Literature DB >> 19190503

From blue jeans to blue genes.

Laurence M Boon1, Miikka Vikkula.   

Abstract

Cutaneous venous anomalies are common. They are blue and vary in size, number, and location and account for most consultations at specialized interdisciplinary clinics for vascular anomalies. Venous lesions are clinically important because they cause pain, dysfunction, destruction of adjacent tissues, and esthetic concern. Only resection and sclerotherapy are helpful, although not always curative. Understanding etiopathogenesis could help design animal models and develop novel therapeutic approaches. John B. Mulliken, MD, envisioned a project to uncover the genetic basis of an inherited form of venous malformation in a large New England family. Recruitment of 2 young fellows resulted in a collaborative project that unraveled the searched-for gene and its mutation. This was an opening for a new era in vascular anomalies. Two blue genes' mutations were discovered, which account for most, if not all, of the inherited forms of venous anomalies, but other genes as well, for rheologically diverse lesions. Differential diagnosis and management has improved, and animal models are being made. This was achieved through the help of Dr Mulliken, who inspired 2 young investigators in blue jeans to find 2 blue genes.

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Year:  2009        PMID: 19190503      PMCID: PMC2901832          DOI: 10.1097/SCS.0b013e318193d7a0

Source DB:  PubMed          Journal:  J Craniofac Surg        ISSN: 1049-2275            Impact factor:   1.046


  22 in total

1.  Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ("glomangiomas").

Authors:  Pascal Brouillard; Laurence M Boon; John B Mulliken; Odile Enjolras; Michella Ghassibé; Matthew L Warman; O T Tan; Bjorn R Olsen; Miikka Vikkula
Journal:  Am J Hum Genet       Date:  2002-02-13       Impact factor: 11.025

2.  Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase.

Authors:  A Irrthum; M J Karkkainen; K Devriendt; K Alitalo; M Vikkula
Journal:  Am J Hum Genet       Date:  2000-06-09       Impact factor: 11.025

3.  KRIT1 is mutated in hyperkeratotic cutaneous capillary-venous malformation associated with cerebral capillary malformation.

Authors:  I Eerola; K H Plate; R Spiegel; L M Boon; J B Mulliken; M Vikkula
Journal:  Hum Mol Genet       Date:  2000-05-22       Impact factor: 6.150

4.  High-resolution physical and transcript map of the locus for venous malformations with glomus cells (VMGLOM) on chromosome 1p21-p22.

Authors:  P Brouillard; B R Olsen; M Vikkula
Journal:  Genomics       Date:  2000-07-01       Impact factor: 5.736

5.  Linkage disequilibrium narrows locus for venous malformation with glomus cells (VMGLOM) to a single 1.48 Mbp YAC.

Authors:  A Irrthum; P Brouillard; O Enjolras; N F Gibbs; L F Eichenfield; B R Olsen; J B Mulliken; L M Boon; M Vikkula
Journal:  Eur J Hum Genet       Date:  2001-01       Impact factor: 4.246

6.  Glomuvenous malformation (glomangioma) and venous malformation: distinct clinicopathologic and genetic entities.

Authors:  Laurence M Boon; John B Mulliken; Odile Enjolras; Miikka Vikkula
Journal:  Arch Dermatol       Date:  2004-08

7.  Glomulin is predominantly expressed in vascular smooth muscle cells in the embryonic and adult mouse.

Authors:  Brendan A S McIntyre; Pascal Brouillard; Virginie Aerts; Ilse Gutierrez-Roelens; Miikka Vikkula
Journal:  Gene Expr Patterns       Date:  2004-05       Impact factor: 1.224

8.  Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia.

Authors:  Alexandre Irrthum; Koenraad Devriendt; David Chitayat; Gert Matthijs; Conrad Glade; Peter M Steijlen; Jean-Pierre Fryns; Maurice A M Van Steensel; Miikka Vikkula
Journal:  Am J Hum Genet       Date:  2003-05-08       Impact factor: 11.025

9.  Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations.

Authors:  Iiro Eerola; Laurence M Boon; John B Mulliken; Patricia E Burrows; Anne Dompmartin; Shoji Watanabe; Romain Vanwijck; Miikka Vikkula
Journal:  Am J Hum Genet       Date:  2003-11-24       Impact factor: 11.025

10.  Locus for susceptibility for familial capillary malformation ('port-wine stain') maps to 5q.

Authors:  Iiro Eerola; Laurence M Boon; Shoji Watanabe; Henri Grynberg; John B Mulliken; Miikka Vikkula
Journal:  Eur J Hum Genet       Date:  2002-06       Impact factor: 4.246

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  1 in total

Review 1.  From germline towards somatic mutations in the pathophysiology of vascular anomalies.

Authors:  Nisha Limaye; Laurence M Boon; Miikka Vikkula
Journal:  Hum Mol Genet       Date:  2009-04-15       Impact factor: 6.150

  1 in total

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