Mattias Moller

Lund, M, Sweden

Last Updated: 09/26/2026

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Found 9 publications

Hypoaldosteronism due to a novel SEC61A1 variant successfully treated with fludrocortisone.

Hypoaldosteronism due to a novel SEC61A1 variant successfully treated with fludrocortisone.

Journal: Clinical kidney journal

Published: March 19, 2024

Elucidation of the low-expressing erythroid CR1 phenotype by bioinformatic mining of the GATA1-driven blood-group regulome.

Elucidation of the low-expressing erythroid CR1 phenotype by bioinformatic mining of the GATA1-driven blood-group regulome.

Journal: Nature communications

Published: November 21, 2022

Missense mutations in the C-terminal portion of the B4GALNT2-encoded glycosyltransferase underlying the Sd(a-) phenotype.

Missense mutations in the C-terminal portion of the B4GALNT2-encoded glycosyltransferase underlying the Sd(a-) phenotype.

Journal: Biochemistry and biophysics reports

Published: May 20, 2019

Disruption of the tumour-associated EMP3 enhances erythroid proliferation and causes the MAM-negative phenotype.

Disruption of the tumour-associated EMP3 enhances erythroid proliferation and causes the MAM-negative phenotype.

Journal: Nature communications

Published: December 11, 2018

Disruption of a GATA1-binding motif upstream of XG/PBDX abolishes Xga expression and resolves the Xg blood group system.

Disruption of a GATA1-binding motif upstream of XG/PBDX abolishes Xga expression and resolves the Xg blood group system.

Journal: Blood

Published: March 30, 2018

Identification of human glycosyltransferase genes expressed in erythroid cells predicts potential carbohydrate blood group loci.

Identification of human glycosyltransferase genes expressed in erythroid cells predicts potential carbohydrate blood group loci.

Journal: Scientific reports

Published: November 23, 2017

GBGT1 is allelically diverse but dispensable in humans and naturally occurring anti-FORS1 shows an ABO-restricted pattern.

GBGT1 is allelically diverse but dispensable in humans and naturally occurring anti-FORS1 shows an ABO-restricted pattern.

Journal: Transfusion

Published: August 31, 2017

Allele-selective RUNX1 binding regulates P1 blood group status by transcriptional control of A4GALT.

Allele-selective RUNX1 binding regulates P1 blood group status by transcriptional control of A4GALT.

Journal: Blood

Published: August 23, 2017

Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project.

Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project.

Journal: Blood advances

Published: October 05, 2016

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Last Updated: 09/26/2026