Clive R. Carter

St James's University Hospital, Beckett Street, LS9 7 TF
Leeds, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 26 publications

Correction to: Inherited CD19 Deficiency Does Not Impair Plasma Cell Formation or Response to CXCL12.

Correction to: Inherited CD19 Deficiency Does Not Impair Plasma Cell Formation or Response to CXCL12.

Journal: Journal of clinical immunology

Published: May 29, 2025

Technical and biological sources of unreliability of Infinium probes on Illumina methylation microarrays.

Technical and biological sources of unreliability of Infinium probes on Illumina methylation microarrays.

Journal: Clinical epigenetics

Published: February 08, 2024

Characterization of Genetic Landscape and Novel Inflammatory Biomarkers in Patients With Adult-Onset Still's Disease.

Characterization of Genetic Landscape and Novel Inflammatory Biomarkers in Patients With Adult-Onset Still's Disease.

Journal: Arthritis & rheumatology (Hoboken, N.J.)

Published: December 10, 2023

Inherited CD19 Deficiency Does Not Impair Plasma Cell Formation or Response to CXCL12.

Inherited CD19 Deficiency Does Not Impair Plasma Cell Formation or Response to CXCL12.

Journal: Journal of clinical immunology

Published: March 28, 2022

Effectiveness of SARS-CoV-2 vaccination in patients with rheumatoid arthritis (RA) on DMARDs: as determined by antibody and T cell responses.

Effectiveness of SARS-CoV-2 vaccination in patients with rheumatoid arthritis (RA) on DMARDs: as determined by antibody and T cell responses.

Journal: RMD open

Published: October 21, 2021

Identification of a novel MAGT1 mutation supports a diagnosis of XMEN disease.

Identification of a novel MAGT1 mutation supports a diagnosis of XMEN disease.

Journal: Genes and immunity

Published: October 05, 2021

Isolated Pre-existing HLA-DP Donor-Specific Antibodies are Associated With Poorer Outcomes in Renal Transplantation.

Isolated Pre-existing HLA-DP Donor-Specific Antibodies are Associated With Poorer Outcomes in Renal Transplantation.

Journal: Kidney international reports

Published: September 27, 2021

Biallelic mutations in calcium release activated channel regulator 2A (CRACR2A) cause a primary immunodeficiency disorder.

Biallelic mutations in calcium release activated channel regulator 2A (CRACR2A) cause a primary immunodeficiency disorder.

Journal: eLife

Published: July 27, 2021

An Atypical Autoinflammatory Disease Due to an LRR Domain NLRP3 Mutation Enhancing Binding to NEK7.

An Atypical Autoinflammatory Disease Due to an LRR Domain NLRP3 Mutation Enhancing Binding to NEK7.

Journal: Journal of clinical immunology

Published: May 24, 2021

Neutralizing Anti-interferon-γ Autoantibodies: an Ameliorating Factor in COVID-19 Infection?

Neutralizing Anti-interferon-γ Autoantibodies: an Ameliorating Factor in COVID-19 Infection?

Journal: Journal of clinical immunology

Published: March 08, 2021

SARS-CoV-2 diagnostics: Towards a more comprehensive approach to routine patient testing.

SARS-CoV-2 diagnostics: Towards a more comprehensive approach to routine patient testing.

Journal: Journal of immunological methods

Published: December 04, 2020

Novel Case of Tripeptidyl Peptidase 2 Deficiency Associated with Mild Clinical Phenotype.

Novel Case of Tripeptidyl Peptidase 2 Deficiency Associated with Mild Clinical Phenotype.

Journal: Journal of clinical immunology

Published: July 15, 2020

Showing 1-12 of 26

Last Updated: 09/26/2026