152 related articles for article (PubMed ID: 36531183)
1. Red blood cell proteomics reveal remnant protein biosynthesis and folding pathways in PIEZO1-related hereditary xerocytosis.
Caulier A; Jankovsky N; Gautier EF; El Nemer W; Guitton C; Ouled-Haddou H; Guillonneau F; Mayeux P; Salnot V; Bruce J; Picard V; Garçon L
Front Physiol; 2022; 13():960291. PubMed ID: 36531183
[TBL] [Abstract][Full Text] [Related]
2. PIEZO1 activation delays erythroid differentiation of normal and hereditary xerocytosis-derived human progenitor cells.
Caulier A; Jankovsky N; Demont Y; Ouled-Haddou H; Demagny J; Guitton C; Merlusca L; Lebon D; Vong P; Aubry A; Lahary A; Rose C; Gréaume S; Cardon E; Platon J; Ouadid-Ahidouch H; Rochette J; Marolleau JP; Picard V; Garçon L
Haematologica; 2020 Mar; 105(3):610-622. PubMed ID: 31413092
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. Inside Out Integrin Activation Mediated by PIEZO1 Signaling in Erythroblasts.
Aglialoro F; Hofsink N; Hofman M; Brandhorst N; van den Akker E
Front Physiol; 2020; 11():958. PubMed ID: 32848880
[TBL] [Abstract][Full Text] [Related]
11. Deciphering and disrupting PIEZO1-TMEM16F interplay in hereditary xerocytosis.
Liang P; Zhang Y; Wan YCS; Ma S; Dong P; Lowry AJ; Francis SJ; Khandelwal S; Delahunty M; Telen MJ; Strouse JJ; Arepally GM; Yang H
Blood; 2024 Jan; 143(4):357-369. PubMed ID: 38033286
[TBL] [Abstract][Full Text] [Related]
12. Hereditary xerocytosis - spectrum and clinical manifestations of variants in the PIEZO1 gene, including co-occurrence with a novel β-globin mutation.
Maciak K; Adamowicz-Salach A; Siwicka A; Poznanski J; Urasinski T; Plochocka D; Gora M; Burzynska B
Blood Cells Mol Dis; 2020 Feb; 80():102378. PubMed ID: 31670187
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. PIEZO1, sensing the touch during erythropoiesis.
Caulier A; Garçon L
Curr Opin Hematol; 2022 May; 29(3):112-118. PubMed ID: 35441597
[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. Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis.
Zarychanski R; Schulz VP; Houston BL; Maksimova Y; Houston DS; Smith B; Rinehart J; Gallagher PG
Blood; 2012 Aug; 120(9):1908-15. PubMed ID: 22529292
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Heterogeneous phenotype of Hereditary Xerocytosis in association with PIEZO1 variants.
de Meira Oliveira P; Balan A; Muto NH; Cervato MC; Fonseca GHH; Suganuma LM; Gualandro S; Pinho JRR; Mohandas N; Silveira PAA; Sitnik R
Blood Cells Mol Dis; 2020 May; 82():102413. PubMed ID: 32109669
[TBL] [Abstract][Full Text] [Related]
20. PIEZO1-gene gain-of-function mutations with lower limb lymphedema onset in an adult: Clinical, scintigraphic, and noncontrast magnetic resonance lymphography findings.
Vignes S; Kaltenbach S; Garçon L; Arrivé L; Asnafi V; Guitton C; Bouligand J; Delarue A; Picard V
Am J Med Genet A; 2022 Jan; 188(1):243-248. PubMed ID: 34477311
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]