1015 Walnut Street
Bluemle Life Sciences Building, Room 430
Philadelphia, PA 19107
(215) 503-0113
Bluemle Life Sciences Building, Room 430
Philadelphia, PA 19107
(215) 503-0113
Most Recent Peer-reviewed Publications
- Visualizing molecular polar order in tissues via electromechanical coupling
- Remodeling of the dermalepidermal junction in bilayered skin constructs after silencing the expression of the p.R2622Q and p.G2623C collagen VII mutants
- Electromechanical properties of dried tendon and isoelectrically focused collagen hydrogels
- Perlecan domain V is neuroprotective and proangiogenic following ischemic stroke in rodents (Journal of Clinical Investigation (2011) 121, 8 (3005-3023) DOI: 10.1172/JCI46358)
- Perlecan domain V is neuroprotective and proangiogenic following ischemic stroke in rodents
- Persistence of intracellular and extracellular changes after incompletely suppressing expression of the R789C (p.R989C) and R992C (p.R1192C) collagen II mutants
- Endostatin binds nerve growth factor and thereby inhibits neurite outgrowth and neuronal migration in-vitro
- Reducing the effects of intracellular accumulation of thermolabile collagen II mutants by increasing their thermostability in cell culture conditions
- Compound heterozygous desmoplakin mutations result in a phenotype with a combination of myocardial, skin, hair, and enamel abnormalities
- Recessive COL6A2 C-globular missense mutations in Ullrich congenital muscular dystrophy: Role of the C2a splice variant
- Fluorescent protein markers to tag collagenous proteins: The paradigm of procollagen VII
- R992C (p.R1192C) Substitution in Collagen II Alters the Structure of Mutant Molecules and Induces the Unfolded Protein Response
- Collagen fibril formation: A new target to limit fibrosis
- Candidate cell and matrix interaction domains on the collagen fibril, the predominant protein of vertebrates
- Cells expressing partially unfolded R789C/p.R989c type II procollagen mutant associated with spondyloepiphyseal dysplasia undergo apoptosis
- Type I collagen and collagen mimetics as angiogenesis promoting superpolymers
- Anchorless keratinocyte survival: An emerging pathogenic mechanism for squamous cell carcinoma in recessive dystrophic epidermolysis bullosa
- Y-position cysteine substitution in type I collagen (α1(I) R888C/p.R1066C) is associated with osteogenesis imperfecta/Ehlers-Danlos Syndrome phenotype
- Molecular basis of organization of collagen fibrils
- High-affinity binding of the NC1 domain of collagen VII to laminin 5 and collagen IV