(Q33801269)

29 July 2017

1 reference

title

Temperature effects on cation transport in hereditary stomatocytosis and allied disorders (English)

1 reference

hereditary stomatocytosis

29 July 2017

1 reference

S E Coles

1

1 reference

PubMed ID

10607015

29 July 2017

G W Stewart

series ordinal

2

1 reference

29 July 2017

1 October 1999

1 reference

International Journal of Experimental Pathology

29 July 2017

1 reference

29 July 2017

80

1 reference

29 July 2017

5

1 reference

29 July 2017

251-258

1 reference

Pseudohyperkalaemia associated with hereditary spherocytosis in four members of a family

29 July 2017

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Opening the gates on ion channel diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter).

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Hereditary hemolytic disease with increased red blood cell phosphatidylcholine and dehydration: one, two, or many disorders?

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Two British families with variants of the 'cryohydrocytosis' form of hereditary stomatocytosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

The permeability and the effect of acyl-chain length for phospholipid bilayers containing cholesterol: theory and experiment

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Altered erythrocyte cation permeability in familial pseudohyperkalaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Hereditary stomatocytosis: consistent association with an integral membrane protein deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Interactions between temperature and tonicity on cation transport in dog red cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Pathophysiology of abnormal cell volume in human red cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Congenital hemolytic anemia associated with dehydrated erythrocytes and increased potassium loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

On phase transitions in erythrocyte membranes and extracted membrane lipids

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

The temperature dependence of passive potassium permeability in mammalian erythrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Cloning and nucleotide sequence of cDNA encoding human erythrocyte band 7 integral membrane protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Hereditary nonspherocytic hemolytic disease associated with an altered phospholipid composition of the erythrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Missing band 7 membrane protein in two patients with high Na, low K erythrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Phase transitions in phospholipid vesicles Fluorescence polarization and permeability measurements concerning the effect of temperature and cholesterol

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Characterization of lipid domains in erythrocyte membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Distributions of proteins and lipids in the erythrocyte membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Biological membranes as bilayer couples. A molecular mechanism of drug-erythrocyte interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Functional rafts in cell membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Familial pseudohyperkalaemia. A new syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

A family with mild hereditary xerocytosis showing high membrane cation permeability at low temperatures

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

The membrane defect in hereditary stomatocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Cold-induced expression of delta 9-desaturase in carp by transcriptional and posttranslational mechanisms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Congenital hemolytic anemia with high sodium, low potassium red cells. I. Studies of membrane permeability

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

A NEW CONGENITAL HEMOLYTIC ANEMIA WITH DEFORMED ERYTHROCYTES ("STOMATOCYTES") AND REMARKABLE SUSCEPTIBILITY OF ERYTHROCYTES TO COLD HEMOLYSIS IN VITRO. I. CLINICAL AND HEMATOLOGIC STUDIES

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517829

Stomatocytosis: a hereditary red cell anomally associated with haemolytic anaemia

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517829

Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis).

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517829

The Caenorhabditis elegans behavioral gene unc-24 encodes a novel bipartite protein similar to both erythrocyte band 7.2 (stomatin) and nonspecific lipid transfer protein.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517829

Isolation of cDNA coding for an ubiquitous membrane protein deficient in high Na+, low K+ stomatocytic erythrocytes

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2517829

Increased human red cell cation passive permeability below 12 °C

30 October 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2613.1999.00120.X

Familial pseudohyperkalaemia

21 January 2018

1 reference

12 December 2020

Possible screening test for familial pseudohyperkalaemia

1 reference

12 December 2020

Temperature sensitivity of potassium flux into red blood cells in the familial pseudohyperkalaemia syndrome

1 reference

12 December 2020

The dependence on external cation of sodium and potassium fluxes across the human red cell membrane at low temperatures

1 reference

12 December 2020

Potassium transport in monkey erythrocytes

1 reference

12 December 2020

[Pseudo-hyperkalemia. Apropos of a familial case]

1 reference

12 December 2020

Conformational order of phospholipids incorporated into human erythrocytes: an FTIR spectroscopy study

1 reference

12 December 2020

Thrombo-embolic disease after splenectomy for hereditary stomatocytosis

1 reference

12 December 2020

Paradoxical temperature dependence of Na and K fluxes in human red cells

1 reference

12 December 2020

Hereditary hemolytic anemia associated with abnormal membrane lipids: mechanism of accumulation of phosphatidyl choline

1 reference

12 December 2020

Human erythrocyte band 7.2b is preferentially labeled by a photoreactive phospholipid

1 reference

12 December 2020

A genetic syndrome associating dehydrated hereditary stomatocytosis, pseudohyperkalaemia and perinatal oedema

1 reference

12 December 2020

A variant of hereditary stomatocytosis with marked pseudohyperkalaemia

1 reference

12 December 2020

10.1046/J.1365-2613.1999.00120.X

Identifiers

DOI

1 reference

29 July 2017

0 references

1 reference

PubMed ID

10607015