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Displaying 15 of 15 results for "CCT3"
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  1. SOLUTION STRUCTURE OF INTRASTRAND CISPLATIN-CROSSLINKED DNA OCTAMER D(CCTG*G*TCC):D(GGACCAGG), NMR, MINIMIZED AVERAGE STRUCTURE PDB

    ID: PDB:1AU5

    Description: 5'-D(*CP*CP*TP*GP*GP*TP*CP*C)-3', 5'-D(*GP*GP*AP*CP*CP*AP*GP*G)-3'

  2. Structure of two CCTG repeats PDB

    ID: PDB:5GWL

    Description: DNA (5'-D(*CP*CP*TP*GP*CP*CP*TP*G)-3')

  3. Transcriptome analysis of Myotonic Dystrophy type 2 (DM2) patients ArrayExpress

    ID: E-GEOD-37084

    Description: mal dominant disease caused by the expansion of a CCTG tetraplet repeat. It is a multisystemic disorder, affecting skeletal muscles, the heart, the eye, the central nervous system and the endocrine system. Whole mRNAs express...

  4. microRNAs expression profile in Myotonic Dystrophy type-2 (DM2) patients ArrayExpress

    ID: E-GEOD-37794

    Description: mal dominant disease caused by the expansion of a CCTG tetraplet repeat. It is a multisystemic disorder, affecting skeletal muscles, the heart, the eye, the central nervous system and the endocrine system The expression of 36...

  5. TCPG_BOVIN UniProt:Swiss-Prot

    ID: Q3T0K2

    Description: T-complex protein 1 subunit gamma N-acetylmethionine Phosphoserine Phosphoserine N6-acetyllysine Phosphoserine Phosphoserine Phospho...

  6. TCPG_RAT UniProt:Swiss-Prot

    ID: Q6P502

    Description: T-complex protein 1 subunit gamma N-acetylmethionine Phosphoserine Phosphoserine N6-acetyllysine Phosphoserine Phosphoserine Phospho...

  7. Homo sapiens : The human myotonic dystrophy type 1 transcriptome BioProject

    ID: PRJNA293977

    Keywords: transcriptome

    Access Type: download

    dataset.description: ly multi-systemic disorder caused by expanded CTG/CCTG repeats. Muscle weakness, myotonia, cardiac arrhythmia, and profound fatigue are common, yet exhibit extreme variability across affected individuals. Many tran...
  8. Transcriptome analysis of Myotonic Dystrophy type 2 (DM2) patients. BioProject

    ID: PRJNA158103

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: mal dominant disease caused by the expansion of a CCTG tetraplet repeat. It is a multisystemic disorder, affecting skeletal muscles, the heart, the eye, the central nervous system and the endocrine system. Whole mRNAs express...
  9. microRNAs expression profile in Myotonic Dystrophy type-2 (DM2) patients BioProject

    ID: PRJNA163353

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: mal dominant disease caused by the expansion of a CCTG tetraplet repeat. It is a multisystemic disorder, affecting skeletal muscles, the heart, the eye, the central nervous system and the endocrine system The expression of 36...
  10. CRYSTAL STRUCTURE OF THE MOUSE CCT GAMMA APICAL DOMAIN (MONOCLINIC) PDB

    ID: PDB:1GN1

    Description: CCT-GAMMA

  11. Molecular architecture of the eukaryotic chaperonin TRiC/CCT derived by a combination of chemical crosslinking and mass-spectrometry, XL-MS PDB

    ID: PDB:4V94

    Description: T-complex protein 1 subunit zeta, T-complex protein 1 subunit theta, T-complex protein 1 subunit eta, T-complex p...

  12. The crystal structure of yeast CCT reveals intrinsic asymmetry of eukaryotic cytosolic chaperonins PDB

    ID: PDB:4V81

    Description: T-complex protein 1 subunit alpha, T-complex protein 1 subunit beta, T-complex protein 1 subunit gamma

  13. microRNAs expression profile in Myotonic Dystrophy type-2 (DM2) patients OmicsDI

    ID: E-GEOD-37794

    Date Released: 06-10-2014

    Description: mal dominant disease caused by the expansion of a CCTG tetraplet repeat. It is a multisystemic disorder, affecting skeletal muscles, the heart, the eye, the central nervous system and the endocrine system The expression of 36...

  14. Transcriptome analysis of Myotonic Dystrophy type 2 (DM2) patients. OmicsDI

    ID: E-GEOD-37084

    Date Released: 04-11-2015

    Description: mal dominant disease caused by the expansion of a CCTG tetraplet repeat. It is a multisystemic disorder, affecting skeletal muscles, the heart, the eye, the central nervous system and the endocrine system. Whole mRNAs express...

  15. Myotonic dystrophy type 2: vastus lateralis biopsies GEO

    ID: geo.datasets:GDS5276

    Description: nts. DM2 is a multisystemic disorder caused by a (CCTG)n repeat expansion in intron 1 of cellular nucleic acid-binding protein. Results provide insight into molecular mechanisms underlying DM2 pathogenesis....

    Types: Expression profiling by array

    Instrument: GPL6102


Displaying 15 of 15 results for "CCT3"