Recent publications published by researchers at the MRC WIMM.
Alpha thalassemia and the hematology of homozygous sickle cell disease in childhood
Stevens MC. et al, (1986), Blood, 67, 411 - 414
DIRECT DETECTION OF HAEMOGLOBIN E WITH SYNTHETIC OLIGONUCLEOTIDES
Thein SL. et al, (1986), The Lancet, 327, 93 - 93
DIRECT MASS-SPECTROMETRIC STUDIES OF THE PYROLYSIS OF CARBONACEOUS FUELS .3. PRIMARY PYROLYSIS OF LIGNIN
EVANS RJ. et al, (1986), JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 9, 207 - 236
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