These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 32109669)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 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. 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]  

  • 7. Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis.
    Glogowska E; Lezon-Geyda K; Maksimova Y; Schulz VP; Gallagher PG
    Blood; 2015 Sep; 126(11):1281-4. PubMed ID: 26198474
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Xerocytosis is caused by mutations that alter the kinetics of the mechanosensitive channel PIEZO1.
    Bae C; Gnanasambandam R; Nicolai C; Sachs F; Gottlieb PA
    Proc Natl Acad Sci U S A; 2013 Mar; 110(12):E1162-8. PubMed ID: 23487776
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hemoglobin C trait accentuates erythrocyte dehydration in hereditary xerocytosis.
    Yang E; Voelkel EB; Lezon-Geyda K; Schulz VP; Gallagher PG
    Pediatr Blood Cancer; 2017 Aug; 64(8):. PubMed ID: 28121068
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Recurrent mutation in the PIEZO1 gene in two families of hereditary xerocytosis with fetal hydrops.
    Beneteau C; Thierry G; Blesson S; Le Vaillant C; Picard V; Béné MC; Eveillard M; Le Caignec C
    Clin Genet; 2014 Mar; 85(3):293-5. PubMed ID: 23581886
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients.
    Andolfo I; Russo R; Rosato BE; Manna F; Gambale A; Brugnara C; Iolascon A
    Am J Hematol; 2018 Dec; 93(12):1509-1517. PubMed ID: 30187933
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary xerocytosis: Diagnostic considerations.
    Risinger M; Glogowska E; Chonat S; Zhang K; Dagaonkar N; Joiner CH; Quinn CT; Kalfa TA; Gallagher PG
    Am J Hematol; 2018 Mar; 93(3):E67-E69. PubMed ID: 29210095
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.