HUGE: a database for human large proteins identified in the Kazusa cDNA sequencing project - Wikidata - awgldk - TriplyDB

HUGE: a database for human large proteins identified in the Kazusa cDNA sequencing project

HUGE: a database for human large proteins identified in the Kazusa cDNA sequencing project

http://www.wikidata.org/entity/Q24548444

about

Cloning of a novel signaling molecule, AMSH-2, that potentiates transforming growth factor beta signaling Human HRD1 is an E3 ubiquitin ligase involved in degradation of proteins from the endoplasmic reticulum Expression and genomic analysis of midasin, a novel and highly conserved AAA protein distantly related to dynein.Limkain b1, a novel human autoantigen localized to a subset of ABCD3 and PXF marked peroxisomes Human CNK1 acts as a scaffold protein, linking Rho and Ras signal transduction pathways Identification of TINO: a new evolutionarily conserved BCL-2 AU-rich element RNA-binding protein A family of RIM-binding proteins regulated by alternative splicing: Implications for the genesis of synaptic active zones.hSnm1 colocalizes and physically associates with 53BP1 before and after DNA damage A transcript finishing initiative for closing gaps in the human transcriptome The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcripts ProtSweep, 2Dsweep and DomainSweep: protein analysis suite at DKFZ Integrative annotation of 21,037 human genes validated by full-length cDNA clones Classification between normal and tumor tissues based on the pair-wise gene expression ratio Widespread A-to-I RNA editing of Alu-containing mRNAs in the human transcriptome Phosphorylation of clock protein PER1 regulates its circadian degradation in normal human fibroblasts.Integrative analysis of kinase networks in TRAIL-induced apoptosis provides a source of potential targets for combination therapy CAST2: identification and characterization of a protein structurally related to the presynaptic cytomatrix protein CAST A PDZ-binding motif as a critical determinant of Rho guanine exchange factor function and cell phenotype Alu mobile elements: from junk DNA to genomic gems Systematic identification of abundant A-to-I editing sites in the human transcriptome ANGLE: a sequencing errors resistant program for predicting protein coding regions in unfinished cDNA.Exome analysis reveals differentially mutated gene signatures of stage, grade and subtype in breast cancers.Widespread RNA editing of embedded alu elements in the human transcriptome.A survey of RNA editing in human brain A bioinformatic screen for novel A-I RNA editing sites reveals recoding editing in BC10.Assessing serotonin receptor mRNA editing frequency by a novel ultra high-throughput sequencing method.Editing of neurotransmitter receptor and ion channel RNAs in the nervous system RNA hairpins in noncoding regions of human brain and Caenorhabditis elegans mRNA are edited by adenosine deaminases that act on RNA.Histone acetyltransferase hALP and nuclear membrane protein hsSUN1 function in de-condensation of mitotic chromosomes.RNA editing level in the mouse is determined by the genomic repeat repertoire.Numerous novel annotations of the human genome sequence supported by a 5'-end-enriched cDNA collection.Human EFO1p exhibits acetyltransferase activity and is a unique combination of linker histone and Ctf7p/Eco1p chromatid cohesion establishment domains.CAFTAN: a tool for fast mapping, and quality assessment of cDNAs.HUGE: a database for human KIAA proteins, a 2004 update integrating HUGEppi and ROUGE.A novel mitochondrial Ca2+-dependent solute carrier in the liver identified by mRNA differential display.A novel de novo microdeletion at 17q11.2 adjacent to NF1 gene associated with developmental delay, short stature, microcephaly and dysmorphic features.Expression and activity of citrullinating peptidylarginine deiminase enzymes in monocytes and macrophages Letter from the editor: Adenosine-to-inosine RNA editing in Alu repeats in the human genome.Editing the message from A to I.Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.

P2860

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P2860

HUGE: a database for human large proteins identified in the Kazusa cDNA sequencing project

http://www.wikidata.org/entity/Q24548444

description

2002 nî lūn-bûn

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2002 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2002 թվականի հունվարին հրատարակված գիտական հոդված

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2002年の論文

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HUGE: a database for human lar ...... Kazusa cDNA sequencing project

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Nucleic Acids Research

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HUGE: a database for human lar ...... Kazusa cDNA sequencing project

@en

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Mina Waki

http://www.w3.org/2001/XMLSchema#string

Osamu Ohara

http://www.w3.org/2001/XMLSchema#string

Reiko Kikuno

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Takahiro Nagase

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P2860

Initial sequencing and analysis of the human genome

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

Prediction of complete gene structures in human genomic DNA

Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro

Construction and characterization of human brain cDNA libraries suitable for analysis of cDNA clones encoding relatively large proteins

RefSeq and LocusLink: NCBI gene-centered resources

The SWISS-PROT protein sequence database and its supplement TrEMBL in 2000.

A computer program for aligning a cDNA sequence with a genomic DNA sequence

GeneCards: a novel functional genomics compendium with automated data mining and query reformulation support.

Inosine exists in mRNA at tissue-specific levels and is most abundant in brain mRNA

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166-8

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scholarly article

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1165839

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10.1093/NAR/30.1.166

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1

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30

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11605606

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11752282

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99081

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