1. Phosphate’s fate made easier

   • Friedrich C. Luft

   Clinical Implications 10 December 2004 Pages: 1 - 2

   

2. Cellular prion protein neuroprotective function: implications in prion diseases

   • Xavier Roucou
   • Andréa C. LeBlanc

   Review 10 November 2004 Pages: 3 - 11

   

3. Autoantigen complementarity: a new theory implicating complementary proteins as initiators of autoimmune disease

   • William F. Pendergraft III
   • Barrak M. Pressler
   • Gloria A. Preston

   Review 11 December 2004 Pages: 12 - 25

   

4. Role of endogenous antisense RNA in cardiac gene regulation

   • Hans Peter Luther

   Review 09 December 2004 Pages: 26 - 32

   

5. Identification of a recurrent mutation in GALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders

   • Yaacov Frishberg
   • Orit Topaz
   • Eli Sprecher

   Original Article 15 December 2004 Pages: 33 - 38

   

6. Site-specific strand bias in gene correction using single-stranded oligonucleotides

   • Charlotte B. Sørensen
   • Anne-Margrethe Krogsdam
   • Thomas G. Jensen

   Original Article 27 October 2004 Pages: 39 - 49

   

7. Association of polymorphisms of the androgen receptor and klotho genes with bone mineral density in Japanese women

   • Yoshiji Yamada
   • Fujiko Ando
   • Hiroshi Shimokata

   Original Article 04 November 2004 Pages: 50 - 57

   

8. Functional analysis of a mutant form of the receptor tyrosine kinase Tie2 causing venous malformations

   • Paul N. Morris
   • Benjamin J. Dunmore
   • Nicholas P. J. Brindle

   Original Article 29 October 2004 Pages: 58 - 63

   

9. Antisense oligonucleotides and short interfering RNAs silencing the cyclin-dependent kinase inhibitor p21 improve proliferation of Duchenne muscular dystrophy patients’ primary skeletal myoblasts

   • Stefanie Endesfelder
   • Alexander Kliche
   • Astrid Speer

   Original Article 05 November 2004 Pages: 64 - 71

   

10. −717A>G polymorphism of human C-reactive protein gene associated with coronary heart disease in ethnic Han Chinese: the Beijing atherosclerosis study

    • Jianhong Chen
    • Jiangong Zhao
    • Dongfeng Gu

    Original Article 28 October 2004 Pages: 72 - 78

    

11. Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?

    • Jop H. van Berlo
    • Willem G. de Voogt
    • Yigal M. Pinto

    Original Article 13 November 2004 Pages: 79 - 83