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Reactome: clear view of a starry sky

Morag Robertson¹

¹m.robertson@elsevier.com

Drug Discovery Today

|September 3, 2004

Summary

No abstract available in PubMed .

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Mouse slc9a8 mutants exhibit retinal defects due to retinal pigmented epithelium dysfunction.

A dominant-negative mutation of mouse Lmx1b causes glaucoma and is semi-lethal via LDB1-mediated dimerization [corrected].

OCT4/SOX2-independent Nanog autorepression modulates heterogeneous Nanog gene expression in mouse ES cells.

The ubiquitin-associated (UBA) 1 domain of Schizosaccharomyces pombe Rhp23 is essential for the recognition of ubiquitin-proteasome system substrates both in vitro and in vivo.

The GP's role in improving the uptake of healthy start vitamins.

Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH.