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1.发明授权Nucleotide and amino acid sequences, and assays and methods of use thereof for diagnosis 有权核苷酸和氨基酸序列，以及用于诊断的测定及其使用方法公开(公告)号：US07842459B2
公开(公告)日：2010-11-30
申请号：US11051646
申请日：2005-01-27
申请人： Michal Ayalon-Soffer , Sarah Pollock , Ronen Shemesh , Rotem Sorek , Zurit Levine , Zipi Shaqed , Amir Toporik , Gad S. Cojocaru , Dvir Dahary , Guy Kol , Pinchas Akiva , Amit Novik , Sergey Nemzer , Alexander Diber , Maxim Shklar , Osnat Sella-Tavor , Lily Bazak , Ariel Farkash , Yossi Cohen
发明人： Michal Ayalon-Soffer , Sarah Pollock , Ronen Shemesh , Rotem Sorek , Zurit Levine , Zipi Shaqed , Amir Toporik , Gad S. Cojocaru , Dvir Dahary , Guy Kol , Pinchas Akiva , Amit Novik , Sergey Nemzer , Alexander Diber , Maxim Shklar , Osnat Sella-Tavor , Lily Bazak , Ariel Farkash , Yossi Cohen
CPC分类号： C12Q1/6886 , C12Q2600/156
摘要： Novel splice variant nucleic acid sequences. The novel splice variants and their nucleic acid sequences according to the present invention may optionally be used for diagnosis of a variant-detectable disease as described herein.
摘要翻译： 新型剪接变体核酸序列。 根据本发明的新型剪接变体及其核酸序列可任选地用于诊断如本文所述的变体可检测的疾病。
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2.发明申请Novel nucleotide and amino acid sequences, and assays and methods of use thereof for diagnosis 有权新型核苷酸和氨基酸序列，以及用于诊断的测定和方法公开(公告)号：US20100120022A1
公开(公告)日：2010-05-13
申请号：US11051646
申请日：2005-01-27
申请人： Michal Ayalon-Soffer , Sarah Pollock , Ronen Shemesh , Rotem Sorek , Zurit Levine , Zipi Shaqed , Amir Toporik , Gad S. Cojocaru , Dvir Dahary , Guy Kol , Pinchas Akiva , Amit Novik , Sergey Nemzer , Alexander Diber , Maxim Shklar , Osnat Sella-Tavor , Lily Bazak , Ariel Farkash , Yossi Cohen
发明人： Michal Ayalon-Soffer , Sarah Pollock , Ronen Shemesh , Rotem Sorek , Zurit Levine , Zipi Shaqed , Amir Toporik , Gad S. Cojocaru , Dvir Dahary , Guy Kol , Pinchas Akiva , Amit Novik , Sergey Nemzer , Alexander Diber , Maxim Shklar , Osnat Sella-Tavor , Lily Bazak , Ariel Farkash , Yossi Cohen
CPC分类号： C12Q1/6886 , C12Q2600/156
摘要： Novel splice variant nucleic acid sequences. The novel splice variants and their nucleic acid sequences according to the present invention may optionally be used for diagnosis of a variant-detectable disease as described herein.
摘要翻译： 新型剪接变体核酸序列。 根据本发明的新型剪接变体及其核酸序列可任选地用于诊断如本文所述的变体可检测的疾病。
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