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Displaying 14 of 14 results for "MRPL9"
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  1. RM09_RAT UniProt:Swiss-Prot

    ID: Q641X9

    Description: Mitochondrion 39S ribosomal protein L9, mitochondrial

  2. RM09_BOVIN UniProt:Swiss-Prot

    ID: Q2TBK2

    Description: Mitochondrion 39S ribosomal protein L9, mitochondrial In isoform 2. In isoform 2....

  3. Structure of the yeast mitochondrial ribosome - Class A PDB

    ID: PDB:5MRC

    Description: 54S ribosomal protein RML2, mitochondrial, 54S ribosomal protein

  4. Structure of the yeast mitochondrial ribosome - Class C PDB

    ID: PDB:5MRF

    Description: 54S ribosomal protein RML2, mitochondrial, 54S ribosomal protein

  5. Structure of the yeast mitochondrial ribosome - Class B PDB

    ID: PDB:5MRE

    Description: 54S ribosomal protein RML2, mitochondrial, 54S ribosomal protein

  6. RM09_PAPAN UniProt:Swiss-Prot

    ID: A9X1A9

    Description: Mitochondrion 39S ribosomal protein L9, mitochondrial

  7. Structure of the large subunit of the mammalian mitoribosome, part 1 of 2 PDB

    ID: PDB:4V19

    Description: MITORIBOSOMAL PROTEIN BL27M, MRPL27, MITORIBOSOMAL PROTEIN BL28M, MRPL28, MITORIBOSOMAL PROTEIN UL29M, MRPL...

  8. 39S large subunit of the porcine mitochondrial ribosome PDB

    ID: PDB:4CE4

    Description: , MRPL30, MRPL32, MRPL33, MRPL34, MRPL35, MRPL36, MRPL9, MRPL13, MRPL14, MRPL15, MRPL16, MRPL17, MRPL18, MRPL19, MRPL20, MRPL21, MRPL22, MRPL23, MRPL24, MRPL38, MRPL39, MRPL44, MRPL45, MRPL49, MRPL52, IC...

  9. RM09_DROME UniProt:Swiss-Prot

    ID: Q9VF89

    Description: Mitochondrion 39S ribosomal protein L9, mitochondrial

  10. RML9_SCHPO UniProt:Swiss-Prot

    ID: Q9P801

    Description: Mitochondrion Probable 54S ribosomal protein L9, mitochondrial

  11. RM09_SCHPO UniProt:Swiss-Prot

    ID: Q9P6P6

    Description: Mitochondrion 54S ribosomal protein L9, mitochondrial

  12. Potentiation of neurotoxicity in double mutant mice with Pink1 ablation and A53T-SNCA overexpression ArrayExpress

    ID: E-GEOD-60414

    Description: sive paralysis at ages >1 year and also exhibited protein aggregates with immunoreactivity for pSer129-SNCA, p62, and ubiquitin in spinal cord and basal brain, contrasting with absence of such features from SM. A brain proteome quantification of ubiquitination sites documented altered degradation of SNCA and the DNA-damage marker H2AX at age 18 months. Global brain transcriptome profiles and qPCR validation experiments identified many consistent transcriptional dysregulations already at age 6 weeks, which were absent from SM. The observed downregulations for Dapk1, Dcaf17, Rab42 and upregulations for Dctn5, Mrpl9, Tmem181a, Xaf1 reflect changes in ubiquitination, mitochondrial / synaptic / microtubular dynamics, and DNA damage. Thus, our study confirmed that SNCA-triggered neurotoxicity is exacerbated by the absence of PINK1, and identified a novel molecular signature that is detectable early in the course of this double pathology. Factorial design comparing Pink1 knock-out/A53T-SNCA double transgenic mice with appropriate wild-type controls (129SvEv+FVB/N...

  13. Potentiation of neurotoxicity in double mutant mice with Pink1 ablation and A53T-SNCA overexpression BioProject

    ID: PRJNA258208

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: sive paralysis at ages >1 year and also exhibited protein aggregates with immunoreactivity for pSer129-SNCA, p62, and ubiquitin in spinal cord and basal brain, contrasting with absence of such features from SM. A brain proteome quantification of ubiquitination sites documented altered degradation of SNCA and the DNA-damage marker H2AX at age 18 months. Global brain transcriptome profiles and qPCR validation experiments identified many consistent transcriptional dysregulations already at age 6 weeks, which were absent from SM. The observed downregulations for Dapk1, Dcaf17, Rab42 and upregulations for Dctn5, Mrpl9, Tmem181a, Xaf1 reflect changes in ubiquitination, mitochondrial / synaptic / microtubular dynamics, and DNA damage. Thus, our study confirmed that SNCA-triggered neurotoxicity is exacerbated by the absence of PINK1, and identified a novel molecular signature that is detectable early in the course of this double pathology. Overall design: Factorial design comparing Pink1 knock-out/A53T-SNCA double transgenic mice with appropriate wild-type control...
  14. Potentiation of neurotoxicity in double mutant mice with Pink1 ablation and A53T-SNCA overexpression OmicsDI

    ID: E-GEOD-60414

    Date Released: 11-08-2014

    Description: sive paralysis at ages >1 year and also exhibited protein aggregates with immunoreactivity for pSer129-SNCA, p62, and ubiquitin in spinal cord and basal brain, contrasting with absence of such features from SM. A brain proteome quantification of ubiquitination sites documented altered degradation of SNCA and the DNA-damage marker H2AX at age 18 months. Global brain transcriptome profiles and qPCR validation experiments identified many consistent transcriptional dysregulations already at age 6 weeks, which were absent from SM. The observed downregulations for Dapk1, Dcaf17, Rab42 and upregulations for Dctn5, Mrpl9, Tmem181a, Xaf1 reflect changes in ubiquitination, mitochondrial / synaptic / microtubular dynamics, and DNA damage. Thus, our study confirmed that SNCA-triggered neurotoxicity is exacerbated by the absence of PINK1, and identified a novel molecular signature that is detectable early in the course of this double pathology. Factorial design comparing Pink1 knock-out/A53T-SNCA double transgenic mice with appropriate wild-type controls (129SvEv+FVB/N...


Displaying 14 of 14 results for "MRPL9"