https://ogma.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 Discovery of 42 genome-wide significant loci associated with dyslexia https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:53505 Thu 30 Nov 2023 15:57:26 AEDT ]]> Bacterial subcellular architecture: recent advances and future prospects https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:2479 Sat 24 Mar 2018 08:27:44 AEDT ]]> The midcell replication factory in Bacillus subtilis is highly mobile: implications for coordinating chromosome replication with other cell cycle events https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:2488 Sat 24 Mar 2018 08:27:44 AEDT ]]> Resequencing and fine-mapping of the chromosome 12q13-14 locus associated with multiple sclerosis refines the number of implicated genes https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:18970 Sat 24 Mar 2018 07:58:53 AEDT ]]> Prometaphase APCcdh¹ activity prevents non-disjunction in mammalian oocytes https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:6537 Sat 24 Mar 2018 07:48:19 AEDT ]]> Essential CDK1-inhibitory role for separase during meiosis I in vertebrate oocytes https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:6562 Sat 24 Mar 2018 07:47:07 AEDT ]]> Subcellular organisation in bacteria https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:6633 Sat 24 Mar 2018 07:46:21 AEDT ]]> Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:276 30% of mutations seem to cluster on proximal Xp and in the pericentric region. In a systematic screen of brain-expressed genes from this region in 210 families with XLMR, we identified seven different mutations in JARID1C, including one frameshift mutation and two nonsense mutations that introduce premature stop codons, as well as four missense mutations that alter evolutionarily conserved amino acids. In two of these families, expression studies revealed the almost complete absence of the mutated JARID1C transcript, suggesting that the phenotype in these families results from functional loss of the JARID1C protein. JARID1C (Jumonji AT-rich interactive domain 1C), formerly known as "SMCX," is highly similar to the Y-chromosomal gene JARID1D/SMCY, which encodes the H-Y antigen. The JARID1C protein belongs to the highly conserved ARID protein family. It contains several DNA-binding motifs that link it to transcriptional regulation and chromatin remodeling, processes that are defective in various other forms of mental retardation. Our results suggest that JARID1C mutations are a relatively common cause of XLMR and that this gene might play an important role in human brain function.]]> Sat 24 Mar 2018 07:43:03 AEDT ]]>