A. Rivera

发表

Erythrocyte ion content and dehydration modulate maximal Gardos channel activity in KCNN4 V282M/+ Hereditary Xerocytosis (HX) red cells.

D. Vandorpe, A. Iolascon, S. Alper, 2019, American journal of physiology. Cell physiology.

Gene Variation of Endoplasmic Reticulum Aminopeptidases 1 and 2, and Risk of Blood Pressure Progression and Incident Hypertension among 17,255 Initially Healthy Women

P. Ridker, D. Chasman, R. Zee, 2018, International journal of genomics.

Aldosterone's rapid, nongenomic effects are mediated by striatin: a modulator of aldosterone's effect on estrogen action.

G. Adler, Gordon H. Williams, J. Romero, 2014, Endocrinology.

Activation of the mineralocorticoid receptor increases striatin levels.

A. Turchin, G. Adler, Gordon H. Williams, 2012, American journal of hypertension.

In vivo reduction of erythrocyte oxidant stress in a murine model of beta-thalassemia.

M. Fleming, A. Bast, L. De Franceschi, 2004, Haematologica.

Combined genetic disruption of K-Cl cotransporters and Gardos channel KCNN4 rescues erythrocyte dehydration in the SAD mouse model of sickle cell disease.

S. Alper, C. Brugnara, M. Trudel, 2019, Blood cells, molecules & diseases.

Endothelin‐1 receptor antagonists regulate cell surface‐associated protein disulfide isomerase in sickle cell disease

J. Romero, A. Rivera, G. Prado, 2013, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

erythrocytes Abnormal regulation of Mg2+ transport via Na/Mg exchanger in sickle

C. Brugnara, J. Romero, A. Rivera, 2013 .

Reduced sickle erythrocyte dehydration in vivo by endothelin-1 receptor antagonists.

A. Rivera, 2007, American journal of physiology. Cell physiology.

Abnormal regulation of Mg2+ transport via Na/Mg exchanger in sickle erythrocytes.

C. Brugnara, J. Romero, A. Rivera, 2005, Blood.

N-ethylmaleimide activates a Cl(-)-independent component of K(+) flux in mouse erythrocytes.

S. Alper, M. Trudel, B. Shmukler, 2013, Blood cells, molecules & diseases.

Biological Sex Modulates the Adrenal and Blood Pressure Responses to Angiotensin II

R. Karas, G. Adler, E. Seely, 2018, Hypertension.

responsiveness expression reveal targets of damage, stress response, and antioxidant SOD2-deficiency anemia: protein oxidation and altered protein

Mary F. Lopez, M. Fleming, S. Doctrow, 2013 .

SOD2-deficiency anemia: protein oxidation and altered protein expression reveal targets of damage, stress response, and antioxidant responsiveness.

Mary F. Lopez, M. Fleming, S. Doctrow, 2004, Blood.

Increased red cell sodium-lithium countertransport and lymphocyte cytosolic calcium are separate phenotypes in patients with essential hypertension

P. Conlin, G. Ceolotto, A. Semplicini, 2002, Journal of Human Hypertension.

RED BLOOD CELL Na+/H+ EXCHANGE ACTIVITY IS INSULIN RESISTANT IN HYPERTENSIVE PATIENTS

P. Conlin, J. Romero, A. Rivera, 2002, Clinical and experimental hypertension.

A physician or group of physicians considers presentation and evolution of a real clinical case, reacting to clinical information and data (boldface type). This is followed by a discussion/commentary Hereditary xerocytosis revisited

M. Fleming, D. Vandorpe, F. Sachs, 2014 .

Hereditary xerocytosis revisited

D. Vandorpe, F. Sachs, A. Iolascon, 2014, American journal of hematology.

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

S. Alper, L. De Franceschi, C. Brugnara, 2019, Blood cells, molecules & diseases.

Plasma Membrane Protein Disulfide Isomerase: Its Role in the Translocation of Diphtheria Toxin and HIV Virus Across Endosomal and Cell Membranes

H. Ryser, A. Rivera, A. Gallina, 1998 .

Calpain-1 knockout reveals broad effects on erythrocyte deformability and physiology.

A. Chishti, L. De Franceschi, C. Brugnara, 2012, The Biochemical journal.

Evidence for a protective role of the Gardos channel against hemolysis in murine spherocytosis.

M. Fleming, P. Gascard, L. De Franceschi, 2005, Blood.

Genetic inactivation of calpain-1 attenuates pain sensitivity in a humanized mouse model of sickle cell disease

Jian Xu, A. Chishti, Jianxun Lei, 2016, Haematologica.

Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65S.

D. Vandorpe, D. E. Bauer, S. Alper, 2011, American journal of physiology. Cell physiology.

Dysregulated Erythroid Mg2+ Efflux in Type 2 Diabetes

S. Alper, J. Wohlgemuth, L. Snyder, 2022, Frontiers in Cell and Developmental Biology.

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

D. Vandorpe, S. Alper, C. Brugnara, 2022, Pflügers Archiv - European Journal of Physiology.

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

S. Alper, H. Wulff, C. Brugnara, 2022, American journal of physiology. Cell physiology.

Effect of complete protein 4.1R deficiency on ion transport properties of murine erythrocytes.

P. Gascard, L. De Franceschi, C. Brugnara, 2006, American journal of physiology. Cell physiology.

Quantitative telomerase activity in circulating human leukocytes: utility of real-time telomeric repeats amplification protocol (RQ-TRAP) in a clinical/epidemiological setting

R. Zee, J. Romero, A. Rivera, 2009, Clinical chemistry and laboratory medicine.

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

S. Alper, C. Brugnara, J. Wohlgemuth, 2022, Physiological reports.

Inhibitory effects of Syzygium jambos extract on biomarkers of endothelial cell activation

J. Romero, A. Rivera, Christopher Vega, 2021, BMC Complementary Medicine and Therapies.

Modulation of Gardos channel activity by cytokines in sickle erythrocytes.

C. Brugnara, P. Jarolim, A. Rivera, 2002, Blood.

Endothelins activate Ca2+-gated K+ channels via endothelin B receptors in CD-1 mouse erythrocytes.

C. Brugnara, M. Rotter, A. Rivera, 1999, American journal of physiology. Cell physiology.

Endothelins activate Ca(2+)-gated K(+) channels via endothelin B receptors in CD-1 mouse erythrocytes.

C. Brugnara, M. Rotter, A. Rivera, 1999, The American journal of physiology.

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

F. Hildebrandt, S. Alper, J. Wohlgemuth, 2022, Physiological reports.

Na+/Mg2+ exchange is functionally coupled to the insulin receptor

J. Romero, A. Rivera, Ana Ferreira, 2004, Journal of cellular physiology.

Cation-leak stomatocytosis in standard schnauzers does not cosegregate with coding mutations in the RhAG, SLC4A1, or GLUT1 genes associated with human disease.

D. Vandorpe, S. Alper, S. Paltrinieri, 2012, Blood cells, molecules & diseases.

Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis.

D. Vandorpe, S. Alper, C. Brugnara, 2011, American journal of physiology. Cell physiology.

Functional expression of beta-chemokine receptors in osteoblasts: role of regulated upon activation, normal T cell expressed and secreted (RANTES) in osteoblasts and regulation of its secretion by osteoblasts and osteoclasts.

Sanghamitra Bandyopadhyay, S. Bandyopadhyay, E. Brown, 2005, Endocrinology.

Sickle Cell Disease and Fetal Hemoglobin

A. Rivera, 2018, Saudi journal of medicine & medical sciences.

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

D. Vandorpe, S. Alper, C. Brugnara, 2021, Blood cells, molecules & diseases.

Pancreatic Homeodomain Transcription Factor IDX1/IPF1 Expressed in Developing Brain Regulates Somatostatin Gene Transcription in Embryonic Neural Cells*

R. Moratalla, B. Perez-Villamil, A. Rivera, 2000, The Journal of Biological Chemistry.

Dehydrated stomatocytic anemia due to the heterozygous mutation R2456H in the mechanosensitive cation channel PIEZO1: a case report.

D. Vandorpe, S. Alper, C. Brugnara, 2014, Blood cells, molecules & diseases.

Na+/Ca2+ Exchanger Activity Modulates Connective Tissue Growth Factor mRNA Expression in Transforming Growth Factor β1- and Des-Arg10-kallidin-stimulated Myofibroblasts*

P. Conlin, J. Romero, M. Bicho, 2005, Journal of Biological Chemistry.

Parathyroid hormone ablation alters erythrocyte parameters that are rescued by calcium‐sensing receptor gene deletion

E. Brown, N. Chattopadhyay, D. Goltzman, 2013, European journal of haematology.

Ablation of the Kell/Xk complex alters erythrocyte divalent cation homeostasis.

Soohee Lee, J. Romero, M. Ho, 2013, Blood cells, molecules & diseases.

Changes in red cell ion transport, reduced intratumoral neovascularization, and some mild motor function abnormalities accompany targeted disruption of the Mouse Kell gene (Kel)

M. Golub, P. Kumarathasan, Soohee Lee, 2009, American journal of hematology.

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

G. Lettre, D. Vandorpe, S. Alper, 2021, Haematologica.

Strain-specific variations in cation content and transport in mouse erythrocytes.

R. Zee, S. Alper, C. Brugnara, 2013, Physiological genomics.

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

D. Vandorpe, S. Alper, C. Brugnara, 2017, American journal of hematology.

in murine spherocytosis Evidence for a protective role of the Gardos channel against hemolysis

M. Fleming, C. Brugnara, N. Mohandas, 2013 .

Abnormal regulation of Mg transport via Na/Mg exchange in sickle erythrocytes

C. Brugnara, J. Romero, A. Rivera, 2004 .

Blockade of endothelin-1 receptor B regulates molecules of the major histocompatibility complex in sickle cell disease

A. Rivera, Yaritza Inostroza-Nieves, J. Romero, 2023, Frontiers in Immunology.

Headpiece domain of dematin is required for the stability of the erythrocyte membrane

P. Low, A. Chishti, C. Brugnara, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Genome-wide association study of erythrocyte density in sickle cell disease patients.

G. Lettre, S. Alper, C. Brugnara, 2017, Blood cells, molecules & diseases.

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

S. Alper, C. Brugnara, J. Niles, 2018, American journal of hematology.

Sex-specific differences in endoplasmic reticulum aminopeptidase 1 modulation influence blood pressure and renin-angiotensin system responses.

Jessica M. Lee, G. Adler, J. Romero, 2019, JCI insight.

Elevated lymphocyte cytosolic calcium in a subgroup of essential hypertensive subjects.

P. Conlin, G. Williams, M. Canessa, 1996, Hypertension.

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

S. Alper, J. Wohlgemuth, L. Snyder, 2022, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Obese first-degree relatives of patients with type 2 diabetes with elevated triglyceride levels exhibit increased β-cell function.

J. Romero, L. Porchia, A. Rivera, 2015, Metabolic syndrome and related disorders.

Serum Amylin Indicates Hypertriglyceridemia in Pre-diabetics

J. Romero, L. Porchia, A. Rivera, 2016 .

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

D. Vandorpe, A. Iolascon, S. Alper, 2018, HemaSphere.

Aldosterone's rapid, nongenomic effects are mediated by striatin: a modulator of aldosterone's effect on estrogen action.

G. Adler, J. Romero, A. Rivera, 2014, Endocrinology.

Obese first-degree relatives of patients with type 2 diabetes with elevated triglyceride levels exhibit increased β-cell function.

J. Romero, L. Porchia, A. Rivera, 2015, Metabolic syndrome and related disorders.

Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis.

D. Vandorpe, S. Alper, C. Brugnara, 2011, American journal of physiology. Cell physiology.

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

S. Alper, L. Snyder, J. Romero, 2023, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

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

D. Vandorpe, C. Brugnara, B. Shmukler, 2017, American journal of hematology.

Modulation of Gardos channel activity by cytokines in sickle erythrocytes.

C. Brugnara, A. Rivera, P. Jarolím, 2002, Blood.