0B68 Fertala, Andrzej - Thomas Jefferson University - Thomas Jefferson University
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Andrzej Fertala, PhD

Contact Dr. Fertala

1015 Walnut Street
Bluemle Life Sciences Building, Room 430
Philadelphia, PA 19107

(215) 503-0113

Most Recent Peer-reviewed Publications

  1. Developmental upregulation of an alternative form of pcp2 with reduced GDI activity
  2. Skeletal diseases caused by mutations that affect collagen structure and function
  3. Kuskokwim syndrome, a recessive congenital contracture disorder, extends the phenotype of FKBP10 mutations
  4. Engineering and characterization of the chimeric antibody that targets the c-terminal telopeptide of the α2 chain of human collagen I: A next step in the quest to reduce localized fibrosis
  5. Visualizing molecular polar order in tissues via electromechanical coupling
  6. Remodeling of the dermalepidermal junction in bilayered skin constructs after silencing the expression of the p.R2622Q and p.G2623C collagen VII mutants
  7. Electromechanical properties of dried tendon and isoelectrically focused collagen hydrogels
  8. 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)
  9. Visualizing molecular polar order in tissues via electromechanical coupling
  10. Comparison of electromechanical properties between tendon and iso-electrically focused collagen
  11. Perlecan domain V is neuroprotective and proangiogenic following ischemic stroke in rodents
  12. Persistence of intracellular and extracellular changes after incompletely suppressing expression of the R789C (p.R989C) and R992C (p.R1192C) collagen II mutants
  13. Endostatin binds nerve growth factor and thereby inhibits neurite outgrowth and neuronal migration in-vitro
  14. Reducing the effects of intracellular accumulation of thermolabile collagen II mutants by increasing their thermostability in cell culture conditions
  15. Compound heterozygous desmoplakin mutations result in a phenotype with a combination of myocardial, skin, hair, and enamel abnormalities
  16. Recessive COL6A2 C-globular missense mutations in Ullrich congenital muscular dystrophy: Role of the C2a splice variant
  17. Fluorescent protein markers to tag collagenous proteins: The paradigm of procollagen VII
  18. R992C (p.R1192C) Substitution in Collagen II Alters the Structure of Mutant Molecules and Induces the Unfolded Protein Response
  19. Collagen fibril formation: A new target to limit fibrosis
  20. Candidate cell and matrix interaction domains on the collagen fibril, the predominant protein of vertebrates
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