Pseudoautosomal linkage of familial Hodgkin's lymphoma: Molecular analysis of a unique family with Leri-Weill dyschondrosteosis and Hodgkins lymphoma [3]

British Journal of Haematology

Volumn 121, Issue 2, 2003, Pages 377-379

  Shears, Deborah J ^a   Endris, Volker ^b   Gokhale, David A ^c   Dearden, Simon P ^c   Radford, John A ^d   Rappold, Gudrun A ^b   Taylor, G Malcolm ^c  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY HOSPITAL HEIDELBERG   (Germany)

^c ST MARY S HOSPITAL   (United Kingdom)

^d CHRISTIE HOSPITAL   (United Kingdom)

Author keywords

Familial Hodgkin's lymphoma; Leri Weill dyschondrosteosis; PAR1 : pseudoautosomal region 1

Indexed keywords

CD99 ANTIGEN; GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR RECEPTOR; INTERLEUKIN 3 RECEPTOR; PROTEIN; PROTEIN MIC2; RECEPTOR SUBUNIT; UNCLASSIFIED DRUG;

CASE REPORT; DYSCHONDROSTEOSIS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE EXPRESSION; GENE STRUCTURE; GENETIC ANALYSIS; GENETIC LINKAGE; HODGKIN DISEASE; HUMAN; LETTER; MICROSATELLITE MARKER; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PSEUDOAUTOSOMAL REGION 1; REED STERNBERG CELL;

FEMALE; GENE DELETION; GENETIC PREDISPOSITION TO DISEASE; HODGKIN DISEASE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LINKAGE (GENETICS); OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PEDIGREE;

EID: 0038216939     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2003.04258.x     Document Type: Letter

References (6)

1. Ferraris, A.M., Racchi, O., Rapezzi, D., Gaetani, G.F. & Boffetta, P. (1997) Familial Hodgkin's disease: a disease of young adulthood? Annals of Hematology, 74, 131-134.
2. Gokhale, D.A., Evans, D.G., Crowther, D., Woll, P., Watson, C.J., Dearden, S.P., Fergusson, W.D., Stevens, R.F. & Taylor, G.M. (1995) Molecular genetic analysis of a family with a history of Hodgkin's disease and dyschondrosteosis. Leukemia, 9, 826-833.
3. Horowitz, M. & Wiernik, P.H. (1999) Pseudoautosomal linkage of Hodgkin disease. American Journal of Human Genetics, 65, 1413-1422.
4. Kim, S.H., Choi, E.Y., Shin, Y.K., Kim, T.J., Chung, D.H., Chang, S.I., Kim, N.K. & Park, S.H. (1998) Generation of cells with Hodgkin's and Reed-Sternberg phenotype through downregulation of CD99 (Mic2). Blood. 92, 4287-4295.
5. Lee, I., Kim, M.K., Choi, E.Y., Mehl, A., Jung, K.C., Gil, M.C., Rowe, M. & Park, S.H. (2001) CD99 expression is positively regulated by Sp1 and is negatively regulated by Epstein-Barr virus latent membrane protein 1 through nuclear factor-kB. Blood. 97, 596-604.
6. Shears, D.J., Vassal, H., Goodman, F.R., Palmer, R.W., Reardon, W., Superti-Furga, A., Scambler, P.J. & Winter, R.M. (1998) Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis. Nature Genetics, 19, 70-73.