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Limaye, Nisha
Limaye, Nisha
在 uclouvain.be 的电子邮件经过验证
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Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome
TC Pansuriya, R van Eijk, P d'Adamo, MAJH van Ruler, ML Kuijjer, ...
Nature genetics 43 (12), 1256-1261, 2011
5792011
Somatic mutations in angiopoietin receptor gene TEK cause solitary and multiple sporadic venous malformations
N Limaye, V Wouters, M Uebelhoer, M Tuominen, R Wirkkala, JB Mulliken, ...
Nature genetics 41 (1), 118-124, 2009
4682009
Suppressed NFAT-dependent VEGFR1 expression and constitutive VEGFR2 signaling in infantile hemangioma
M Jinnin, D Medici, L Park, N Limaye, Y Liu, E Boscolo, J Bischoff, ...
Nature medicine 14 (11), 1236-1246, 2008
4282008
Association of extensive polymorphisms in the SLAM/CD2 gene cluster with murine lupus
AE Wandstrat, C Nguyen, N Limaye, AY Chan, S Subramanian, XH Tian, ...
Immunity 21 (6), 769-780, 2004
3212004
Somatic activating PIK3CA mutations cause venous malformation
N Limaye, J Kangas, A Mendola, C Godfraind, MJ Schlögel, R Helaers, ...
The American Journal of Human Genetics 97 (6), 914-921, 2015
3042015
Rapamycin improves TIE2-mutated venous malformation in murine model and human subjects
E Boscolo, N Limaye, L Huang, KT Kang, J Soblet, M Uebelhoer, ...
The Journal of clinical investigation 125 (9), 3491-3504, 2015
2442015
Blue rubber bleb nevus (BRBN) syndrome is caused by somatic TEK (TIE2) mutations
J Soblet, J Kangas, M Nätynki, A Mendola, R Helaers, M Uebelhoer, ...
Journal of Investigative Dermatology 137 (1), 207-216, 2017
2062017
Variable somatic TIE2 mutations in half of sporadic venous malformations
J Soblet, N Limaye, M Uebelhoer, LM Boon, M Vikkula
Molecular syndromology 4 (4), 179-183, 2013
1772013
Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylating effects
V Wouters, N Limaye, M Uebelhoer, A Irrthum, LM Boon, JB Mulliken, ...
European Journal of Human Genetics 18 (4), 414-420, 2010
1772010
From germline towards somatic mutations in the pathophysiology of vascular anomalies
N Limaye, LM Boon, M Vikkula
Human molecular genetics 18 (R1), R65-R74, 2009
1332009
Venous malformation-causative TIE2 mutations mediate an AKT-dependent decrease in PDGFB
M Uebelhoer, M Nätynki, J Kangas, A Mendola, HL Nguyen, J Soblet, ...
Human molecular genetics 22 (17), 3438-3448, 2013
1132013
Classification of vascular anomalies: an update
JE Steiner, BA Drolet
Seminars in Interventional Radiology 34 (03), 225-232, 2017
1052017
Common and specific effects of TIE2 mutations causing venous malformations
M Nätynki, J Kangas, I Miinalainen, R Sormunen, R Pietilä, J Soblet, ...
Human molecular genetics 24 (22), 6374-6389, 2015
1012015
PDGFRB gain-of-function mutations in sporadic infantile myofibromatosis
FA Arts, R Sciot, B Brichard, M Renard, A de Rocca Serra, G Dachy, ...
Human molecular genetics 26 (10), 1801-1810, 2017
922017
Susceptibility genes in the pathogenesis of murine lupus
C Nguyen, N Limaye, EK Wakeland
Arthritis Research 4 (Suppl 3), S255-63, 2002
832002
Vascular anomalies caused by abnormal signaling within endothelial cells: targets for novel therapies
HL Nguyen, LM Boon, M Vikkula
Seminars in interventional radiology 34 (03), 233-238, 2017
642017
Liquid biopsy for mutational profiling of locoregional recurrent and/or metastatic head and neck squamous cell carcinoma
R Galot, C van Marcke, R Helaers, A Mendola, RM Goebbels, X Caignet, ...
Oral oncology 104, 104631, 2020
542020
Association of PDGFRB mutations with pediatric myofibroma and myofibromatosis
G Dachy, RR De Krijger, S Fraitag, I Théate, B Brichard, SB Hoffman, ...
JAMA dermatology 155 (8), 946-950, 2019
542019
B cell–intrinsic CD84 and Ly108 maintain germinal center B cell tolerance
EB Wong, C Soni, AY Chan, PP Domeier, S Shwetank, T Abraham, ...
The Journal of Immunology 194 (9), 4130-4143, 2015
512015
Outcomes of venous malformation sclerotherapy: a review of study methodology and long-term results
S Ali, SE Mitchell
Seminars in Interventional Radiology 34 (03), 288-293, 2017
432017
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