233 South Tenth Street
Bluemle Life Sciences Building, Suite 450
Philadelphia, PA 19107
(215) 503-5785
Bluemle Life Sciences Building, Suite 450
Philadelphia, PA 19107
(215) 503-5785
Most Recent Peer-reviewed Publications
- Pseudoxanthoma elasticum: The paradigm of ectopic mineralization disorders - Diagnosis and treatment
- Expression of p53 protein after nonablative rejuvenation: The other side of the coin
- Pseudoxanthoma elasticum: Progress in research toward treatment: Summary of the 2012 PXE international research meeting
- Clinical and histopathological characteristics of a family with R1141X mutation of pseudoxanthoma elasticum - presymptomatic testing and lack of carrier phenotypes
- Topical Application of Recombinant Type VII Collagen Incorporates Into the Dermal-Epidermal Junction and Promotes Wound Closure
- Warfarin accelerates ectopic mineralization in Abcc6-/- mi Clinical relevance to pseudoxanthoma elasticum
- Vitamin K-dependent carboxylation of matrix Gla-protein: A crucial switch to control ectopic mineralization
- A single-nucleotide polymorphism in the Abcc6 gene associates with connective tissue mineralization in mice similar to targeted models for pseudoxanthoma elasticum
- Analysis of chemotactic molecules in bone marrow-derived mesenchymal stem cells and the skin: Ccl27-Ccr10 axis as a basis for targeting to cutaneous tissues
- The complexity of elastic fibre biogenesis in the skin - a perspective to the clinical heterogeneity of cutis laxa
- Intravenously Injected Recombinant Human Type VII Collagen Homes to Skin Wounds and Restores Skin Integrity of Dystrophic Epidermolysis Bullosa
- Administration of bone marrow derived mesenchymal stem cells into the liver: Potential to rescue pseudoxanthoma elasticum in a mouse model (Abcc6 -/-)
- Type VII collagen deficiency causes defective tooth enamel formation due to poor differentiation of ameloblasts
- Cell-based therapies for epidermolysis bullosa-From bench to bedside | Zellbasierte Therapien bei Epidermolysis bullosa-vom Labor zum Patienten
- Erratum: Early intra-amniotic gene transfer using lentiviral vector improves skin blistering phenotype in a murine model of Herlitz junctional epidermolysis bullosa (Gene Therapy (2012) 19 (561-569) DOI :10.1038/gt.2011. 135)
- Rare heritable skin diseases: Targets for regenerative medicine
- A novel animal model for pseudoxanthoma elasticum: The KK/HlJ mouse
- Magnesium: Novel applications in cardiovascular disease - A review of the literature
- Keratinocyte-Targeted Expression of Human Laminin γ2 Rescues Skin Blistering and Early Lethality of Laminin γ2 Deficient Mice
- Revertant mosaicism in heritable skin diseases: mechanisms of natural gene therapy.