M E Elder

Summary

Affiliation: University of California
Country: USA

Publications

  1. ncbi Distinct T cell developmental consequences in humans and mice expressing identical mutations in the DLAARN motif of ZAP-70
    M E Elder
    Department of Pediatrics, University of California, San Francisco, CA 94143, USA
    J Immunol 166:656-61. 2001
  2. ncbi Human severe combined immunodeficiency due to a defect in ZAP-70, a T cell tyrosine kinase
    M E Elder
    Department of Pediatrics, University of California, San Francisco 94143 0110
    Science 264:1596-9. 1994
  3. ncbi Association between beta2-glycoprotein I gene polymorphisms and pediatric SLE and antiphospholipid antibodies
    E von Scheven
    Pediatric Rheumatology, University of California, San Francisco, CA 94143, USA
    Lupus 14:440-4. 2005
  4. ncbi A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)
    J Zonana
    Department of Molecular and Medical Genetics, Oregon Health Sciences University, Portland, OR 97221, USA
    Am J Hum Genet 67:1555-62. 2000

Collaborators

  • J Wu
  • E von Scheven
  • J Zonana
  • S J Orlow
  • B M Ferguson
  • M Golabi
  • S K Shapira
  • D W Wara
  • S A Emmal
  • P A Farndon
  • C Moss
  • L C Schneider

Detail Information

Publications4

  1. ncbi Distinct T cell developmental consequences in humans and mice expressing identical mutations in the DLAARN motif of ZAP-70
    M E Elder
    Department of Pediatrics, University of California, San Francisco, CA 94143, USA
    J Immunol 166:656-61. 2001
    ....
  2. ncbi Human severe combined immunodeficiency due to a defect in ZAP-70, a T cell tyrosine kinase
    M E Elder
    Department of Pediatrics, University of California, San Francisco 94143 0110
    Science 264:1596-9. 1994
    ..These findings demonstrate that ZAP-70 is essential for human T cell function and suggest that CD4+ and CD8+ T cells depend on different intracellular signaling pathways to support their development or survival...
  3. ncbi Association between beta2-glycoprotein I gene polymorphisms and pediatric SLE and antiphospholipid antibodies
    E von Scheven
    Pediatric Rheumatology, University of California, San Francisco, CA 94143, USA
    Lupus 14:440-4. 2005
    ..Neither novel exon 7 beta2GPI mutations or the previously described C306G polymorphism was identified in this pediatric cohort...
  4. ncbi A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)
    J Zonana
    Department of Molecular and Medical Genetics, Oregon Health Sciences University, Portland, OR 97221, USA
    Am J Hum Genet 67:1555-62. 2000
    ....