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    • 3. 发明授权
    • HPV E6, E7 MRNA assay and methods of use thereof
    • HPV E6,E7 MRNA测定及其使用方法
    • US08653250B2
    • 2014-02-18
    • US12645202
    • 2009-12-22
    • Bruce K. Patterson
    • Bruce K. Patterson
    • C07H21/04
    • C12Q1/708C12Q1/6841C12Q2600/158G06F19/00
    • Provided is an HPV E6, E7 mRNA assay, referenced herein as the “In Cell HPV Assay,” that is capable of sensitive and specific detection of normal cervical cells undergoing malignant transformation as well as abnormal cervical cells with pre-malignant or malignant lesions. The In Cell HPV Assay identifies HPV E6, E7 mRNA via in situ hybridization with oligonucleotides specific for HPV E6, E7 mRNA and quantitates the HPV E6, E7 mRNA via flow cytometry. The In Cell HPV Assay can be carried out in less than three hours directly from liquid-based cervical (“LBC”) cytology specimens. The In Cell HPV Assay provides an efficient and highly sensitive alternative to the Pap smear for determining abnormal cervical cytology.
    • 提供了HPV E6,E7mRNA测定法,其在本文中被称为“In Cell HPV Assay”,其能够敏感和特异性检测经历恶性转化的正常宫颈细胞以及具有恶性前或恶性病变的异常宫颈细胞。 In Cell HPV Assay通过与HPV E6,E7 mRNA特异性寡核苷酸的原位杂交鉴定HPV E6,E7 mRNA,并通过流式细胞术定量HPV E6,E7 mRNA。 In Cell HPV Assay可以在不到三个小时的时间内直接从液体宫颈(“LBC”)细胞学标本中进行。 In Cell HPV Assay提供了一种有效和高度敏感的替代方法,用于确定宫颈细胞学异常的Pap涂片。
    • 4. 发明申请
    • HPV E6, E7 MRNA Assay and Methods of Use Thereof
    • HPV E6,E7 MRNA测定及其使用方法
    • US20100120021A1
    • 2010-05-13
    • US12645202
    • 2009-12-22
    • Bruce K. Patterson
    • Bruce K. Patterson
    • C12Q1/70
    • C12Q1/708C12Q1/6841C12Q2600/158G06F19/00
    • Provided is an HPV E6, E7 mRNA assay, referenced herein as the “In Cell HPV Assay,” that is capable of sensitive and specific detection of normal cervical cells undergoing malignant transformation as well as abnormal cervical cells with pre-malignant or malignant lesions. The In Cell HPV Assay identifies HPV E6, E7 mRNA via in situ hybridization with oligonucleotides specific for HPV E6, E7 mRNA and quantitates the HPV E6, E7 mRNA via flow cytometry. The In Cell HPV Assay can be carried out in less than three hours directly from liquid-based cervical (“LBC”) cytology specimens. The In Cell HPV Assay provides an efficient and highly sensitive alternative to the Pap smear for determining abnormal cervical cytology.
    • 提供了HPV E6,E7mRNA测定法,其在本文中被称为“In Cell HPV Assay”,其能够敏感和特异性检测经历恶性转化的正常宫颈细胞以及具有恶性前或恶性病变的异常宫颈细胞。 In Cell HPV Assay通过与HPV E6,E7 mRNA特异性寡核苷酸的原位杂交鉴定HPV E6,E7 mRNA,并通过流式细胞术定量HPV E6,E7 mRNA。 In Cell HPV Assay可以在不到三个小时的时间内直接从液体宫颈(“LBC”)细胞学标本中进行。 In Cell HPV Assay提供了一种有效和高度敏感的替代方法,用于确定宫颈细胞学异常的Pap涂片。
    • 5. 发明授权
    • Method of testing adequacy of cells in a specimen
    • 测试样本中细胞充分性的方法
    • US06939687B2
    • 2005-09-06
    • US10341094
    • 2003-01-13
    • Bruce K. Patterson
    • Bruce K. Patterson
    • G01N15/14G01N33/50C12Q1/04C12N13/00C12Q1/02
    • G01N33/5005G01N15/14
    • The present invention provides a device and method for determining the adequacy of squamous (ectocervical) cells, columnar (endocervical) cells, neutrophils, and noncellular material in a liquid based cytology specimen. The invention first analyzes a liquid based cytology specimen using light scatter to create a light scatter characteristic representing a predetermined cell. Next the invention determines the presence of squamous (ectocervical) cells versus columnar (endocervical) cells versus neutrophils versus noncellular material using the results of the light scatter. The light scatter characteristic that may be used may be forward light scatter, side light scatter, or both side and forward light scatter.
    • 本发明提供了一种用于确定液体细胞学样本中鳞状(宫颈外)细胞,柱状(宫颈内)细胞,嗜中性粒细胞和非细胞材料的适宜性的装置和方法。 本发明首先分析使用光散射的基于液体的细胞学标本,以产生表示预定细胞的光散射特性。 接下来,本发明使用光散射的结果确定鳞状(宫颈外)细胞与柱状(子宫颈内)细胞对嗜中性粒细胞与非细胞材料的存在。 可以使用的光散射特性可以是向前的光散射,侧面光散射或者两侧和向前的光散射。
    • 7. 发明申请
    • HPV E6, E7 mRNA ASSAY AND METHODS OF USE THEREOF
    • HPV E6,E7 mRNA测定及其使用方法
    • US20090220945A1
    • 2009-09-03
    • US12391634
    • 2009-02-24
    • Bruce K. Patterson
    • Bruce K. Patterson
    • C12Q1/70
    • C12Q1/708C12Q1/6841C12Q2600/158G06F19/00
    • Provided is an HPV E6, E7 mRNA assay, referenced herein as the “In Cell HPV Assay,” that is capable of sensitive and specific detection of normal cervical cells undergoing malignant transformation as well as abnormal cervical cells with pre-malignant or malignant lesions. The In Cell HPV Assay identifies HPV E6, E7 mRNA via in situ hybridization with oligonucleotides specific for HPV E6, E7 mRNA and quantitates the HPV E6, E7 mRNA via flow cytometry. The In Cell HPV Assay can be carried out in less than three hours directly from liquid-based cervical (“LBC”) cytology specimens. The In Cell HPV Assay provides an efficient and highly sensitive alternative to the Pap smear for determining abnormal cervical cytology.
    • 提供了HPV E6,E7mRNA测定法,其在本文中被称为“In Cell HPV Assay”,其能够敏感和特异性检测经历恶性转化的正常宫颈细胞以及具有恶性前或恶性病变的异常宫颈细胞。 In Cell HPV Assay通过与HPV E6,E7 mRNA特异性寡核苷酸的原位杂交鉴定HPV E6,E7 mRNA,并通过流式细胞术定量HPV E6,E7 mRNA。 In Cell HPV Assay可以在不到三个小时的时间内直接从液体宫颈(“LBC”)细胞学标本中进行。 In Cell HPV Assay提供了一种有效和高度敏感的替代方法,用于确定宫颈细胞学异常的Pap涂片。