-Deficient Myoblasts via Hetero Ligand Nanoclusters on Biomaterial Surface: Effects of Integrin-Syndecan or Dystroglycan CrosstalkSemantic proximity Read ↗

Albumin-derived nanocarriers: substrates for enhanced cell adhesive ligand display and cell motility.Semantic proximity Read ↗

Alginate type and RGD density control myoblast phenotype.Semantic proximity Read ↗

Biomaterial arrays with defined adhesion ligand densities and matrix stiffness identify distinct phenotypes for tumorigenic and non-tumorigenic human mesenchymal cell typesSemantic proximity Read ↗

Interplay between integrins and cadherins to control bone differentiation upon BMP-2 stimulationSemantic proximity Read ↗

Interplay of Geometric Cues and RGD/BMP-2 Crosstalk in Directing Stem Cell FateSemantic proximity Read ↗

Real-Time Quantification of Cell Mechanics and Functions by Double Resonator Piezoelectric Cytometry — Theory and Study of Cellular Adhesion of HUVECsSemantic proximity Read ↗

Presenting multiple adhesion ligands on hydrogels for control of PC12 phenotype.Semantic proximity Read ↗

RGD peptides immobilized on a mechanically deformable surface promote osteoblast differentiation.Semantic proximity Read ↗

Arginine-glycine-glutamine and serine-isoleucine-lysine-valine-alanine-valine modified poly(l-lactide) films: bioactive molecules used for surface grafting to guide cellular contractile phenotype.Semantic proximity Read ↗

Interrogating cellular fate decisions with high-throughput arrays of multiplexed cellular communities.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.