Is a rare CXCL8 gene variant a new possible cause or course factor of inflammatory bowel disease?
This suggest that the <i>CXCL8</i> c.91T allele may influence IBD manifestation and the course of the disorders in Polish patients, potentially serving as a novel target for future studies and therapeutic approaches.
Authors
- Marcin Gabryel (ORCID: https://orcid.org/0000-0002-6701-0460)
- Marzena Skrzypczak-Zielińska (ORCID: https://orcid.org/0000-0001-5313-107X)
- Magdalena Hryhorowicz (ORCID: https://orcid.org/0000-0002-1496-1502)
- Agnieszka Dobrowolska (ORCID: https://orcid.org/0000-0002-3647-5070)
- Alina Baturo
- Joanna Suszyńska-Zajczyk (ORCID: https://orcid.org/0000-0002-7560-9350)
- Oliwia Zakerska‐Banaszak (ORCID: https://orcid.org/0000-0002-2223-3767)
- Karolina Ladziak
- Katarzyna Anna Hubert
Institutions
- Poznan University of Medical Sciences (PL)
- Institute of Human Genetics (PL)
- University of Life Sciences in Poznań (PL)
- Polish Academy of Sciences (PL)
Publication Details
- Journal
- Frontiers in Immunology
- Published
- 2025-03-19
- DOI
- https://doi.org/10.3389/fimmu.2025.1562618
- Citations
- 1
- Primary Topic
- Inflammatory Bowel Disease
- Type
- article
- Field-Weighted Citation Impact
- 1.82