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Investigation of biomarkers in esophageal squamous cell carcinomaChung, Man-fai, Yvonne. January 2009 (has links)
Thesis (Ph. D.)--University of Hong Kong, 2010. / Includes bibliographical references (leaves 121-150). Also available in print.
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Gene expression biomarkers for colorectal neoplasia /LaPointe, Lawrence Charles, January 2008 (has links)
Thesis (Ph. D.)--Flinders University, School of Medicine, Dept. of Medicine. / Typescript bound. Includes bibliographical references (leaves 308-361). Also available electronically via the World Wide Web.
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Tumour marker CA-50 in pancreatic cancerPålsson, Birger. January 1993 (has links)
Thesis (doctoral)--Lund University, 1993. / Added t.p. with thesis statement inserted.
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Tumour marker CA-50 in pancreatic cancerPålsson, Birger. January 1993 (has links)
Thesis (doctoral)--Lund University, 1993. / Added t.p. with thesis statement inserted.
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Investigation of biomarkers in esophageal squamous cell carcinomaChung, Man-fai, Yvonne., 鍾文暉. January 2009 (has links)
published_or_final_version / Surgery / Doctoral / Doctor of Philosophy
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identification of potential tumor markers and suppressor genes by cDNA microarray data mining and high-throughput gene expression in hepatocellular carcinomaPeng, Chung-Min 28 July 2003 (has links)
Hepatocellular carcinoma (HCC) is one of the most common malignant tumors in the world, especially in Asia and Africa countries. The distribution pattern shows geographical variation and pathogesis in multifactors as environment, infection, nutrition, metabolism, and endocrine contribute to hepatocarcinogenesis. Alpha fetal protein (AFP), the major tumor marker used at present accounts only 50% HCC diagnostic efficiency. This study aims to identify potential tumor markers or suppressor genes for further application in early HCC diagnoses and treatments. Therefore we utilized available cDNA microarray databases in conjunction with other bioinformatic resources to identify our candidate genes related to HCCs. cDNA microarray technology and bioinformatic resources which enable investigators to obtain comprehensive data with respect to gene-expression profiles, is progressing rapidly. The Okabe¡¦s and Stanford¡¦s HCC database were our major data-mining material. A total of 85 potential tumor markers and 106 potential tumor suppressors were found via preliminary in silico datamining. We furthermore narrowed down to 14 candidate tumor markers and 7 candidate tumor suppressor genes by the way of quantitative RT-PCR technologies were applied in various HCC cancer cell lines and 21 patient¡¦s in pair, tumor/non-tumor tissues to confirm gene expression profile. The results revealed that 6 genes (PRO2000, PYGB, STMN1, AFM, C8FW, NNMT) conformed to our data-mining studies.
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A study of Twist and DJ-1 expressions and their clinical significance in renal cell carcinoma of clear cell typeLi, Tak-kin., 李德健. January 2010 (has links)
published_or_final_version / Medicine / Master / Master of Medical Sciences
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Protein expression in prostate cancer /Lexander, Helena, January 2006 (has links)
Diss. (sammanfattning) Stockholm : Karol. inst., 2006. / Härtill 4 uppsatser.
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Modulating liposomal stealth properties to evade RES and target tumorsMcNeeley, Kathleen Margaret. January 2008 (has links)
Thesis (Ph.D)--Biomedical Engineering, Georgia Institute of Technology, 2009. / Committee Chair: Ravi V. Bellamkonda; Committee Member: Ananth V. Annapragada; Committee Member: Andrew Lyon; Committee Member: Gang Bao; Committee Member: Niren Murthy. Part of the SMARTech Electronic Thesis and Dissertation Collection.
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Anti-p53 and c-erbB2 as prognostic markers in South African breast cancer patientsWinchester, Carolyn Margaret January 2000 (has links)
Thesis (DTech(Biomedical Technology))--Cape Technikon, Cape Town, 2000 / The diagnosis of breast cancer is not possible using currently available serological
detection of cancer markers as these lack adequate sensitivity or specificity. This study
investigates the prevalence and significance of anti-p53 antibody and c-erbB-2 protein in
the post-surgical sera of South African breast cancer patients and correlates these
features with the clinicopathological characteristics of breast cancer. Further, this study
investigates the possibilityofimproving prognostic sensitivityby combining the two subject
markers to monitor each patient. Further, this study will provide the opportunity to
investigate lNhether only certain types of breast cancer can elicit an immunological
response and at what stage and grade of tumour antibodies are present in the postoperative
serum. The study also establishes a foundation for determining in South Africa
lNhether there is a genetic influence in the response to p53 mutation and INhther this
response is higher in the indigenous African women compared to other South African
women. The purpose of the study is to determine if the resulting findings can be used to
enhance our ability to diagnose breast cancer and to identify node-negative breast cancer
patients at high risk for early disease recurrence and or death, for 1Nh0m adjuvant therapy
is unequivocally justified.
The study accrued 92 South African breast cancer patients who were essentially women
of colour 62 [67%] indigenous African women and 20 [22%] Caucasian of Indian descent,
6 [6%J of mixed [ColouredJ background and only 4 [4%J Caucasian of White descent. A
predominantly indigenous African populationwas chosen becausethey are the group most
likely to benefitfrom an easily repeatable, affordable serological cancer marker.
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