Red cell membrane disorders. (Q39266347)

10 September 2017

Red cell membrane disorders. (English)

1 reference

10 September 2017

J Narla

1

1 reference

PubMed ID

28447420

10 September 2017

N Mohandas

series ordinal

2

1 reference

10 September 2017

1 May 2017

1 reference

International Journal of Laboratory Hematology

10 September 2017

1 reference

10 September 2017

39 Suppl 1

1 reference

10 September 2017

47-52

1 reference

Quantitative assessment of sensing and sequestration of spherocytic erythrocytes by the human spleen

10 September 2017

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

The molecular basis of hereditary red cell membrane disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

New insights into erythrocyte membrane organization and microelasticity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Red cell membrane: past, present, and future

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Mechanical properties of the red cell membrane in relation to molecular structure and genetic defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Phosphatidylserine binding sites in erythroid spectrin: location and implications for membrane stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

An Unrecognized Function of Cholesterol: Regulating the Mechanism Controlling Membrane Phospholipid Asymmetry

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Identification of a functional role for lipid asymmetry in biological membranes: Phosphatidylserine-skeletal protein interactions modulate membrane stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Phosphatidylinositol-4,5-biphosphate (PIP2) differentially regulates the interaction of human erythrocyte protein 4.1 (4.1R) with membrane proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Red blood cell blood group antigens: structure and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Rh-RhAG/ankyrin-R, a new interaction site between the membrane bilayer and the red cell skeleton, is impaired by Rh(null)-associated mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Cooperative action between band 3 and glycophorin A in human erythrocytes: immobilization of band 3 induced by antibodies to glycophorin A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Conformational stabilities of the structural repeats of erythroid spectrin and their functional implications.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Forced unfolding of proteins within cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Shear-response of the spectrin dimer-tetramer equilibrium in the red blood cell membrane.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Hereditary spherocytosis--defects in proteins that connect the membrane skeleton to the lipid bilayer

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

21 January 2018

Hereditary spherocytosis

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Hereditary elliptocytosis: spectrin and protein 4.1R.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

A Congenital Haemolytic Anaemia with Thermal Sensitivity of the Erythrocyte Membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

The hereditary stomatocytoses: genetic disorders of the red cell membrane permeability to monovalent cations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

An extreme consequence of splenectomy in dehydrated hereditary stomatocytosis: gradual thrombo-embolic pulmonary hypertension and lung-heart transplantation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

Diagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometer

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12657

21 January 2018

Identifiers

DOI

10.1111/IJLH.12657

1 reference

10 September 2017

1 reference

PubMed ID

28447420