Zobrazeno 1 - 10
of 17
pro vyhledávání: '"D S, Millar"'
Autor:
A, Chetcuti, S H, Margan, P, Russell, S, Mann, D S, Millar, S J, Clark, J, Rogers, D J, Handelsman, Q, Dong
Publikováno v:
Cancer research. 61(17)
Annexin II mRNA coding for a calcium binding protein was found to be absent in prostate cancer by subtractive hybridization and Northern analysis. In contrast to high expression in normal and benign hyperplastic glandular and basal epithelium, Annexi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e4c789838aec956b90163420c2f0d388
https://pubmed.ncbi.nlm.nih.gov/11522620
https://pubmed.ncbi.nlm.nih.gov/11522620
Publikováno v:
Thrombosis and haemostasis. 78(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9ebd0225eaba9c6587b2c1f5a79f18d7
https://pubmed.ncbi.nlm.nih.gov/9198147
https://pubmed.ncbi.nlm.nih.gov/9198147
Publikováno v:
Thrombosis and haemostasis. 78(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2a4b6051cbe26eee685da26db91e5620
https://pubmed.ncbi.nlm.nih.gov/9198146
https://pubmed.ncbi.nlm.nih.gov/9198146
Autor:
C, Stirzaker, D S, Millar, C L, Paul, P M, Warnecke, J, Harrison, P C, Vincent, M, Frommer, S J, Clark
Publikováno v:
Cancer research. 57(11)
The retinoblastoma gene (Rb) is one of the best characterized tumor suppressor genes, and its inactivation is associated with a number of cancers. Previous studies have shown, by restriction enzyme analysis, that the promoter region of the Rb gene is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::66c1017fcc7a5aa492c8f6f457d76c83
https://pubmed.ncbi.nlm.nih.gov/9187126
https://pubmed.ncbi.nlm.nih.gov/9187126
Autor:
D A, Lane, T, Bayston, R J, Olds, A C, Fitches, D N, Cooper, D S, Millar, K, Jochmans, D J, Perry, K, Okajima, S L, Thein, J, Emmerich
Publikováno v:
Thrombosis and haemostasis. 77(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ab7b266033dfca349d1dc350babd684a
https://pubmed.ncbi.nlm.nih.gov/9031473
https://pubmed.ncbi.nlm.nih.gov/9031473
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 5(4)
A novel homozygous mutation in the protein C (PROC) gene was detected in an individual with severe type I protein C deficiency who presented with neonatal Purpura fulminans. The deletion/insertion mutation found [3351del4, 3350insA] resulted in an As
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1f39542ceeb8980689157997f9071a37
https://pubmed.ncbi.nlm.nih.gov/7841323
https://pubmed.ncbi.nlm.nih.gov/7841323
Autor:
C B, Grundy, F, Thomas, D S, Millar, M, Krawczak, E, Melissari, V, Lindo, E, Moffat, V V, Kakkar, D N, Cooper
Publikováno v:
Blood. 78(4)
Eight unrelated patients with recurrent thromboembolism, a family history of thrombosis, and plasma antithrombin III (ATIII) activity/antigen levels consistent with a diagnosis of heterozygous type I ATIII deficiency were studied by polymerase chain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::72f90c2a9630d947067e0164885848ee
https://pubmed.ncbi.nlm.nih.gov/1868237
https://pubmed.ncbi.nlm.nih.gov/1868237
Autor:
J K, Pattinson, D S, Millar, J H, McVey, C B, Grundy, K, Wieland, R S, Mibashan, U, Martinowitz, K, Tan-Un, M, Vidaud, M, Goossens
Publikováno v:
Blood. 76(11)
A directed-search strategy for point mutations in the factor VIII gene causing hemophilia A was used to screen eight potentially hypermutable CpG dinucleotides occurring at sites deemed to be of functional importance. Polymerase chain reaction-amplif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d2e19097885e3a323aa45a1d4652f661
https://pubmed.ncbi.nlm.nih.gov/1979502
https://pubmed.ncbi.nlm.nih.gov/1979502
Publikováno v:
Prenatal Diagnosis. 5:367-373
Samples of pure fetal blood from 116 fetuses of 15-21 weeks' gestation were obtained by direct vision fetoscopy. Ninety nine of these fetuses, presumed to be haematologically normal, were suitable for analysis. The data obtained show that the erythro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f54c006e7dbee653ad2ae32b88bc1657
https://doi.org/10.1002/pd.1970050602
https://doi.org/10.1002/pd.1970050602