CLN5 | bioCADDIE Data Discovery Index
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Displaying 19 of 19 results for "CLN5"
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  1. CLN5_BOVIN UniProt:Swiss-Prot

    ID: Q1ZYR0

    Description: Ceroid-lipofuscinosis neuronal protein 5 N-linked (GlcNAc...) N-linked (Gl...

  2. CLN5_SHEEP UniProt:Swiss-Prot

    ID: A2TJ54

    Description: Ceroid-lipofuscinosis neuronal protein 5 N-linked (GlcNAc...) N-linked (Gl...

  3. Palmitoyl protein thioesterase-1 knockout mice hofma-affy-mouse-370000 BioProject

    ID: PRJNA98609

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: Infantile neuronal ceroid lipofuscinosis (aka infantile Batten disease) is a severe neurodegenerative d...
  4. 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) share clinical and pathological features, including lys...
  5. 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) share clinical and pathological features, including lys...

  6. Brain gene expression profiles of Cln1 and Cln5 deficient mice unravels common molecular pathways underlying neuronal degeneration in NCL diseases OmicsDI

    ID: E-MEXP-1333

    Date Released: 09-09-2014

    Description: The neuronal ceroid lipofuscinoses (NCL) are a group of childhood inherited neurodegenerative disorders characterize...

  7. Brain gene expression profiles of Cln1 and Cln5 deficient mice unravels common molecular pathways underlying neuronal degeneration in NCL diseases ArrayExpress

    ID: E-MEXP-1333

    Description: The neuronal ceroid lipofuscinoses (NCL) are a group of childhood inherited neurodegenerative disorders characterize...

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

    ID: E-GEOD-6678

    Description: Infantile neuronal ceroid lipofuscinosis (aka infantile Batten disease) is a severe neurodegenerative d...

  9. 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 ceroid

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

    ID: 454

    Keywords: functional genomics

    Description: Infantile neuronal ceroid lipofuscinosis (aka infantile Batten disease) is a severe neurodegenerative d...

  11. 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 ceroid

  12. 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) share clinical and pathological features, including lys...

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

    ID: PRJNA162369

    Keywords: Transcriptome or Gene expression

    Access Type: download

  14. 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 Batten disease) is a severe neurodegenerative d...

  15. CLN5B_DICDI UniProt:Swiss-Prot

    ID: Q54WC3

    Description: Cln5-like protein 2 N-linked (GlcNAc...) N-linked (GlcNAc...) N-linked (GlcNAc...) N-linked (GlcNAc...) N-linked (GlcNAc...) N-link...

  16. CLN5C_DICDI UniProt:Swiss-Prot

    ID: Q54C37

    Description: Cln5-like protein 3 Helical Poly-Gly N-linked (GlcNAc...) N-linked (GlcNAc...) N-linked (GlcNAc...) N-linked (GlcNAc...) N-linked (...

  17. Yeast W303 yox1yhp1 mutant cell cycle BioProject

    ID: PRJNA96391

    Keywords: Transcriptome or Gene expression

    Access Type: download

  18. Many obesity-associated SNPs strongly associate with DNA methylation changes at proximal promoters and enhancers ArrayExpress

    ID: E-GEOD-73103

    Description: Background: The mechanisms of how genetic variants (SNPs) identified in genome-wide association studies act to influence body mass remain unknown for ...

  19. Many obesity-associated SNPs strongly associate with DNA methylation changes at proximal promoters and enhancers BioProject

    ID: PRJNA296032

    Keywords: Epigenomics

    Access Type: download


Displaying 19 of 19 results for "CLN5"