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Displaying 10 of 32 results for "NDN"
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  1. Expression data from Mvt-1 clonal isolates over-expressing Ndn 50T or Ndn 50C BioProject

    ID: PRJNA275143

    Keywords: Transcriptome or Gene expression

    Access Type: download

  2. The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome ArrayExpress

    ID: E-GEOD-56136

    Description: -of-origin differential gene expression. To study Prader-Willi syndrome (PWS), a developmental imprinting disorder, we generated patient-derived induced pluripotent stem cells (iPSCs) harboring distinct deletions in the ...

  3. The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome BioProject

    ID: PRJNA242529

    Keywords: Transcriptome or Gene expression

    Access Type: download

  4. Expression data from Mvt-1 clonal isolates over-expressing Ndn 50T or Ndn 50C ArrayExpress

    ID: E-GEOD-65824

    Description: Ndn is a candidate metastasis suppressor gene that has been reported to regulate transcription. We examined the changes in gene exp...

  5. The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome OmicsDI

    ID: E-GEOD-56136

    Date Released: 04-09-2014

    Description: -of-origin differential gene expression. To study Prader-Willi syndrome (PWS), a developmental imprinting disorder, we generated patient-derived induced pluripotent stem cells (iPSCs) harboring distinct deletions in the ...

  6. Recurrent 15q13 microdeletions ArrayExpress

    ID: E-GEOD-10189

    Description: We report a recurrent microdeletion syndrome causing mental retardation, epilepsy and variable facial and digital dysmorphisms. We describe nine patients, including si...

  7. Expression data from Mvt-1 clonal isolates over-expressing Ndn 50T or Ndn 50C OmicsDI

    ID: E-GEOD-65824

    Date Released: 02-22-2016

    Description: Ndn is a candidate metastasis suppressor gene that has been reported to regulate transcription. We examined the changes in gene exp...

  8. Recurrent 15q13 microdeletions BioProject

    ID: PRJNA108297

    Keywords: Variation

    Access Type: download

    dataset.description: We report a recurrent microdeletion syndrome causing mental retardation, epilepsy and variable facial and digital dysmorphisms. We describe nine patients, including si...
  9. Homo sapiens : snoRD116HG transcript regulates the chromatin architecture of MAGEL2 and NDN locus over long distance BioProject

    ID: PRJNA304479

    Keywords: epigenomics

    Access Type: download

  10. PWS Natural History Protocol dbGaP

    ID: phs000575.v1.p1

    Description: ory and the clinical features of individuals with Prader-Willi syndrome and individuals with features of PWS-like/EMO. A blood sample will be obtained from the participants in order to create a DNA and RNA repository. In those PWS participants with a known ...

    Study Types: Case Set


Displaying 10 of 32 results for "NDN"