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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 08 Dec 2016.

Luc7 homolog

LUC7L, hLuc7B1, LUC7-LIKE, Luc7 homolog (S. cerevisiae)-like
The LUC7L gene may represent a mammalian heterochromatic gene, encoding a putative RNA-binding protein similar to the yeast Luc7p subunit of the U1 snRNP splicing complex that is normally required for 5-prime splice site selection (Tufarelli et al., 2001 [PubMed 11170747]).[supplied by OMIM, Mar 2008] (from NCBI)
Top mentioned proteins: V1a, AAG, HAD, GILZ, MKP-1
Papers on LUC7L
High Incidence of Malaria Along the Sino-Burmese Border Is Associated With Polymorphisms of CR1, IL-1A, IL-4R, IL-4, NOS, and TNF, But Not With G6PD Deficiency.
New
Zhu et al., Saint Helena. In Medicine (baltimore), Oct 2015
Logistic regression was used to calculate the prevalence odds ratio (POR) and 95% confidence interval (CI) of malaria for the T520C SNP of CR1 and SNPs of G6PD, IL-4, IL-4R, IL-1A, NOS, CD40LG, TNF, and LUC7L.
Fish Myogenic Regulatory Protein LUC7L: Characterization and Expression Analysis in Korean Rose Bitterling (Rhodeus uyekii).
An et al., Pusan, South Korea. In Dev Reprod, 2014
Serine-arginine-rich nuclear protein LUC7L plays an important role in the regulation of myogenesis in mice.
Globin gene structure in a reptile supports the transpositional model for amniote α- and β-globin gene evolution.
Graves et al., Canberra, Australia. In Chromosome Res, 2010
According to this model, all jawed vertebrates share one ancient region containing α- and β-globin genes and several flanking genes in the order MPG-C16orf35-(α-β)-GBY-LUC7L that has been conserved for more than 410 million years, whereas amniotes evolved a distinct β-globin cluster by insertion of a transposed β-globin gene from this ancient region into a cluster of olfactory receptors flanked by CCKBR and RRM1.
Increase in dual specificity phosphatase 1, TGF-beta stimulated gene 22, domain family protein 3 and Luc7 homolog (S. cerevisiae)-like messenger RNA after mechanical asphyxiation in the mouse lung.
Nakasono et al., Nagasaki, Japan. In Leg Med (tokyo), 2009
Of those genes, quantitative real-time PCR revealed that dual specificity phosphatase 1 (Dusp1), TGF-beta stimulated gene 22, domain family protein 3 (TSC22d3) and Luc7 homolog (Saccharomyces cerevisiae)-like (Luc7l) after asphyxia were more significantly increased than those after decapitation.
The Diasporin Pathway: a tumor progression-related transcriptional network that predicts breast cancer survival.
Hunter et al., Bethesda, United States. In Clin Exp Metastasis, 2007
Seven candidates were identified (Ndn, Pi16, Luc7l, Rrp1b, Brd4, Centd3 and Csf1r).
Platypus globin genes and flanking loci suggest a new insertional model for beta-globin evolution in birds and mammals.
Graves et al., Canberra, Australia. In Bmc Biol, 2007
Comparison of flanking sequences revealed that all jawed vertebrate alpha-globin clusters are flanked by MPG-C16orf35 and LUC7L, whereas all bird and mammal beta-globin clusters are embedded in olfactory genes.
The U1 snRNP-associated factor Luc7p affects 5' splice site selection in yeast and human.
Séraphin et al., Heidelberg, Germany. In Nucleic Acids Res, 2006
Database searches identified three putative human yLuc7p homologs (hLuc7A, hLuc7B1 and hLuc7B2).
Sequencing and mapping hemoglobin gene clusters in the Australian model dasyurid marsupial Sminthopsis macroura.
Graves et al., Melbourne, Australia. In Cytogenet Genome Res, 2004
The LUC7L gene was found 3' of the S. macroura alpha locus, a gene order shared with humans but not mouse, chicken or fugu.
Serine-arginine-rich nuclear protein Luc7l regulates myogenesis in mice.
GeneRIF
Morisaki et al., Suita, Japan. In Gene, 2004
Luc7l is thought to play an important role in the regulation of muscle differentiation.
Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease.
Impact
Higgs et al., Oxford, United Kingdom. In Nat Genet, 2003
We recently described an individual with an inherited form of anemia (alpha-thalassemia) who has a deletion that results in a truncated, widely expressed gene (LUC7L) becoming juxtaposed to a structurally normal alpha-globin gene (HBA2).
Characterization of a widely expressed gene (LUC7-LIKE; LUC7L) defining the centromeric boundary of the human alpha-globin domain.
Higgs et al., Oxford, United Kingdom. In Genomics, 2001
The gene, called 16pHQG;16 (HGMW-approved symbol LUC7L), is widely transcribed and lies in the opposite orientation with respect to the alpha-globin genes.
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