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Molecular mechanism of P1 antigen expression

Blood, 2018-04, Vol.131 (14), p.1505-1506

Bruce, Lesley J.

2018

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Reticulocyte Maturation and Variant Red Blood Cells

Frontiers in physiology, 2022-03, Vol.13, p.834463-834463

2022

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Hereditary stomatocytosis and cation leaky red cells — Recent developments

Blood cells, molecules, & diseases, 2009-05, Vol.42 (3), p.216-222

Bruce, Lesley J.

2009

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The Molecular Basis for Altered Cation Permeability in Hereditary Stomatocytic Human Red Blood Cells

Frontiers in physiology, 2018-04, Vol.9, p.367-367

2018

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Reticulocyte Maturation

Membranes (Basel), 2022-03, Vol.12 (3), p.311

2022

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The involvement of cation leaks in the storage lesion of red blood cells

Frontiers in physiology, 2014-06, Vol.5, p.214-214

2014

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Homozygous Southeast Asian ovalocytosis in five live-born neonates

Haematologica (Roma), 2021-06, Vol.106 (6), p.1758-1761

2021

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Vesiculation in irradiated and cation‐leaky‐stored red blood cells

Transfusion (Philadelphia, Pa.), 2024-01, Vol.64 (1), p.150-161

2024

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Modelling the structure of the red cell membrane

Biochemistry and cell biology, 2011-04, Vol.89 (2), p.200

2011

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The compound effect of irradiation and familial pseudohyperkalemia on potassium leak from red blood cells

Transfusion (Philadelphia, Pa.), 2022-12, Vol.62 (12), p.2587-2595

2022

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Familial pseudohyperkalemia induces significantly higher levels of extracellular potassium in early storage of red cell concentrates without affecting other standard measures of quality: A case control and allele frequency study

Transfusion (Philadelphia, Pa.), 2021-08, Vol.61 (8), p.2439-2449

2021

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Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome

Blood, 2011-11, Vol.118 (19), p.5267-5277

2011

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Expression of South East Asian Ovalocytic Band 3 Disrupts Erythroblast Cytokinesis and Reticulocyte Maturation

Frontiers in physiology, 2020-04, Vol.11, p.357

2020

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Unconventional cell death in erythroid cells

Blood, 2016-01, Vol.127 (1), p.12-14

2016

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The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein

Blood, 2009-02, Vol.113 (6), p.1350-1357

2009

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Red cell membrane proteins

HemaSphere, 2019-06, Vol.3 (Suppl), p.154-156

2019

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Red cell membrane transport abnormalities

Current opinion in hematology, 2008-05, Vol.15 (3), p.184-190

Bruce, Lesley J

2008

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Familial pseudohyperkalemia in blood donors: a novel mutation with implications for transfusion practice

Transfusion (Philadelphia, Pa.), 2014-12, Vol.54 (12), p.3043-3050

2014

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Homozygous Southeast Asian ovalocytosis is a severe dyserythropoietic anemia associated with distal renal tubular acidosis

Blood, 2014-03, Vol.123 (12), p.1963-1965

2014

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A band 3–based macrocomplex of integral and peripheral proteins in the RBC membrane

Blood, 2003-05, Vol.101 (10), p.4180-4188

2003

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An Infant with Pseudohyperkalemia, Hemolysis, and Seizures: Cation-Leaky GLUT1-Deficiency Syndrome due to a SLC2A1 Mutation

The journal of clinical endocrinology and metabolism, 2012-06, Vol.97 (6), p.E987-E993

2012

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Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1

Nature genetics, 2005-11, Vol.37 (11), p.1258-1263

2005

Volltextzugriff (PDF)

Band 3 nullVIENNA, a novel homozygous SLC4A1 p.Ser477X variant causing severe hemolytic anemia, dyserythropoiesis and complete distal renal tubular acidosis

Pediatric blood & cancer, 2017-03, Vol.64 (3), p.n/a

2017

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Band 3 null VIENNA , a novel homozygous SLC4A1 p.Ser477X variant causing severe hemolytic anemia, dyserythropoiesis and complete distal renal tubular acidosis

Pediatric blood & cancer, 2017-03, Vol.64 (3)

2017

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Distal renal tubular acidosis with hereditary spherocytosis

Indian pediatrics, 2013-07, Vol.50 (7), p.693-695

2013

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Molecular mechanism of P1 antigen expression

Reticulocyte Maturation and Variant Red Blood Cells

Hereditary stomatocytosis and cation leaky red cells — Recent developments

The Molecular Basis for Altered Cation Permeability in Hereditary Stomatocytic Human Red Blood Cells

Reticulocyte Maturation

The involvement of cation leaks in the storage lesion of red blood cells

Homozygous Southeast Asian ovalocytosis in five live-born neonates

Vesiculation in irradiated and cation‐leaky‐stored red blood cells

Modelling the structure of the red cell membrane

The compound effect of irradiation and familial pseudohyperkalemia on potassium leak from red blood cells

Familial pseudohyperkalemia induces significantly higher levels of extracellular potassium in early storage of red cell concentrates without affecting other standard measures of quality: A case control and allele frequency study

Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome

Expression of South East Asian Ovalocytic Band 3 Disrupts Erythroblast Cytokinesis and Reticulocyte Maturation

Unconventional cell death in erythroid cells

The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein

Red cell membrane proteins

Red cell membrane transport abnormalities

Familial pseudohyperkalemia in blood donors: a novel mutation with implications for transfusion practice

Homozygous Southeast Asian ovalocytosis is a severe dyserythropoietic anemia associated with distal renal tubular acidosis

A band 3–based macrocomplex of integral and peripheral proteins in the RBC membrane

An Infant with Pseudohyperkalemia, Hemolysis, and Seizures: Cation-Leaky GLUT1-Deficiency Syndrome due to a SLC2A1 Mutation

Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1

Band 3 nullVIENNA, a novel homozygous SLC4A1 p.Ser477X variant causing severe hemolytic anemia, dyserythropoiesis and complete distal renal tubular acidosis

Band 3 null VIENNA , a novel homozygous SLC4A1 p.Ser477X variant causing severe hemolytic anemia, dyserythropoiesis and complete distal renal tubular acidosis

Distal renal tubular acidosis with hereditary spherocytosis

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