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Serveur d'exploration sur le lymphœdème - Curation (Ncbi)

Index « Keywords » - entrée « Lymphatic Abnormalities (genetics) »
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Lymphatic Abnormalities (diagnostic imaging) < Lymphatic Abnormalities (genetics) < Lymphatic Abnormalities (parasitology)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 11.
Ident.Authors (with country if any)Title
000D44 (2003) Benjamin M. Kriederman [États-Unis] ; Teressa L. Myloyde ; Marlys H. Witte ; Susan L. Dagenais ; Charles L. Witte ; Margaret Rennels ; Michael J. Bernas ; Michelle T. Lynch ; Robert P. Erickson ; Mark S. Caulder ; Naoyuki Miura ; David Jackson ; Brian P. Brooks ; Thomas W. GloverFOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.
001B00 (2004) Tatiana V. Petrova [Finlande] ; Terhi Karpanen ; Camilla Norrmén ; Russell Mellor ; Tomoki Tamakoshi ; David Finegold ; Robert Ferrell ; Dontscho Kerjaschki ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; Seppo Yl Herttuala ; Naoyuki Miura ; Kari Alitalo [Finlande]Defective valves and abnormal mural cell recruitment underlie lymphatic vascular failure in lymphedema distichiasis.
001C67 (2003) Michael S. Pepper [Suisse]Literature watch. FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.
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 EricksonComparative lymphatic, ocular, and metabolic phenotypes of Foxc2 haploinsufficient and aP2-FOXC2 transgenic mice.
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. MortimerMutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limb.
002824 (2007) Pascal Brouillard [Belgique] ; Miikka VikkulaGenetic causes of vascular malformations.
004971 (2012) F C Connell ; K. Kalidas ; P. Ostergaard ; G. Brice ; V. Murday ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; I. Jeffrey ; S. Jeffery ; Sahar MansourCCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non-immune hydrops fetalis.
005059 (2012) Alice Frigerio [Italie] ; David A. Stevenson ; J Fredrik GrimmerThe genetics of vascular anomalies.
005D12 (????) Prashant Yadav [États-Unis] ; Dawn K. De Castro ; Milton Waner ; Lutz Meyer ; Aaron FayVascular anomalies of the head and neck: a review of genetics.
006380 (2014) Pascal Brouillard ; Laurence Boon ; Miikka Vikkula [Belgique]Genetics of lymphatic anomalies
007314 (2014) R P EricksonNext generation sequencing is here now.

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