NOD2/CARD15 single nucleotide polymorphism 13 (3020insC) is associated with risk of sepsis and single nucleotide polymorphism 8 (2104C>T) with herpes viruses reactivation in patients after allogeneic hematopoietic stem cell transplantation.

doi:10.1016/j.bbmt.2013.12.558

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Article

NOD2/CARD15 single nucleotide polymorphism 13 (3020insC) is associated with risk of sepsis and single nucleotide polymorphism 8 (2104C>T) with herpes viruses reactivation in patients after allogeneic hematopoietic stem cell transplantation.

Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation - 1 Mar 2014

Jaskula Emilia, Lange Andrzej, Kyrcz-Krzemien Slawomira, Markiewicz Miroslaw, Dzierzak-Mietla Monika, Jedrzejczak Wieslaw Wiktor, Czajka Przemyslaw, Mordak-Domagala Monika, Lange Janusz, Gronkowska Anna, Nowak Jacek, Warzocha Krzysztof, Hellmann Andrzej, Kowalczyk Jerzy, Drabko Katarzyna, Gozdzik Jolanta, Mizia Sylwia

Abstract excerpt

Three NOD2 polymorphisms (single nucleotide polymorphism [SNP]8 [2104C>T, Arg702Trp], SNP12 [2722G>C, Gly908Arg], and SNP13 [3020insC, Leu1007 fsins C]), identified as disease-associated variants in Crohn's disease, have recently been suggested as gene markers of the outcome of hematopoietic stem...

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PMID: 24345423
DOI: 10.1016/j.bbmt.2013.12.558

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NOD2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24345423-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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