173 related articles for article (PubMed ID: 18780836)
21. Heme metabolism and in vitro erythropoiesis in anemia associated with hypochromic microcytosis.
Brown AC; Lutton JD; Pearson HA; Nelson JC; Levere RD; Abraham NG
Am J Hematol; 1988 Jan; 27(1):1-6. PubMed ID: 3354554
[TBL] [Abstract][Full Text] [Related]
22. Evidence for and consequences of chronic heme deficiency in Belgrade rat reticulocytes.
Garrick MD; Scott D; Kulju D; Romano MA; Dolan KG; Garrick LM
Biochim Biophys Acta; 1999 Mar; 1449(2):125-36. PubMed ID: 10082971
[TBL] [Abstract][Full Text] [Related]
23. Regulation and tissue-specific expression of δ-aminolevulinic acid synthases in non-syndromic sideroblastic anemias and porphyrias.
Peoc'h K; Nicolas G; Schmitt C; Mirmiran A; Daher R; Lefebvre T; Gouya L; Karim Z; Puy H
Mol Genet Metab; 2019 Nov; 128(3):190-197. PubMed ID: 30737140
[TBL] [Abstract][Full Text] [Related]
24. A novel ENU-induced Cpox mutation causes microcytic hypochromic anemia in mice.
Miyasaka Y; Okuda K; Miura I; Motegi H; Wakana S; Ohno T
Exp Anim; 2022 Nov; 71(4):433-441. PubMed ID: 35527013
[TBL] [Abstract][Full Text] [Related]
25. Anti-Correlation between the Dynamics of the Active Site Loop and C-Terminal Tail in Relation to the Homodimer Asymmetry of the Mouse Erythroid 5-Aminolevulinate Synthase.
Na I; Catena D; Kong MJ; Ferreira GC; Uversky VN
Int J Mol Sci; 2018 Jun; 19(7):. PubMed ID: 29958424
[TBL] [Abstract][Full Text] [Related]
26. Strong correlation of ferrochelatase enzymatic activity with Mitoferrin-1 mRNA in lymphoblasts of patients with protoporphyria.
Phillips J; Farrell C; Wang Y; Singal AK; Anderson K; Balwani M; Bissell M; Bonkovsky H; Seay T; Paw B; Desnick R; Bloomer J
Mol Genet Metab; 2019 Nov; 128(3):391-395. PubMed ID: 30391163
[TBL] [Abstract][Full Text] [Related]
27. Non-transferrin-bound iron uptake in Belgrade and normal rat erythroid cells.
Garrick LM; Dolan KG; Romano MA; Garrick MD
J Cell Physiol; 1999 Mar; 178(3):349-58. PubMed ID: 9989781
[TBL] [Abstract][Full Text] [Related]
28. Results of a pilot study of isoniazid in patients with erythropoietic protoporphyria.
Parker CJ; Desnick RJ; Bissel MD; Bloomer JR; Singal A; Gouya L; Puy H; Anderson KE; Balwani M; Phillips JD
Mol Genet Metab; 2019 Nov; 128(3):309-313. PubMed ID: 31395332
[TBL] [Abstract][Full Text] [Related]
29. Increased plasma transferrin, altered body iron distribution, and microcytic hypochromic anemia in ferrochelatase-deficient mice.
Lyoumi S; Abitbol M; Andrieu V; Henin D; Robert E; Schmitt C; Gouya L; de Verneuil H; Deybach JC; Montagutelli X; Beaumont C; Puy H
Blood; 2007 Jan; 109(2):811-8. PubMed ID: 17003376
[TBL] [Abstract][Full Text] [Related]
30. Induction of hepatic aminolevulinate acid synthetase activity by isoflurane in a genetic model for erythropoietic protoporphyria.
Buzaleh AM; Morán-Jiménez MJ; Garcia-Bravo M; Sampedro A; Batlle AM; Enriquez de Salamanca R; Fontanellas A
Cell Mol Biol (Noisy-le-grand); 2009 Feb; 55(1):38-44. PubMed ID: 19268000
[TBL] [Abstract][Full Text] [Related]
31. Anemia and impaired stress-induced erythropoiesis in aceruloplasminemic mice.
Cherukuri S; Tripoulas NA; Nurko S; Fox PL
Blood Cells Mol Dis; 2004; 33(3):346-55. PubMed ID: 15528156
[TBL] [Abstract][Full Text] [Related]
32. Disturbed iron metabolism in erythropoietic protoporphyria and association of GDF15 and gender with disease severity.
Barman-Aksoezen J; Girelli D; Aurizi C; Schneider-Yin X; Campostrini N; Barbieri L; Minder EI; Biolcati G
J Inherit Metab Dis; 2017 May; 40(3):433-441. PubMed ID: 28185024
[TBL] [Abstract][Full Text] [Related]
33. Molecular pathophysiology and genetic mutations in congenital sideroblastic anemia.
Fujiwara T; Harigae H
Free Radic Biol Med; 2019 Mar; 133():179-185. PubMed ID: 30098397
[TBL] [Abstract][Full Text] [Related]
34. Targeted deletion of the mouse Mitoferrin1 gene: from anemia to protoporphyria.
Troadec MB; Warner D; Wallace J; Thomas K; Spangrude GJ; Phillips J; Khalimonchuk O; Paw BH; Ward DM; Kaplan J
Blood; 2011 May; 117(20):5494-502. PubMed ID: 21310927
[TBL] [Abstract][Full Text] [Related]
35. Late-onset X-linked sideroblastic anemia. Missense mutations in the erythroid delta-aminolevulinate synthase (ALAS2) gene in two pyridoxine-responsive patients initially diagnosed with acquired refractory anemia and ringed sideroblasts.
Cotter PD; May A; Fitzsimons EJ; Houston T; Woodcock BE; al-Sabah AI; Wong L; Bishop DF
J Clin Invest; 1995 Oct; 96(4):2090-6. PubMed ID: 7560104
[TBL] [Abstract][Full Text] [Related]
36. Mild iron deficiency does not ameliorate the phenotype of a murine erythropoietic protoporphyria model.
Schmidt PJ; Hollowell ML; Fitzgerald K; Butler JS; Fleming MD
Am J Hematol; 2020 May; 95(5):492-496. PubMed ID: 31990410
[TBL] [Abstract][Full Text] [Related]
37. GLRX5 mutations impair heme biosynthetic enzymes ALA synthase 2 and ferrochelatase in Human congenital sideroblastic anemia.
Daher R; Mansouri A; Martelli A; Bayart S; Manceau H; Callebaut I; Moulouel B; Gouya L; Puy H; Kannengiesser C; Karim Z
Mol Genet Metab; 2019 Nov; 128(3):342-351. PubMed ID: 30660387
[TBL] [Abstract][Full Text] [Related]
38. Clinical and molecular epidemiology of erythropoietic protoporphyria in Italy.
Ventura P; Brancaleoni V; Di Pierro E; Graziadei G; Macrì A; Carmine Guida C; Nicolli A; Rossi MT; Granata F; Fiorentino V; Fustinoni S; Sala R; Pinton PC; Trevisan A; Marchini S; Cuoghi C; Marcacci M; Corradini E; Sorge F; Aurizi C; Savino MG; Cappellini MD; Pietrangelo A
Eur J Dermatol; 2020 Oct; 30(5):532-540. PubMed ID: 33021473
[TBL] [Abstract][Full Text] [Related]
39. Oxidative stress modulates heme synthesis and induces peroxiredoxin-2 as a novel cytoprotective response in β-thalassemic erythropoiesis.
De Franceschi L; Bertoldi M; De Falco L; Santos Franco S; Ronzoni L; Turrini F; Colancecco A; Camaschella C; Cappellini MD; Iolascon A
Haematologica; 2011 Nov; 96(11):1595-604. PubMed ID: 21750082
[TBL] [Abstract][Full Text] [Related]
40. A mutation in the iron-responsive element of
Ducamp S; Luscieti S; Ferrer-Cortès X; Nicolas G; Manceau H; Peoc'h K; Yien YY; Kannengiesser C; Gouya L; Puy H; Sanchez M
Haematologica; 2021 Jul; 106(7):2030-2033. PubMed ID: 33596641
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
