Defective valves and abnormal mural cell recruitment underlie lymphatic vascular failure in lymphedema distichiasis-Reference-Cited by-同舟云学术

Defective valves and abnormal mural cell recruitment underlie lymphatic vascular failure in lymphedema distichiasis

Published:2004-08-22 Issue:9 Volume:10 Page:974-981
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Petrova Tatiana V,Karpanen Terhi,Norrmén Camilla,Mellor Russell,Tamakoshi Tomoki,Finegold David,Ferrell Robert,Kerjaschki Dontscho,Mortimer Peter,Ylä-Herttuala Seppo,Miura Naoyuki,Alitalo Kari

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm1094.pdf

Reference51 articles.

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2. Karkkainen, M.J. et al. Missense mutations interfere with VEGFR-3 signaling in primary lymphoedema. Nat. Genet. 25, 153–159 (2000).

3. Irrthum, A. et al. Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia. Am. J. Hum. Genet. 72, 1470–1478 (2003).

4. Fang, J. et al. Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome. Am. J. Hum. Genet. 67, 1382–1388 (2000).

5. Finegold, D.N. et al. Truncating mutations in FOXC2 cause multiple lymphedema syndromes. Hum. Mol. Genet. 10, 1185–1189 (2001).

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