Dzamila M. Boguslawska
Prof. Szafrana St. 1
Zielona Gora, LB 65516, Poland
Zielona Gora, LB 65516, Poland
Last Updated: 09/26/2026
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Found 17 publications
Two Variants of the ANK1 Gene Associated with Hereditary Spherocytosis.
Journal: Biomedicines
Published: December 31, 2024
Novel Variant of the SLC4A1 Gene Associated with Hereditary Spherocytosis.
Journal: Biomedicines
Published: February 02, 2023
Spherocytosis-Related L1340P Mutation in Ankyrin Affects Its Interactions with Spectrin.
Journal: Life (Basel, Switzerland)
Published: October 19, 2022
A rare mutation (p.F149del) of the NT5C3A gene is associated with pyrimidine 5'-nucleotidase deficiency.
Journal: Cellular & molecular biology letters
Published: September 28, 2022
Identification of a Novel Mutation of β-Spectrin in Hereditary Spherocytosis Using Whole Exome Sequencing.
Journal: International journal of molecular sciences
Published: September 03, 2021
Role of Extrinsic Apoptotic Signaling Pathway during Definitive Erythropoiesis in Normal Patients and in Patients with β-Thalassemia.
Journal: International journal of molecular sciences
Published: April 11, 2020
The role of spectrin in cell adhesion and cell-cell contact.
Journal: Experimental biology and medicine (Maywood, N.J.)
Published: June 23, 2019
Efficient method for isolation of reticulocyte RNA from healthy individuals and hemolytic anaemia patients.
Journal: Journal of cellular and molecular medicine
Published: March 29, 2018
Palmitoylation of MPP1 (membrane-palmitoylated protein 1)/p55 is crucial for lateral membrane organization in erythroid cells.
Journal: The Journal of biological chemistry
Published: February 25, 2018
A new frameshift mutation of the β-spectrin gene associated with hereditary spherocytosis.
Journal: Annals of hematology
Published: June 17, 2016
A novel L1340P mutation in the ANK1 gene is associated with hereditary spherocytosis?
Journal: British journal of haematology
Published: June 07, 2014
Last Updated: 09/26/2026