132 related articles for article (PubMed ID: 16140868)
1. Analysis of the E399D mutation in SLC11A2.
Gunshin H; Jin J; Fujiwara Y; Andrews NC; Mims M; Prchal J
Blood; 2005 Sep; 106(6):2221; author reply 2221-2. PubMed ID: 16140868
[No Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. Severe hypochromic microcytic anemia caused by a congenital defect of the iron transport pathway in erythroid cells.
Priwitzerova M; Pospisilova D; Prchal JT; Indrak K; Hlobilkova A; Mihal V; Ponka P; Divoky V
Blood; 2004 May; 103(10):3991-2. PubMed ID: 15121718
[No Abstract] [Full Text] [Related]
9. Slc11a2 is required for intestinal iron absorption and erythropoiesis but dispensable in placenta and liver.
Gunshin H; Fujiwara Y; Custodio AO; Direnzo C; Robine S; Andrews NC
J Clin Invest; 2005 May; 115(5):1258-66. PubMed ID: 15849611
[TBL] [Abstract][Full Text] [Related]
10. Intestinal DMT1 is critical for iron absorption in the mouse but is not required for the absorption of copper or manganese.
Shawki A; Anthony SR; Nose Y; Engevik MA; Niespodzany EJ; Barrientos T; Öhrvik H; Worrell RT; Thiele DJ; Mackenzie B
Am J Physiol Gastrointest Liver Physiol; 2015 Oct; 309(8):G635-47. PubMed ID: 26294671
[TBL] [Abstract][Full Text] [Related]
11. The zebrafish mutant gene chardonnay (cdy) encodes divalent metal transporter 1 (DMT1).
Donovan A; Brownlie A; Dorschner MO; Zhou Y; Pratt SJ; Paw BH; Phillips RB; Thisse C; Thisse B; Zon LI
Blood; 2002 Dec; 100(13):4655-9. PubMed ID: 12393445
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Recently identified molecular aspects of intestinal iron absorption.
Wood RJ; Han O
J Nutr; 1998 Nov; 128(11):1841-4. PubMed ID: 9808632
[TBL] [Abstract][Full Text] [Related]
15. Divalent metal transporter 1.
Mims MP; Prchal JT
Hematology; 2005 Aug; 10(4):339-45. PubMed ID: 16085548
[TBL] [Abstract][Full Text] [Related]
16. Gene symbol: SLC40A1. Disease: Primary iron overload.
Zaahl MG; Merryweather-Clarke AT; Kotze MJ; van der Merwe S; Warnich L; Robson KJ
Hum Genet; 2005 May; 116(6):541. PubMed ID: 15991323
[No Abstract] [Full Text] [Related]
17. Nramp2 is mutated in the anemic Belgrade (b) rat: evidence of a role for Nramp2 in endosomal iron transport.
Fleming MD; Romano MA; Su MA; Garrick LM; Garrick MD; Andrews NC
Proc Natl Acad Sci U S A; 1998 Feb; 95(3):1148-53. PubMed ID: 9448300
[TBL] [Abstract][Full Text] [Related]
18. Gene symbol: SLC40A1. Disease: primary iron overload.
Zaahl MG; Merryweather-Clarke AT; Kotze MJ; van der Merwe S; Warnich L; Robson KJ
Hum Genet; 2005 Dec; 118(3-4):547. PubMed ID: 16521305
[No Abstract] [Full Text] [Related]
19. 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]
20. Quantitative evaluation of expression of iron-metabolism genes in ceruloplasmin-deficient mice.
Yamamoto K; Yoshida K; Miyagoe Y; Ishikawa A; Hanaoka K; Nomoto S; Kaneko K; Ikeda S; Takeda S
Biochim Biophys Acta; 2002 Dec; 1588(3):195-202. PubMed ID: 12393173
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]