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Exhaustion of the CD8+ T Cell Compartment in Patients with Mutations in Phosphoinositide 3-Kinase Delta.
Published in:
Frontiers in Immunology, 2018, p. 1, doi. 10.3389/fimmu.2018.00446
By:
- Wentink, Marjolein W. J.;
- Mueller, Yvonne M.;
- Dalm, Virgil A. S. H.;
- Driessen, Gertjan J.;
- van Hagen, P. Martin;
- van Montfrans, Joris M.;
- van der Burg, Mirjam;
- Katsikis, Peter D.
Publication type:
Article
Delineating Human B Cell Precursor Development With Genetically Identified PID Cases as a Model.
Published in:
Frontiers in Immunology, 2019, v. 10, p. 1, doi. 10.3389/fimmu.2019.02680
By:
- Wentink, Marjolein W. J.;
- Kalina, Tomas;
- Perez-Andres, Martin;
- del Pino Molina, Lucia;
- IJspeert, Hanna;
- Kavelaars, François G.;
- Lankester, Arjan C.;
- Lecrevisse, Quentin;
- van Dongen, Jacques J. M.;
- Orfao, Alberto;
- van der Burg, Mirjam
Publication type:
Article
EuroFlow-Based Flowcytometric Diagnostic Screening and Classification of Primary Immunodeficiencies of the Lymphoid System.
Published in:
Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.01271
By:
- van Dongen, Jacques J. M.;
- van der Burg, Mirjam;
- Kalina, Tomas;
- Perez-Andres, Martin;
- Mejstrikova, Ester;
- Vlkova, Marcela;
- Lopez-Granados, Eduardo;
- Wentink, Marjolein;
- Kienzler, Anne-Kathrin;
- Philippé, Jan;
- Sousa, Ana E.;
- van Zelm, Menno C.;
- Blanco, Elena;
- Orfao, Alberto
Publication type:
Article
The EuroFlow PID Orientation Tube for Flow Cytometric Diagnostic Screening of Primary Immunodeficiencies of the Lymphoid System.
Published in:
Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.00246
By:
- van der Burg, Mirjam;
- Kalina, Tomas;
- Perez-Andres, Martin;
- Vlkova, Marcela;
- Lopez-Granados, Eduardo;
- Blanco, Elena;
- Bonroy, Carolien;
- Sousa, Ana E.;
- Kienzler, Anne-Kathrin;
- Wentink, Marjolein;
- Mejstríková, Ester;
- Šinkorova, Vendula;
- Stuchly, Jan;
- van Zelm, Menno C.;
- Orfao, Alberto;
- van Dongen, Jacques J. M.
Publication type:
Article
The expansion of human T-bethighCD21low B cells is T cell dependent.
Published in:
Science Immunology, 2021, v. 6, n. 64, p. 1, doi. 10.1126/sciimmunol.abh0891
By:
- Keller, Baerbel;
- Strohmeier, Valentina;
- Harder, Ina;
- Unger, Susanne;
- Payne, Kathryn J.;
- Andrieux, Geoffroy;
- Boerries, Melanie;
- Felixberger, Peter Tobias;
- Landry, Jonathan J. M.;
- Nieters, Alexandra;
- Rensing-Ehl, Anne;
- Salzer, Ulrich;
- Frede, Natalie;
- Usadel, Susanne;
- Elling, Roland;
- Speckmann, Carsten;
- Hainmann, Ina;
- Ralph, Elizabeth;
- Gilmour, Kimberly;
- Wentink, Marjolein W. J.
Publication type:
Article
Dissection of the Pre-Germinal Center B-Cell Maturation Pathway in Common Variable Immunodeficiency Based on Standardized Flow Cytometric EuroFlow Tools.
Published in:
Frontiers in Immunology, 2021, v. 11, p. N.PAG, doi. 10.3389/fimmu.2020.603972
By:
- del Pino-Molina, Lucía;
- López-Granados, Eduardo;
- Lecrevisse, Quentin;
- Torres Canizales, Juan;
- Pérez-Andrés, Martín;
- Blanco, Elena;
- Wentink, Marjolein;
- Bonroy, Carolien;
- Nechvatalova, Jana;
- Milota, Tomas;
- Kienzler, Anne-Kathrin;
- Philippé, Jan;
- Sousa, Ana E.;
- van der Burg, Mirjam;
- Kalina, Tomas;
- van Dongen, Jacques J.M.;
- Orfao, Alberto
Publication type:
Article
Variants Within TSC2 Exons 25 and 31 Are Very Unlikely to Cause Clinically Diagnosable Tuberous Sclerosis.
Published in:
Human Mutation, 2016, v. 37, n. 4, p. 364, doi. 10.1002/humu.22951
By:
- Ekong, Rosemary;
- Nellist, Mark;
- Hoogeveen‐Westerveld, Marianne;
- Wentink, Marjolein;
- Panzer, Jessica;
- Sparagana, Steven;
- Emmett, Warren;
- Dawson, Natalie L.;
- Malinge, Marie Claire;
- Nabbout, Rima;
- Carbonara, Caterina;
- Barberis, Marco;
- Padovan, Sergio;
- Futema, Marta;
- Plagnol, Vincent;
- Humphries, Steve E.;
- Migone, Nicola;
- Povey, Sue
Publication type:
Article
Functional assessment of variants in the TSC1 and TSC2 genes identified in individuals with Tuberous Sclerosis Complex.
Published in:
Human Mutation, 2011, v. 32, n. 4, p. 424, doi. 10.1002/humu.21451
By:
- Hoogeveen-Westerveld, Marianne;
- Wentink, Marjolein;
- van den Heuvel, Diana;
- Mozaffari, Melika;
- Ekong, Rosemary;
- Povey, Sue;
- den Dunnen, Johan T.;
- Metcalfe, Kay;
- Vallee, Stephanie;
- Krueger, Stefan;
- Bergoffen, JoAnn;
- Shashi, Vandana;
- Elmslie, Frances;
- Kwiatkowski, David;
- Sampson, Julian;
- Vidales, Concha;
- Dzarir, Jacinta;
- Garcia-Planells, Javier;
- Dies, Kira;
- Maat-Kievit, Anneke
Publication type:
Article
Adaptive immune defects in a patient with leukocyte adhesion deficiency type III with a novel mutation in FERMT3.
Published in:
Pediatric Allergy & Immunology, 2016, v. 27, n. 2, p. 214, doi. 10.1111/pai.12485
By:
- Suratannon, Narissara;
- Yeetong, Patra;
- Srichomthong, Chalurmpon;
- Amarinthnukrowh, Pramuk;
- Chatchatee, Pantipa;
- Sosothikul, Darintr;
- Hagen, P. Martin;
- Burg, Mirjam;
- Wentink, Marjolein;
- Driessen, Gertjan J.;
- Suphapeetiporn, Kanya;
- Shotelersuk, Vorasuk
Publication type:
Article
Strategies for B-cell receptor repertoire analysis in primary immunodeficiencies: from severe combined immunodeficiency to common variable immunodeficiency.
Published in:
Frontiers in Immunology, 2015, v. 6, p. 1, doi. 10.3389/fimmu.2015.00157
By:
- IJspeert, Hanna;
- Wentink, Marjolein;
- van Zessen, David;
- Driessen, Gertjan J.;
- Dalm, Virgil A. S. H.;
- van Hagen, Martin P.;
- Pico-Knijnenburg, Ingrid;
- Simons, Erik J.;
- van Dongen, Jacques J. M.;
- Stubbs, Andrew P.;
- van der Burg, Mirjam
Publication type:
Article

Found: 10

Exhaustion of the CD8<sup>+</sup> T Cell Compartment in Patients with Mutations in Phosphoinositide 3-Kinase Delta.

Delineating Human B Cell Precursor Development With Genetically Identified PID Cases as a Model.

EuroFlow-Based Flowcytometric Diagnostic Screening and Classification of Primary Immunodeficiencies of the Lymphoid System.

The EuroFlow PID Orientation Tube for Flow Cytometric Diagnostic Screening of Primary Immunodeficiencies of the Lymphoid System.

The expansion of human T-bet<sup>high</sup>CD21<sup>low</sup> B cells is T cell dependent.

Dissection of the Pre-Germinal Center B-Cell Maturation Pathway in Common Variable Immunodeficiency Based on Standardized Flow Cytometric EuroFlow Tools.

Variants Within TSC2 Exons 25 and 31 Are Very Unlikely to Cause Clinically Diagnosable Tuberous Sclerosis.

Functional assessment of variants in the TSC1 and TSC2 genes identified in individuals with Tuberous Sclerosis Complex.

Adaptive immune defects in a patient with leukocyte adhesion deficiency type III with a novel mutation in FERMT3.

Strategies for B-cell receptor repertoire analysis in primary immunodeficiencies: from severe combined immunodeficiency to common variable immunodeficiency.