Literature DB >> 8475063

A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7.

A K Ewart1, C A Morris, G J Ensing, J Loker, C Moore, M Leppert, M Keating.   

Abstract

The pathogenesis of vascular disease is unclear, but genetic factors play an important role. In this study we performed linkage analyses in two families with supravalvular aortic stenosis, an inherited vascular disorder that causes narrowing of major arteries and may lead to cardiac overload and failure. DNA markers on the long arm of chromosome 7 (D7S371, D7S395, D7S448, and ELN) were linked to supravalvular aortic stenosis in both families with a combined logarithm of likelihood for linkage (lod score) of 5.9 at the ELN locus. These findings indicate that a gene for supravalvular aortic stenosis is located in the same chromosomal subunit as elastin, which becomes a candidate for the disease gene.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8475063      PMCID: PMC46272          DOI: 10.1073/pnas.90.8.3226

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  24 in total

1.  D7S448 detects a HindIII polymorphism located in the centromere region of chromosome 7.

Authors:  M Dean; C Stewart; A Perry; D Stauffer; B Otterud; R White; M Leppert
Journal:  Nucleic Acids Res       Date:  1991-01-11       Impact factor: 16.971

2.  Twenty-five loci form a continuous linkage map of markers for human chromosome 7.

Authors:  G M Lathrop; P O'Connell; M Leppert; Y Nakamura; M Farrall; L C Tsui; J M Lalouel; R White
Journal:  Genomics       Date:  1989-11       Impact factor: 5.736

3.  Familial supravalvular aortic stenosis: a genetic study.

Authors:  F Chiarella; F D Bricarelli; G Lupi; P Bellotti; S Domenicucci; C Vecchio
Journal:  J Med Genet       Date:  1989-02       Impact factor: 6.318

4.  Spectrum of findings in a family with nonsyndromic autosomal dominant supravalvular aortic stenosis: a Doppler echocardiographic study.

Authors:  G J Ensing; M A Schmidt; D J Hagler; V V Michels; G A Carter; R H Feldt
Journal:  J Am Coll Cardiol       Date:  1989-02       Impact factor: 24.094

5.  Adults with Williams syndrome.

Authors:  C A Morris; C O Leonard; C Dilts; S A Demsey
Journal:  Am J Med Genet Suppl       Date:  1990

6.  Isolation and mapping of a polymorphic DNA sequence (pTHH28) on chromosome 7p [D7S371].

Authors:  T Holm; Y Nakamura; L Ballard; P O'Connell; M Leppert; G M Lathrop; J M Lalouel; R White
Journal:  Nucleic Acids Res       Date:  1988-10-25       Impact factor: 16.971

7.  "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1984-02       Impact factor: 3.365

8.  Supravalvular aortic stenosis. Clinical and pathologic observations in six patients.

Authors:  W N O'Connor; J B Davis; R Geissler; C M Cottrill; J A Noonan; E P Todd
Journal:  Arch Pathol Lab Med       Date:  1985-02       Impact factor: 5.534

9.  Human elastin gene: new evidence for localization to the long arm of chromosome 7.

Authors:  M J Fazio; M G Mattei; E Passage; M L Chu; D Black; E Solomon; J M Davidson; J Uitto
Journal:  Am J Hum Genet       Date:  1991-04       Impact factor: 11.025

10.  Natural history of Williams syndrome: physical characteristics.

Authors:  C A Morris; S A Demsey; C O Leonard; C Dilts; B L Blackburn
Journal:  J Pediatr       Date:  1988-08       Impact factor: 4.406

View more
  37 in total

1.  Induced chromosome deletion in a Williams-Beuren syndrome mouse model causes cardiovascular abnormalities.

Authors:  Craig J Goergen; Hong-Hua Li; Uta Francke; Charles A Taylor
Journal:  J Vasc Res       Date:  2010-10-07       Impact factor: 1.934

2.  Fluorescent in situ hybridisation (FISH) for hemizygous deletion at the elastin locus in patients with isolated supravalvular aortic stenosis.

Authors:  H Fryssira; R Palmer; K A Hallidie-Smith; J Taylor; D Donnai; W Reardon
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

Review 3.  Insights into brain development from neurogenetic syndromes: evidence from fragile X syndrome, Williams syndrome, Turner syndrome and velocardiofacial syndrome.

Authors:  E Walter; P K Mazaika; A L Reiss
Journal:  Neuroscience       Date:  2009-04-17       Impact factor: 3.590

Review 4.  Genetics of the extracellular matrix in aortic aneurysmal diseases.

Authors:  Chien-Jung Lin; Chieh-Yu Lin; Nathan O Stitziel
Journal:  Matrix Biol       Date:  2018-04-12       Impact factor: 11.583

5.  Surgical repair of supravalvular aortic stenosis with use of Brom's technique: short-term results in 9 children.

Authors:  Brenda Fabiola Cruz-Castañeda; Fernando Carrillo-Llamas; Saúl Ramos-Higuera; Jaime Gilberto López-Taylor; Eliseo Portilla-de Buen
Journal:  Tex Heart Inst J       Date:  2009

6.  Genome-wide association study of severity in multiple sclerosis.

Authors: 
Journal:  Genes Immun       Date:  2011-06-09       Impact factor: 2.676

7.  Aortic stiffness with the Williams-Beuren syndrome.

Authors:  A Wessel; R Pankau; W Berdau; P Löns
Journal:  Pediatr Cardiol       Date:  1997 May-Jun       Impact factor: 1.655

Review 8.  Vascular wall extracellular matrix proteins and vascular diseases.

Authors:  Junyan Xu; Guo-Ping Shi
Journal:  Biochim Biophys Acta       Date:  2014-07-18

Review 9.  The extracellular matrix during heart development.

Authors:  C D Little; B J Rongish
Journal:  Experientia       Date:  1995-09-29

10.  Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome.

Authors:  Timothy A Hinsley; Pamela Cunliffe; Hannah J Tipney; Andrew Brass; May Tassabehji
Journal:  Protein Sci       Date:  2004-10       Impact factor: 6.725

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.