Hereditary lymphedema: evidence for linkage and genetic heterogeneity.
about
GJC2 missense mutations cause human lymphedemaProtein tyrosine phosphatase PTPN14 is a regulator of lymphatic function and choanal development in humansAnalysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinaseA juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2A gene for lymphedema-distichiasis maps to 16q24.3.Lymphangiogenesis and Lesion Heterogeneity in Interstitial Lung DiseasesA novel mutation in CELSR1 is associated with hereditary lymphedemaA model for gene therapy of human hereditary lymphedemaSomatic mutation of vascular endothelial growth factor receptors in juvenile hemangiomaCharacterization of indolinones which preferentially inhibit VEGF-C- and VEGF-D-induced activation of VEGFR-3 rather than VEGFR-2Mapping of the locus for cholestasis-lymphedema syndrome (Aagenaes syndrome) to a 6.6-cM interval on chromosome 15qStimulation of beta 1 integrin induces tyrosine phosphorylation of vascular endothelial growth factor receptor-3 and modulates cell migration.Lymphedema-lymphangiectasia-mental retardation (Hennekam) syndrome: a review.Current views on the function of the lymphatic vasculature in health and diseaseVascular endothelial growth factor receptor-2 promotes the development of the lymphatic vasculature.Connexin37 and Connexin43 deficiencies in mice disrupt lymphatic valve development and result in lymphatic disorders including lymphedema and chylothoraxAn overview of lymphatic vessels and their emerging role in cardiovascular diseaseMilroy disease and the VEGFR-3 mutation phenotype.Possible genetic predisposition to lymphedema after breast cancer.Albumin-binding domain conjugate for near-infrared fluorescence lymphatic imaging.Current concepts in lymphatic malformation.Novel Mechanisms of Compromised Lymphatic Endothelial Cell Homeostasis in Obesity: The Role of Leptin in Lymphatic Endothelial Cell Tube Formation and ProliferationPrimary congenital lymphedema complicated by hydrops fetalis: a case report and review of the literatureConnexin 47 mutations increase risk for secondary lymphedema following breast cancer treatmentBiomarkers of lymphatic function and disease: state of the art and future directions.Circulating lymphangiogenic growth factors in gastrointestinal solid tumors, could they be of any clinical significance?Integrin-alpha9 is required for fibronectin matrix assembly during lymphatic valve morphogenesis.New developments in clinical aspects of lymphatic disease.Massively parallel sequencing and identification of genes for primary lymphoedema: a perfect fit.FLT4/VEGFR3 and Milroy disease: novel mutations, a review of published variants and database update.The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings.Gene and protein therapies utilizing VEGF for ALS.Morphogenesis of the lymphatic vasculature: A focus on new progenitors and cellular mechanisms important for constructing lymphatic vessels.Routine genetic screening with a multi-gene panel in patients with pheochromocytomas.The lymphatic vasculature: development and role in shaping immunity.VEGF-C gene therapy augments postnatal lymphangiogenesis and ameliorates secondary lymphedema.A Novel Mutation in the FOXC2 Gene: A Heterozygous Insertion of Adenosine (c.867insA) in a Family with Lymphoedema of Lower Limbs without Distichiasis.AA amyloidosis as a complication of primary lymphedema.Methicillin-resistant Staphylococcus aureus causes sustained collecting lymphatic vessel dysfunction.
P2860
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P2860
Hereditary lymphedema: evidence for linkage and genetic heterogeneity.
description
1998 nî lūn-bûn
@nan
1998 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Hereditary lymphedema: evidence for linkage and genetic heterogeneity.
@ast
Hereditary lymphedema: evidence for linkage and genetic heterogeneity.
@en
Hereditary lymphedema: evidence for linkage and genetic heterogeneity.
@nl
type
label
Hereditary lymphedema: evidence for linkage and genetic heterogeneity.
@ast
Hereditary lymphedema: evidence for linkage and genetic heterogeneity.
@en
Hereditary lymphedema: evidence for linkage and genetic heterogeneity.
@nl
prefLabel
Hereditary lymphedema: evidence for linkage and genetic heterogeneity.
@ast
Hereditary lymphedema: evidence for linkage and genetic heterogeneity.
@en
Hereditary lymphedema: evidence for linkage and genetic heterogeneity.
@nl
P2093
P356
P1476
Hereditary lymphedema: evidence for linkage and genetic heterogeneity.
@en
P2093
Barmada MM
Ferrell RE
Finegold DN
Lawrence EC
Levinson KL
P304
P356
10.1093/HMG/7.13.2073
P577
1998-12-01T00:00:00Z