174 related articles for article (PubMed ID: 16439678)
1. Two new human DMT1 gene mutations in a patient with microcytic anemia, low ferritinemia, and liver iron overload.
Beaumont C; Delaunay J; Hetet G; Grandchamp B; de Montalembert M; Tchernia G
Blood; 2006 May; 107(10):4168-70. PubMed ID: 16439678
[TBL] [Abstract][Full Text] [Related]
2. A novel N491S mutation in the human SLC11A2 gene impairs protein trafficking and in association with the G212V mutation leads to microcytic anemia and liver iron overload.
Bardou-Jacquet E; Island ML; Jouanolle AM; Détivaud L; Fatih N; Ropert M; Brissot E; Mosser A; Maisonneuve H; Brissot P; Loréal O
Blood Cells Mol Dis; 2011 Dec; 47(4):243-8. PubMed ID: 21871825
[TBL] [Abstract][Full Text] [Related]
3. Not all DMT1 mutations lead to iron overload.
Blanco E; Kannengiesser C; Grandchamp B; Tasso M; Beaumont C
Blood Cells Mol Dis; 2009; 43(2):199-201. PubMed ID: 19553145
[TBL] [Abstract][Full Text] [Related]
4. Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2).
Iolascon A; d'Apolito M; Servedio V; Cimmino F; Piga A; Camaschella C
Blood; 2006 Jan; 107(1):349-54. PubMed ID: 16160008
[TBL] [Abstract][Full Text] [Related]
5. A novel R416C mutation in human DMT1 (SLC11A2) displays pleiotropic effects on function and causes microcytic anemia and hepatic iron overload.
Lam-Yuk-Tseung S; Camaschella C; Iolascon A; Gros P
Blood Cells Mol Dis; 2006; 36(3):347-54. PubMed ID: 16584902
[TBL] [Abstract][Full Text] [Related]
6. Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload.
Mims MP; Guan Y; Pospisilova D; Priwitzerova M; Indrak K; Ponka P; Divoky V; Prchal JT
Blood; 2005 Feb; 105(3):1337-42. PubMed ID: 15459009
[TBL] [Abstract][Full Text] [Related]
7. Functional characterization of the E399D DMT1/NRAMP2/SLC11A2 protein produced by an exon 12 mutation in a patient with microcytic anemia and iron overload.
Lam-Yuk-Tseung S; Mathieu M; Gros P
Blood Cells Mol Dis; 2005; 35(2):212-6. PubMed ID: 16023393
[TBL] [Abstract][Full Text] [Related]
8. Natural history of recessive inheritance of DMT1 mutations.
Iolascon A; Camaschella C; Pospisilova D; Piscopo C; Tchernia G; Beaumont C
J Pediatr; 2008 Jan; 152(1):136-9. PubMed ID: 18154916
[TBL] [Abstract][Full Text] [Related]
9. Mutations in the gene encoding DMT1: clinical presentation and treatment.
Iolascon A; De Falco L
Semin Hematol; 2009 Oct; 46(4):358-70. PubMed ID: 19786204
[TBL] [Abstract][Full Text] [Related]
10. Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overload.
Casale M; Borriello A; Scianguetta S; Roberti D; Caiazza M; Bencivenga D; Tartaglione I; Ladogana S; Maruzzi M; Della Ragione F; Perrotta S
Am J Hematol; 2018 Mar; 93(3):E58-E60. PubMed ID: 29178181
[No Abstract] [Full Text] [Related]
11. New Cases of Hypochromic Microcytic Anemia Due to Mutations in the
Romero-Cortadellas L; Hernández G; Ferrer-Cortès X; Zalba-Jadraque L; Fuster JL; Bermúdez-Cortés M; Galera-Miñarro AM; Pérez-Montero S; Tornador C; Sánchez M
Int J Mol Sci; 2022 Apr; 23(8):. PubMed ID: 35457224
[TBL] [Abstract][Full Text] [Related]
12. Previously uncharacterized isoforms of divalent metal transporter (DMT)-1: implications for regulation and cellular function.
Hubert N; Hentze MW
Proc Natl Acad Sci U S A; 2002 Sep; 99(19):12345-50. PubMed ID: 12209011
[TBL] [Abstract][Full Text] [Related]
13. A Japanese family with ferroportin disease caused by a novel mutation of SLC40A1 gene: hyperferritinemia associated with a relatively low transferrin saturation of iron.
Koyama C; Wakusawa S; Hayashi H; Ueno T; Suzuki R; Yano M; Saito H; Okazaki T
Intern Med; 2005 Sep; 44(9):990-3. PubMed ID: 16258219
[TBL] [Abstract][Full Text] [Related]
14. The homozygous mutation G75R in the human SLC11A2 gene leads to microcytic anaemia and iron overload.
Barrios M; Moreno-Carralero MI; Cuadrado-Grande N; Baro M; Vivanco JL; Morán-Jiménez MJ
Br J Haematol; 2012 May; 157(4):514-6. PubMed ID: 22313374
[No Abstract] [Full Text] [Related]
15. Functional consequences of the human DMT1 (SLC11A2) mutation on protein expression and iron uptake.
Priwitzerova M; Nie G; Sheftel AD; Pospisilova D; Divoky V; Ponka P
Blood; 2005 Dec; 106(12):3985-7. PubMed ID: 16091455
[TBL] [Abstract][Full Text] [Related]
16. DMT1: a mammalian transporter for multiple metals.
Garrick MD; Dolan KG; Horbinski C; Ghio AJ; Higgins D; Porubcin M; Moore EG; Hainsworth LN; Umbreit JN; Conrad ME; Feng L; Lis A; Roth JA; Singleton S; Garrick LM
Biometals; 2003 Mar; 16(1):41-54. PubMed ID: 12572663
[TBL] [Abstract][Full Text] [Related]
17. Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3).
Devalia V; Carter K; Walker AP; Perkins SJ; Worwood M; May A; Dooley JS
Blood; 2002 Jul; 100(2):695-7. PubMed ID: 12091367
[TBL] [Abstract][Full Text] [Related]
18. Divalent metal transporter 1.
Mims MP; Prchal JT
Hematology; 2005 Aug; 10(4):339-45. PubMed ID: 16085548
[TBL] [Abstract][Full Text] [Related]
19. Iron overload in Africans and African-Americans and a common mutation in the SCL40A1 (ferroportin 1) gene.
Gordeuk VR; Caleffi A; Corradini E; Ferrara F; Jones RA; Castro O; Onyekwere O; Kittles R; Pignatti E; Montosi G; Garuti C; Gangaidzo IT; Gomo ZA; Moyo VM; Rouault TA; MacPhail P; Pietrangelo A
Blood Cells Mol Dis; 2003; 31(3):299-304. PubMed ID: 14636642
[TBL] [Abstract][Full Text] [Related]
20. Identification of mutations in SLC40A1 that affect ferroportin function and phenotype of human ferroportin iron overload.
Mayr R; Griffiths WJ; Hermann M; McFarlane I; Halsall DJ; Finkenstedt A; Douds A; Davies SE; Janecke AR; Vogel W; Cox TM; Zoller H
Gastroenterology; 2011 Jun; 140(7):2056-63, 2063.e1. PubMed ID: 21396368
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]