Zobrazeno 1 - 10
of 58
pro vyhledávání: '"S. S. Zail"'
Publikováno v:
Scandinavian Journal of Haematology. 14:81-85
The administration of vitamin E, a natural antioxidant, to a patient with paroxysmal nocturnal haemoglobinuria (PNH) failed to diminish the urinary excretion of 59-Fe as monitored by 59-Fe whole body counting and urinary loss of isotope. However, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74d0a01f8972679174e8eec4cd667e2a
https://doi.org/10.1111/j.1600-0609.1975.tb00299.x
https://doi.org/10.1111/j.1600-0609.1975.tb00299.x
Publikováno v:
British medical journal. 3(5562)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff7b376e83187bd9fedaf1748c129068
https://pubmed.ncbi.nlm.nih.gov/20791302
https://pubmed.ncbi.nlm.nih.gov/20791302
Publikováno v:
Blood. 92(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6d4780dda547353298b89df40cda5146
https://pubmed.ncbi.nlm.nih.gov/9746802
https://pubmed.ncbi.nlm.nih.gov/9746802
Autor:
S S Zail, T L Coetzer
Publikováno v:
Journal of Clinical Investigation. 74:753-762
The interaction of spectrin with spectrin-depleted inside-out membrane vesicles was studied in a kindred with an atypical variant of hereditary elliptocytosis inherited in a recessive manner. The probands are characterized by prominent elliptocytosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c455bb307ba17038e61c467dc04d2a7f
https://doi.org/10.1172/jci111491
https://doi.org/10.1172/jci111491
Autor:
S. S. Zail, Stephen Lambert
Publikováno v:
Blood. 69:473-478
A kindred is described in which two brothers with a poikilocytic variant of hereditary elliptocytosis (HE) were found to have a defect of spectrin dimer association and a decreased spectrin-band 3 ratio. Two-dimensional gel electrophoresis of limited
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::593ca20ba6e1aaaaea46d12e6defc15b
https://doi.org/10.1182/blood.v69.2.473.473
https://doi.org/10.1182/blood.v69.2.473.473
Publikováno v:
Blood. 72:1926-1929
Genomic DNA from five kindreds and two individuals with hereditary elliptocytosis [HE(4.1+)] and a partial deficiency of protein 4.1 [HE(4.1+)] was extracted and probed with a cDNA for protein 4.1. When using a fragment of the cDNA that encompassed t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20dd793e9f0b7f5109cb3e8f6310f7e6
https://doi.org/10.1182/blood.v72.6.1926.1926
https://doi.org/10.1182/blood.v72.6.1926.1926
Autor:
Theresa L. Coetzer, S. S. Zail
Publikováno v:
Blood. 59:900-905
The proportion of spectrin tetramers and dimers in 4 degrees C low ionic strength extracts of red cell membranes of 9 subjects with 4 different variants of hereditary elliptocytosis (HE) and 2 subjects with hereditary spherocytosis (HS) was determine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::423ac296c46f1dc3dcf2f32a3e1f4467
https://doi.org/10.1182/blood.v59.5.900.bloodjournal595900
https://doi.org/10.1182/blood.v59.5.900.bloodjournal595900
Autor:
S. S. Zail, Theresa L. Coetzer
Publikováno v:
Blood. 56:159-167
G6PD-deficient red cells (nonhemolytic variants) incubated for 24 hr in medium containing glucose maintain their adenosine triphosphate (ATP) levels but show a pronounced fall in reduced glutathione (GSH) levels. Membranes of such ATP-replete, GSH-de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9928dcc17378559a794d6e90a43de78f
https://doi.org/10.1182/blood.v56.2.159.159
https://doi.org/10.1182/blood.v56.2.159.159
Publikováno v:
British Journal of Haematology. 18:79-88
Summary. The combination of iron overload and hexachlorobenzene (HCB) feeding in rats produces an ‘experimental symptomatic porphyria’. Studies of hepatic haem biosynthesis in this model showed a decrease in total liver haem and cytochromes P450
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c51bb1f177aab936e7f9dfba3691759
https://doi.org/10.1111/j.1365-2141.1970.tb01420.x
https://doi.org/10.1111/j.1365-2141.1970.tb01420.x
Autor:
S. M. Joubert, S. S. Zail
Publikováno v:
British Journal of Haematology. 15:123-130
Hepatic ALA synthetase activity was determined on biopsy material from 12 patients with symptomatic porphyria. Five patients had values at least 1.5 times greater than the highest normal value whilst the remaining seven had values within or slightly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::486b1c5ddcc9eba986f6382579cba999
https://doi.org/10.1111/j.1365-2141.1968.tb01521.x
https://doi.org/10.1111/j.1365-2141.1968.tb01521.x