List of bibliographic references
Number of relevant bibliographic references: 45.
[0-20] [
0 - 20][
0 - 45][
20-40]
| Ident. | Authors (with country if any) | Title |
|---|
| 001D41 (2005) |
M. Ng ; T. Andrew ; T. Spector ; S. Jeffery | Linkage to the FOXC2 region of chromosome 16 for varicose veins in otherwise healthy, unselected sibling pairs |
| 001F19 (2005) |
Fred B. Berry [Canada] ; Yahya Tamimi ; Michelle V. Carle ; Ordan J. Lehmann ; Michael A. Walter | The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis. |
| 002132 (2006) |
Subash Babu [États-Unis] ; Carla P. Blauvelt ; V. Kumaraswami ; Thomas B. Nutman | Regulatory networks induced by live parasites impair both Th1 and Th2 pathways in patent lymphatic filariasis: implications for parasite persistence. |
| 002354 (2007) |
Amy E. Young [États-Unis] ; Leslie P. Bower ; Verena K. Affolter ; Hilde E V. De Cock ; Gregory L. Ferraro ; Danika L. Bannasch | Evaluation of FOXC2 as a candidate gene for chronic progressive lymphedema in draft horses. |
| 002367 (2006) |
A. Noon [États-Unis] ; R J Hunter ; M H Witte ; B. Kriederman ; M. Bernas ; M. Rennels ; D. Percy ; S. Enerb Ck ; R P Erickson | Comparative lymphatic, ocular, and metabolic phenotypes of Foxc2 haploinsufficient and aP2-FOXC2 transgenic mice. |
| 002582 (2007) |
S. Kumar ; C. Carver ; S. Mccall ; G. Brice ; P. Ostergaard ; Peter Mortimer (dermatologue) [Royaume-Uni] ; S. Jeffery | A family with lymphoedema-distichiasis where identical twins have a discordant phenotype. |
| 002628 (2007) |
Russell H. Mellor [Royaume-Uni] ; Glen Brice ; Anthony W B. Stanton ; Jane French ; Alberto Smith ; Steve Jeffery ; J Rodney Levick ; Kevin G. Burnand ; Peter S. Mortimer | Mutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limb. |
| 002899 (2007) |
M A M. Van Steensel [Pays-Bas] ; M. Van Geel ; C. Schrander-Stumpel ; P M Steijlen ; J C J M. Veraart | Lymphedema, cardiac septal defects, and characteristic facies: possible new case of Irons-Bianchi syndrome. |
| 002B19 (2008) |
Sajid Malik [Allemagne] ; Karl-Heinz Grzeschik | Congenital, low penetrance lymphedema of lower limbs maps to chromosome 6q16.2-q22.1 in an inbred Pakistani family. |
| 002B22 (2008) |
Tayebeh Rezaie [États-Unis] ; Rose Ghoroghchian ; Rachel Bell ; Glen Brice ; Ali Hasan ; Kevin Burnand ; Steve Vernon ; Sahar Mansour ; Peter Mortimer (dermatologue) [Royaume-Uni] ; Steve Jeffery ; Anne Child ; Mansoor Sarfarazi | Primary non-syndromic lymphoedema (Meige disease) is not caused by mutations in FOXC2. |
| 002B53 (2008) |
Glen Brice | Perinatal diagnosis of a lymphoedema-distichiasis syndrome. |
| 002D37 (2008) |
Robert E. Ferrell [États-Unis] ; David N. Finegold | Research perspectives in inherited lymphatic disease: an update. |
| 002D98 (2008) |
K. Rutscher [Allemagne] ; J. Wilting | Transcription factor FOXC2 demarcates the jugular lymphangiogenic region in avian embryos. |
| 003051 (2008) |
Maaike Vreeburg [Pays-Bas] ; Martijn V. Heitink ; Robert J. Damstra ; Ute Moog ; Michel Van Geel ; Maurice A M. Van Steensel | Lymphedema-distichiasis syndrome: a distinct type of primary lymphedema caused by mutations in the FOXC2 gene. |
| 003069 (2008) |
M T Dellinger [États-Unis] ; K. Thome ; M J Bernas ; R P Erickson ; M H Witte | Novel FOXC2 missense mutation identified in patient with lymphedema-distichiasis syndrome and review. |
| 003367 (2009) |
Arash Ghalamkarpour [Belgique] ; Christian Debauche ; Eric Haan ; Nicole Van Regemorter ; Yves Sznajer ; Dominique Thomas ; Nicole Revencu ; Yves Gillerot ; Laurence M. Boon ; Miikka Vikkula | Sporadic in utero generalized edema caused by mutations in the lymphangiogenic genes VEGFR3 and FOXC2. |
| 003620 (2009) |
M A M. Van Steensel [Pays-Bas] ; R J Damstra ; M V Heitink ; R S Bladergroen ; J. Veraart ; Peter M. Steijlen ; M. Van Geel | Novel missense mutations in the FOXC2 gene alter transcriptional activity. |
| 003936 (2010) |
Pranoot Tanpaiboon [Thaïlande] ; Piranit Kantaputra ; Karn Wejathikul ; Wirawit Piyamongkol | c. 595-596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and Robin sequence in a Thai patient. |
| 003957 (2009) |
M H Witte [États-Unis] ; R P Erickson ; M. Khalil ; M. Dellinger ; M. Bernas ; T. Grogan ; H. Nitta ; J. Feng ; D. Duggan ; C L Witte | Lymphedema-distichiasis syndrome without FOXC2 mutation: evidence for chromosome 16 duplication upstream of FOXC2. |
| 003A96 (2010) |
Antonella Fabretto [Italie] ; Alison Shardlow ; Flavio Faletra ; Loredana Lepore ; Uros Hladnik ; Paolo Gasparini | A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation. |
| 003B62 (2010) |
Rocío Sánchez-Carpintero [Espagne] ; Pablo Dominguez ; María Teresa Nú Ez ; Ana Pati O-García | Spinal extradural arachnoid cysts in lymphedema-distichiasis syndrome. |
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