Publications
204 results found
Almeida AM, Murakami Y, Layton DM, et al., 2006, Hypomorphic promoter mutation in <i>PIGM</i> causes inherited glycosylphosphatidylinositol deficiency, NATURE MEDICINE, Vol: 12, Pages: 846-851, ISSN: 1078-8956
- Author Web Link
- Cite
- Citations: 163
Ghorashian S, Pancham S, Howard J, et al., 2006, Prospective screening of patients with sickle cell disease for the presence of pulmonary arterial hypertension as determined by tricuspid regurgitant jet velocity at echocardiography, 46th Annual Scientific Meetign of the British-Society-for-Haematology, Publisher: BLACKWELL PUBLISHING, Pages: 71-71, ISSN: 0007-1048
Almeida A, Murakami Y, Hillmen P, et al., 2006, Characterisation of the biochemical and genetic defect in congenital glycosylphosphatidylinositol (GPI) deficiency, 46th Annual Scientific Meetign of the British-Society-for-Haematology, Publisher: BLACKWELL PUBLISHING, Pages: 23-23, ISSN: 0007-1048
Stockford IM, Morgan SP, Crowe JA, et al., 2006, Comparison of methods for surface reflection and short path scatter removal in tissue imaging
Cross-polar detection and a dark-field technique to remove surface reflections and short path light from scattering media are compared. Simulations indicate that the dark-field technique exhibits better resolution at the expense of SNR. © 2006 Optical Society of America.
Percy MJ, Crowley LJ, Roper D, et al., 2005, Identification and characterization of the novel FAD-binding lobe G75S mutation in cytochrome <i>b</i><sub>5</sub> reductase:: An aid to determine recessive congenital methemoglobinernia status in an infant, BLOOD CELLS MOLECULES AND DISEASES, Vol: 36, Pages: 81-90, ISSN: 1079-9796
- Author Web Link
- Cite
- Citations: 18
Percy MJ, Crowley LJ, Davis CA, et al., 2005, A novel heterologous expression system for characterization of individual NADH-cytochrome b5 reductase variants in recessive congenital methemoglobinemia., 47th Annual Meeting of the American-Society-of-Hematology, Publisher: AMER SOC HEMATOLOGY, Pages: 478A-478A, ISSN: 0006-4971
Almeida AM, Hillmen P, Richards SJ, et al., 2005, Defective modification of mannose residues by terminal phosphoethanolamine underlies inherited GPI deficiency., 47th Annual Meeting of the American-Society-of-Hematology, Publisher: AMER SOC HEMATOLOGY, Pages: 41A-41A, ISSN: 0006-4971
Bruce LJ, Robinson HC, Guizouarn H, et al., 2005, Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1, NATURE GENETICS, Vol: 37, Pages: 1258-1263, ISSN: 1061-4036
- Author Web Link
- Cite
- Citations: 124
Hepburn AL, Ng WF, Layton M, et al., 2005, In vivo evidence for apoptosis in the bone marrow in SLE, Joint Meeting of the British-Society-for-Rheumatology/Deutsche-Gesellschaft-fur-Rheumatologie and Spring Meeting of the British-Health-Professionals-in-Rheumatology, Publisher: OXFORD UNIV PRESS, Pages: I135-I135, ISSN: 1462-0324
Repiso A, Corrons JLV, Vulliamy T, et al., 2005, New haplotype for the Glu104Asp mutation in triose-phosphate isomerase deficiency and prenatal diagnosis in a Spanish family, JOURNAL OF INHERITED METABOLIC DISEASE, Vol: 28, Pages: 807-809, ISSN: 0141-8955
- Author Web Link
- Cite
- Citations: 3
Laurence AD, Layton M, Duley JA, et al., 2004, Elevated erythrocyte CDP-choline levels associated with β-thalassaemia in patients with transfusion independent anaemia, NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS, Vol: 23, Pages: 1265-1267, ISSN: 1525-7770
- Author Web Link
- Cite
- Citations: 2
Bain BJ, Thomas A, Clough V, et al., 2004, Report on slide session, British Society for Haematology, 44th Annual Scientific Meeting, Cardiff, 2004, CLINICAL AND LABORATORY HAEMATOLOGY, Vol: 26, Pages: 309-314, ISSN: 0141-9854
Politou M, Terpos E, Anagnostopoulos A, et al., 2004, Role of receptor activator of nuclear factor-kappa B ligand (RANKL), osteoprotegerin and macrophage protein 1-alpha (MIP-1a) in monoclonal gammopathy of undetermined significance (MGUS), BRITISH JOURNAL OF HAEMATOLOGY, Vol: 126, Pages: 686-689, ISSN: 0007-1048
- Author Web Link
- Cite
- Citations: 87
Gomez K, Laffan MA, Kemball-Cook G, et al., 2004, Two novel mutations in severe factor VII deficiency, BRITISH JOURNAL OF HAEMATOLOGY, Vol: 126, Pages: 105-110, ISSN: 0007-1048
- Author Web Link
- Cite
- Citations: 11
Gore DA, Layton M, Sinha AK, et al., 2004, Four pedigrees of the cation-leaky hereditary stomatocytosis class presenting with pseudohyperkalaemia.: Novel profile of temperature dependence of Na<SUP>+</SUP>-K<SUP>+</SUP> leak in a xerocytic form, BRITISH JOURNAL OF HAEMATOLOGY, Vol: 125, Pages: 521-527, ISSN: 0007-1048
- Author Web Link
- Cite
- Citations: 9
Bain BJ, Goldman JM, Lucie NP, et al., 2004, Report on slide session, British Society for Haematology, 43rd Annual Scientific Meeting, Glasgow, 2003, CLINICAL AND LABORATORY HAEMATOLOGY, Vol: 26, Pages: 87-93, ISSN: 0141-9854
Dahl KN, Parthasarathy R, Westhoff CM, et al., 2004, Protein 4.2 is critical to CD47-membrane skeleton attachment in human red cells, BLOOD, Vol: 103, Pages: 1131-1136, ISSN: 0006-4971
- Author Web Link
- Cite
- Citations: 37
Ofori-Acquah SF, Lalloz MRA, Serjeant G, et al., 2004, Dominant influence of gamma-globin promoter polymorphisms on fetal haemoglobin expression in sickle cell disease, CELLULAR AND MOLECULAR BIOLOGY, Vol: 50, Pages: 35-42, ISSN: 0145-5680
- Author Web Link
- Cite
- Citations: 11
Politou M, Terpos E, Szydlo R, et al., 2003, Role of RankL, osteoprotegerin and macrophage inflammatory protein-1 alpha in monoclonal gammopathy of undetermined significance (MGUS)., 45th Annual Meeting of the American-Society-of-Hematology, Publisher: AMER SOC HEMATOLOGY, Pages: 442A-442A, ISSN: 0006-4971
Bain BJ, Vassiliou G, Owen R, et al., 2003, British Society for Haematology Slide Session, Annual Scientific Meeting, Harrogate, 2001, CLINICAL AND LABORATORY HAEMATOLOGY, Vol: 25, Pages: 1-8, ISSN: 0141-9854
Clarke JL, Vulliamy TJ, Roper D, et al., 2003, Combined glucose-6-phosphate dehydrogenase and glucosephosphate isomerase deficiency can alter clinical outcome, BLOOD CELLS MOLECULES AND DISEASES, Vol: 30, Pages: 258-263, ISSN: 1079-9796
- Author Web Link
- Cite
- Citations: 5
Bruce LJ, Ghosh S, King MJ, et al., 2002, Absence of CD47 in protein 4.2-deficient hereditary spherocytosis in man: an interaction between the Rh complex and the band 3 complex, BLOOD, Vol: 100, Pages: 1878-1885, ISSN: 0006-4971
- Author Web Link
- Cite
- Citations: 89
Samyn M, Dhawan A, Layton M, et al., 2002, Giant cell hepatitis with Coombs' positive haemolytic anaemia in childhood: A single centre experience, JOURNAL OF HEPATOLOGY, Vol: 36, Pages: 263-263, ISSN: 0168-8278
Hadzic N, Layton M, Baker A, et al., 2002, Multiorgan and acute liver failure related to haemophagocytic lymphohistiocytosis in children, JOURNAL OF HEPATOLOGY, Vol: 36, Pages: 263-263, ISSN: 0168-8278
Layton M, Lalloz M, Lambert C, et al., 2001, Resolution of the locus for familial haemophagocytic lymphohistiocytosis on chromosome 9 and identification of perforin gene mutation in virus-associated haemophagocytic syndrome., BLOOD, Vol: 98, Pages: 505A-505A, ISSN: 0006-4971
Bruce LJ, Ghosh S, King MJ, et al., 2001, Severe deficiency of CD47 and reduction of RHAG associated with the absence of protein 4.2 in the red blood cell membrane., BLOOD, Vol: 98, Pages: 10A-10A, ISSN: 0006-4971
- Author Web Link
- Cite
- Citations: 2
Ofori-Acquah SF, Green BN, Davies SC, et al., 2001, Mass spectral analysis of asymmetric hemoglobin hybrids:: Demonstration of Hb FS (α<sub>2</sub>γβ<SUP>s</SUP>) in sickle cell disease, ANALYTICAL BIOCHEMISTRY, Vol: 298, Pages: 76-82, ISSN: 0003-2697
- Author Web Link
- Cite
- Citations: 13
Samyn M, Dhawan A, Layton M, et al., 2001, Giant cell hepatitis with Coombs' positive haemolytic anaemia in childhood: A single centre experience., HEPATOLOGY, Vol: 34, Pages: 528A-528A, ISSN: 0270-9139
Ofori-Acquah SF, Lalloz MRA, Layton DM, 2001, Nucleotide variation regulates the level of enhancement by hypersensitive site 2 of the β-globin locus control region, BLOOD CELLS MOLECULES AND DISEASES, Vol: 27, Pages: 803-811, ISSN: 1079-9796
- Author Web Link
- Cite
- Citations: 10
Wild BJ, Green BN, Cooper EK, et al., 2001, Rapid identification of hemoglobin variants by electrospray ionization mass spectrometry, BLOOD CELLS MOLECULES AND DISEASES, Vol: 27, Pages: 691-704, ISSN: 1079-9796
- Author Web Link
- Cite
- Citations: 87
This data is extracted from the Web of Science and reproduced under a licence from Thomson Reuters. You may not copy or re-distribute this data in whole or in part without the written consent of the Science business of Thomson Reuters.