(Q28287132)

1

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Hirotake Kitaura

2

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T Jeffrey Keen

3

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Hiroyoshi Ariga

5

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Sanae M M Iguchi-Ariga

Experimental Cell Research

6

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language of work or name

English

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publication date

1 November 2004

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published in

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volume

300

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issue

2

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page(s)

283-96

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cites work

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The PIM-1 serine kinase prolongs survival and inhibits apoptosis-related mitochondrial dysfunction in part through a bcl-2-dependent pathway

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Pim-1 kinase and p100 cooperate to enhance c-Myb activity

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Physical and functional interactions between Pim-1 kinase and Cdc25A phosphatase. Implications for the Pim-1-mediated activation of the c-Myc signaling pathway

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Identification of heterochromatin protein 1 (HP1) as a phosphorylation target by Pim-1 kinase and the effect of phosphorylation on the transcriptional repression function of HP1(1)

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Pim-1 translocates sorting nexin 6/TRAF4-associated factor 2 from cytoplasm to nucleus

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Pim-1 associates with protein complexes necessary for mitosis

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Retinitis pigmentosa: defined from a molecular point of view

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Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa

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A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11)

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Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa

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A new technique for the assay of infectivity of human adenovirus 5 DNA

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MM-1, a novel c-Myc-associating protein that represses transcriptional activity of c-Myc

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ORC1 interacts with c-Myc to inhibit E-box-dependent transcription by abrogating c-Myc-SNF5/INI1 interaction

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Core filaments of the nuclear matrix

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SR proteins and splicing control

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Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei

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Normal and mutant human β-globin pre-mRNAs are faithfully and efficiently spliced in vitro

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The role of exon sequences in splice site selection.

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The cellular organization of gene expression

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Factor required for mammalian spliceosome assembly is localized to discrete regions in the nucleus

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Isolation of a complementary DNA that encodes the mammalian splicing factor SC35

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Both subunits of U2AF recognize the 3' splice site in Caenorhabditis elegans

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Regulation of alternative splicing in vivo by overexpression of antagonistic splicing factors

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Disease mechanism for retinitis pigmentosa (RP11) caused by mutations in the splicing factor gene PRPF31

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Protein 61K, encoded by a gene (PRPF31) linked to autosomal dominant retinitis pigmentosa, is required for U4/U6*U5 tri-snRNP formation and pre-mRNA splicing

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CIR, a corepressor linking the DNA binding factor CBF1 to the histone deacetylase complex

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A role for SKIP in EBNA2 activation of CBF1-repressed promoters

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10.1016/J.YEXCR.2004.07.029

7 January 2021

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

15474994

1 reference

Consolidated OpenCitations Corpus – April 2017