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Displaying 20 of 86 results for "LAMA2"
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  1. Expression data from laminin alpha 2 chain deficient mice vs wild type BioProject

    ID: PRJNA113373

    Keywords: Transcriptome or Gene expression

    Access Type: download

  2. Transcription profiling of mouse laminin alpha 2 chain deficient animals vs wild type ArrayExpress

    ID: E-GEOD-12049

    Description: Mutations in the gene encoding laminin a2 chain cause congenital muscular dystrophy, MDC1A. In skeletal m...

  3. The Congenital Muscular Dystrophy Genotype and Phenotype Study BioProject

    ID: PRJNA75791

    Keywords: Phenotype or Genotype

    Access Type: download

  4. Expression data from laminin alpha 2 chain deficient mice vs wild type GEMMA

    ID: 1632

    Keywords: functional genomics

    Description: Mutations in the gene encoding laminin a2 chain cause congenital muscular dystrophy, MDC1A. In skeletal m...

  5. Genetics of Inherited Muscle Disease BioProject

    ID: PRJNA215657

    Access Type: download

    dataset.description: geneous set of neuromuscular disorders, including congenital muscular dystrophy, congenital myopathy, limb-girdle muscular dystrophy, Emery-Dreifuss
  6. Genetics of Inherited Muscle Disease BioProject

    ID: PRJNA215658

    Keywords: Phenotype or Genotype

    Access Type: download

    dataset.description: geneous set of neuromuscular disorders, including congenital muscular dystrophy, congenital myopathy, limb-girdle muscular dystrophy, Emery-Dreifuss
  7. Homo sapiens : The Congenital Muscular Dystrophy Genotype and Phenotype Study BioProject

    ID: PRJNA75789

    Access Type: download

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

    ID: E-GEOD-43698

    Description: uscle samples from patients with various forms of muscular dystrophy and mitochondrial myopathies in order to identify specific gene expression changes associated with collagen VI deficiency (leading to Ullrich´s C

  9. 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

  10. L4b Domain of Human Laminin alpha-2 PDB

    ID: PDB:4YEQ

    Description: L4b Domain of Human Laminin alpha-2

  11. L4b Domain of Human Laminin alpha-2 PDB

    ID: PDB:4YEP

    Description: L4b Domain of Human Laminin alpha-2

  12. iption profiling of diaphragm muscles from alpha2-laminin (merosin)-deficient dy/dy dystrophic mice and wild type mice to study differential gene expression... ArrayExpress

    ID: E-GEOD-3252

    Description: Laminin (merosin) deficient muscular dystrophy in dy/dy mouse diaphragm mu...

  13. Genetics of Inherited Muscle Disease dbGaP

    ID: phs000655.v1.p1

    Description: geneous set of neuromuscular disorders, including congenital muscular dystrophy, congenital myopathy, limb-girdle muscular dystrophy, Emery-Dreifuss

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

    ID: PRJNA92901

    Keywords: Transcriptome or Gene expression

    Access Type: download

  15. Transcription profiling of mouse laminin alpha 2 chain deficient animals vs wild type OmicsDI

    ID: E-GEOD-12049

    Date Released: 06-10-2011

    Description: Mutations in the gene encoding laminin a2 chain cause congenital muscular dystrophy, MDC1A. In skeletal m...

  16. SG196_HUMAN UniProt:Swiss-Prot

    ID: Q9H5K3

    Description: Protein O-mannose kinase Cytoplasmic Helical; Signal-anchor for type II membrane protein Lumenal Protein kinase N-acetylmethionine N-linked (GlcNAc......

    dataset.keywords: Congenital muscular dystrophy
  17. Laminin A2LG45 C-form, G6/7 bound. PDB

    ID: PDB:5IK5

    Description: Laminin subunit alpha-2

  18. Laminin A2LG45 C-form, Apo. PDB

    ID: PDB:5IK4

    Description: Laminin subunit alpha-2

  19. Genetics of Inherited Muscle Disease dbGaP

    ID: phs000655.v3.p1

    Description: geneous set of neuromuscular disorders, including congenital muscular dystrophy, congenital myopathy, limb-girdle muscular dystrophy, Emery-Dreifuss

  20. Laminin A2LG45 I-form, G6/7 bound. PDB

    ID: PDB:5IK8

    Description: Laminin subunit alpha-2


Displaying 20 of 86 results for "LAMA2"