Ulrich Pannicke

Ulm, BW 89081, Germany

Last Updated: 09/26/2026

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Found 33 publications

Posttransplant B cell Development and Function in Patients with B cell Positive SCID Caused by Pathogenic Variants in IL2RG and JAK3.

Posttransplant B cell Development and Function in Patients with B cell Positive SCID Caused by Pathogenic Variants in IL2RG and JAK3.

Journal: Journal of clinical immunology
Published: August 08, 2025

RAG recombinase expression discriminates the development of natural killer cells.

RAG recombinase expression discriminates the development of natural killer cells.

Journal: Frontiers in immunology
Published: April 07, 2025

A noncoding mutation in the NOTCH1 gene initiates oncogenic NOTCH signaling via wild-type NICD stabilization in CLL.

A noncoding mutation in the NOTCH1 gene initiates oncogenic NOTCH signaling via wild-type NICD stabilization in CLL.

Journal: Blood
Published: January 22, 2025

AK2-Deficient Mice Recapitulate Impaired Lymphopoiesis of Reticular Dysgenesis Patients, but Also Lack Erythropoiesis.

AK2-Deficient Mice Recapitulate Impaired Lymphopoiesis of Reticular Dysgenesis Patients, but Also Lack Erythropoiesis.

Journal: European journal of immunology
Published: August 19, 2024

Non-Skewed X-inactivation Results in NF-κB Essential Modulator (NEMO) Δ-exon 5-autoinflammatory Syndrome (NEMO-NDAS) in a Female with Incontinentia Pigmenti.

Non-Skewed X-inactivation Results in NF-κB Essential Modulator (NEMO) Δ-exon 5-autoinflammatory Syndrome (NEMO-NDAS) in a Female with Incontinentia Pigmenti.

Journal: Journal of clinical immunology
Published: February 01, 2024

Chemotherapy for a secondary malignancy nearly restores complete chimerism in an SCID-patient after HSCT.

Chemotherapy for a secondary malignancy nearly restores complete chimerism in an SCID-patient after HSCT.

Journal: Clinical immunology (Orlando, Fla.)
Published: November 17, 2023

A partial human LCK defect causes a T cell immunodeficiency with intestinal inflammation.

A partial human LCK defect causes a T cell immunodeficiency with intestinal inflammation.

Journal: The Journal of experimental medicine
Published: May 29, 2023

Transcriptional reprogramming by mutated IRF4 in lymphoma.

Transcriptional reprogramming by mutated IRF4 in lymphoma.

Journal: Nature communications
Published: November 29, 2022

Compound heterozygous variants in OTULIN are associated with fulminant atypical late-onset ORAS.

Compound heterozygous variants in OTULIN are associated with fulminant atypical late-onset ORAS.

Journal: EMBO molecular medicine
Published: July 26, 2021

Biomarkers of DNA Damage Response Enable Flow Cytometry-Based Diagnostic to Identify Inborn DNA Repair Defects in Primary Immunodeficiencies.

Biomarkers of DNA Damage Response Enable Flow Cytometry-Based Diagnostic to Identify Inborn DNA Repair Defects in Primary Immunodeficiencies.

Journal: Journal of clinical immunology
Published: July 01, 2021

A Novel Non-Coding Variant in DCLRE1C Results in Deregulated Splicing and Induces SCID Through the Generation of a Truncated ARTEMIS Protein That Fails to Support V(D)J Recombination and DNA Damage Repair.

A Novel Non-Coding Variant in DCLRE1C Results in Deregulated Splicing and Induces SCID Through the Generation of a Truncated ARTEMIS Protein That Fails to Support V(D)J Recombination and DNA Damage Repair.

Journal: Frontiers in immunology
Published: March 01, 2021

Author Correction: Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells.

Author Correction: Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells.

Journal: Nature communications
Published: April 22, 2020
Showing 1-12 of 33

Last Updated: 09/26/2026