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Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis)

American journal of hematology, 2015-10, Vol.90 (10), p.921-926

2015

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The erythroid K-Cl cotransport inhibitor [(dihydroindenyl)oxy]acetic acid blocks erythroid Ca2+-activated K+ channel KCNN4

American Journal of Physiology: Cell Physiology, 2022-09, Vol.323 (3), p.C694-C705

2022

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Purinergic signaling is essential for full Psickle activation by hypoxia and by normoxic acid pH in mature human sickle red cells and in vitro-differentiated cultured human sickle reticulocytes

Pflügers Archiv, 2022-05, Vol.474 (5), p.553-565

2022

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Erythroid‐specific inactivation of Slc12a6/Kcc3 by EpoR promoter‐driven Cre expression reduces K‐Cl cotransport activity in mouse erythrocytes

Physiological reports, 2022-03, Vol.10 (5), p.e15186-n/a

2022

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Development of a Commercial Reference Laboratory Elective Rotation for Residents in Clinical Pathology

American journal of clinical pathology, 2018-10, Vol.150 (6), p.485-490

2018

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A Grammastola spatulata mechanotoxin-4 (GsMTx4)-sensitive cation channel mediates increased cation permeability in human hereditary spherocytosis of multiple genetic etiologies

Haematologica (Roma), 2021-10, Vol.106 (10), p.2759-2762

2021

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Activation of 2‐oxoglutarate receptor 1 (OXGR1) by α‐ketoglutarate (αKG) does not detectably stimulate Pendrin‐mediated anion exchange in Xenopus oocytes

Physiological reports, 2022-07, Vol.10 (14), p.e15362-n/a

2022

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An Intact Dissecting Baker’s Cyst Mimicking Recurrent Deep Vein Thrombosis

JIM - high impact case reports, 2016-04, Vol.4 (2), p.2324709616650703-2324709616650703

2016

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Dysregulated Erythroid Mg2+ Efflux in Type 2 Diabetes

Frontiers in cell and developmental biology, 2022-04, Vol.10, p.861644-861644

2022

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Evaluation of an automated digital imaging system, Nextslide Digital Review Network, for examination of peripheral blood smears

Archives of pathology & laboratory medicine (1976), 2012-06, Vol.136 (6), p.660-667

2012

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Increased Red Cell KCNN4 Activity in Sporadic Hereditary Xerocytosis Associated With Enhanced Single Channel Pressure Sensitivity of PIEZO1 Mutant V598M

HemaSphere, 2018-10, Vol.2 (5), p.e55-n/a

2018

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Magnesium homeostasis in deoxygenated sickle erythrocytes is modulated by endothelin‐1 via Na+/Mg2+ exchange

The FASEB journal, 2022-12, Vol.36 (12), p.e22638-n/a

2022

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Blockade of the mineralocorticoid receptor improves markers of human endothelial cell dysfunction and hematological indices in a mouse model of sickle cell disease

The FASEB journal, 2023-08, Vol.37 (8), p.e23092-n/a

2023

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Magnesium homeostasis in deoxygenated sickle erythrocytes is modulated by endothelin-1 via Na + /Mg 2+ exchange

The FASEB journal, 2022-12, Vol.36 (12), p.e22638

2022

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Erythrocyte ion content and dehydration modulate maximal Gardos channel activity in KCNN4 V282M/+ hereditary xerocytosis red cells

American Journal of Physiology: Cell Physiology, 2019-08, Vol.317 (2), p.C287-C302

2019

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Analytical validation of an HPLC assay for urinary albumin

Clinica chimica acta, 2006-05, Vol.367 (1), p.150-155

2006

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Trpv1 and Trpa1 are not essential for Psickle-like activity in red cells of the SAD mouse model of sickle cell disease

Blood cells, molecules, & diseases, 2021-12, Vol.92, p.102619-102619, Article 102619

2021

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Revised prevalence estimate of possible Hereditary Xerocytosis as derived from a large U.S. Laboratory database

American journal of hematology, 2018-01, Vol.93 (1), p.E9-E12

2018

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Erythrocytes from hereditary xerocytosis patients heterozygous for KCNN4 V282M exhibit increased spontaneous Gardos channel‐like activity inhibited by senicapoc

American journal of hematology, 2017-06, Vol.92 (6), p.E108-E110

2017

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Genetic disruption of KCC cotransporters in a mouse model of thalassemia intermedia

Blood cells, molecules, & diseases, 2020-03, Vol.81, p.102389-102389, Article 102389

2020

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Oxidation and erythrocyte senescence

Current opinion in hematology, 2000-03, Vol.7 (2), p.113-116

2000

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Early verification of myocardial ischemia with a novel biomarker of acute tissue damage: C-reactive protein fractional forms

Clinica chimica acta, 2012-10, Vol.413 (19-20), p.1536-1541

2012

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Accuracy evaluation of a new glucometer with automated hematocrit measurement and correction

Clinica chimica acta, 2005-06, Vol.356 (1), p.178-183

2005

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Membrane Phospholipid Asymmetry in Human Thalassemia

Blood, 1998-04, Vol.91 (8), p.3044-3051

1998

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Pulse pressure-driven neutral lipid accumulation and correlative proinflammatory markers of accelerated atherogenesis

Atherosclerosis, 2005-11, Vol.183 (1), p.17-24

2005

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Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis)

The erythroid K-Cl cotransport inhibitor [(dihydroindenyl)oxy]acetic acid blocks erythroid Ca2+-activated K+ channel KCNN4

Purinergic signaling is essential for full Psickle activation by hypoxia and by normoxic acid pH in mature human sickle red cells and in vitro-differentiated cultured human sickle reticulocytes

Erythroid‐specific inactivation of Slc12a6/Kcc3 by EpoR promoter‐driven Cre expression reduces K‐Cl cotransport activity in mouse erythrocytes

Development of a Commercial Reference Laboratory Elective Rotation for Residents in Clinical Pathology

A Grammastola spatulata mechanotoxin-4 (GsMTx4)-sensitive cation channel mediates increased cation permeability in human hereditary spherocytosis of multiple genetic etiologies

Activation of 2‐oxoglutarate receptor 1 (OXGR1) by α‐ketoglutarate (αKG) does not detectably stimulate Pendrin‐mediated anion exchange in Xenopus oocytes

An Intact Dissecting Baker’s Cyst Mimicking Recurrent Deep Vein Thrombosis

Dysregulated Erythroid Mg2+ Efflux in Type 2 Diabetes

Evaluation of an automated digital imaging system, Nextslide Digital Review Network, for examination of peripheral blood smears

Increased Red Cell KCNN4 Activity in Sporadic Hereditary Xerocytosis Associated With Enhanced Single Channel Pressure Sensitivity of PIEZO1 Mutant V598M

Magnesium homeostasis in deoxygenated sickle erythrocytes is modulated by endothelin‐1 via Na+/Mg2+ exchange

Blockade of the mineralocorticoid receptor improves markers of human endothelial cell dysfunction and hematological indices in a mouse model of sickle cell disease

Magnesium homeostasis in deoxygenated sickle erythrocytes is modulated by endothelin-1 via Na + /Mg 2+ exchange

Erythrocyte ion content and dehydration modulate maximal Gardos channel activity in KCNN4 V282M/+ hereditary xerocytosis red cells

Analytical validation of an HPLC assay for urinary albumin

Trpv1 and Trpa1 are not essential for Psickle-like activity in red cells of the SAD mouse model of sickle cell disease

Revised prevalence estimate of possible Hereditary Xerocytosis as derived from a large U.S. Laboratory database

Erythrocytes from hereditary xerocytosis patients heterozygous for KCNN4 V282M exhibit increased spontaneous Gardos channel‐like activity inhibited by senicapoc

Genetic disruption of KCC cotransporters in a mouse model of thalassemia intermedia

Oxidation and erythrocyte senescence

Early verification of myocardial ischemia with a novel biomarker of acute tissue damage: C-reactive protein fractional forms

Accuracy evaluation of a new glucometer with automated hematocrit measurement and correction

Membrane Phospholipid Asymmetry in Human Thalassemia

Pulse pressure-driven neutral lipid accumulation and correlative proinflammatory markers of accelerated atherogenesis

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