List of works - Lesley J Bruce

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

scientific article published on 16 January 2003

A novel insertion mutation (1286insC) in exon 9 of the factor XIII-A subunit gene.

scientific article

A red cell band 3 variant with altered stilbene disulphonate binding is associated with the Diego (Dia) blood group antigen

scientific article published on December 1992

Absence of CD47 in protein 4.2-deficient hereditary spherocytosis in man: an interaction between the Rh complex and the band 3 complex

scientific article published on 01 September 2002

Altered band 3 structure and function in glycophorin A- and B-deficient (MkMk) red blood cells

scientific article published on 01 August 1994

Altered structure and anion transport properties of band 3 (AE1, SLC4A1) in human red cells lacking glycophorin A

scientific article published on 05 November 2003

An infant with pseudohyperkalemia, hemolysis, and seizures: cation-leaky GLUT1-deficiency syndrome due to a SLC2A1 mutation.

scientific article published on 6 April 2012

Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin A.

scientific article published on 03 January 2008

Band 3 HT, a human red-cell variant associated with acanthocytosis and increased anion transport, carries the mutation Pro-868-->Leu in the membrane domain of band 3.

scientific article

Band 3 Memphis variant II. Altered stilbene disulfonate binding and the Diego (Dia) blood group antigen are associated with the human erythrocyte band 3 mutation Pro854-->Leu

scientific journal article

Band 3 Walton, a C-terminal deletion associated with distal renal tubular acidosis, is expressed in the red cell membrane but retained internally in kidney cells.

scientific article

Band 3 mutations, renal tubular acidosis and South-East Asian ovalocytosis in Malaysia and Papua New Guinea: loss of up to 95% band 3 transport in red cells

scientific article

Changes in the blood group Wright antigens are associated with a mutation at amino acid 658 in human erythrocyte band 3: a site of interaction between band 3 and glycophorin A under certain conditions

scientific article published on 01 January 1995

Distal renal tubular acidosis in Filipino children, caused by mutations of the anion-exchanger SLC4A1 (AE1, Band 3) gene

scientific article published on 08 January 2010

Distal renal tubular acidosis with hereditary spherocytosis

scientific article published in July 2013

Erythroid band 3 variants and disease

scientific article published on 01 December 1999

Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene

scientific article

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

scientific article published on 19 June 2014

Glycophorin A mutation Ala65 --> Pro gives rise to a novel pair of MNS alleles ENEP (MNS39) and HAG (MNS41) and altered Wrb expression: direct evidence for GPA/band 3 interaction necessary for normal Wrb expression

scientific article published on 01 June 1999

Hereditary stomatocytosis and cation-leaky red cells--recent developments.

scientific article published on 03 March 2009

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

scientific article published on 01 March 2014

Investigating the key membrane protein changes during in vitro erythropoiesis of protein 4.2 (-) cells (mutations Chartres 1 and 2).

scientific article

Melanesian hereditary ovalocytes have a deletion in red cell band 3

scientific article published on 01 November 1991

Modelling the structure of the red cell membrane

scientific article

Molecular basis and functional consequences of the dominant effects of the mutant band 3 on the structure of normal band 3 in Southeast Asian ovalocytosis

scientific article published in March 2002

Molecular mechanism of P1 antigen expression

scientific article published on 01 April 2018

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

scientific article

Mutations in band 3 and cation leaky red cells.

scientific article

Recessive distal renal tubular acidosis in Sarawak caused by AE1 mutations

scientific article published on 27 October 2005

Review. Leaky Cl--HCO3- exchangers: cation fluxes via modified AE1.

scientific article published on January 2009

South-east Asian ovalocytosis and the cryohydrocytosis form of hereditary stomatocytosis show virtually indistinguishable cation permeability defects.

scientific article published on 23 January 2011

South-east asian ovalocytic (SAO) erythrocytes have a cold sensitive cation leak: implications for in vitro studies on stored SAO red cells.

scientific article

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

scientific journal article

Structure-function relationships of band 3 variants.

scientific article published on November 1996

Study of the D-- phenotype reveals erythrocyte membrane alterations in the absence of RHCE.

scientific article

The defective red cell anion transporter (band 3) in hereditary South East Asian ovalocytosis and the role of glycophorin A in the expression of band 3 anion transport activity in Xenopus oocytes

scientific article published in August 1992

The hereditary stomatocytoses

scientific article published on August 2009

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

scientific article

The low-incidence blood group antigen, Wda, is associated with the substitution Val557-->Met in human erythrocyte band 3 (AE1)

scientific article published on 01 January 1996

The mutant erythrocyte band 3 protein in Southeast Asian ovalocytosis does not bind eosin-5-maleimide

scientific article published in February 2009

Tropical distal renal tubular acidosis: clinical and epidemiological studies in 78 patients.

scientific article published on September 2012

Unconventional cell death in erythroid cells.

scientific article published in January 2016

alpha-Hemoglobin stabilizing protein is not a suitable marker for a screening test for variant Creutzfeldt-Jakob disease.

scientific article published on 22 May 2008

List of works by Lesley J Bruce

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

A novel insertion mutation (1286insC) in exon 9 of the factor XIII-A subunit gene.

A red cell band 3 variant with altered stilbene disulphonate binding is associated with the Diego (Dia) blood group antigen

Absence of CD47 in protein 4.2-deficient hereditary spherocytosis in man: an interaction between the Rh complex and the band 3 complex

Altered band 3 structure and function in glycophorin A- and B-deficient (MkMk) red blood cells

Altered structure and anion transport properties of band 3 (AE1, SLC4A1) in human red cells lacking glycophorin A

An infant with pseudohyperkalemia, hemolysis, and seizures: cation-leaky GLUT1-deficiency syndrome due to a SLC2A1 mutation.

Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin A.

Band 3 HT, a human red-cell variant associated with acanthocytosis and increased anion transport, carries the mutation Pro-868-->Leu in the membrane domain of band 3.

Band 3 Memphis variant II. Altered stilbene disulfonate binding and the Diego (Dia) blood group antigen are associated with the human erythrocyte band 3 mutation Pro854-->Leu

Band 3 Walton, a C-terminal deletion associated with distal renal tubular acidosis, is expressed in the red cell membrane but retained internally in kidney cells.

Band 3 mutations, renal tubular acidosis and South-East Asian ovalocytosis in Malaysia and Papua New Guinea: loss of up to 95% band 3 transport in red cells

Changes in the blood group Wright antigens are associated with a mutation at amino acid 658 in human erythrocyte band 3: a site of interaction between band 3 and glycophorin A under certain conditions

Distal renal tubular acidosis in Filipino children, caused by mutations of the anion-exchanger SLC4A1 (AE1, Band 3) gene

Distal renal tubular acidosis with hereditary spherocytosis

Erythroid band 3 variants and disease

Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene

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

Glycophorin A mutation Ala65 --> Pro gives rise to a novel pair of MNS alleles ENEP (MNS39) and HAG (MNS41) and altered Wrb expression: direct evidence for GPA/band 3 interaction necessary for normal Wrb expression

Hereditary stomatocytosis and cation-leaky red cells--recent developments.

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

Investigating the key membrane protein changes during in vitro erythropoiesis of protein 4.2 (-) cells (mutations Chartres 1 and 2).

Melanesian hereditary ovalocytes have a deletion in red cell band 3

Modelling the structure of the red cell membrane

Molecular basis and functional consequences of the dominant effects of the mutant band 3 on the structure of normal band 3 in Southeast Asian ovalocytosis

Molecular mechanism of P1 antigen expression

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

Mutations in band 3 and cation leaky red cells.

Recessive distal renal tubular acidosis in Sarawak caused by AE1 mutations

Review. Leaky Cl--HCO3- exchangers: cation fluxes via modified AE1.

South-east Asian ovalocytosis and the cryohydrocytosis form of hereditary stomatocytosis show virtually indistinguishable cation permeability defects.

South-east asian ovalocytic (SAO) erythrocytes have a cold sensitive cation leak: implications for in vitro studies on stored SAO red cells.

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

Structure-function relationships of band 3 variants.

Study of the D-- phenotype reveals erythrocyte membrane alterations in the absence of RHCE.

The defective red cell anion transporter (band 3) in hereditary South East Asian ovalocytosis and the role of glycophorin A in the expression of band 3 anion transport activity in Xenopus oocytes

The hereditary stomatocytoses

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

The low-incidence blood group antigen, Wda, is associated with the substitution Val557-->Met in human erythrocyte band 3 (AE1)

The mutant erythrocyte band 3 protein in Southeast Asian ovalocytosis does not bind eosin-5-maleimide

Tropical distal renal tubular acidosis: clinical and epidemiological studies in 78 patients.

Unconventional cell death in erythroid cells.

alpha-Hemoglobin stabilizing protein is not a suitable marker for a screening test for variant Creutzfeldt-Jakob disease.