Effects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell trait (Q24629836)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1752955%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

title

Effects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell trait (English)

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17 September 2019

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7

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17 September 2019

author name string

Gupta AK

1

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17 September 2019

Kirchner KA

2

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17 September 2019

Nicholson R

3

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17 September 2019

Adams JG 3rd

4

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17 September 2019

Schechter AN

5

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17 September 2019

Noguchi CT

6

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17 September 2019

language of work or name

English

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publication date

1 December 1991

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Journal of Clinical Investigation

17 September 2019

published in

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17 September 2019

volume

88

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17 September 2019

issue

6

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17 September 2019

page(s)

1963-1968

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Detection of specific sequences among DNA fragments separated by gel electrophoresis

17 September 2019

cites work

1 reference

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A general method for isolation of high molecular weight DNA from eukaryotes

7 April 2017

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Sickling phenomenon produced by hypertonic solutions: a possible explanation for the hyposthenuria of sicklemia

7 April 2017

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Two different molecular organizations account for the single alpha-globin gene of the alpha-thalassemia-2 genotype

27 September 2017

1 reference

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The intracellular polymerization of sickle hemoglobin and its relevance to sickle cell disease

27 September 2017

1 reference

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Molecular and cellular pathogenesis of hemoglobin SC disease

27 September 2017

1 reference

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Determination of deoxyhemoglobin S polymer in sickle erythrocytes upon deoxygenation

27 September 2017

1 reference

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Intracellular polymerization of sickle hemoglobin. Effects of cell heterogeneity

27 September 2017

1 reference

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Polymerization in erythrocytes containing S and non-S hemoglobins

27 September 2017

1 reference

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Concurrent sickle cell anemia and alpha-thalassemia. Effect on pathological properties of sickle erythrocytes

27 September 2017

1 reference

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Renal ischemia: a new perspective

27 September 2017

1 reference

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Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions

27 September 2017

1 reference

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Molecular basis for nondeletion alpha-thalassemia in American blacks. Alpha 2(116GAG----UAG).

27 September 2017

1 reference

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Subunit assembly of hemoglobin: an important determinant of hematologic phenotype

27 September 2017

1 reference

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Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin gene.

27 September 2017

1 reference

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Polymerization of sickle cell hemoglobin at arterial oxygen saturation impairs erythrocyte deformability

27 September 2017

1 reference

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Hemoglobin S gelation and sickle cell disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295777

Sickle cell trait revisited

27 September 2017

1 reference

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Beyond hemoglobin polymerization: the red blood cell membrane and sickle disease pathophysiology

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295777

Negro alpha-thalassaemia is caused by deletion of a single alpha-globin gene

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295777

Impaired Renal Tubular Potassium Secretion in Sickle Cell Disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295777

Determinants of red cell sickling. Effects of varying pH and of increasing intracellular hemoglobin concentration by osmotic shrinkage

27 September 2017

1 reference

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Renal acidification in sickle cell trait

27 September 2017

1 reference

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Prevalence and molecular heterogeneity of alfa+ thalassemia in two tribal populations from Andhra Pradesh, India

27 September 2017

1 reference

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The urinary concentrating mechanism

30 May 2018

1 reference

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Trimodality in the percentages of beta chain variants in heterozygotes: the effect of the number of active Hbalpha structural loci

30 May 2018

1 reference

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alpha-Globin gene organisation in blacks precludes the severe form of alpha-thalassaemia

30 May 2018

1 reference

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Clinical Implications of Sickle-Cell Trait and Glucose-6-Phosphate Dehydrogenase Deficiency in Hospitalized Black Male Patients

30 May 2018

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Some statistical methods useful in circulation research.

30 May 2018

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Effect of polymerization tendency on haematological, rheological and clinical parameters in sickle cell anaemia

28 November 2018

1 reference

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A New Sickling Disorder Resulting from Interaction of the Genes for Haemoglobin S and α-Thalassaemia

28 November 2018

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12 December 2020

A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait

1 reference

12 December 2020

Dense cells in sickle cell anemia: the effects of gene interaction

1 reference

12 December 2020

Influence of HbS levels upon the hematological and clinical characteristics of sickle cell trait

1 reference

12 December 2020

Regulation of erythrocyte cation and water content in sickle cell anemia

1 reference

12 December 2020

A new high-performance liquid chromatographic procedure for the separation and quantitation of various hemoglobin variants in adults and newborn babies

1 reference

12 December 2020

Electrostatic interactions in the assembly of haemoglobin

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12 December 2020

Polymerization of hemoglobin in sickle trait erythrocytes and lysates

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12 December 2020

Nature of concentrating defect in sickle-cell nephropathy. Microradioangiographic studies

1 reference

12 December 2020

Genetic Determination of Phenotypic Variation in Sickle Cell Trait

1 reference

12 December 2020

Alpha Thalassaemia in Adults with Sickle-Cell Trait

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12 December 2020

Studies on acid excretion in adults with sickle-cell anaemia

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12 December 2020

Identifiers

DOI

10.1172/JCI115521

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1752955%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1752955%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

PubMed publication ID

1752955

2 references