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Items: 4

1.
Bi-allelic Variants in METTL5 Cause Autosomal-Recessive Intellectual Disability and Microcephaly
Elodie M. Richard, Daniel L. Polla, Muhammad Zaman Assir, Minerva Contreras, Mohsin Shahzad, Asma A. Khan, Attia Razzaq, Javed Akram, Moazzam N. Tarar, Thomas A. Blanpied, Zubair M. Ahmed, Rami Abou Jamra, Dagmar Wieczorek, Hans van Bokhoven, Sheikh Riazuddin, Saima Riazuddin
Am J Hum Genet. 2019 Oct 3; 105(4): 869–878. Published online 2019 Sep 26. doi: 10.1016/j.ajhg.2019.09.007
PMCID:
PMC6817559
AbstractArticlePDF–1.7M
2.
The human 18S rRNA m6A methyltransferase METTL5 is stabilized by TRMT112
Nhan van Tran, Felix G M Ernst, Ben R Hawley, Christiane Zorbas, Nathalie Ulryck, Philipp Hackert, Katherine E Bohnsack, Markus T Bohnsack, Samie R Jaffrey, Marc Graille, Denis L J Lafontaine
Nucleic Acids Res. 2019 Sep 5; 47(15): 7719–7733. Published online 2019 Jul 22. doi: 10.1093/nar/gkz619
PMCID:
PMC6735865
AbstractArticlePDF–4.3M
3.
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences
Mammalian Gene Collection (MGC) Program Team
Proc Natl Acad Sci U S A. 2002 Dec 24; 99(26): 16899–16903. Published online 2002 Dec 11. doi: 10.1073/pnas.242603899
PMCID:
PMC139241
AbstractArticlePDF–118K
4.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas
Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042
PMCID:
PMC3178059
AbstractArticlePDF–1.0M

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