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Fatima Dhalla

Showing results (11-20 of 24) with videos related to

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The New England Journal of Medicine|July 3, 2024
Normalization of C1 Inhibitor in a Patient with Hereditary AngioedemaNicholas E Peters, Dylan J Mac Lochlainn, Fatima Dhalla, et al.
Science Advances|May 13, 2022
Developmental dynamics of the neural crest-mesenchymal axis in creating the thymic microenvironmentAdam E Handel, Stanley Cheuk, Fatima Dhalla, et al.
Clinical Immunology (Orlando, Fla.)|December 18, 2021
Resolving the polygenic aetiology of a late onset combined immune deficiency caused by NFKB1 haploinsufficiency and modified by PIK3R1 and TNFRSF13B variantsChantal E Hargreaves, Fatima Dhalla, Arzoo M Patel, et al.
The Journal of Allergy and Clinical Immunology|September 20, 2024
European Society for Immunodeficiencies guidelines for the management of patients with congenital athymiaAlexandra Y Kreins, Fatima Dhalla, Aisling M Flinn, et al.
Nature Communications|July 10, 2023
Combined multidimensional single-cell protein and RNA profiling dissects the cellular and functional heterogeneity of thymic epithelial cellsFabian Klein, Clara Veiga-Villauriz, Anastasiya Börsch, et al.
Journal of Clinical Immunology|December 16, 2014
Identification of a novel mutation in MAGT1 and progressive multifocal leucoencephalopathy in a 58-year-old man with XMEN diseaseFatima Dhalla, Sarah Murray, Ross Sadler, et al.
Elife|August 26, 2020
Ageing compromises mouse thymus function and remodels epithelial cell differentiationJeanette Baran-Gale, Michael D Morgan, Stefano Maio, et al.
Nature Communications|April 25, 2019
Sequencing of human genomes with nanopore technologyRory Bowden, Robert W Davies, Andreas Heger, et al.
Journal of Clinical Immunology|January 19, 2021
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous MutationsGiuliana Giardino, Svetlana O Sharapova, Peter Ciznar, et al.
Science Advances|December 3, 2021
FOXN1 forms higher-order nuclear condensates displaced by mutations causing immunodeficiencyIoanna A Rota, Adam E Handel, Stefano Maio, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
The New England Journal of Medicine|July 3, 2024
Normalization of C1 Inhibitor in a Patient with Hereditary AngioedemaNicholas E Peters, Dylan J Mac Lochlainn, Fatima Dhalla, et al.
Science Advances|May 13, 2022
Developmental dynamics of the neural crest-mesenchymal axis in creating the thymic microenvironmentAdam E Handel, Stanley Cheuk, Fatima Dhalla, et al.
Clinical Immunology (Orlando, Fla.)|December 18, 2021
Resolving the polygenic aetiology of a late onset combined immune deficiency caused by NFKB1 haploinsufficiency and modified by PIK3R1 and TNFRSF13B variantsChantal E Hargreaves, Fatima Dhalla, Arzoo M Patel, et al.
The Journal of Allergy and Clinical Immunology|September 20, 2024
European Society for Immunodeficiencies guidelines for the management of patients with congenital athymiaAlexandra Y Kreins, Fatima Dhalla, Aisling M Flinn, et al.
Nature Communications|July 10, 2023
Combined multidimensional single-cell protein and RNA profiling dissects the cellular and functional heterogeneity of thymic epithelial cellsFabian Klein, Clara Veiga-Villauriz, Anastasiya Börsch, et al.
Journal of Clinical Immunology|December 16, 2014
Identification of a novel mutation in MAGT1 and progressive multifocal leucoencephalopathy in a 58-year-old man with XMEN diseaseFatima Dhalla, Sarah Murray, Ross Sadler, et al.
Elife|August 26, 2020
Ageing compromises mouse thymus function and remodels epithelial cell differentiationJeanette Baran-Gale, Michael D Morgan, Stefano Maio, et al.
Nature Communications|April 25, 2019
Sequencing of human genomes with nanopore technologyRory Bowden, Robert W Davies, Andreas Heger, et al.
Journal of Clinical Immunology|January 19, 2021
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous MutationsGiuliana Giardino, Svetlana O Sharapova, Peter Ciznar, et al.
Science Advances|December 3, 2021
FOXN1 forms higher-order nuclear condensates displaced by mutations causing immunodeficiencyIoanna A Rota, Adam E Handel, Stefano Maio, et al.
Pageof 3