Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Linda A. D. Bradley"'
Autor:
Ruth C. Lovering, Christine Kinnon, F. Katz, Gareth J. Morgan, Roland J. Levinsky, Linda A. D. Bradley, Chaim M. Roifman, Hubert B. Gaspar
Publikováno v:
Human Molecular Genetics. 4:755-757
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9b8eec0354085c770bacf83a7a731b6
https://doi.org/10.1093/hmg/4.4.755
https://doi.org/10.1093/hmg/4.4.755
Autor:
Christine Kinnon, Roland J. Levinsky, Marie-Anne J. O'Reilly, Linda A. D. Bradley, Angela K. Sweatman, Ruth C. Lovering
Publikováno v:
Human genetics. 94(6)
We have produced physical maps of the proximal part of Xq22, containing the Bruton's tyrosine kinase (BTK) and alpha-galactosidase A (GLA) gene loci, using long range physical mapping techniques and yeast artificial chromosomes (YACs). These maps rev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::915729c51ed48e7cae304a3e8b1ccae3
https://pubmed.ncbi.nlm.nih.gov/7989038
https://pubmed.ncbi.nlm.nih.gov/7989038
Autor:
Roland J. Levinsky, Angela K. Sweatman, Christine Kinnon, Linda A. D. Bradley, Gareth Morgan, Alison Jones, Ruth C. Lovering
Publikováno v:
Human molecular genetics. 3(1)
The gene defective in X-linked agammaglobulinemia (XLA) has recently been isolated and identified as btk, a non-receptor protein tyrosine kinase. We have utilized the technique of single strand conformation polymorphism (SSCP) analysis for the btk ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d64b2d08b64c0a448868bf722304ea1
https://pubmed.ncbi.nlm.nih.gov/8162056
https://pubmed.ncbi.nlm.nih.gov/8162056
Autor:
Angela K. Sweatman, Helen Middleton-Price, Ruth C. Lovering, Sue Malcolm, Christine Kinnon, Roland J. Levinsky, Lesley A. Alterman, Marie-Anne J. O'Reilly, Gareth Morgan, M.H. Parkar, Sally Genet, Linda A. D. Bradley
Publikováno v:
Human molecular genetics. 2(2)
Genetic linkage analysis has been instrumental in mapping the gene for X-linked agammaglobulinemia (XLA) to the proximal long arm of the human X chromosome, to Xq22. Due to the relative rarity of this disease the localization of the gene within Xq22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::caca07624c0d47cf21a2a988f90596f3
https://pubmed.ncbi.nlm.nih.gov/8499902
https://pubmed.ncbi.nlm.nih.gov/8499902
Autor:
Linda A. D. Bradley, Lesley A. Alterman, M Tarlow, R.B. Thompson, Alison Jones, Christine Kinnon, Gareth Morgan
Publikováno v:
Archives of Disease in Childhood. 74:548-549
Typical X linked agammaglobulinaemia (XLA) is characterised by absence of immunoglobulin production and lack of mature B cells. The gene responsible for XLA has recently been identified, and codes for a B cell tyrosine kinase, BTK. A family affected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dce4f5b5568974a6f7f561a497875055
https://doi.org/10.1136/adc.74.6.548
https://doi.org/10.1136/adc.74.6.548