Long human-mouse sequence alignments reveal novel regulatory elements: a reason to sequence the mouse genome

Genome Res. 1997 Oct;7(10):959-66. doi: 10.1101/gr.7.10.959.
No abstract available

Publication types

  • Comparative Study

MeSH terms

  • Agammaglobulinaemia Tyrosine Kinase
  • Animals
  • Base Sequence
  • DNA Helicases*
  • DNA-Binding Proteins / genetics
  • Gene Expression Regulation
  • Genome
  • Globins / genetics
  • Hominidae / genetics*
  • Humans
  • Kinesins
  • Mice / genetics*
  • Microtubule-Associated Proteins / genetics
  • Models, Genetic
  • Molecular Sequence Data
  • Myosins / genetics
  • Protein-Tyrosine Kinases / genetics
  • Proteins / genetics
  • Receptors, Antigen, T-Cell / genetics
  • Regulatory Sequences, Nucleic Acid*
  • Sequence Alignment*
  • Transcription Factors*
  • X-ray Repair Cross Complementing Protein 1
  • Xeroderma Pigmentosum Group D Protein

Substances

  • DNA-Binding Proteins
  • Microtubule-Associated Proteins
  • Proteins
  • Receptors, Antigen, T-Cell
  • Transcription Factors
  • X-ray Repair Cross Complementing Protein 1
  • Globins
  • Protein-Tyrosine Kinases
  • Agammaglobulinaemia Tyrosine Kinase
  • DNA Helicases
  • Myosins
  • Xeroderma Pigmentosum Group D Protein
  • Kinesins
  • ERCC2 protein, human
  • Ercc2 protein, mouse