These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 38713105)

  • 21. Rare Variants in LAMA5 Gene associated with FLT4 and FOXC2 Mutations in Primary Lymphedema May Contribute to Severity.
    Liu NF; Yu ZY; Sun D; Lou Y
    Lymphology; 2016 Dec; 49(4):192-204. PubMed ID: 29908552
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Milroy's primary congenital lymphedema in a male infant and review of the literature.
    Kitsiou-Tzeli S; Vrettou C; Leze E; Makrythanasis P; Kanavakis E; Willems P
    In Vivo; 2010; 24(3):309-14. PubMed ID: 20555004
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Vegfc/Flt4 signalling is suppressed by Dll4 in developing zebrafish intersegmental arteries.
    Hogan BM; Herpers R; Witte M; Heloterä H; Alitalo K; Duckers HJ; Schulte-Merker S
    Development; 2009 Dec; 136(23):4001-9. PubMed ID: 19906867
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A family with Milroy disease caused by the FLT4/VEGFR3 gene variant c.2774 T > A.
    Sui Y; Lu Y; Lin M; Ni X; Chen X; Li H; Jiang M
    BMC Med Genomics; 2021 Jun; 14(1):151. PubMed ID: 34103024
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Antagonistic Activities of Vegfr3/Flt4 and Notch1b Fine-tune Mechanosensitive Signaling during Zebrafish Cardiac Valvulogenesis.
    Fontana F; Haack T; Reichenbach M; Knaus P; Puceat M; Abdelilah-Seyfried S
    Cell Rep; 2020 Jul; 32(2):107883. PubMed ID: 32668254
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentations.
    Ghalamkarpour A; Morlot S; Raas-Rothschild A; Utkus A; Mulliken JB; Boon LM; Vikkula M
    Clin Genet; 2006 Oct; 70(4):330-5. PubMed ID: 16965327
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Lymphatic dysfunction, not aplasia, underlies Milroy disease.
    Mellor RH; Hubert CE; Stanton AW; Tate N; Akhras V; Smith A; Burnand KG; Jeffery S; Mäkinen T; Levick JR; Mortimer PS
    Microcirculation; 2010 May; 17(4):281-96. PubMed ID: 20536741
    [TBL] [Abstract][Full Text] [Related]  

  • 28. DNA methylation regulates expression of VEGF-R2 (KDR) and VEGF-R3 (FLT4).
    Quentmeier H; Eberth S; Romani J; Weich HA; Zaborski M; Drexler HG
    BMC Cancer; 2012 Jan; 12():19. PubMed ID: 22251800
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A Novel Missense Mutation in FLT4 Causes Autosomal Recessive Hereditary Lymphedema.
    Melikhan-Revzin S; Kurolap A; Dagan E; Mory A; Gershoni-Baruch R
    Lymphat Res Biol; 2015 Jun; 13(2):107-11. PubMed ID: 26091405
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A Milroy case with FLT4/VEGFR3 mutation and an unusual skin biopsy.
    Liu NF; Yu ZY; Lou Y; Sun D
    Br J Dermatol; 2019 Jan; 180(1):223-224. PubMed ID: 30169892
    [No Abstract]   [Full Text] [Related]  

  • 31. Two novel variations p.(Ser1275Thr) and p.(Ser1275Arg) in FLT4 causing prenatal hereditary lymphedema type 1.
    Lajmi Y; Loeuillet L; Petrilli G; Egloff C; Nectoux J; Molac C; Roux N; Pannier E; Achaiaa A; Arkoub ZA; Chuon S; Coussement A; Dupont JM; Malan V; Spaggiari E; Razavi F; Amiel J; Bessières B; Grotto S; Attié-Bitach T
    Birth Defects Res; 2023 Mar; 115(5):563-571. PubMed ID: 36538874
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Gene-environment regulatory circuits of right ventricular pathology in tetralogy of fallot.
    Zhao Y; Kang X; Gao F; Guzman A; Lau RP; Biniwale R; Wadehra M; Reemtsen B; Garg M; Halnon N; Quintero-Rivera F; Van Arsdell G; Coppola G; Nelson SF; Touma M;
    J Mol Med (Berl); 2019 Dec; 97(12):1711-1722. PubMed ID: 31834445
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Distinct genetic interactions between multiple Vegf receptors are required for development of different blood vessel types in zebrafish.
    Covassin LD; Villefranc JA; Kacergis MC; Weinstein BM; Lawson ND
    Proc Natl Acad Sci U S A; 2006 Apr; 103(17):6554-9. PubMed ID: 16617120
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A novel mutation in the conserved sequence of vascular endothelial growth factor receptor 3 leads to primary lymphoedema.
    Dai T; Li B; He B; Yan L; Gu L; Liu X; Qi J; Li P; Zhou X
    J Int Med Res; 2018 Aug; 46(8):3162-3171. PubMed ID: 29896974
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Rspo1/Wnt signaling promotes angiogenesis via Vegfc/Vegfr3.
    Gore AV; Swift MR; Cha YR; Lo B; McKinney MC; Li W; Castranova D; Davis A; Mukouyama YS; Weinstein BM
    Development; 2011 Nov; 138(22):4875-86. PubMed ID: 22007135
    [TBL] [Abstract][Full Text] [Related]  

  • 36. BVES downregulation in non-syndromic tetralogy of fallot is associated with ventricular outflow tract stenosis.
    Shi Y; Li Y; Wang Y; Zhu P; Chen Y; Wang H; Yue S; Xia X; Chen J; Jiang Z; Zhou C; Cai W; Yuan H; Wu Y; Wan Y; Li X; Zhu X; Zhou Z; Dai G; Li F; Mo X; Ye X; Fan X; Zhuang J; Wu X; Yuan W
    Sci Rep; 2020 Aug; 10(1):14167. PubMed ID: 32843646
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The heparan sulfate editing enzyme Sulf1 plays a novel role in zebrafish VegfA mediated arterial venous identity.
    Gorsi B; Liu F; Ma X; Chico TJ; v A; Kramer KL; Bridges E; Monteiro R; Harris AL; Patient R; Stringer SE
    Angiogenesis; 2014 Jan; 17(1):77-91. PubMed ID: 23959107
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function.
    Alpaslan M; Fastré E; Mestre S; van Haeringen A; Repetto GM; Keymolen K; Boon LM; Belva F; Giacalone G; Revencu N; Sznajer Y; Riches K; Keeley V; Mansour S; Gordon K; Martin-Almedina S; Dobbins S; Ostergaard P; Quere I; Brouillard P; Vikkula M
    Hum Mol Genet; 2024 Jul; 33(14):1250-1261. PubMed ID: 38676400
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Case Report: The compound heterozygotes variants in
    Xiang Q; Chen J; Xiao X; Xu B; Xie H; Wang H; Yang M; Liu S
    Front Genet; 2023; 14():1140406. PubMed ID: 37035731
    [No Abstract]   [Full Text] [Related]  

  • 40. A novel VEGFR3 mutation causes Milroy disease.
    Butler MG; Dagenais SL; Rockson SG; Glover TW
    Am J Med Genet A; 2007 Jun; 143A(11):1212-7. PubMed ID: 17458866
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.