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  • 1
    UID:
    almahu_9947381963202882
    Format: 1 online resource (97 pages) : , illustrations; digital, PDF file(s).
    ISBN: 9782889193806
    Series Statement: Frontiers Research Topics
    Content: In the past decade, significant progresses have taken place in the field of cancer immunotherapeutics. Tumor-targeting or adjuvant immunotherapies are being developed for most human cancers including melanoma, prostate cancer, glioblastoma, sarcoma, lung carcinoma and hepatocellular carcinoma. New immunotherapeutics, such as Ipilimumab (anti-CTLA-4), have finished human trials and are approved by the US Food and Drug Administration (FDA) for clinical treatment; cell-based immunotherapies such as adoptive cell transfer (ACT) have either been approved (i.e., sipuleucel-T) for the treatment of selected neoplastic malignancies or reached the stage of phase II/III clinical trials. Immunotherapetics has become a sophisticated field. Multimodal therapeutic regimens comprising several functional modules (up to 5 in the case of ACT) have been developed to provide more focused therapeutic responses with improved efficacy and reduced side effects. Despite the tremendous developments, a major challenge mains: the lack of effective and clinically-applicable methods. Due to the complex immunological responses of patients that involve both the organs with neoplastic lesion and the whole immune system, it is difficult to provide comprehensive assessment of therapeutic efficacy and mechanism in patients. Despite the rapid adaptation of advanced medical imaging modalities such as MRI and PET/CT scan and the gold standard pathological examination, there is still unmet demand in the clinic to best evaluate cancer-specific cellular immunity and functions. Flow cytometry analysis has modernized hematology and immunology, and is currently being adapted to clinical immune monitoring through a multi-center endeavour in the US. The study aims to normalize, standardize, and implement flow cytometry-based cellular immunity assay in routine clinical tests. In parallel, new technologies including single cell polyfunctional analysis and immunophenotyping microchip are being developed for rapid, informative, and longitudinal monitoring of immune response to anti-cancer treatment in the clinical settings, shedding new light to future clinical trials of cancer immunotherapies. These technologies were designed to address the major challenges caused by the complexity and functional heterogeneity of cancer biology and cellular immunity, and allow for comprehensive survey of both tumor and the immune system to identify their mechanistic interplay in response to cancer immunotherapy. In addition, new computational tools are required to integrate high dimensional data sets from comprehensive, single-cell level measurements of patient’s immune responses and render most accurate and definitive diagnostic decision facilitated by new immune monitoring tools. This new generation of informative, personalized clinical diagnostic tools will likely contribute to new understanding of therapy mechanism, pre-treatment stratification of patients, ongoing therapeutic monitoring and assessment.
    Note: Bibliographic Level Mode of Issuance: Monograph , English
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    UID:
    gbv_624588076
    Format: 432 S , Ill
    Edition: Mikrofiche-Ausg. 2 Mikrofiches
    Note: Paris, Univ., Diss., 2005
    Language: French
    Keywords: Hochschulschrift
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    Online Resource
    Online Resource
    Qing dao
    UID:
    gbv_1812540760
    Format: 19 Seiten
    Edition: Online-Ausgabe Bei jing 2012 1 Online-Ressource Min guo tu shu shu ju ku = Early Twentieth Century Book in China, 1911-1949. tu shu ; yi qi
    Original writing title: 美丽的青岛
    Original writing publisher: 青岛 : 青岛市繁荣促进会
    Content: 收风景图片44幅. 有说明.
    Note: Pinyin-Umschrift und Langzeichen wurden automatisiert erstellt , System requirements: Internet browser, Acrobat reader with Adobe simplified Chinese fonts.
    Language: Chinese
    Library Location Call Number Volume/Issue/Year Availability
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  • 4
    UID:
    edocfu_9958106863302883
    Format: 1 online resource (97 pages) : , illustrations; digital, PDF file(s).
    ISBN: 9782889193806
    Series Statement: Frontiers Research Topics
    Content: In the past decade, significant progresses have taken place in the field of cancer immunotherapeutics. Tumor-targeting or adjuvant immunotherapies are being developed for most human cancers including melanoma, prostate cancer, glioblastoma, sarcoma, lung carcinoma and hepatocellular carcinoma. New immunotherapeutics, such as Ipilimumab (anti-CTLA-4), have finished human trials and are approved by the US Food and Drug Administration (FDA) for clinical treatment; cell-based immunotherapies such as adoptive cell transfer (ACT) have either been approved (i.e., sipuleucel-T) for the treatment of selected neoplastic malignancies or reached the stage of phase II/III clinical trials. Immunotherapetics has become a sophisticated field. Multimodal therapeutic regimens comprising several functional modules (up to 5 in the case of ACT) have been developed to provide more focused therapeutic responses with improved efficacy and reduced side effects. Despite the tremendous developments, a major challenge mains: the lack of effective and clinically-applicable methods. Due to the complex immunological responses of patients that involve both the organs with neoplastic lesion and the whole immune system, it is difficult to provide comprehensive assessment of therapeutic efficacy and mechanism in patients. Despite the rapid adaptation of advanced medical imaging modalities such as MRI and PET/CT scan and the gold standard pathological examination, there is still unmet demand in the clinic to best evaluate cancer-specific cellular immunity and functions. Flow cytometry analysis has modernized hematology and immunology, and is currently being adapted to clinical immune monitoring through a multi-center endeavour in the US. The study aims to normalize, standardize, and implement flow cytometry-based cellular immunity assay in routine clinical tests. In parallel, new technologies including single cell polyfunctional analysis and immunophenotyping microchip are being developed for rapid, informative, and longitudinal monitoring of immune response to anti-cancer treatment in the clinical settings, shedding new light to future clinical trials of cancer immunotherapies. These technologies were designed to address the major challenges caused by the complexity and functional heterogeneity of cancer biology and cellular immunity, and allow for comprehensive survey of both tumor and the immune system to identify their mechanistic interplay in response to cancer immunotherapy. In addition, new computational tools are required to integrate high dimensional data sets from comprehensive, single-cell level measurements of patient’s immune responses and render most accurate and definitive diagnostic decision facilitated by new immune monitoring tools. This new generation of informative, personalized clinical diagnostic tools will likely contribute to new understanding of therapy mechanism, pre-treatment stratification of patients, ongoing therapeutic monitoring and assessment.
    Note: Bibliographic Level Mode of Issuance: Monograph , English
    Language: English
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  • 5
    UID:
    edoccha_9958106863302883
    Format: 1 online resource (97 pages) : , illustrations; digital, PDF file(s).
    ISBN: 9782889193806
    Series Statement: Frontiers Research Topics
    Content: In the past decade, significant progresses have taken place in the field of cancer immunotherapeutics. Tumor-targeting or adjuvant immunotherapies are being developed for most human cancers including melanoma, prostate cancer, glioblastoma, sarcoma, lung carcinoma and hepatocellular carcinoma. New immunotherapeutics, such as Ipilimumab (anti-CTLA-4), have finished human trials and are approved by the US Food and Drug Administration (FDA) for clinical treatment; cell-based immunotherapies such as adoptive cell transfer (ACT) have either been approved (i.e., sipuleucel-T) for the treatment of selected neoplastic malignancies or reached the stage of phase II/III clinical trials. Immunotherapetics has become a sophisticated field. Multimodal therapeutic regimens comprising several functional modules (up to 5 in the case of ACT) have been developed to provide more focused therapeutic responses with improved efficacy and reduced side effects. Despite the tremendous developments, a major challenge mains: the lack of effective and clinically-applicable methods. Due to the complex immunological responses of patients that involve both the organs with neoplastic lesion and the whole immune system, it is difficult to provide comprehensive assessment of therapeutic efficacy and mechanism in patients. Despite the rapid adaptation of advanced medical imaging modalities such as MRI and PET/CT scan and the gold standard pathological examination, there is still unmet demand in the clinic to best evaluate cancer-specific cellular immunity and functions. Flow cytometry analysis has modernized hematology and immunology, and is currently being adapted to clinical immune monitoring through a multi-center endeavour in the US. The study aims to normalize, standardize, and implement flow cytometry-based cellular immunity assay in routine clinical tests. In parallel, new technologies including single cell polyfunctional analysis and immunophenotyping microchip are being developed for rapid, informative, and longitudinal monitoring of immune response to anti-cancer treatment in the clinical settings, shedding new light to future clinical trials of cancer immunotherapies. These technologies were designed to address the major challenges caused by the complexity and functional heterogeneity of cancer biology and cellular immunity, and allow for comprehensive survey of both tumor and the immune system to identify their mechanistic interplay in response to cancer immunotherapy. In addition, new computational tools are required to integrate high dimensional data sets from comprehensive, single-cell level measurements of patient’s immune responses and render most accurate and definitive diagnostic decision facilitated by new immune monitoring tools. This new generation of informative, personalized clinical diagnostic tools will likely contribute to new understanding of therapy mechanism, pre-treatment stratification of patients, ongoing therapeutic monitoring and assessment.
    Note: Bibliographic Level Mode of Issuance: Monograph , English
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
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  • 6
    UID:
    gbv_1036197115
    Format: 2, 2, 232 S. , 图
    Original writing title: 苏州作家研究
    Original writing person/organisation: 徐国强
    Original writing publisher: 上海 : 复旦大学出版社
    ISBN: 9787309061796
    Note: 附参考文献、附索引 , SBB-PK Berlin
    Language: Chinese
    Library Location Call Number Volume/Issue/Year Availability
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  • 7
    UID:
    gbv_1036197034
    Format: 2, 3, 234 S. , 图
    Original writing title: 苏州作家研究
    Original writing person/organisation: 徐国强
    Original writing publisher: 上海 : 复旦大学出版社
    ISBN: 9787309061796
    Note: 附参考文献、附索引 , SBB-PK Berlin
    Language: Chinese
    Library Location Call Number Volume/Issue/Year Availability
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  • 8
    Book
    Book
    bei jing
    UID:
    gbv_1038825636
    Format: 3,3,298 S.
    Original writing title: 新闻评论学
    Original writing person/organisation: 范荣康
    Original writing publisher: 北京 : 人民日报出版社
    ISBN: 7800020347
    Note: SBB-PK Berlin
    Language: Chinese
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  • 9
    Book
    Book
    chong qing, si chuan
    UID:
    gbv_1038769817
    Format: 2,5,450 S.
    Original writing title: 四十年间
    Original writing person/organisation: 范荣康
    Original writing publisher: 重庆 : 重庆出版社
    ISBN: 7536617186
    Content: 本书共分四辑, 是作者1945年至1985年发表过的新闻通讯和新闻评论. 内容主要反映了解放前至粉碎 '四人帮' 后不同时期的社会生活
    Note: SBB-PK Berlin
    Language: Chinese
    Library Location Call Number Volume/Issue/Year Availability
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  • 10
    Book
    Book
    Paris : L'Harmattan
    UID:
    gbv_543980391
    Format: 248 S. , 22 cm
    ISBN: 2296029698 , 9782296029699
    Series Statement: Critiques littéraires
    Note: Includes bibliographical references (p. [235]-243) , Teilw. zugl.: Paris, Univ. Paris 8, Diss., 2005 u.d.T.: Fan, Rong: La rélation frère-soeur chez Marguerite Duras
    Language: French
    Subjects: Romance Studies
    RVK:
    Keywords: Duras, Marguerite 1914-1996 ; Geschwister ; Inzest ; Ödipuskomplex ; Aufsatzsammlung ; Hochschulschrift
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