Search research articles
Contact Us
Filters
Showing results (21-30 of 44) with videos related to
Page
of 5
Sort By:
BMC Cancer
|
August 20, 2024
Spatial transcriptomics profiling of gallbladder adenocarcinoma: a detailed two-case study of progression from precursor lesions to cancer
Sophie Pirenne, Fátima Manzano-Núñez, Axelle Loriot, et al.
Immunity
|
December 14, 2004
Association of extensive polymorphisms in the SLAM/CD2 gene cluster with murine lupus
Amy E Wandstrat, Charles Nguyen, Nisha Limaye, et al.
JAMA Dermatology
|
April 25, 2019
Association of PDGFRB Mutations With Pediatric Myofibroma and Myofibromatosis
Guillaume 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 synovitis
Clément 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 tolerance
Eric 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 inhibitor
Natasha 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 Arthritis
Clément 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 subjects
Elisa 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 effects
Vinciane Wouters, Nisha Limaye, Melanie Uebelhoer, et al.
Human Molecular Genetics
|
March 24, 2017
PDGFRB gain-of-function mutations in sporadic infantile myofibromatosis
Florence A Arts, Raf Sciot, Bénédicte Brichard, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 44) with videos related to
Sort By:
Page
of 5
BMC Cancer
|
August 20, 2024
Spatial transcriptomics profiling of gallbladder adenocarcinoma: a detailed two-case study of progression from precursor lesions to cancer
Sophie Pirenne, Fátima Manzano-Núñez, Axelle Loriot, et al.
Immunity
|
December 14, 2004
Association of extensive polymorphisms in the SLAM/CD2 gene cluster with murine lupus
Amy E Wandstrat, Charles Nguyen, Nisha Limaye, et al.
JAMA Dermatology
|
April 25, 2019
Association of PDGFRB Mutations With Pediatric Myofibroma and Myofibromatosis
Guillaume 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 synovitis
Clément 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 tolerance
Eric 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 inhibitor
Natasha 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 Arthritis
Clément 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 subjects
Elisa 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 effects
Vinciane Wouters, Nisha Limaye, Melanie Uebelhoer, et al.
Human Molecular Genetics
|
March 24, 2017
PDGFRB gain-of-function mutations in sporadic infantile myofibromatosis
Florence A Arts, Raf Sciot, Bénédicte Brichard, et al.
Page
of 5