hmg.oxfordjournals.org
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URLs from hmg.oxfordjournals.org:
URL: http://hmg.oxfordjournals.org/cgi/reprint/13/21/2625.pdf URL: http://hmg.oxfordjournals.org/cgi/content/full/12/21/2837 URL: http://hmg.oxfordjournals.org/cgi/reprint/12/5/527.pdf URL: http://hmg.oxfordjournals.orgTweets 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