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Alexandre Bolze

Showing results (21-30 of 56) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|December 23, 2024
Dominant negative <i>ADA2</i> mutations cause ADA2 deficiency in heterozygous carriersMarjon Wouters, Lisa Ehlers, Wout Van Eynde, et al.
The Journal of Experimental Medicine|January 9, 2026
Correction: Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriersMarjon Wouters, Lisa Ehlers, Wout Van Eynde, et al.
American Journal of Human Genetics|November 27, 2010
Whole-exome-sequencing-based discovery of human FADD deficiencyAlexandre Bolze, Minji Byun, David McDonald, et al.
The Journal of Experimental Medicine|August 27, 2025
Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriersMarjon Wouters, Lisa Ehlers, Wout Van Eynde, et al.
Developmental Cell|May 8, 2012
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 moduleMatthew Koss, Alexandre Bolze, Andrea Brendolan, et al.
The Journal of Experimental Medicine|April 29, 2015
Inherited IL-17RC deficiency in patients with chronic mucocutaneous candidiasisYun Ling, Sophie Cypowyj, Caner Aytekin, et al.
The Journal of Pediatrics|September 18, 2010
Isolated congenital asplenia: a French nationwide retrospective survey of 20 casesNizar Mahlaoui, Veronique Minard-Colin, Capucine Picard, et al.
Journal of Clinical Immunology|October 7, 2022
Decoding the Human Genetic and Immunological Basis of COVID-19 mRNA Vaccine-Induced MyocarditisAlexandre Bolze, Trine H Mogensen, Shen-Ying Zhang, et al.
Genetics in Medicine Open|December 13, 2024
Combining rare and common genetic variants improves population risk stratification for breast cancerAlexandre Bolze, Daniel Kiser, Kelly M Schiabor Barrett, et al.
Journal of Human Immunity|December 5, 2025
The seven enigmas of SARS-CoV-2: from the past to the futureEvangelos Andreakos, Lisa Arkin, Paul Bastard, et al.
Pageof 6

Showing results (21-30 of 56) with videos related to

Sort By:
Pageof 6
Medrxiv : the Preprint Server for Health Sciences|December 23, 2024
Dominant negative <i>ADA2</i> mutations cause ADA2 deficiency in heterozygous carriersMarjon Wouters, Lisa Ehlers, Wout Van Eynde, et al.
The Journal of Experimental Medicine|January 9, 2026
Correction: Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriersMarjon Wouters, Lisa Ehlers, Wout Van Eynde, et al.
American Journal of Human Genetics|November 27, 2010
Whole-exome-sequencing-based discovery of human FADD deficiencyAlexandre Bolze, Minji Byun, David McDonald, et al.
The Journal of Experimental Medicine|August 27, 2025
Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriersMarjon Wouters, Lisa Ehlers, Wout Van Eynde, et al.
Developmental Cell|May 8, 2012
Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 moduleMatthew Koss, Alexandre Bolze, Andrea Brendolan, et al.
The Journal of Experimental Medicine|April 29, 2015
Inherited IL-17RC deficiency in patients with chronic mucocutaneous candidiasisYun Ling, Sophie Cypowyj, Caner Aytekin, et al.
The Journal of Pediatrics|September 18, 2010
Isolated congenital asplenia: a French nationwide retrospective survey of 20 casesNizar Mahlaoui, Veronique Minard-Colin, Capucine Picard, et al.
Journal of Clinical Immunology|October 7, 2022
Decoding the Human Genetic and Immunological Basis of COVID-19 mRNA Vaccine-Induced MyocarditisAlexandre Bolze, Trine H Mogensen, Shen-Ying Zhang, et al.
Genetics in Medicine Open|December 13, 2024
Combining rare and common genetic variants improves population risk stratification for breast cancerAlexandre Bolze, Daniel Kiser, Kelly M Schiabor Barrett, et al.
Journal of Human Immunity|December 5, 2025
The seven enigmas of SARS-CoV-2: from the past to the futureEvangelos Andreakos, Lisa Arkin, Paul Bastard, et al.
Pageof 6