148 related articles for article (PubMed ID: 33519508)
21. 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]
22. PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus.
Imashuku S; Muramatsu H; Sugihara T; Okuno Y; Wang X; Yoshida K; Kato A; Kato K; Tatsumi Y; Hattori A; Kita S; Oe K; Sueyoshi A; Usui T; Shiraishi Y; Chiba K; Tanaka H; Miyano S; Ogawa S; Kojima S; Kanno H
Int J Hematol; 2016 Jul; 104(1):125-9. PubMed ID: 26971963
[TBL] [Abstract][Full Text] [Related]
23. 'Gardos Channelopathy': a variant of hereditary Stomatocytosis with complex molecular regulation.
Fermo E; Bogdanova A; Petkova-Kirova P; Zaninoni A; Marcello AP; Makhro A; Hänggi P; Hertz L; Danielczok J; Vercellati C; Mirra N; Zanella A; Cortelezzi A; Barcellini W; Kaestner L; Bianchi P
Sci Rep; 2017 May; 7(1):1744. PubMed ID: 28496185
[TBL] [Abstract][Full Text] [Related]
24. Utility of mean sphered cell volume and mean reticulocyte volume for the diagnosis of hereditary spherocytosis.
Arora RD; Dass J; Maydeo S; Arya V; Kotwal J; Bhargava M
Hematology; 2018 Aug; 23(7):413-416. PubMed ID: 29338606
[TBL] [Abstract][Full Text] [Related]
25. Hematologic and biochemical abnormalities indicating iron deficiency are associated with decreased reticulocyte hemoglobin content (CHr) and reticulocyte volume (rMCV) in dogs.
Steinberg JD; Olver CS
Vet Clin Pathol; 2005; 34(1):23-7. PubMed ID: 15732013
[TBL] [Abstract][Full Text] [Related]
26. Hereditary xerocytosis: a report of six unrelated Spanish families with leaky red cell syndrome and increased heat stability of the erythrocyte membrane.
Vives Corrons JL; Besson I; Aymerich M; Ayala S; Alloisio N; Delaunay J; Gonzalez I; Manrubia E
Br J Haematol; 1995 Aug; 90(4):817-22. PubMed ID: 7669659
[TBL] [Abstract][Full Text] [Related]
27. Reticulocyte parameters of delta beta thalassaemia trait, beta thalassaemia trait and iron deficiency anaemia.
Velasco-Rodríguez D; Alonso-Domínguez JM; González-Fernández FA; Villarrubia J; Sopeña M; Abalo L; Ropero P; Martínez-Nieto J; de la Fuente Gonzalo F; Cava F
J Clin Pathol; 2016 Feb; 69(2):149-54. PubMed ID: 26265587
[TBL] [Abstract][Full Text] [Related]
28. New insights on hereditary erythrocyte membrane defects.
Andolfo I; Russo R; Gambale A; Iolascon A
Haematologica; 2016 Nov; 101(11):1284-1294. PubMed ID: 27756835
[TBL] [Abstract][Full Text] [Related]
29. Mechanistic ion channel interactions in red cells of patients with Gárdos channelopathy.
Jansen J; Qiao M; Hertz L; Wang X; Fermo E; Zaninoni A; Colombatti R; Bernhardt I; Bianchi P; Kaestner L
Blood Adv; 2021 Sep; 5(17):3303-3308. PubMed ID: 34468723
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. 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]
32. 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]
33. PIEZO1 gain-of-function mutations delay reticulocyte maturation in hereditary xerocytosis.
Moura PL; Hawley BR; Dobbe JGG; Streekstra GJ; Rab MAE; Bianchi P; van Wijk R; Toye AM; Satchwell TJ
Haematologica; 2020 Jun; 105(6):e268-e271. PubMed ID: 31624108
[No Abstract] [Full Text] [Related]
34. Red blood cell Gardos channel (KCNN4): the essential determinant of erythrocyte dehydration in hereditary xerocytosis.
Rapetti-Mauss R; Picard V; Guitton C; Ghazal K; Proulle V; Badens C; Soriani O; Garçon L; Guizouarn H
Haematologica; 2017 Oct; 102(10):e415-e418. PubMed ID: 28619848
[No Abstract] [Full Text] [Related]
35. 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]
36. Stomatocytosis in 7 related Standard Schnauzers.
Bonfanti U; Comazzi S; Paltrinieri S; Bertazzolo W
Vet Clin Pathol; 2004; 33(4):234-9. PubMed ID: 15570561
[TBL] [Abstract][Full Text] [Related]
37. Different reticulocyte volume in diabetes mellitus patients with and without hypercholesterolemia and/or hypertriglyceridemia.
Bunyaratvej P; Komindr S; Wisedpanichkij R
J Med Assoc Thai; 2000 Jul; 83(7):790-6. PubMed ID: 10932515
[TBL] [Abstract][Full Text] [Related]
38. Variant spectrum of PIEZO1 and KCNN4 in Japanese patients with dehydrated hereditary stomatocytosis.
Nakahara E; Yamamoto KS; Ogura H; Aoki T; Utsugisawa T; Azuma K; Akagawa H; Watanabe K; Muraoka M; Nakamura F; Kamei M; Tatebayashi K; Shinozuka J; Yamane T; Hibino M; Katsura Y; Nakano-Akamatsu S; Kadowaki N; Maru Y; Ito E; Ohga S; Yagasaki H; Morioka I; Yamamoto T; Kanno H
Hum Genome Var; 2023 Mar; 10(1):8. PubMed ID: 36864026
[TBL] [Abstract][Full Text] [Related]
39. Use of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) in the Diagnosis of RBC Membrane Disorders, Enzyme Defects, and Congenital Dyserythropoietic Anemias: A Monocentric Study on 202 Patients.
Zaninoni A; Fermo E; Vercellati C; Consonni D; Marcello AP; Zanella A; Cortelezzi A; Barcellini W; Bianchi P
Front Physiol; 2018; 9():451. PubMed ID: 29755372
[TBL] [Abstract][Full Text] [Related]
40. Calcium Channels and Calcium-Regulated Channels in Human Red Blood Cells.
Kaestner L; Bogdanova A; Egee S
Adv Exp Med Biol; 2020; 1131():625-648. PubMed ID: 31646528
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]