Associated Papers
Accurate affinity models for SH2 domains from peptide binding assays and free-energy regression.
Gagoski D et al.
Protein Science : a Publication of the Protein Society, 2025
Accurate sequence-to-affinity models for SH2 domains from multi-round peptide binding assays coupled with free-energy regression.
Gagoski D et al.
Biorxiv : the Preprint Server for Biology, 2025
Inherited CARD9 Deficiency Due to a Founder Effect in East Asia.
Tomomasa D et al.
Journal of Clinical Immunology, 2024
Concurrent infection of Exophiala dermatitidis and Angiostrongylus cantonensis in central nervous system of a child with inherited CARD9 deficiency: A case report and literature review.
Ma N et al.
Journal De Mycologie Medicale, 2024
A nucleation barrier spring-loads the CBM signalosome for binary activation.
Rodriguez Gama A et al.
Elife, 2022
The role and mechanism of CARD9 gene polymorphism in diseases.
Ji C et al.
Biomedical Journal, 2021
Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings.
Imanaka Y et al.
Journal of Clinical Immunology, 2021
The role of mycobiota-genotype association in inflammatory bowel diseases: a narrative review.
Mahmoudi E et al.
Gut Pathogens, 2021
The Role of CARD9 Deficiency in Neutrophils.
Sheng R et al.
Mediators of Inflammation, 2021
CARD9 Deficiency in a Chinese Man with Cutaneous Mucormycosis, Recurrent Deep Dermatophytosis and a Review of the Literature.
Wang X et al.
Mycopathologia, 2020
The Phytopathogenic Fungus Pallidocercospora crystallina-Caused Localized Subcutaneous Phaeohyphomycosis in a Patient with a Homozygous Missense CARD9 Mutation.
Guo Y et al.
Journal of Clinical Immunology, 2019
Recurrent fungal infections in a Chinese patient with CARD9 deficiency and a review of 48 cases.
Quan C et al.
The British Journal of Dermatology, 2019
Cerebral Phaeohyphomycosis Caused by Exophiala dermatitidis in a Chinese CARD9-Deficient Patient: A Case Report and Literature Review.
Wang C et al.
Frontiers in Neurology, 2019
Inherited CARD9 Deficiency: Invasive Disease Caused by Ascomycete Fungi in Previously Healthy Children and Adults.
Corvilain E et al.
Journal of Clinical Immunology, 2018
Prototheca zopfii Colitis in Inherited CARD9 Deficiency.
Sari S et al.
The Journal of Infectious Diseases, 2018
Molecular and physiological roles of the adaptor protein CARD9 in immunity.
Zhong X et al.
Cell Death & Disease, 2018
Novel bi-allelic splice mutations in CARD9 causing adult-onset Candida endophthalmitis.
Gavino C et al.
Mycoses, 2018
Frequency and Geographic Distribution of CARD9 Mutations in Patients With Severe Fungal Infections.
Vaezi A et al.
Frontiers in Microbiology, 2018
Impaired RASGRF1/ERK-mediated GM-CSF response characterizes CARD9 deficiency in French-Canadians.
Gavino C et al.
The Journal of Allergy and Clinical Immunology, 2016
CARD9 mutation linked to Corynespora cassiicola infection in a Chinese patient.
Yan XX et al.
The British Journal of Dermatology, 2016
Genetic errors of the human caspase recruitment domain-B-cell lymphoma 10-mucosa-associated lymphoid tissue lymphoma-translocation gene 1 (CBM) complex: Molecular, immunologic, and clinical heterogeneity.
Pérez de Diego R et al.
The Journal of Allergy and Clinical Immunology, 2015
Inherited CARD9 deficiency in otherwise healthy children and adults with Candida species-induced meningoencephalitis, colitis, or both.
Lanternier F et al.
The Journal of Allergy and Clinical Immunology, 2015
Inherited CARD9 deficiency in 2 unrelated patients with invasive Exophiala infection.
Lanternier F et al.
The Journal of Infectious Diseases, 2015
CARD9 deficiency and spontaneous central nervous system candidiasis: complete clinical remission with GM-CSF therapy.
Gavino C et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America, 2014
Deep dermatophytosis and inherited CARD9 deficiency.
Lanternier F et al.
The New England Journal of Medicine, 2013
Invasive fungal infection and impaired neutrophil killing in human CARD9 deficiency.
Drewniak A et al.
Blood, 2013