hmg.oxfordjournals.org

     
Concentrates on full-length research papers covering a wide range of topics in all aspects of human molecular genetics. Subscription required for full-text papers.

Tweets about hmg.oxfordjournals.org

  • RT @KrisGevaert_VIB: N-terminal acetylation defects: trying to understand the Ogden syndrome; #UGent #VIB #Proteomics
  • thanks to @UUtah Clinical Genetics Research Program: Phenotyping Core at University of Utah (CCTS grant UL1RR025764).
  • N-terminal acetylation defects: trying to understand the Ogden syndrome; #UGent #VIB #Proteomics
  • Provisional PDF now out for this paper on Ogden Syndrome we worked on for past three years.
  • RT @YiXing77: @aloraine205 @EduEyras have been doing this for a while. works very well. see this and this
  • @aloraine205 @EduEyras have been doing this for a while. works very well. see this and this
  • Our recent work featured on the cover page of #hmg
  • Ion channels: structural bioinformatics and modelling
  • Italian Scientists reveal how SEPN-1 mutation causes muscle disease and possible treatment avenue
  • A new, improved mouse model for SOD1-related amyotrophic lateral sclerosis via @feedly
  • Non-coding RNA #ncRNA research "...small ncRNAs ...in prokaryotes that appear to regulate mRNA translation/stability"
  • Interesting article on HIV & mutant genes @timesnewsdesk
  • Non-coding #RNA - Human Molecular Genetics: Abstract. The term non-coding #RNA (ncRNA) is commonly employed… #bing
  • New #HMG paper on SEPN1 counteracts hyper-oxidation by means of redox-regulating SERCA2 pump activity in sk. muscle
  • genetics and #SkinColor: #race
  • RT @Matt_Muscle_Guy: New #HMG paper linking dystrophin protein structure to Becker Muscular Dystrophy (BMD) disease severity
  • @MaRianaGlezC if you want to specifically read my research, you can find it at
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