序号 | 专利名 | 申请号 | 申请日 | 公开(公告)号 | 公开(公告)日 | 发明人 |
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181 | NOVEL METHOD | EP13808199.7 | 2013-12-17 | EP2931881A1 | 2015-10-21 | REIK, Wolf; PEAT, Julian; HORE, Timothy; KRUEGER, Christel |
The invention relates to a method of enhancing the potency of a cell (for example, to a totipotent state), by introducing a TET family gene, derivative or fragment thereof into the cell. The invention also relates to methods and kits for preparing cells with enhanced potency, and uses of said cells. | ||||||
182 | NOVEL CLASS OF GLYPHOSATE RESISTANCE GENES | EP13743493 | 2013-02-01 | EP2809144A4 | 2015-10-21 | LIRA JUSTIN M; CICCHILLO ROBERT M; NAIR SATISH K |
The present disclosure relates to nucleic acid molecules encoding a having 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) activity and transgenic plants, cells or tissues containing the same. | ||||||
183 | Plants having enhanced yield-related traits and a method for making the same | EP11192693.7 | 2008-05-02 | EP2505652B1 | 2015-10-14 | Sanz Molinero, Ana Isabel; Hatzfeld, Yves; Vandenabeele, Steven; Shirley, Amber; Darnielle, Lalitree; McKersie, Bryan; Frankard, Valerie |
The present invention relates generally to the field of molecular biology and concerns a method for enhancing yield-related traits and/or improving various plant growth characteristics by modulating expression in a plant of a nucleic acid encoding a GRP (Growth Regulating Protein). The GRP is selected from a LOB-domain comprising protein (LOB: Lateral Organ Boundaries), herein abbreviated as LBD polypeptide, a JMJC (JUMONJI-C) polypeptide, a CKI 10 (Casein Kinase I) polypeptide, a bHLH11-like (basic Helix-Loop-Helix 11) protein, a plant homeodomain finger-homeodomain (PHDf-HD) polypeptide, an ASR (abscisic acid-, stress-, and ripening-induced) polypeptide and/or a Squamosa promoter binding protein-like (SPL11) transcription factor polypeptide. The present invention also concerns plants having modulated expression of a nucleic acid encoding a GRP, which plants have improved growth characteristics relative to corresponding wild type plants or other control plants. The invention also provides novel GRP nucleic acids and GRP polypeptides as well as constructs useful in the methods of the invention. | ||||||
184 | METHOD OF MANUFACTURING DIFFERENTIATED PLURIPOTENT STEM CELL | EP13851495.5 | 2013-10-29 | EP2913396A1 | 2015-09-02 | KATO, Hidemasa; MORIYAMA, Yosuke; HIRAKI, Keiko; OKUDA, Akihiko |
The present invention allows a TET1 protein to be more stably expressed in human pluripotent stem cells than in the past by, inter alia, substituting the second amino acid from the amino terminal of a TET1 protein with a different amino acid. Furthermore upon differentiation of said pluripotent stem cells, it is possible to quickly eliminate the expression of, inter alia, NANOG, which is an inhibitor of differentiation and promote the expression of factors related to differentiation by introducing a variant TET1 protein to a pluripotent stem cell. The present invention provides a method for manufacturing pluripotent stem cells with increased differentiation potential, and a substance that is useful to said method. |
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185 | BIOLOGICAL METHOD FOR PRODUCING CIS-5-HYDROXY-L-PIPECOLINIC ACID | EP13804143.9 | 2013-06-12 | EP2873730A1 | 2015-05-20 | FUJII, Tadashi; TAMURA, Keisuke |
The present invention provides a method for producing cis-5-hydroxy-L-pipecolic acid. In the production method of the present invention, a gene recombinant microorganism enabling direct production of cis-5-hydroxy-L-pipecolic acid can be used. The present invention also provides such a gene recombinant microorganism. A preferred embodiment of the present invention is characterized in that a gene recombinant microorganism having DNAs encoding proteins involved in the biosynthesis of L-pipecolic acid and a DNA encoding a protein having the L-pipecolic acid cis-5-hydroxylase activity is cultured in a medium, and cis-5-hydroxy-L-pipecolic acid is collected from the medium. |
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186 | METHODS AND COMPOSITIONS FOR DISCRIMINATION BETWEEN CYTOSINE AND MODIFICATIONS THEREOF, AND FOR METHYLOME ANALYSIS | EP13715047.0 | 2013-03-14 | EP2825645A2 | 2015-01-21 | VAISVILA, Romualdas; JOHNSON, Heidi, Erika; VAINAUSKAS, Saulius; DAVIS, Theodore B. |
Compositions and methods are provided for discrimination between cytosine and modifications thereof using cytidine deaminases. Variants of wild type cytidine deaminases are described which show reduced bias with respect to adjacent nucleotides upstream of the cytosine. The methods provide a rapid and convenient use of enzymes to obtain methylomes. | ||||||
187 | SYNTHETIC BRASSICA-DERIVED CHLOROPLAST TRANSIT PEPTIDES | EP13744313.1 | 2013-02-01 | EP2809148A1 | 2014-12-10 | LIRA, Justin, M.; CICCHILLO, Robert, M.; YERKES, Carla; ROBINSON, Andrew, E. |
The present disclosure relates to nucleic acid molecules encoding a having 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) activity and transgenic plants, cells or tissues containing the same. | ||||||
188 | GLYPHOSATE RESISTANT PLANTS AND ASSOCIATED METHODS | EP13743263.9 | 2013-02-01 | EP2809143A1 | 2014-12-10 | LIRA, Justin M.; CICCHILLO, Robert M.; YERKES, Carla; ROBINSON, Andrew E. |
The present disclosure relates to nucleic acid molecules encoding a having 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) activity and transgenic plants, cells or tissues containing the same. | ||||||
189 | SYNTHETIC CHLOROPLAST TRANSIT PEPTIDES | EP13743027.8 | 2013-02-01 | EP2809142A1 | 2014-12-10 | LIRA, Justin M.; CICCHILLO, Robert M.; YERKES, Carla; ROBINSON, Andrew E. |
The present disclosure relates to nucleic acid molecules encoding a having 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) activity and transgenic plants, cells or tissues containing the same. | ||||||
190 | MICROORGANISM ABLE TO PRODUCE L-AMINO ACID, AND METHOD FOR PRODUCING L-AMINO ACID BY USING SAME | EP13733718.4 | 2013-01-07 | EP2801611A2 | 2014-11-12 | CHEONG, Ki Yong; LEE, Seok Myung; HWANG, Young Bin; LEE, Keun Cheol; LEE, Kwang Ho |
The present invention relates to a microorganism able to produce L-threonine or L-tryptophan, and to a method for producing L-threonine or L-tryptophan by using same. More specifically, the present invention relates to: recombinant Escherichia coli which is more efficient in producing L-threonine or L-tryptophan by increasing the ability to produce ATP which is used as the most plentiful energy source in cells when producing L-threonine or L-tryptophan; and a method for producing L-threonine or L-tryptophan by using same. |
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191 | Plants having enhanced yield-related traits and a method for making the same | EP09178578.2 | 2008-05-02 | EP2230310B1 | 2013-01-16 | Hatzfeld, Yves; Sanz Molinero, Ana Isabel; Shirley, Amber; Darnielle, Lalitree; Frankard, Valerie; Vandenabeele, Steven; McKersie, Bryan |
The present invention relates generally to the field of molecular biology and concerns a method for enhancing yield-related traits and/or improving various plant growth characteristics by modulating expression in a plant of a nucleic acid encoding a GRP (Growth Regulating Protein). The GRP is selected from a LOB-domain comprising protein (LOB: Lateral Organ Boundaries), herein abbreviated as LBD polypeptide, a JMJC (JUMONJI-C) polypeptide, a CKI 10 (Casein Kinase I) polypeptide, a bHLH11-like (basic Helix-Loop-Helix 11) protein, a plant homeodomain finger-homeodomain (PHDf-HD) polypeptide, an ASR (abscisic acid-, stress-, and ripening-induced) polypeptide and/or a Squamosa promoter binding protein-like (SPL11) transcription factor polypeptide. The present invention also concerns plants having modulated expression of a nucleic acid encoding a GRP, which plants have improved growth characteristics relative to corresponding wild type plants or other control plants. The invention also provides novel GRP nucleic acids and GRP polypeptides as well as constructs useful in the methods of the invention. | ||||||
192 | Plants having enhanced yield-related traits and a method for making the same | EP10181988.6 | 2008-05-02 | EP2316956A3 | 2011-08-24 | Sanz Molinero, Ana Isabel |
The present invention relates generally to the field of molecular biology and concerns a method for enhancing various economically important yield-related traits in plants. More specifically, the present invention concerns a method for enhancing yield-related traits in plants by modulating expression in a plant of a nucleic acid encoding a JMJC polypeptide. The present invention also concerns plants having modulated expression of a nucleic acid encoding a JMJC polypeptide, which plants have enhanced yield-related traits relative to control plants. The invention also provides constructs comprising JMJC nucleic acids, useful in performing the methods of the invention. |
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193 | CAS9 PROTEINS INCLUDING LIGAND-DEPENDENT INTEINS | PCT/US2015042770 | 2015-07-30 | WO2016022363A3 | 2016-05-26 | LIU DAVID R; DAVIS KEVIN |
Some aspects of this disclosure provide compositions, methods, systems, and kits for controlling the activity of RNA-programmable endonucleases, such as Cas9, or for controlling the activity of proteins comprising a Cas9 variant fused to a functional effector domain, such as a nuclease, nickase, recombinase, deaminase, transcriptional activator, transcriptional repressor, or epigenetic modifying domain. For example, the inventive proteins provided comprise a ligand-dependent intein, the presence of which inhibits one or more activities of the protein (e.g., gRNA binding, enzymatic activity, target DNA binding). The binding of a ligand to the intein results in self-excision of the intein, restoring the activity of the protein. | ||||||
194 | RNA-GUIDED TARGETING OF GENETIC AND EPIGENOMIC REGULATORY PROTEINS TO SPECIFIC GENOMIC LOCI | PCT/US2014027335 | 2014-03-14 | WO2014152432A3 | 2015-10-29 | JOUNG J KEITH; MAEDER MORGAN |
Methods and constructs for RNA-guided targeting of heterologous functional domains such as transcriptional activators to specific genomic loci. This invention relates to methods and constructs for RNA-guided targeting of genetic and epigenomic regulatory proteins, e.g., transcriptional activators, histone modification enzymes, DNA methylation modifiers, to specific genomic loci. At least in part, the present invention is based on the development of a fusion protein including a heterologous functional domain (e.g., a transcriptional activation domain) fused to a Cas9 nuclease that has had its nuclease activity inactivated by mutations (also known as "dCas9"). | ||||||
195 | USING TRUNCATED GUIDE RNAS (TRU-GRNAS) TO INCREASE SPECIFICITY FOR RNA-GUIDED GENOME EDITING | PCT/US2014029068 | 2014-03-14 | WO2014144592A3 | 2014-12-31 | JOUNG J KEITH; SANDER JEFFRY D; FU YANFANG; MAEDER MORGAN |
CRISPR-Cas genome editing uses a guide RNA, which includes both a complementarity region, which binds the target DNA by base- pairing, and a Cas9-binding region, to direct a Cas9 nuclease to a target DNA. Further disclosed are methods for increasing specificity of RNA-guided genome editing using CRISPR/Cas9 systems by using truncated guide RNAs (tru-gRNAs). | ||||||
196 | METHODS AND COMPOSITIONS FOR DISCRIMINATION BETWEEN CYTOSINE AND MODIFICATIONS THEREOF, AND FOR METHYLOME ANALYSIS | PCT/US2013031620 | 2013-03-14 | WO2013138644A3 | 2013-11-07 | VAISVILA ROMUALDAS; JOHNSON HEIDI ERIKA; VAINAUSKAS SAULIUS; DAVIS THEODORE B |
Compositions and methods are provided for discrimination between cytosine and modifications thereof using cytidine deaminases and/or oxygenases. Variants of wild type cytidine deaminases are described which show reduced bias with respect to adjacent nucleotides upstream of the cytosine. The methods provide a rapid and convenient use of enzymes to obtain methylomes. |