188 related articles for article (PubMed ID: 34737711)
1. Hereditary Xerocytosis: Differential Behavior of PIEZO1 Mutations in the N-Terminal Extracellular Domain Between Red Blood Cells and HEK Cells.
Yamaguchi Y; Allegrini B; Rapetti-Mauss R; Picard V; Garçon L; Kohl P; Soriani O; Peyronnet R; Guizouarn H
Front Physiol; 2021; 12():736585. PubMed ID: 34737711
[TBL] [Abstract][Full Text] [Related]
2. Erythrocyte ion content and dehydration modulate maximal Gardos channel activity in KCNN4 V282M/+ hereditary xerocytosis red cells.
Rivera A; Vandorpe DH; Shmukler BE; Andolfo I; Iolascon A; Archer NM; Shabani E; Auerbach M; Hamerschlak N; Morton J; Wohlgemuth JG; Brugnara C; Snyder LM; Alper SL
Am J Physiol Cell Physiol; 2019 Aug; 317(2):C287-C302. PubMed ID: 31091145
[TBL] [Abstract][Full Text] [Related]
3. Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels.
Albuisson J; Murthy SE; Bandell M; Coste B; Louis-Dit-Picard H; Mathur J; Fénéant-Thibault M; Tertian G; de Jaureguiberry JP; Syfuss PY; Cahalan S; Garçon L; Toutain F; Simon Rohrlich P; Delaunay J; Picard V; Jeunemaitre X; Patapoutian A
Nat Commun; 2013; 4():1884. PubMed ID: 23695678
[TBL] [Abstract][Full Text] [Related]
4. Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis.
Glogowska E; Schneider ER; Maksimova Y; Schulz VP; Lezon-Geyda K; Wu J; Radhakrishnan K; Keel SB; Mahoney D; Freidmann AM; Altura RA; Gracheva EO; Bagriantsev SN; Kalfa TA; Gallagher PG
Blood; 2017 Oct; 130(16):1845-1856. PubMed ID: 28716860
[TBL] [Abstract][Full Text] [Related]
5. Mild erythrocytosis as a presenting manifestation of
Knight T; Zaidi AU; Wu S; Gadgeel M; Buck S; Ravindranath Y
Pediatr Hematol Oncol; 2019 Aug; 36(5):317-326. PubMed ID: 31298594
[TBL] [Abstract][Full Text] [Related]
6. Recent advances in the pathophysiology of PIEZO1-related hereditary xerocytosis.
Jankovsky N; Caulier A; Demagny J; Guitton C; Djordjevic S; Lebon D; Ouled-Haddou H; Picard V; Garçon L
Am J Hematol; 2021 Aug; 96(8):1017-1026. PubMed ID: 33848364
[TBL] [Abstract][Full Text] [Related]
7. Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis).
Andolfo I; Russo R; Manna F; Shmukler BE; Gambale A; Vitiello G; De Rosa G; Brugnara C; Alper SL; Snyder LM; Iolascon A
Am J Hematol; 2015 Oct; 90(10):921-6. PubMed ID: 26178367
[TBL] [Abstract][Full Text] [Related]
8. Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in India.
More TA; Dongerdiye R; Devendra R; Warang PP; Kedar PS
Ann Hematol; 2020 Apr; 99(4):715-727. PubMed ID: 32112123
[TBL] [Abstract][Full Text] [Related]
9. Rapid Gardos Hereditary Xerocytosis Diagnosis in 8 Families Using Reticulocyte Indices.
Picard V; Guitton C; Mansour-Hendili L; Jondeau B; Bendélac L; Denguir M; Demagny J; Proulle V; Galactéros F; Garçon L
Front Physiol; 2020; 11():602109. PubMed ID: 33519508
[TBL] [Abstract][Full Text] [Related]
10. The Molecular Basis for Altered Cation Permeability in Hereditary Stomatocytic Human Red Blood Cells.
Flatt JF; Bruce LJ
Front Physiol; 2018; 9():367. PubMed ID: 29713289
[TBL] [Abstract][Full Text] [Related]
11. Gain-of-function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathway.
Andolfo I; Rosato BE; Manna F; De Rosa G; Marra R; Gambale A; Girelli D; Russo R; Iolascon A
Am J Hematol; 2020 Feb; 95(2):188-197. PubMed ID: 31737919
[TBL] [Abstract][Full Text] [Related]
12. Common PIEZO1 Allele in African Populations Causes RBC Dehydration and Attenuates Plasmodium Infection.
Ma S; Cahalan S; LaMonte G; Grubaugh ND; Zeng W; Murthy SE; Paytas E; Gamini R; Lukacs V; Whitwam T; Loud M; Lohia R; Berry L; Khan SM; Janse CJ; Bandell M; Schmedt C; Wengelnik K; Su AI; Honore E; Winzeler EA; Andersen KG; Patapoutian A
Cell; 2018 Apr; 173(2):443-455.e12. PubMed ID: 29576450
[TBL] [Abstract][Full Text] [Related]
13. New KCNN4 Variants Associated With Anemia: Stomatocytosis Without Erythrocyte Dehydration.
Allegrini B; Jedele S; David Nguyen L; Mignotet M; Rapetti-Mauss R; Etchebest C; Fenneteau O; Loubat A; Boutet A; Thomas C; Durin J; Petit A; Badens C; Garçon L; Da Costa L; Guizouarn H
Front Physiol; 2022; 13():918620. PubMed ID: 36003639
[TBL] [Abstract][Full Text] [Related]
14. Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.
Andolfo I; Alper SL; De Franceschi L; Auriemma C; Russo R; De Falco L; Vallefuoco F; Esposito MR; Vandorpe DH; Shmukler BE; Narayan R; Montanaro D; D'Armiento M; Vetro A; Limongelli I; Zuffardi O; Glader BE; Schrier SL; Brugnara C; Stewart GW; Delaunay J; Iolascon A
Blood; 2013 May; 121(19):3925-35, S1-12. PubMed ID: 23479567
[TBL] [Abstract][Full Text] [Related]
15. Proteome alterations in erythrocytes with PIEZO1 gain-of-function mutations.
Andolfo I; Monaco V; Cozzolino F; Rosato BE; Marra R; Cerbone V; Pinto VM; Forni GL; Unal S; Iolascon A; Monti M; Russo R
Blood Adv; 2023 Jun; 7(12):2681-2693. PubMed ID: 36595486
[TBL] [Abstract][Full Text] [Related]
16. Piezo1 links mechanical forces to red blood cell volume.
Cahalan SM; Lukacs V; Ranade SS; Chien S; Bandell M; Patapoutian A
Elife; 2015 May; 4():. PubMed ID: 26001274
[TBL] [Abstract][Full Text] [Related]
17. Clinical and biological features in
Picard V; Guitton C; Thuret I; Rose C; Bendelac L; Ghazal K; Aguilar-Martinez P; Badens C; Barro C; Bénéteau C; Berger C; Cathébras P; Deconinck E; Delaunay J; Durand JM; Firah N; Galactéros F; Godeau B; Jaïs X; de Jaureguiberry JP; Le Stradic C; Lifermann F; Maffre R; Morin G; Perrin J; Proulle V; Ruivard M; Toutain F; Lahary A; Garçon L
Haematologica; 2019 Aug; 104(8):1554-1564. PubMed ID: 30655378
[TBL] [Abstract][Full Text] [Related]
18. A novel PIEZO1 mutation in a patient with dehydrated hereditary stomatocytosis: a case report and a brief review of literature.
Zama D; Giulietti G; Muratore E; Andolfo I; Russo R; Iolascon A; Pession A
Ital J Pediatr; 2020 Jul; 46(1):102. PubMed ID: 32703298
[TBL] [Abstract][Full Text] [Related]
19. Genetic Diseases of PIEZO1 and PIEZO2 Dysfunction.
Alper SL
Curr Top Membr; 2017; 79():97-134. PubMed ID: 28728825
[TBL] [Abstract][Full Text] [Related]
20.
Andolfo I; De Rosa G; Errichiello E; Manna F; Rosato BE; Gambale A; Vetro A; Calcaterra V; Pelizzo G; De Franceschi L; Zuffardi O; Russo R; Iolascon A
Front Physiol; 2019; 10():258. PubMed ID: 30930797
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
