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Human C3 deficiency associated with impairments in dendritic cell differentiation, memory B cells, and regulatory T cells.

Arije Ghannam , Martine Pernollet , Jean-Luc Fauquert , Nicole Monnier , Denise Ponard , et al.
Journal of Immunology, 2008, 181 (7), pp.5158-66
Journal articles inserm-00381929v1
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SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypes

Denise Ponard , Christine Gaboriaud , Delphine Charignon , Arije Ghannam , Ineke Wagenaar-Bos , et al.
Human Mutation, 2020, 41 (1), pp.38-57. ⟨10.1002/humu.23917⟩
Journal articles hal-02429966v1
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Characterisation of a new C1 inhibitor mutant in a patient with hepatocellular carcinoma.

Nicole Monnier , Denise Ponard , Christiane Duponchel , Françoise Csopaki , Laurence Bouillet , et al.
Molecular Immunology, 2006, 43 (14), pp.2161-8. ⟨10.1016/j.molimm.2006.01.006⟩
Journal articles inserm-00383902v1
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Mutational spectrum and phenotypes in Danish families with hereditary angioedema because of C1 inhibitor deficiency.

Anette Bygum , Christina R. Fagerberg , D. Ponard , Nicole Monnier , Joel Lunardi , et al.
Allergy, 2011, 66 (1), pp.76-84. ⟨10.1111/j.1398-9995.2010.02456.x⟩
Journal articles inserm-00567441v1

Human C3 deficiency associated with impairments in dendritic cell differentiation, memory B cells, and regulatory T cells.

Arije Ghannam , Martine Pernollet , Jean-Luc Fauquert , Nicole Monnier , Denise Ponard , et al.
Journal of Immunology, 2008, 181 (7), pp.5158-66
Journal articles inserm-00325814v1