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Nisha Limaye

Showing results (21-30 of 44) with videos related to

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BMC Cancer|August 20, 2024
Spatial transcriptomics profiling of gallbladder adenocarcinoma: a detailed two-case study of progression from precursor lesions to cancerSophie Pirenne, Fátima Manzano-Núñez, Axelle Loriot, et al.
Immunity|December 14, 2004
Association of extensive polymorphisms in the SLAM/CD2 gene cluster with murine lupusAmy E Wandstrat, Charles Nguyen, Nisha Limaye, et al.
JAMA Dermatology|April 25, 2019
Association of PDGFRB Mutations With Pediatric Myofibroma and MyofibromatosisGuillaume Dachy, Ronald R de Krijger, Sylvie Fraitag, et al.
Annals of the Rheumatic Diseases|July 28, 2023
Disease activity drives transcriptomic heterogeneity in early untreated rheumatoid synovitisClément Triaille, Gaëlle Tilman, Tatiana Sokolova, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 25, 2015
B cell-intrinsic CD84 and Ly108 maintain germinal center B cell toleranceEric B Wong, Chetna Soni, Alice Y Chan, et al.
European Journal of Cancer (Oxford, England : 1990)|November 1, 2023
Tumour-agnostic plasma assay for circulating tumour DNA predicts outcome in recurrent and/or metastatic squamous cell carcinoma of the head and neck treated with a PD-1 inhibitorNatasha Honoré, Athenaïs van der Elst, Anna Dietz, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|May 23, 2024
Two Broad Categories Overlapping With Rheumatoid Arthritis Observed in Synovial Biopsies from Patients With Juvenile Idiopathic ArthritisClément Triaille, Gaëlle Tilman, Charlotte A Baert, et al.
The Journal of Clinical Investigation|August 11, 2015
Rapamycin improves TIE2-mutated venous malformation in murine model and human subjectsElisa Boscolo, Nisha Limaye, Lan Huang, et al.
European Journal of Human Genetics : EJHG|November 6, 2009
Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylating effectsVinciane Wouters, Nisha Limaye, Melanie Uebelhoer, et al.
Human Molecular Genetics|March 24, 2017
PDGFRB gain-of-function mutations in sporadic infantile myofibromatosisFlorence A Arts, Raf Sciot, Bénédicte Brichard, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
BMC Cancer|August 20, 2024
Spatial transcriptomics profiling of gallbladder adenocarcinoma: a detailed two-case study of progression from precursor lesions to cancerSophie Pirenne, Fátima Manzano-Núñez, Axelle Loriot, et al.
Immunity|December 14, 2004
Association of extensive polymorphisms in the SLAM/CD2 gene cluster with murine lupusAmy E Wandstrat, Charles Nguyen, Nisha Limaye, et al.
JAMA Dermatology|April 25, 2019
Association of PDGFRB Mutations With Pediatric Myofibroma and MyofibromatosisGuillaume Dachy, Ronald R de Krijger, Sylvie Fraitag, et al.
Annals of the Rheumatic Diseases|July 28, 2023
Disease activity drives transcriptomic heterogeneity in early untreated rheumatoid synovitisClément Triaille, Gaëlle Tilman, Tatiana Sokolova, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 25, 2015
B cell-intrinsic CD84 and Ly108 maintain germinal center B cell toleranceEric B Wong, Chetna Soni, Alice Y Chan, et al.
European Journal of Cancer (Oxford, England : 1990)|November 1, 2023
Tumour-agnostic plasma assay for circulating tumour DNA predicts outcome in recurrent and/or metastatic squamous cell carcinoma of the head and neck treated with a PD-1 inhibitorNatasha Honoré, Athenaïs van der Elst, Anna Dietz, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|May 23, 2024
Two Broad Categories Overlapping With Rheumatoid Arthritis Observed in Synovial Biopsies from Patients With Juvenile Idiopathic ArthritisClément Triaille, Gaëlle Tilman, Charlotte A Baert, et al.
The Journal of Clinical Investigation|August 11, 2015
Rapamycin improves TIE2-mutated venous malformation in murine model and human subjectsElisa Boscolo, Nisha Limaye, Lan Huang, et al.
European Journal of Human Genetics : EJHG|November 6, 2009
Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylating effectsVinciane Wouters, Nisha Limaye, Melanie Uebelhoer, et al.
Human Molecular Genetics|March 24, 2017
PDGFRB gain-of-function mutations in sporadic infantile myofibromatosisFlorence A Arts, Raf Sciot, Bénédicte Brichard, et al.
Pageof 5