LIM–kinase deleted in Williams syndrome

No abstract is available for this paper.

• Publication year

  1996

• Venue

  Nature Genetics

• Publication date

  1996-07-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1038/NG0796-272PMID 8673124
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Limk1 is predominantly expressed in neural tissues and phosphorylates serine, threonine and tyrosine residues in vitro.

  1995cited by this paper
• Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patients.

  1995cited by this paper
• LIMK-1 and LIMK-2, two members of a LIM motif-containing protein kinase family.

  1995cited by this paper
• Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndrome.

  1995cited by this paper
• Classification of LIM proteins.

  1995cited by this paper
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  1994cited by this paper
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  1993cited by this paper
• The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis.

  1993cited by this paper
• Williams syndrome: autosomal dominant inheritance.

  1993cited by this paper
• Supravalvular aortic stenosis cosegregates with a familial 6; 7 translocation which disrupts the elastin gene.

  1993cited by this paper
• Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

  1988cited by this paper
• Natural history of Williams syndrome: physical characteristics.

  1988cited by this paper

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  2007cites this paper
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  2006influential citation
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  2006cites this paper
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  2006cites this paper
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  2005cites this paper
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  2005cites this paper
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  1999cites this paper