Recent publications published by researchers at the MRC WIMM.
The Regulation of the Differential Expression of the Human Globin Genes During Development
WEATHERALL DJ., (1986), Journal of Cell Science, 1986, 319 - 336
The relationship between the common mutations of the alpha gene cluster and its evolutionary history.
Weatherall DJ. et al, (1986), Prog Clin Biol Res, 218, 47 - 62
Prenatal diagnosis of the common haemoglobin disorders.
Weatherall DJ. et al, (1985), Journal of Medical Genetics, 22, 422 - 430
Direct cloning of specific genomic DNA sequences in plasmid libraries following fragment enrichment.
Nicholls RD. et al, (1985), Nucleic Acids Res, 13, 7569 - 7578
Relative roles of genetic factors, dietary deficiency, and infection in anaemia in Vanuatu, South-West Pacific.
Bowden DK. et al, (1985), Lancet, 2, 1025 - 1028
A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16.
Reeders ST. et al, (1985), Nature, 317, 542 - 544
Recombination within the human embryonic xi-globin locus: a common xi-xi chromosome produced by gene conversion of the psi xi gene.
Hill AV. et al, (1985), Cell, 42, 809 - 819
Cytotoxic T cells recognize fragments of the influenza nucleoprotein.
Townsend AR. et al, (1985), Cell, 42, 457 - 467
A new method for the rapid purification of both the membrane-bound and released forms of the variant surface glycoprotein from Trypanosoma brucei.
Jackson DG. et al, (1985), Biochem J, 230, 195 - 202
Acute splenic sequestration in homozygous sickle cell disease: natural history and management.
Emond AM. et al, (1985), J Pediatr, 107, 201 - 206
Rearrangement of the T-cell-receptor beta-chain gene in the diagnosis of lymphoproliferative disorders.
O'Connor NT. et al, (1985), Lancet, 1, 1295 - 1297
A genetic marker for elevated levels of haemoglobin F in homozygous sickle cell disease?
Wainscoat JS. et al, (1985), Br J Haematol, 60, 261 - 268
Alpha zero-thalassemia due to recombination between the alpha 1-globin gene and an AluI repeat.
Nicholls RD. et al, (1985), Blood, 65, 1434 - 1438
Analysis of Globin Gene Inversion Reveals Similarities with Immunoglobulin Rearrangement
JENNINGS MW. et al, (1985), Annals of the New York Academy of Sciences, 445, 212 - 217
Clinical presentation of homozygous sickle cell disease.
Bainbridge R. et al, (1985), J Pediatr, 106, 881 - 885
First Trimester Diagnosis of the Hemoglobin Disorders
OLD JM. et al, (1985), Annals of the New York Academy of Sciences, 445, 349 - 356
Vascular occlusion and infarction in sickle cell crisis and the sickle chest syndrome.
Athanasou NA. et al, (1985), J Clin Pathol, 38, 659 - 664
a thalassaemia in British people
Higgs DR. et al, (1985), British Medical Journal (Clinical research ed.), 290
Alpha thalassaemia in British people.
Higgs DR. et al, (1985), Br Med J (Clin Res Ed), 290, 1303 - 1306
Alpha thalassemia changes erythrocyte heterogeneity in sickle cell disease.
Noguchi CT. et al, (1985), J Clin Invest, 75, 1632 - 1637