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PubMed 10021330 The surface ectoderm is essential for nephric duct formation in intermediate mesoderm. The nephric duct is the first epithelial tubule to differentiate from intermediate mesoderm that is essential for 1.29 KB 2015-11-20 2 131
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PubMed 10021369 Identification of APC2, a homologue of the adenomatous polyposis coli tumour suppressor. The adenomatous polyposis coli (APC) tumour-suppressor protein controls the Wnt signalling pathway by forming a 1.07 KB 2019-12-21 13 87
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PubMed 10022127 TIF1gamma, a novel member of the transcriptional intermediary factor 1 family. We report the cloning and characterization of a novel member of the Transcriptional Intermediary Factor 1 (TIF1) gene fam 1.39 KB 2015-11-20 2 123
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PubMed 10022831 Role of alphavbeta3 integrin in the activation of vascular endothelial growth factor receptor-2. Interaction between integrin alphavbeta3 and extracellular matrix is crucial for endothelial cells spro 1.7 KB 2015-10-30 6 152
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PubMed 10022888 A novel genetic screen for snRNP assembly factors in yeast identifies a conserved protein, Sad1p, also required for pre-mRNA splicing. The assembly pathway of spliceosomal snRNPs in yeast is poorly un 1.73 KB 2015-11-20 3 128
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PubMed 10022904 Activation of IkappaB kinase beta by protein kinase C isoforms. The atypical protein kinase C (PKC) isotypes (lambda/iotaPKC and zetaPKC) have been shown to be critically involved in important cell fu 2.05 KB 2015-10-30 4 124
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PubMed 10022909 Mammalian staufen is a double-stranded-RNA- and tubulin-binding protein which localizes to the rough endoplasmic reticulum. Staufen (Stau) is a double-stranded RNA (dsRNA)-binding protein involved in 1.2 KB 2015-11-20 3 95
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PubMed 10022914 Identification of a novel family of targets of PYK2 related to Drosophila retinal degeneration B (rdgB) protein. The protein tyrosine kinase PYK2 has been implicated in signaling pathways activated by 1.69 KB 2015-10-30 4 111
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PubMed 10023043 Genomic organization and promoter characterization of two human UHS keratin genes. TTD is a rare human genetic disease caused by mutations in XPB and XPD, two subunits of the transcription/repair fact 960 Bytes 2015-10-30 5 47
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PubMed 10023073 The human genome has only one functional hsp47 gene (CBP2) and a pseudogene (pshsp47). Among all the species investigated to date, only in humans is hsp47 reported to exist as two separate genes. Here 1.09 KB 2015-11-20 2 49
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