0B68 Li, Qiaoli - Thomas Jefferson University - Thomas Jefferson University
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Qiaoli Li, PhD

Contact Dr. Li

233 South Tenth Street
Bluemle Life Sciences Building, Suite 430
Philadelphia, PA 19107

(215) 503-5713
(215) 503-5788 fax

Most Recent Peer-reviewed Publications

  1. Mutations in the ABCC6 gene as a cause of generalized arterial calcification of infancy: Genotypic overlap with pseudoxanthoma elasticum
  2. Changes in Dermal Fibroblasts from Abcc6-/- Mice Are Present before and after the Onset of Ectopic Tissue Mineralization
  3. Analysis of pseudoxanthoma elasticum-causing missense mutants of ABCC6 in vivo; Pharmacological correction of the mislocalized proteins
  4. Mouse alopecia areata and heart disease: Know your mouse!
  5. Zebrafish as a model system to study heritable skin diseases
  6. Clinical phenotypes and ABCC6 gene mutations in brazilian families with pseudoxanthoma elasticum
  7. Mutant Enpp1asj mice as a model for generalized arterial calcification of infancy
  8. Mineralization/anti-mineralization networks in the skin and vascular connective tissues
  9. Pseudoxanthoma elasticum: The paradigm of ectopic mineralization disorders - Diagnosis and treatment
  10. Warfarin accelerates ectopic mineralization in Abcc6-/- mi Clinical relevance to pseudoxanthoma elasticum
  11. Up-Regulated Expression and Aberrant DNA Methylation of LEP and SH3PXD2A in Pre-Eclampsia
  12. A single-nucleotide polymorphism in the Abcc6 gene associates with connective tissue mineralization in mice similar to targeted models for pseudoxanthoma elasticum
  13. Quantitative analysis of follistatin (FST) promoter methylation in peripheral blood of patients with polycystic ovary syndrome
  14. The complexity of elastic fibre biogenesis in the skin - a perspective to the clinical heterogeneity of cutis laxa
  15. Identification and Functional Study of a New Missense Mutation in the Motor Head Domain of Myosin VIIA in a Family with Autosomal Dominant Hearing Impairment (DFNA11)
  16. Heritable ectopic mineralization disorders: the paradigm of pseudoxanthoma elasticum.
  17. A novel animal model for pseudoxanthoma elasticum: The KK/HlJ mouse
  18. Lack of support for association between the copy number variants in the FCGR locus and schizophrenia: A case control study
  19. Mouse Samd9l is not a functional paralogue of the human SAMD9, the gene mutated in normophosphataemic familial tumoral calcinosis
  20. HLA-B*58:01 allele is associated with augmented risk for both mild and severe cutaneous adverse reactions induced by allopurinol in Han Chinese
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