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Displaying 20 of 24 results for "LAMA2"
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  1. Identification of GABRA1 and LAMA2 as new DNA methylation markers in colorectal cancer ArrayExpress

    ID: E-GEOD-26799

    Description: This SuperSeries is composed of the following subset Series: GSE19659: Indirect expression microarray from 5 pairs of tissues from colorectal cancer p...

  2. RNA-sequencing analysis of a wildtype CHO cell line (CHO-K1), a mutant CHO cell line (pgsA745) that lacks xylosyltransferase (XylT) activity, and pgsA... BioProject

    ID: PRJNA304606

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: ion in the gene encoding for laminin subunit α2 (Lama2) in CHO pgsA745. Overall design: RNA of three different cell lines was extracted and analyzed....
  3. Identification of GABRA1 and LAMA2 as new DNA methylation markers in colorectal cancer OmicsDI

    ID: E-GEOD-26799

    Date Released: 05-04-2014

    Description: This SuperSeries is composed of the following subset Series: GSE19659: Indirect expression microarray from 5 pairs of tissues from colorectal cancer p...

  4. Transcription profiling of diaphragm muscles from alpha2-laminin (merosin)-deficient dy/dy dystrophic mice and wild type mice to study differential ge... ArrayExpress

    ID: E-GEOD-3252

    Description: Laminin (merosin) deficient muscular dystrophy in dy/dy mouse diaphragm muscle, 8 weeks old Experiment Overall Design: 4 normal samples; 4 dystrophic ...

  5. Laminin-deficient muscular dystrophy, dy/dy diaphragm BioProject

    ID: PRJNA92901

    Keywords: Transcriptome or Gene expression

    Access Type: download

  6. Laminin A2LG45 C-form, Apo. PDB

    ID: PDB:5IK4

    Description: Laminin subunit alpha-2

    gene.name: Lama2
  7. Laminin A2LG45 C-form, G6/7 bound. PDB

    ID: PDB:5IK5

    Description: Laminin subunit alpha-2

    gene.name: Lama2
  8. Muscle from patients with mitochondrial myopathies and congenital muscular dystrophies versus normal human muscle ArrayExpress

    ID: E-GEOD-43698

    Description: Global gene expression analysis was performed comparing human skeletal muscle samples from patients with various forms of muscular dystrophy and mitoc...

  9. Laminin A2LG45 I-form, Apo. PDB

    ID: PDB:5IK7

    Description: Laminin subunit alpha-2

    gene.name: Lama2
  10. Laminin A2LG45 I-form, G6/7 bound. PDB

    ID: PDB:5IK8

    Description: Laminin subunit alpha-2

    gene.name: Lama2
  11. L4b Domain of Human Laminin alpha-2 PDB

    ID: PDB:4YEQ

    Description: L4b Domain of Human Laminin alpha-2

    gene.name: LAMA2, LAMM
  12. L4b Domain of Human Laminin alpha-2 PDB

    ID: PDB:4YEP

    Description: L4b Domain of Human Laminin alpha-2

    gene.name: LAMA2, LAMM
  13. Genetics of Inherited Muscle Disease BioProject

    ID: PRJNA215657

    Access Type: download

  14. Genetics of Inherited Muscle Disease BioProject

    ID: PRJNA215658

    Keywords: Phenotype or Genotype

    Access Type: download

  15. The Congenital Muscular Dystrophy Genotype and Phenotype Study BioProject

    ID: PRJNA75791

    Keywords: Phenotype or Genotype

    Access Type: download

  16. Homo sapiens : The Congenital Muscular Dystrophy Genotype and Phenotype Study BioProject

    ID: PRJNA75789

    Access Type: download

  17. Genetics of Inherited Muscle Disease dbGaP

    ID: phs000655.v1.p1

    Description: The samples are drawn from a collection of patients with a heterogeneous set of neuromuscular disorders, including congenital muscular dystrophy, cong...

  18. Muscle from patients with mitochondrial myopathies and congenital muscular dystrophies versus normal human muscle BioProject

    ID: PRJNA187082

    Keywords: Transcriptome or Gene expression

    Access Type: download

  19. Genetics of Inherited Muscle Disease dbGaP

    ID: phs000655.v3.p1

    Description: The samples are drawn from a collection of patients with a heterogeneous set of neuromuscular disorders, including congenital muscular dystrophy, cong...

  20. Genetics of Inherited Muscle Disease dbGaP

    ID: phs000655.v2.p1

    Description: The samples are drawn from a collection of patients with a heterogeneous set of neuromuscular disorders, including congenital muscular dystrophy, cong...


Displaying 20 of 24 results for "LAMA2"