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Displaying 20 of 169 results for "PPT1"
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  1. Palmitoyl protein thioesterase-1 knockout mice hofma-affy-mouse-370000 BioProject

    ID: PRJNA98609

    Keywords: Transcriptome or Gene expression

    Access Type: download

  2. Transcription profiling of palmitoyl protein thioesterase-1 knockout mice ArrayExpress

    ID: E-GEOD-6678

    Description: Infantile neuronal ceroid lipofuscinosis (aka infantile...

  3. Transcription profiling of palmitoyl protein thioesterase-1 knockout mice OmicsDI

    ID: E-GEOD-6678

    Date Released: 06-10-2011

    Description: Infantile neuronal ceroid lipofuscinosis (aka infantile...

  4. Palmitoyl protein thioesterase-1 knockout mice hofma-affy-mouse-370000 GEMMA

    ID: 454

    Keywords: functional genomics

    Description: Infantile neuronal ceroid lipofuscinosis (aka infantile...

  5. CRYSTAL STRUCTURE OF PALMITOYL PROTEIN THIOESTERASE 1 PDB

    ID: PDB:1EI9

    Description: PALMITOYL PROTEIN THIOESTERASE 1 (E.C.3.1.2.22)

  6. CRYSTAL STRUCTURE OF PALMITOYL PROTEIN THIOESTERASE 1 COMPLEXED WITH PALMITATE PDB

    ID: PDB:1EH5

    Description: PALMITOYL PROTEIN THIOESTERASE (E.C.3.1.2.22)

  7. The crystal structure of palmitoyl protein thioesterase-2 reveals the basis for divergent substrate specificities of t... PDB

    ID: PDB:1PJA

    Description: Palmitoyl-protein thioesterase 2 precursor (E.C.3.1.2.22)

  8. Human palmitoyl-protein thioesterase 1 PDB

    ID: PDB:3GRO

    Description: Palmitoyl-protein thioesterase 1 (E.C.3.1.2.22)

  9. Distinct Early Molecular Responses to Mutations Causing vLINCL and JNCL Presage ATP Synthase Subunit c Accumulation in Cerebellar Cells ArrayExpress

    ID: E-GEOD-24368

    Description: Variant late-infantile (vLINCL) and juvenile neuronal ceroid lipofuscinosis (JNCL) shar...

  10. Distinct Early Molecular Responses to Mutations Causing vLINCL and JNCL Presage ATP Synthase Subunit c Accumulation in Cerebellar Cells BioProject

    ID: PRJNA132961

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: Variant late-infantile (vLINCL) and juvenile neuronal ceroid lipofuscinosis (JNCL) shar...
  11. Hypo-osmotic shock - ppt1 and wildtype BioProject

    ID: PRJNA84955

    Keywords: Transcriptome or Gene expression

    Access Type: download

  12. Crystal Structure Analysis of Tripeptidyl peptidase -I PDB

    ID: PDB:3EE6

    Description: Tripeptidyl-peptidase 1 (E.C.3.4.14.9)

  13. Crystal Structure of the Precursor Form of Human Tripeptidyl-Peptidase 1 PDB

    ID: PDB:3EDY

    Description: Crystal Structure of the Precursor Form of Human Tripeptidyl-Peptidase 1

  14. Distinct Early Molecular Responses to Mutations Causing vLINCL and JNCL Presage ATP Synthase Subunit c Accumulation in Cerebellar Cells GEMMA

    ID: 2689

    Keywords: functional genomics

    Description: Variant late-infantile (vLINCL) and juvenile neuronal ceroid lipofuscinosis (JNCL) shar...

  15. CRYSTAL STRUCTURE OF PALMITOYL PROTEIN THIOESTERASE 1 COMPLEXED WITH HEXADECYLSULFONYL FLUORIDE PDB

    ID: PDB:1EXW

    Description: PALMITOYL PROTEIN THIOESTERASE 1 (E.C.3.1.2.22)

  16. Exacerbated neuronal ceroid lipofuscinosos phenotype in Cln1/5 double knock-out mice OmicsDI

    ID: E-GEOD-37643

    Date Released: 11-08-2012

    Description: Both CLN1 and CLN5 deficiency leads to severe neurodegenerative diseases of childhood, known as neuronal

  17. Distinct Early Molecular Responses to Mutations Causing vLINCL and JNCL Presage ATP Synthase Subunit c Accumulation in Cerebellar Cells OmicsDI

    ID: E-GEOD-24368

    Date Released: 02-01-2011

    Description: Variant late-infantile (vLINCL) and juvenile neuronal ceroid lipofuscinosis (JNCL) shar...

  18. Exacerbated neuronal ceroid lipofuscinosos phenotype in Cln1/5 double knock-out mice BioProject

    ID: PRJNA162369

    Keywords: Transcriptome or Gene expression

    Access Type: download

  19. Exacerbated neuronal ceroid lipofuscinosos phenotype in Cln1/5 double knock-out mice ArrayExpress

    ID: E-GEOD-37643

    Description: Both CLN1 and CLN5 deficiency leads to severe neurodegenerative diseases of childhood, known as neuronal

  20. PDF1_SCHPO UniProt:Swiss-Prot

    ID: O59747

    Description: Palmitoyl-protein thioesterase-dolichyl pyrophosphate phosphatase fusion 1...


Displaying 20 of 169 results for "PPT1"