Prediction of the coding sequences of unidentified human genes. I. The coding sequences of 40 new genes (KIAA0001-KIAA0040) deduced by analysis of randomly sampled cDNA clones from human immature myeloid cell line KG-1
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The novel MMS-inducible gene Mif1/KIAA0025 is a target of the unfolded protein response pathwayA G protein-coupled receptor for UDP-glucoseMutations of MLC1 (KIAA0027), encoding a putative membrane protein, cause megalencephalic leukoencephalopathy with subcortical cystsA HECT domain E3 enzyme assembles novel polyubiquitin chainsMutations in the 3beta-hydroxysterol Delta24-reductase gene cause desmosterolosis, an autosomal recessive disorder of cholesterol biosynthesisThe Caenorhabditis elegans sex-determining protein FEM-2 and its human homologue, hFEM-2, are Ca2+/calmodulin-dependent protein kinase phosphatases that promote apoptosisRegulation of the multifunctional Ca2+/calmodulin-dependent protein kinase II by the PP2C phosphatase PPM1F in fibroblastsSilencing of KIF14 interferes with cell cycle progression and cytokinesis by blocking the p27(Kip1) ubiquitination pathway in hepatocellular carcinomaA human homolog of the mitochondrial protein import receptor Mom19 can assemble with the yeast mitochondrial receptor complexHuman helicase gene SKI2W in the HLA class III region exhibits striking structural similarities to the yeast antiviral gene SKI2 and to the human gene KIAA0052: emergence of a new gene familyPurification and characterization of a new eukaryotic protein translation factor. Eukaryotic initiation factor 4HA family of human receptors structurally related to Drosophila TollThe AML1-MTG8 leukemic fusion protein forms a complex with a novel member of the MTG8(ETO/CDR) family, MTGR1Structure of the highly conserved HERC2 gene and of multiple partially duplicated paralogs in humanMolecular pathogenesis of megalencephalic leukoencephalopathy with subcortical cysts: mutations in MLC1 cause folding defectsP2Y-like receptor, GPR105 (P2Y14), identifies and mediates chemotaxis of bone-marrow hematopoietic stem cellsThe immunogenicity of a new human minor histocompatibility antigen results from differential antigen processingShotgun sequencing of the human transcriptome with ORF expressed sequence tagsIntegrative annotation of 21,037 human genes validated by full-length cDNA clonesThe role of toll like receptors in pregnancyToward a protein-protein interaction map of the budding yeast: A comprehensive system to examine two-hybrid interactions in all possible combinations between the yeast proteinsLinking the 3' poly(A) tail to the subunit joining step of translation initiation: relations of Pab1p, eukaryotic translation initiation factor 5b (Fun12p), and Ski2p-Slh1p3' poly(A) is dispensable for translation.A link between secretion and pre-mRNA processing defects in Saccharomyces cerevisiae and the identification of a novel splicing gene, RSE1Interaction between Cannabinoid System and Toll-Like Receptors Controls InflammationInhibition of apoptosis by oncogenic hepatitis B virus X protein: Implications for the treatment of hepatocellular carcinomaAssociation between Toll-Like Receptor 4 Polymorphisms and Systemic Lupus Erythematosus Susceptibility: A Meta-AnalysisFurther biochemical and kinetic characterization of human eukaryotic initiation factor 4HHERC3 binding to and regulation by ubiquitinHodgkin's lymphoma cell lines express a fusion protein encoded by intergenically spliced mRNA for the multilectin receptor DEC-205 (CD205) and a novel C-type lectin receptor DCL-1A missense mutation in a novel gene encoding a putative cation channel is associated with catatonic schizophrenia in a large pedigreeCreation of genome-wide protein expression libraries using random activation of gene expressionMolecular cloning of a 74-kDa regulatory subunit (B" or delta) of human protein phosphatase 2AIL-1Rrp is a novel receptor-like molecule similar to the type I interleukin-1 receptor and its homologues T1/ST2 and IL-1R AcPPlant and animal sensors of conserved microbial signaturesIdentification of a human cDNA clone for lysosomal type Ca2+-independent phospholipase A2 and properties of the expressed proteinGene identification in 1.6-Mb region of the Down syndrome region on chromosome 21Wobble modification defect in tRNA disturbs codon-anticodon interaction in a mitochondrial diseasePhospholipid hydroperoxides are substrates for non-selenium glutathione peroxidase.Directional cDNA library construction assisted by the in vitro recombination reaction.
P2860
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P2860
Prediction of the coding sequences of unidentified human genes. I. The coding sequences of 40 new genes (KIAA0001-KIAA0040) deduced by analysis of randomly sampled cDNA clones from human immature myeloid cell line KG-1
description
1994 nî lūn-bûn
@nan
1994 թուականին հրատարակուած գիտական յօդուած
@hyw
1994 թվականին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Prediction of the coding seque ...... mmature myeloid cell line KG-1
@ast
Prediction of the coding seque ...... mmature myeloid cell line KG-1
@en
Prediction of the coding seque ...... mmature myeloid cell line KG-1
@nl
type
label
Prediction of the coding seque ...... mmature myeloid cell line KG-1
@ast
Prediction of the coding seque ...... mmature myeloid cell line KG-1
@en
Prediction of the coding seque ...... mmature myeloid cell line KG-1
@nl
prefLabel
Prediction of the coding seque ...... mmature myeloid cell line KG-1
@ast
Prediction of the coding seque ...... mmature myeloid cell line KG-1
@en
Prediction of the coding seque ...... mmature myeloid cell line KG-1
@nl
P2093
P3181
P356
P1433
P1476
Prediction of the coding seque ...... mmature myeloid cell line KG-1
@en
P2093
K Ishikawa
N Miyajima
Y Kawarabayasi
P3181
P356
10.1093/DNARES/1.1.27
P407
P50
P577
1994-01-01T00:00:00Z