Britt-sabina S. Petersen

Kiel, SH 24105, Germany

Last Updated: 09/26/2026

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Found 43 publications

Author Correction: CEACAM1 regulates TIM-3-mediated tolerance and exhaustion.

Author Correction: CEACAM1 regulates TIM-3-mediated tolerance and exhaustion.

Journal: Nature

Published: February 09, 2024

Deficiency in X-linked inhibitor of apoptosis protein promotes susceptibility to microbial triggers of intestinal inflammation.

Deficiency in X-linked inhibitor of apoptosis protein promotes susceptibility to microbial triggers of intestinal inflammation.

Journal: Science immunology

Published: November 05, 2021

Monocytes as Potential Mediators of Pathogen-Induced T-Helper 17 Differentiation in Patients With Primary Sclerosing Cholangitis (PSC).

Monocytes as Potential Mediators of Pathogen-Induced T-Helper 17 Differentiation in Patients With Primary Sclerosing Cholangitis (PSC).

Journal: Hepatology (Baltimore, Md.)

Published: June 24, 2019

Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

Journal: PLoS genetics

Published: May 31, 2019

First known case of paediatric inflammatory bowel disease in a western lowland gorilla may be linked to a familial mutation in the MEFV gene.

First known case of paediatric inflammatory bowel disease in a western lowland gorilla may be linked to a familial mutation in the MEFV gene.

Journal: Gut

Published: May 08, 2019

Identifying Crohn's disease signal from variome analysis.

Identifying Crohn's disease signal from variome analysis.

Journal: Genome medicine

Published: February 18, 2019

Compound heterozygous mutations in IL10RA combined with a complement factor properdin mutation in infantile-onset inflammatory bowel disease.

Compound heterozygous mutations in IL10RA combined with a complement factor properdin mutation in infantile-onset inflammatory bowel disease.

Journal: European journal of gastroenterology & hepatology

Published: September 11, 2018

IL-17A is functionally relevant and a potential therapeutic target in bullous pemphigoid.

IL-17A is functionally relevant and a potential therapeutic target in bullous pemphigoid.

Journal: Journal of autoimmunity

Published: July 23, 2018

Whole-exome sequencing identifies rare genetic variations in German families with pulmonary sarcoidosis.

Whole-exome sequencing identifies rare genetic variations in German families with pulmonary sarcoidosis.

Journal: Human genetics

Published: March 29, 2018

IKZF1plus Defines a New Minimal Residual Disease-Dependent Very-Poor Prognostic Profile in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia.

IKZF1plus Defines a New Minimal Residual Disease-Dependent Very-Poor Prognostic Profile in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia.

Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology

Published: March 03, 2018

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

Journal: PLoS genetics

Published: November 09, 2017

Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2.

Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2.

Journal: Cold Spring Harbor molecular case studies

Published: November 08, 2017

Showing 1-12 of 43

Last Updated: 09/26/2026