Literature DB >> 9544492

Iron deficiency: lessons from anemic mice.

N C Andrews1.   

Abstract

Iron is an essential nutrient, and disorders of iron metabolism are common. Nonetheless, intestinal iron absorption and cellular iron transport are poorly understood. Biochemical approaches to elucidating these processes have yielded little in the past decade. As an alternative approach, we have begun to study spontaneous mouse mutants, that have inherited defects in key steps in iron transport. We have undertaken positional cloning of the gene responsible for microcytic anemia (gene symbol mk). This report describes the important characteristics of these mice, and our progress in studying them.

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Year:  1997        PMID: 9544492      PMCID: PMC2589100     

Source DB:  PubMed          Journal:  Yale J Biol Med        ISSN: 0044-0086


  15 in total

1.  A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis.

Authors:  J N Feder; A Gnirke; W Thomas; Z Tsuchihashi; D A Ruddy; A Basava; F Dormishian; R Domingo; M C Ellis; A Fullan; L M Hinton; N L Jones; B E Kimmel; G S Kronmal; P Lauer; V K Lee; D B Loeb; F A Mapa; E McClelland; N C Meyer; G A Mintier; N Moeller; T Moore; E Morikang; C E Prass; L Quintana; S M Starnes; R C Schatzman; K J Brunke; D T Drayna; N J Risch; B R Bacon; R K Wolff
Journal:  Nat Genet       Date:  1996-08       Impact factor: 38.330

2.  Characterization and genetic studies of microcytic anemia in house mouse.

Authors:  E S Russell; D J Nash; S E Bernstein; E L Kent; E C McFarland; S M Matthews; M S Norwood
Journal:  Blood       Date:  1970-06       Impact factor: 22.113

3.  A comprehensive genetic map of the mouse genome.

Authors:  W F Dietrich; J Miller; R Steen; M A Merchant; D Damron-Boles; Z Husain; R Dredge; M J Daly; K A Ingalls; T J O'Connor
Journal:  Nature       Date:  1996-03-14       Impact factor: 49.962

4.  Mouse microcytic anaemia caused by a defect in the gene encoding the globin enhancer-binding protein NF-E2.

Authors:  L L Peters; N C Andrews; E M Eicher; M B Davidson; S H Orkin; S E Lux
Journal:  Nature       Date:  1993-04-22       Impact factor: 49.962

5.  Microcytic anemia in mk/mk mice is not corrected by retroviral-mediated gene transfer of wild-type p45 NF-E2.

Authors:  P A Ney; S F Farina; D M Bodine; N C Andrews; S H Orkin; A W Neinhuis
Journal:  Exp Hematol       Date:  1995-01       Impact factor: 3.084

6.  Purification of the human NF-E2 complex: cDNA cloning of the hematopoietic cell-specific subunit and evidence for an associated partner.

Authors:  P A Ney; N C Andrews; S M Jane; B Safer; M E Purucker; S Weremowicz; C C Morton; S C Goff; S H Orkin; A W Nienhuis
Journal:  Mol Cell Biol       Date:  1993-09       Impact factor: 4.272

7.  The human transcription factor CP2 (TFCP2), a component of the human gamma-globin stage selector protein, maps to chromosome region 12q13 and is within 250 kb of the NF-E2 gene.

Authors:  J M Cunningham; E F Vanin; N Tran; M Valentine; S M Jane
Journal:  Genomics       Date:  1995-11-20       Impact factor: 5.736

8.  Microcytic anemia with iron malabsorption: an inherited disorder of iron metabolism.

Authors:  K R Hartman; J A Barker
Journal:  Am J Hematol       Date:  1996-04       Impact factor: 10.047

9.  Retroviral integration within the Fli-2 locus results in inactivation of the erythroid transcription factor NF-E2 in Friend erythroleukemias: evidence that NF-E2 is essential for globin expression.

Authors:  S J Lu; S Rowan; M R Bani; Y Ben-David
Journal:  Proc Natl Acad Sci U S A       Date:  1994-08-30       Impact factor: 11.205

10.  Co-operative regulation of endocytosis by three Rab5 isoforms.

Authors:  C Bucci; A Lütcke; O Steele-Mortimer; V M Olkkonen; P Dupree; M Chiariello; C B Bruni; K Simons; M Zerial
Journal:  FEBS Lett       Date:  1995-06-05       Impact factor: 4.124

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  5 in total

1.  A novel TMPRSS6 mutation that prevents protease auto-activation causes IRIDA.

Authors:  Sandro Altamura; Flavia D'Alessio; Barbara Selle; Martina U Muckenthaler
Journal:  Biochem J       Date:  2010-11-01       Impact factor: 3.857

2.  Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA).

Authors:  Karin E Finberg; Matthew M Heeney; Dean R Campagna; Yeşim Aydinok; Howard A Pearson; Kip R Hartman; Mary M Mayo; Stewart M Samuel; John J Strouse; Kyriacos Markianos; Nancy C Andrews; Mark D Fleming
Journal:  Nat Genet       Date:  2008-04-13       Impact factor: 38.330

3.  Polymorphisms and mutations of human TMPRSS6 in iron deficiency anemia.

Authors:  E Beutler; C Van Geet; D M W M te Loo; T Gelbart; K Crain; J Truksa; P L Lee
Journal:  Blood Cells Mol Dis       Date:  2009-10-08       Impact factor: 3.039

Review 4.  Iron refractory iron deficiency anemia.

Authors:  Luigia De Falco; Mayka Sanchez; Laura Silvestri; Caroline Kannengiesser; Martina U Muckenthaler; Achille Iolascon; Laurent Gouya; Clara Camaschella; Carole Beaumont
Journal:  Haematologica       Date:  2013-06       Impact factor: 9.941

5.  Iron-refractory iron deficiency anemia.

Authors:  Ebru Yılmaz Keskin; İdil Yenicesu
Journal:  Turk J Haematol       Date:  2015-03-05       Impact factor: 1.831

  5 in total

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