Publications
204 results found
Modell B, Khan M, Darlison M, et al., 2001, A national register for surveillance of inherited disorders:: β thalassaemia in the United Kingdom, BULLETIN OF THE WORLD HEALTH ORGANIZATION, Vol: 79, Pages: 1006-1013, ISSN: 0042-9686
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- Citations: 44
Bain BJ, Swirsky D, Bhavnani, et al., 2001, British Society for Haematology Slide Session, Annual Scientific Meeting of BSH, Bournemouth, 2000, Clin Lab Haematol, Vol: 23, Pages: 1-5
Old J, Petrou M, Varnavides L, et al., 2000, Accuracy of prenatal diagnosis for haemoglobin disorders in the UK: 25 years' experience, PRENATAL DIAGNOSIS, Vol: 20, Pages: 986-991, ISSN: 0197-3851
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- Citations: 24
Tung J, Hadzic N, Layton M, et al., 2000, Bone marrow failure in children with acute liver failure, JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, Vol: 31, Pages: 557-561, ISSN: 0277-2116
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- Citations: 39
Chowdhury MR, Herrmann FH, Schroder W, et al., 2000, Factor VIII gene polymorphisms in the Asian Indian population, HAEMOPHILIA, Vol: 6, Pages: 625-630, ISSN: 1351-8216
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- Citations: 22
Modell B, Harris R, Lane B, et al., 2000, Informed choice in genetic screening for thalassaemia during pregnancy: audit from a national confidential inquiry, BMJ-BRITISH MEDICAL JOURNAL, Vol: 320, Pages: 337-341, ISSN: 1756-1833
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- Citations: 84
Millar DS, Elliston L, Deex P, et al., 2000, Molecular analysis of the genotype-phenotype relationship in factor X deficiency, HUMAN GENETICS, Vol: 106, Pages: 249-257, ISSN: 0340-6717
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- Citations: 67
Ofori-Acquah SF, Lalloz MRA, Layton DM, 1999, Transcriptional regulation by haplotype-specific LCR-HS2 and <SUP>G</SUP>γ promoter alleles reveals distinct mechanisms for persistent gamma-globin expression on β<SUP>S</SUP> chromosomes., BLOOD, Vol: 94, Pages: 197A-197A, ISSN: 0006-4971
Ationu A, Humphries A, Lalloz MRA, et al., 1999, Reversal of metabolic block in glycolysis by enzyme replacement in triosephosphate isomerase-deficient cells, BLOOD, Vol: 94, Pages: 3193-3198, ISSN: 0006-4971
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- Citations: 22
Lambert C, Layton DM, Lalloz MRA, 1999, Maternal somatic mosaicism for a novel factor VIII gene mutation, JOURNAL OF MEDICAL GENETICS, Vol: 36, Pages: S99-S99, ISSN: 0022-2593
Thompson LJ, Lalloz MRA, Layton DM, 1999, Unique and recurrent WAS gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia, BLOOD CELLS MOLECULES AND DISEASES, Vol: 25, Pages: 218-226, ISSN: 1079-9796
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- Citations: 13
Humphries A, Ationu A, Wild B, et al., 1999, The consequence of nucleotide substitutions in the triosephosphate isomerase (TPI) gene promoter, BLOOD CELLS MOLECULES AND DISEASES, Vol: 25, Pages: 210-217, ISSN: 1079-9796
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- Citations: 7
Humphries A, Ationu A, Lalloz MRA, et al., 1999, Ancestral origin of variation in the triosephosphate isomerase gene promoter, HUMAN GENETICS, Vol: 104, Pages: 486-491, ISSN: 0340-6717
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- Citations: 8
Ationu A, Humphries A, Wild B, et al., 1999, Towards enzyme-replacement treatment in triosephosphate isomerase deficiency, LANCET, Vol: 353, Pages: 1155-1156, ISSN: 0140-6736
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- Citations: 8
Layton DM, Lambert CT, Ribases M, et al., 1999, Hereditary microcytic anaemia due to a defect of cellular iron utilisation: A novel disorder., BRITISH JOURNAL OF HAEMATOLOGY, Vol: 105, Pages: 80-80, ISSN: 0007-1048
Hillmen P, Richards SJ, Baker AJ, et al., 1999, Congenital paroxysmal nocturnal haemoglobinuria, BRITISH JOURNAL OF HAEMATOLOGY, Vol: 105, Pages: 64-64, ISSN: 0007-1048
Wild BJ, Green BN, Lalloz MRA, et al., 1999, Molecular characterisation of hybrid haemoglobins by mass spectrometry, BRITISH JOURNAL OF HAEMATOLOGY, Vol: 105, Pages: 81-81, ISSN: 0007-1048
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- Citations: 2
Erten S, Ofori-Acquah SF, Boothe H, et al., 1999, <i>In vivo</i> globin switching and identification of zinc finger proteins in human fetal erythroid cells., BRITISH JOURNAL OF HAEMATOLOGY, Vol: 105, Pages: 65-65, ISSN: 0007-1048
Ohadi M, Lalloz MRA, Sham P, et al., 1999, Localisation of a gene at chromosome 9q21.3-22 and evidence for locus heterogeneity in familial haemophagocytic lymphohistiocytosis., BRITISH JOURNAL OF HAEMATOLOGY, Vol: 105, Pages: 65-65, ISSN: 0007-1048
Lambert CT, Thompson LJ, Lalloz MRA, et al., 1999, Prenatal diagnosis of factor VII and factor X deficiencies by combined analysis of F7 and F10 gene polymorphisms., BRITISH JOURNAL OF HAEMATOLOGY, Vol: 105, Pages: 36-36, ISSN: 0007-1048
Hickman M, Modell B, Greengross P, et al., 1999, Mapping the prevalence of sickle cell and beta thalassaemia in England: estimating and validating ethnic-specific rates, BRITISH JOURNAL OF HAEMATOLOGY, Vol: 104, Pages: 860-867, ISSN: 0007-1048
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- Citations: 70
Ofori-Acquah SF, Lalloz MRA, Layton DM, 1999, Localisation of <i>cis</i> regulatory elements at the β-globin locus:: Analysis of hybrid haplotype chromosomes, BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, Vol: 254, Pages: 181-187, ISSN: 0006-291X
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- Citations: 18
Ohadi M, Lalloz MRA, Sham P, et al., 1999, Localization of a gene for familial hemophagocytic lymphohistiocytosis at chromosome 9q21.3-22 by homozygosity mapping, AMERICAN JOURNAL OF HUMAN GENETICS, Vol: 64, Pages: 165-171, ISSN: 0002-9297
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- Citations: 155
Ationu A, Humphries A, Layton DM, 1999, Regulation of triosephosphate isomerase (TPI) gene expression in TPI deficient lymphoblastoid cells, INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, Vol: 3, Pages: 21-24, ISSN: 1107-3756
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- Citations: 3
Wonke B, Jensen C, Hanslip JJ, et al., 1998, Genetic and acquired predisposing factors and treatment of osteoporosis in thalassaemia major, JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, Vol: 11, Pages: 795-801, ISSN: 0334-018X
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- Citations: 61
Hillmen P, Richards SJ, Baker AJ, et al., 1998, Congenital paroxysmal nocturnal haemoglobinuria., BLOOD, Vol: 92, Pages: 154A-154A, ISSN: 0006-4971
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- Citations: 2
Hollan S, Layton M, Horanyi M, et al., 1998, Decrease in plasmalogen content in triosephosphate isomerase (TPI) deficiency: A potential target for therapy., BLOOD, Vol: 92, Pages: 6B-6B, ISSN: 0006-4971
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- Citations: 2
Ofori-Acquah SF, Green BN, Wild BJ, et al., 1998, Quantification of <SUP>G</SUP>γ- and <SUP>A</SUP>γ-globins by electrospray ionisation mass spectrometry, INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, Vol: 2, Pages: 451-453, ISSN: 1107-3756
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- Citations: 4
Tung J, Hadzic N, Layton M, et al., 1998, Aplastic anemia associated with fulminant liver failure in children., HEPATOLOGY, Vol: 28, Pages: 495A-495A, ISSN: 0270-9139
McVey JH, Boswell EJ, Takamiya O, et al., 1998, Exclusion of the first EGF domain of factor VII by a splice site mutation causes lethal factor VII deficiency, BLOOD, Vol: 92, Pages: 920-926, ISSN: 0006-4971
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- Citations: 39
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