Zobrazeno 1 - 10 of 490 pro vyhledávání: '"D S, Millar"'
2
Loss of annexin II heavy and light chains in prostate cancer and its precursors
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
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5
Extensive DNA methylation spanning the Rb promoter in retinoblastoma tumors
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
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7
A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancy
Autor: D S, Millar, J, Allgrove, C, Rodeck, V V, Kakkar, D N, Cooper
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
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8
Recurrent deletion in the human antithrombin III gene
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
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9
The molecular genetic analysis of hemophilia A: a directed search strategy for the detection of point mutations in the human factor VIII gene
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
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10
Akademický článek
Integrative approach for classifying male tumors based on DNA methylation 450K data.
Autor: Wu, Ji-Ming1 (AUTHOR), Qiu, Wang-Ren1 (AUTHOR) qiuone@163.com, Liu, Zi1 (AUTHOR), Xu, Zhao-Chun1 (AUTHOR), Zhang, Shou-Hua2 (AUTHOR)
Publikováno v: Electronic Research Archive. 2023, Vol. 31 Issue 11, p1-19. 19p.
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