Publications by authors named "Nisha Limaye"

31Publications

Liquid biopsy for mutational profiling of locoregional recurrent and/or metastatic head and neck squamous cell carcinoma.

Oral Oncol 2020 05 10;104:104631. Epub 2020 Mar 10.

Department of Medical Oncology, Institut Roi Albert II - Cliniques universitaires Saint-Luc, Brussels, Belgium; Institute for Clinical and Experimental Research (MIRO), Université catholique de Louvain, Brussels, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.oraloncology.2020.104631DOI Listing
May 2020

[Rapamycin opens the era of targeted molecular therapy of venous malformations].

Med Sci (Paris) 2016 Jun-Jul;32(6-7):574-8. Epub 2016 Jul 12.

Génétique Moléculaire Humaine, institut de Duve, université catholique de Louvain, Bruxelles, DDUV, Avenue Hippocrate 75, 1200 Woluwe-Saint-Lambert, Belgique - Centre des anomalies vasculaires, division de chirurgie plastique, cliniques universitaires Saint-Luc, université catholique de Louvain, Bruxelles, Belgique.

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http://dx.doi.org/10.1051/medsci/20163206016DOI Listing
July 2017

Somatic Activating PIK3CA Mutations Cause Venous Malformation.

Am J Hum Genet 2015 Dec;97(6):914-21

Human Molecular Genetics, de Duve Institute, Université Catholique de Louvain, 1200 Brussels, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2015.11.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678782PMC
December 2015

Common and specific effects of TIE2 mutations causing venous malformations.

Hum Mol Genet 2015 Nov 28;24(22):6374-89. Epub 2015 Aug 28.

Oulu Center for Cell-Matrix Research, Biocenter Oulu and Faculty of Biochemistry and Molecular Medicine, University of Oulu, Oulu, Finland,

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http://dx.doi.org/10.1093/hmg/ddv349DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614705PMC
November 2015

B cell-intrinsic CD84 and Ly108 maintain germinal center B cell tolerance.

J Immunol 2015 May 23;194(9):4130-43. Epub 2015 Mar 23.

Department of Microbiology and Immunology, Pennsylvania State University College of Medicine, Hershey, PA 17033;

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http://dx.doi.org/10.4049/jimmunol.1403023DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4402266PMC
May 2015

Venous malformation-causative TIE2 mutations mediate an AKT-dependent decrease in PDGFB.

Hum Mol Genet 2013 Sep 30;22(17):3438-48. Epub 2013 Apr 30.

Laboratory of Human Molecular Genetics, de Duve Institute, Université catholique de Louvain, 1200 Brussels, Belgium.

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http://dx.doi.org/10.1093/hmg/ddt198DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3736867PMC
September 2013

Ligand oligomerization state controls Tie2 receptor trafficking and angiopoietin-2-specific responses.

J Cell Sci 2012 May 22;125(Pt 9):2212-23. Epub 2012 Feb 22.

Oulu Center for Cell-Matrix Research, Biocenter Oulu and Department of Medical Biochemistry and Molecular Biology, University of Oulu, Oulu, Finland.

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http://jcs.biologists.org/cgi/doi/10.1242/jcs.098020
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http://dx.doi.org/10.1242/jcs.098020DOI Listing
May 2012

From germline towards somatic mutations in the pathophysiology of vascular anomalies.

Hum Mol Genet 2009 Apr;18(R1):R65-74

de Duve Institute, Division of Plastic Surgery, Cliniques universitaires Saint-Luc, Université catholique de Louvain, Brussels, Belgium.

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http://dx.doi.org/10.1093/hmg/ddp002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2657941PMC
April 2009

Cutaneous venous malformations in familial cerebral cavernomatosis caused by KRIT1 gene mutations.

Dermatology 2009 31;218(4):307-13. Epub 2009 Jan 31.

Department of Dermatology, Hospital del Mar, IMAS, Barcelona ES-08003, Spain.

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http://dx.doi.org/10.1159/000199461DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2889683PMC
October 2009

Suppressed NFAT-dependent VEGFR1 expression and constitutive VEGFR2 signaling in infantile hemangioma.

Nat Med 2008 Nov 19;14(11):1236-46. Epub 2008 Oct 19.

Department of Developmental Biology, Harvard School of Dental Medicine, Boston, Massachusetts 02115, USA.

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http://www.nature.com/articles/nm.1877
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http://dx.doi.org/10.1038/nm.1877DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2593632PMC
November 2008

Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.

Hum Genet 2007 Dec;122(5):552

Institute of Cellular Pathology, Université Catholique de Louvain, Laboratory of Human Molecular Genetics, Avenue Hippocrate 74(+5), bp. 75.39, B-1200, Brussels, Belgium.

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December 2007

Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.

Hum Genet 2007 Dec;122(5):552

Institute of Cellular Pathology, Université Catholique de Louvain, Laboratory of Human Molecular Genetics, Avenue Hippocrate 74(+5), bp. 75.39, B-1200, Brussels, Belgium.

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December 2007

Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.

Hum Genet 2007 Dec;122(5):551

Institute of Cellular Pathology, Université Catholique de Louvain, Laboratory of Human Molecular Genetics, Avenue Hippocrate 74(+5), bp. 75.39, B-1200, Brussels, Belgium.

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December 2007

Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.

Hum Genet 2007 Dec;122(5):552

Institute of Cellular Pathology, Université Catholique de Louvain, Laboratory of Human Molecular Genetics, Avenue Hippocrate 74(+5), bp. 75.39, B-1200, Brussels, Belgium.

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December 2007

Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.

Hum Genet 2007 Dec;122(5):551

Institute of Cellular Pathology, Université Catholique de Louvain, Laboratory of Human Molecular Genetics, Avenue Hippocrate, Brussels, Belgium.

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December 2007

Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.

Hum Genet 2007 Dec;122(5):551

Institute of Cellular Pathology, Université Catholique de Louvain, Laboratory of Human Molecular Genetics, Avenue Hippocrate, Brussels, Belgium.

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December 2007

Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.

Hum Genet 2007 Dec;122(5):550

Institute of Cellular Pathology, Université Catholique de Louvain, Laboratory of Human Molecular Genetics, Avenue Hippocrate, Brussels, Belgium.

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December 2007

Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.

Hum Genet 2007 Dec;122(5):550

Institute of Cellular Pathology, Université Catholique de Louvain, Laboratory of Human Molecular Genetics, Avenue Hippocrate, Brussels, Belgium.

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December 2007

Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.

Hum Genet 2007 Dec;122(5):550

Institute of Cellular Pathology, Université Catholique de Louvain, Laboratory of Human Molecular Genetics, Avenue Hippocrate, Brussels, Belgium.

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December 2007

Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.

Hum Genet 2007 Dec;122(5):549-50

Institute of Cellular Pathology, Université Catholique de Louvain, Laboratory of Human Molecular Genetics, Avenue Hippocrate, Brussels, Belgium.

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December 2007

Susceptibility genes in the pathogenesis of murine lupus.

Arthritis Res 2002 9;4 Suppl 3:S255-63. Epub 2002 May 9.

Center for Immunology, University of Texas Southwestern Medical Center, Dallas 75290, USA.

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http://arthritis-research.biomedcentral.com/articles/10.1186
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3240158PMC
http://dx.doi.org/10.1186/ar583DOI Listing
May 2003