Recent publications published by researchers at the MRC WIMM.
The Molecular Basis for Phenotypic Diversity of Genetic Disease
WEATHERALL DJ., (1995), Annals of the New York Academy of Sciences, 758, 245 - 260
The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains.
Hughes J. et al, (1995), Nat Genet, 10, 151 - 160
Novel reagents for chemical cleavage at abasic sites and UV photoproducts in DNA.
McHugh PJ. and Knowland J., (1995), Nucleic Acids Res, 23, 1664 - 1670
Increased expression of CD44v6 and CD44v3 in ulcerative colitis but not colonic Crohn's disease.
Rosenberg WM. et al, (1995), Lancet, 345, 1205 - 1209
Functions of fibroblast growth factors and their receptors.
Wilkie AO. et al, (1995), Curr Biol, 5, 500 - 507
Repeated ECS differentially affects rat brain 5-HT1A and 5-HT2A receptor expression.
Burnet PW. et al, (1995), Neuroreport, 6, 901 - 904
Contrasting effects of alpha and beta globin regulatory elements on chromatin structure may be related to their different chromosomal environments.
Craddock CF. et al, (1995), EMBO J, 14, 1718 - 1726
Bone marrow transplantation. Review articles must accurately reflect current practice.
Rule SA. et al, (1995), BMJ, 310
Processing of major histocompatibility class I-restricted antigens in the endoplasmic reticulum.
Elliott T. et al, (1995), J Exp Med, 181, 1481 - 1491
Regulation of growth and dissemination of a human lymphoma by CD44 splice variants.
Bartolazzi A. et al, (1995), J Cell Sci, 108 ( Pt 4), 1723 - 1733
The molecular basis for phenotypic variability of the common thalassaemias
Weatherall D., (1995), Molecular Medicine Today, 1, 15 - 20
Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome).
Gibbons RJ. et al, (1995), Cell, 80, 837 - 845
Saethre-Chotzen syndrome associated with balanced translocations involving 7p21: three further families.
Wilkie AO. et al, (1995), J Med Genet, 32, 174 - 180
Thalassaemia in Vanuatu, south-west Pacific: frequency and haematological phenotypes of young children.
Ganczakowski M. et al, (1995), Br J Haematol, 89, 485 - 495
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome.
Wilkie AO. et al, (1995), Nat Genet, 9, 165 - 172
CD44 isoforms containing exon V3 are responsible for the presentation of heparin-binding growth factor.
Bennett KL. et al, (1995), J Cell Biol, 128, 687 - 698
Genes encoded in the major histocompatibility complex affecting the generation of peptides for TAP transport.
Cerundolo V. et al, (1995), Eur J Immunol, 25, 554 - 562
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes.
Rutland P. et al, (1995), Nat Genet, 9, 173 - 176