Hereditary xerocytosis revisited-Reference-Cited by-同舟云学术

Hereditary xerocytosis revisited

Published:2014-07-21 Issue:12 Volume:89 Page:1142-1146
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Archer Natasha M.¹²,Shmukler Boris E.³⁴,Andolfo Immacolata⁵⁶,Vandorpe David H.³⁴,Gnanasambandam Radhakrishnan⁷,Higgins John M.⁸⁹,Rivera Alicia¹⁰¹¹,Fleming Mark D.¹¹,Sachs Frederick⁷,Gottlieb Philip A.⁷,Iolascon Achille⁵⁶,Brugnara Carlo¹⁰¹¹,Alper Seth L.³⁴¹²,Nathan David G.¹²¹³

Affiliation:

1. Division of Hematology and Oncology; Boston Children's Hospital; Boston Massachusetts

2. Dana-Farber Cancer Center; Boston Massachusetts

3. Renal Division; Beth Israel Deaconess Medical Center; Boston Massachusetts

4. Molecular and Vascular Medicine Division; Beth Israel Deaconess Medical Center; Boston Massachusetts

5. Department of Molecular Medicine and Medical Biotechnologies; Federico II University of Naples; Naples Italy

6. CEINGE, Advanced Biotechnologies; Naples Italy

7. Department of Physiology and Biophysics; University of Buffalo; Buffalo New York

8. Department of Systems Biology; Harvard Medical School; Boston Massachusetts

9. Center for Systems Biology and Department of Pathology; Massachusetts General Hospital; Boston Massachusetts

10. Department of Laboratory Medicine; Boston Children's Hospital; Boston Massachusetts

11. Department of Pathology; Harvard Medical School; Boston Massachusetts

12. Department of Medicine; Harvard Medical School; Boston Massachusetts

13. Department of Pediatrics; Harvard Medical School; Boston Massachusetts

Funder

NIH

MIUR and Telethon (Italy)

Doris Duke Charitable Foundation

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.23799/fullpdf

Reference26 articles.

1. Exercise-induced hemolysis in xerocytosis. Erythrocyte dehydration and shear sensitivity;Platt;J Clin Invest,1981

2. A new variant of hereditary hemolytic anemia with stomatocytosis and erythrocyte cation abnormality;Miller;Blood,1971

3. Congenital hemolytic anemia associated with dehydrated erythrocytes and increased potassium loss;Glader;N Engl J Med,1974

4. Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia;Andolfo;Am J Hematol,2013

5. Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis;Zarychanski;Blood,2012

Cited by 47 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Deciphering and disrupting PIEZO1-TMEM16F interplay in hereditary xerocytosis;Blood;2024-01-25

2. The protein-bound uremic solute 3-carboxy-4-methyl-5-propyl-2-furanpropionate (CMPF) increases erythrocyte osmotic fragility through interaction with the mechanosensitive channel Piezo1;2023-05-27

3. Piezo1 activation augments sickling propensity and the adhesive properties of sickle red blood cells in a calcium‐dependent manner;British Journal of Haematology;2023-04-03

4. Congenital Defects with Impaired Red Blood Cell Deformability – The Role of Next-Generation Ektacytometry;The Erythrocyte - A Unique Cell;2023-03-29

5. Pseudohyperkalemia: Three Cases and a Review of Literature;The American Journal of Medicine;2022-07