GDI1 gene

Rare copy-number variation (CNV) is an important source of risk for autism spectrum disorders (ASDs). We analyzed 2,446 ASD… (More)

Selection of reference genes in Brassica napus, a tetraploid (4×) species, is a very difficult task without information on genome… (More)

X-linked intellectual disability (XLID) is a heterogeneous disorder, and mutations in more than 90 genes have been associated… (More)

We report on the identification of a 0.3 Mb inherited recurrent but variable copy-number gain at Xq28 in affected males of four… (More)

Rho GDP-dissociation inhibitors (RhoGDIs) modulate the cycling of Rho GTPases between active GTP-bound and inactive GDP-bound… (More)

X-linked forms of mental retardation (XLMR) include a variety of different disorders and may account for up to 25% of all… (More)

Rab is a family of small Ras-like GTPases regulating intracellular vesicle transport. We have previously reported that prenylated… (More)

The most likely cause of the Rett syndrome (RTT) is an X-linked dominant mutation lethal in hemizygous males. Previous exclusion… (More)

GTP binding proteins of the Sec4/Ypt/rab family regulate distinct vesicular traffic events in eukaryotic cells. We have cloned… (More)

After the development of efficient methods for the construction of transcription maps of defined genomic regions, the rate… (More)