Vascular Endothelial Growth Factor Receptor-3 (deficiency) < Vascular Endothelial Growth Factor Receptor-3 (genetics) < Vascular Endothelial Growth Factor Receptor-3 (immunology)

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List of bibliographic references

Number of relevant bibliographic references: 59.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000C07 (2002)	Robert E. Ferrell [États-Unis]	Research perspectives in inherited lymphatic disease.
000C59 (2003)	Young-Sup Yoon ; Toshinori Murayama ; Edwin Gravereaux ; Tengiz Tkebuchava ; Marcy Silver ; Cynthia Curry ; Andrea Wecker ; Rudolf Kirchmair ; Chun Song Hu ; Marianne Kearney ; Alan Ashare [États-Unis] ; David G. Jackson [Royaume-Uni] ; Hajime Kubo [Finlande] ; Jeffrey M. Isner ; Douglas W. Losordo	VEGF-C gene therapy augments postnatal lymphangiogenesis and ameliorates secondary lymphedema
000D95 (2003)	Kara L. Levinson [États-Unis] ; Eleanor Feingold ; Robert E. Ferrell ; Thomas W. Glover ; Elias I. Traboulsi ; David N. Finegold	Age of onset in hereditary lymphedema.
000E05 (2002)	T. M Kinen [Finlande] ; Kari Alitalo [Finlande]	Molecular mechanisms of lymphangiogenesis.
000E31 (2003)	Anita Rauch [Allemagne] ; Maike Beese ; Ertan Mayatepek ; Helmut-Günther Dörr ; Dieter Wenzel ; André Reis ; Udo Trautmann	A novel 5q35.3 subtelomeric deletion syndrome.
000E67 (2003)	Michael Jeltsch [Finlande] ; Tuomas Tammela ; Kari Alitalo [Finlande] ; Jörg Wilting	Genesis and pathogenesis of lymphatic vessels.
000E72 (2003)	A. Evans ; R. Bell ; G. Brice ; P. Comeglio ; C. Lipede ; S. Jeffery ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; M. Sarfarazi ; A. Child	Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema
001755 (2004)	Marika J. Karkkainen [Finlande] ; Paula Haiko ; Kirsi Sainio ; Juha Partanen ; Jussi Taipale ; Tatiana V. Petrova ; Michael Jeltsch ; David G. Jackson ; Marja Talikka ; Heikki Rauvala ; Christer Betsholtz ; Kari Alitalo [Finlande]	Vascular endothelial growth factor C is required for sprouting of the first lymphatic vessels from embryonic veins.
001974 (2004)	Jian Feng Wang [États-Unis] ; Xuefeng Zhang ; Jerome E. Groopman	Activation of vascular endothelial growth factor receptor-3 and its downstream signaling promote cell survival under oxidative stress.
001C97 (2005)	G. Brice ; A. Child ; A. Evans ; R. Bell ; S. Mansour ; K. Burnand ; M. Sarfarazi ; S. Jeffery ; Peter Mortimer (dermatologue)‎ [Royaume-Uni]	Milroy disease and the VEGFR-3 mutation phenotype
001D07 (2004)	A M Fink [Autriche] ; I. Kaltenegger ; B. Schneider ; J. Frühauf ; W. Jurecka ; A. Steiner	Serum level of VEGF-D in patients with primary lymphedema.
001E38 (2005)	Seiji Mizuno [Japon] ; Yasukazu Yamada ; Kenichiro Yamada ; Noriko Nomura ; Nobuaki Wakamatsu	Clinical variability in a Japanese hereditary lymphedema type I family with an FLT4 mutation.
002256 (2006)	Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; J R Levick [Royaume-Uni]	Of mice and men; the translational physiology of a genetic form of lymphoedema
002380 (2006)	Ronen Spiegel [Israël] ; Arash Ghalamkarpour ; Etty Daniel-Spiegel ; Miikka Vikkula ; Stavit A. Shalev	Wide clinical spectrum in a family with hereditary lymphedema type I due to a novel missense mutation in VEGFR3.
002399 (2006)	A. Ghalamkarpour [Belgique] ; S. Morlot ; A. Raas-Rothschild ; A. Utkus ; J B Mulliken ; L M Boon ; M. Vikkula	Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentations.
002551 (2007)	C. Carver ; G. Brice ; S. Mansour ; P. Ostergaard ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; S. Jeffery	Three children with Milroy disease and de novo mutations in VEGFR3.
002675 (2007)	Matthew G. Butler [États-Unis] ; Susan L. Dagenais ; Stanley G. Rockson ; Thomas W. Glover	A novel VEGFR3 mutation causes Milroy disease.
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.
002975 (2007)	Zhengya Yu ; Jingjing Wang ; Shuling Peng ; Bing Dong ; Yang Li	Identification of a novel VEGFR-3 missense mutation in a Chinese family with hereditary lymphedema type I.
002B74 (2008)	Takeshi Futatani [Japon] ; Eiji Nii ; Makoto Obata ; Fukiko Ichida ; Yoshie Okabe ; Hirokazu Kanegane ; Toshio Miyawaki	Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease.
002C96 (2008)	Annelii Ny [Belgique] ; Marta Koch ; Wouter Vandevelde ; Martin Schneider ; Christian Fischer ; Antonio Diez-Juan ; Elke Neven ; Ilse Geudens ; Sunit Maity ; Lieve Moons ; Stéphane Plaisance ; Diether Lambrechts ; Peter Carmeliet ; Mieke Dewerchin	Role of VEGF-D and VEGFR-3 in developmental lymphangiogenesis, a chemicogenetic study in Xenopus tadpoles.

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