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
- The complexity of elastic fibre biogenesis in the skin - a perspective to the clinical heterogeneity of cutis laxa
- Vitamin K-dependent carboxylation of matrix Gla-protein: a crucial switch to control ectopic mineralization
- 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
- A Single-Nucleotide Polymorphism in the Abcc6 Gene Associates with Connective Tissue Mineralization in Mice Similar to Targeted Models for Pseudoxanthoma Elasticum
- Keratinocyte-Targeted Expression of Human Laminin γ2 Rescues Skin Blistering and Early Lethality of Laminin γ2 Deficient Mice
- Restricting dietary magnesium accelerates ectopic connective tissue mineralization in a mouse model of pseudoxanthoma elasticum (Abcc6 -/-)
- Magnesium: Novel Applications in Cardiovascular Disease - A Review of the Literature.
- Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutation
- Efficacy of mesotherapy in facial rejuvenation: A histological and immunohistochemical evaluation
- Familial pityriasis rubra pilaris is caused by mutations in CARD14
- Mouse Samd9l is not a functional paralogue of the human SAMD9, the gene mutated 07AF in normophosphataemic familial tumoral calcinosis
- Progress in epidermolysis bullosa: Summary of a workshop in CILAD-2010
- Magnesium Reduces Carotid Intima-Media Thickness in a Mouse Model of Pseudoxanthoma Elasticum: A Novel Treatment Biomarker
- Multiple minimally invasive Erbium: Yttrium Aluminum Garnet laser mini-peels for skin rejuvenation: An objective assessment
- Early intra-amniotic gene transfer using lentiviral vector improves skin blistering phenotype in a murine model of Herlitz junctional epidermolysis bullosa