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| 2. |
- Herbert, Roger, et al.
(författare)
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Surface chemistry and morphology of poorly crystalline iron sulfides precipitated in media containing sulfate-reducing bacteria
- 1998
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Ingår i: Chemical Geology. - 0009-2541 .- 1872-6836. ; 144:1-2, s. 87-97
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Tidskriftsartikel (refereegranskat)abstract
- This study characterizes the surface chemistry and morphology of poorly crystalline iron sulfides precipitated in a chemically defined growth media for sulfate-reducing bacteria. The precipitates were analyzed by X-ray diffractometry (XRD), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). Based on XRD results, the precipitates exhibit only incipient crystallization with a single broad diffraction peak at about 5 Angstrom, characteristic of disordered mackinawite. The iron sulfides generally exhibit a platy habit with particles 100 to 300 nm in diameter; these particles appear often in 1 to 2 mu m spherical aggregates. The XPS results indicate that the Fe(2p(3/2)) spectrum for poorly crystalline iron sulfide can be fitted with Fe(II) and Fe(III) components, both corresponding to Fe-S bond types, The absence of oxide oxygen in the O(1s) spectrum and Fe(III)-O bond types in the Fe(2p(3/2)) spectrum supports the conclusion that the poorly crystalline iron sulfides are composed of both ferric and ferrous iron coordinated with monosulfide, with lesser amounts of disulfide and polysulfides also present. These results suggest that the precipitates possess a surface composition similar to greigite, with the remaining mineral mass composed of disordered mackinawite.
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| 3. |
- Lind, L, et al.
(författare)
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Localization of the gene for congenital dyserythropoietic anemia type III, CDAN3, to chromosome 15q21-q25.
- 1995
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Ingår i: Human Molecular Genetics. - 0964-6906 .- 1460-2083. ; 4:1, s. 109-12
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Tidskriftsartikel (refereegranskat)abstract
- Congenital dyserythropoietic anemia, type III (CDA III) is a rare autosomal dominant disorder characterized by macrocytic anemia, bone marrow erythroid hyperplasia and giant multinucleate erythroblasts. We have genetically characterized a large Swedish family in which the concurrence of CDA III and myeloma or benign monoclonal gammopathy is significantly higher than expected and have found that the causative genetic defect for CDA III maps to an 11 cM interval within 15q21-q25.
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| 4. |
- Sandström, Herbert, et al.
(författare)
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[Localized gene of the rare "Norrland disease". CDA-III blood disease with dominant heredity].
- 1999
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Ingår i: Läkartidningen. - 0023-7205 .- 1652-7518. ; 96:4, s. 343-7
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Tidskriftsartikel (refereegranskat)abstract
- The article consists in a review of available knowledge of the rare blood disorder, congenital dyserythropoietic anaemia, type III (CDA-III), a disease characterised by autosomal dominant heredity, and mild to moderate haemolytic anaemia. The gene causing CDA-III has been localised on chromosome 15q22. Most patients are adapted to their disease, and have few or no overt manifestations. Bone marrow examination yields a characteristic picture of erythroid hyperplasia and multinucleate erythroblasts. A Swedish family affected with CDA-III has been reported to be characterised by a high prevalence of monoclonal gammopathy and angioid streaks, a triad suggested by the authors to represent a hitherto unreported syndrome.
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