Literature DB >> 20667188

Genetic aspects of cerebrovascular malformations.

C L Shovlin1.   

Abstract

SUMMARY: In the last decade there have been fundamental advances in our understanding of the pathogenesis of vascular malformations. These advances have resulted from the application of molecular methods to identify disease genes, rather than from immunohistochemical or physiological studies. This presentation reviews the genetic basis of a variety of cerebral vascular malformations which occur as part of well-characterised diseases inherited in an autosomal dominant manner. These highlight the diversity of mechanisms which can perturb vascular development, and should have significant implications for the development of new therapies.

Entities:  

Year:  2001        PMID: 20667188      PMCID: PMC3679585          DOI: 10.1177/159101990000600204

Source DB:  PubMed          Journal:  Interv Neuroradiol        ISSN: 1591-0199            Impact factor:   1.610


  24 in total

Review 1.  Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms.

Authors:  C L Shovlin; M Letarte
Journal:  Thorax       Date:  1999-08       Impact factor: 9.139

Review 2.  Type 1 neurofibromatosis and the pediatric patient.

Authors:  V M Riccardi
Journal:  Curr Probl Pediatr       Date:  1992-02

3.  A gene responsible for cavernous malformations of the brain maps to chromosome 7q.

Authors:  J Dubovsky; J M Zabramski; J Kurth; R F Spetzler; S S Rich; H T Orr; J L Weber
Journal:  Hum Mol Genet       Date:  1995-03       Impact factor: 6.150

4.  Assignment of transforming growth factor beta1 and beta3 and a third new ligand to the type I receptor ALK-1.

Authors:  A Lux; L Attisano; D A Marchuk
Journal:  J Biol Chem       Date:  1999-04-09       Impact factor: 5.157

5.  Allelic and locus heterogeneity in inherited venous malformations.

Authors:  J T Calvert; T J Riney; C D Kontos; E H Cha; V G Prieto; C R Shea; J N Berg; N C Nevin; S A Simpson; K A Pasyk; M C Speer; K G Peters; D A Marchuk
Journal:  Hum Mol Genet       Date:  1999-07       Impact factor: 6.150

6.  Association of Krev-1/rap1a with Krit1, a novel ankyrin repeat-containing protein encoded by a gene mapping to 7q21-22.

Authors:  I Serebriiskii; J Estojak; G Sonoda; J R Testa; E A Golemis
Journal:  Oncogene       Date:  1997-08-28       Impact factor: 9.867

7.  Endoglin is an accessory protein that interacts with the signaling receptor complex of multiple members of the transforming growth factor-beta superfamily.

Authors:  N P Barbara; J L Wrana; M Letarte
Journal:  J Biol Chem       Date:  1999-01-08       Impact factor: 5.157

8.  Hereditary haemorrhagic telangiectasia with extensive liver involvement is not caused by either HHT1 or HHT2.

Authors:  M Piantanida; E Buscarini; C Dellavecchia; A Minelli; A Rossi; L Buscarini; C Danesino
Journal:  J Med Genet       Date:  1996-06       Impact factor: 6.318

9.  Endothelial receptor tyrosine kinases activate the STAT signaling pathway: mutant Tie-2 causing venous malformations signals a distinct STAT activation response.

Authors:  E I Korpelainen; M Kärkkäinen; Y Gunji; M Vikkula; K Alitalo
Journal:  Oncogene       Date:  1999-01-07       Impact factor: 9.867

10.  Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27.

Authors:  H D Craig; M Günel; O Cepeda; E W Johnson; L Ptacek; G K Steinberg; C S Ogilvy; M J Berg; S C Crawford; R M Scott; E Steichen-Gersdorf; R Sabroe; C T Kennedy; G Mettler; M J Beis; A Fryer; I A Awad; R P Lifton
Journal:  Hum Mol Genet       Date:  1998-11       Impact factor: 6.150

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