Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Marie Anne J. O'Reilly"'
Publikováno v:
Development. 125:3887-3894
Brachyury is a member of the T-box gene family and is required for formation of posterior mesoderm and notochord during vertebrate development. The ability of Brachyury to activate transcription is essential for its biological function, but nothing i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43e8ae1f224ab1c57f0df73ff69df0d5
https://doi.org/10.1242/dev.125.19.3887
https://doi.org/10.1242/dev.125.19.3887
Autor:
C. Ross Pinkerton, Barry A. Gusterson, Marie-Anne J. O'reilly, Kathryn Pritchard Jones, Aidan McManus, Janet Shipley, Chris Mitchell
Publikováno v:
The Journal of Pathology. 178:410-414
The identification of t(2;13)(q35;q14) is a useful aid in the accurate diagnosis of rhabdomyosarcoma, distinguishing it from other small round cell tumours and supporting the distinction between alveolar and embryonal forms. Cytogenetic analysis is d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::728f2db1430bfcd7d1c38cc1c5708956
https://doi.org/10.1002/(sici)1096-9896(199604)178:4<410::aid-path508>3.0.co
https://doi.org/10.1002/(sici)1096-9896(199604)178:4<410::aid-path508>3.0.co
Autor:
Lesley A. Alterman, Roland J. Levinsky, Christine Kinnon, S. Malcolm, Marie-Anne J. O'Reilly, Jantine Zijlstra
Publikováno v:
Genomics. 15:275-282
The Xq22 region of the human X chromosome encompasses the loci of several genes and random DNA markers whose relative positions have not been determined. By a combination of PFGE mapping and the analysis of a selected panel of X chromosome radiation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74ccb4d42baecf0f2357b70ba5630be2
https://doi.org/10.1006/geno.1993.1057
https://doi.org/10.1006/geno.1993.1057
Publikováno v:
Blood. 76:820-824
The molecular basis of X-linked chronic granulomatous disease (X-CGD) has recently been elucidated and the defective gene identified and isolated. Two restriction fragment-length polymorphisms have been identified using the X-CGD cDNA probe. We have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a994d6e246a1346bb5585bc9b6e39fa
https://doi.org/10.1182/blood.v76.4.820.bloodjournal764820
https://doi.org/10.1182/blood.v76.4.820.bloodjournal764820
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:
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:
Roland J. Levinsky, Sue Malcolm, Christine Kinnon, Lesley A. Alterman, Marie-Anne J. O'Reilly
Publikováno v:
Human Genetics. 90
The X-linked agammaglobulinaemia (XLA) gene locus has previously been mapped to Xq22. Genetic linkage analysis has shown tight linkage between the disease and the DXS178 locus and that DXS3 and DXS94 are the closest proximal and distal flanking marke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0070858df5ac9cee17a67d31b57342fc
https://doi.org/10.1007/bf00220078
https://doi.org/10.1007/bf00220078
Publikováno v:
Journal of immunological methods. 131(1)
In this review, we have attempted to describe the methodology involved in PFGE mapping and to review how this technique has contributed to the mapping of the major histocompatibility loci, the multiply rearranging genes of the immunoglobulin heavy ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::061954d61e42df04ef6f03aaa73bcde4
https://pubmed.ncbi.nlm.nih.gov/2116481
https://pubmed.ncbi.nlm.nih.gov/2116481
Autor:
Helen Middleton-Price, Marie-Anne J. O'Reilly, Ruth C. Lovering, S. Malcolm, Angela K. Sweatman, Roland J. Levinsky, Sally Genet, Christine Kinnon
Publikováno v:
Europe PubMed Central
The gene responsible for X-linked agammaglobulinemia (XLA) has not been identified; however, in the course of genetic linkage studies designed to map the locus more precisely, a number of closely linked polymorphic loci have been identified. These ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7742094bc3aee32c99f8adda7b8b2f8
http://europepmc.org/abstract/med/8462977
http://europepmc.org/abstract/med/8462977
