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1 / 68,884
1.1020230150219ECOSYSTEM EXTINCTION RISK DIAGNOSIS SYSTEM AND OPERATING METHOD THEREOF
KR - 30.10.2023
Int.Class G06Q 50/26
GPHYSICS
06COMPUTING; CALCULATING OR COUNTING
QINFORMATION AND COMMUNICATION TECHNOLOGY SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES; SYSTEMS OR METHODS SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES, NOT OTHERWISE PROVIDED FOR
50Information and communication technology specially adapted for implementation of business processes of specific business sectors, e.g. utilities or tourism
10Services
26Government or public services
 Appl.No 1020230051968 Applicant 고려대학교 산학협력단 Inventor LEE MINYOUNG
The present invention relates to an ecosystem extinction risk diagnosis system and an operating method thereof. The operating method of the ecosystem extinction risk diagnosis system, according to an embodiment of the present invention, comprises the steps of: (a) selecting, as areas to be evaluated, one or more locations where one or more endangered species appear among a plurality of species included in a specific ecosystem; (b) for each of the areas to be evaluated, constructing a first food web network for the specific ecosystem; (c) for each of the areas to be evaluated, constructing an extinction scenario including an extinction sequence, in which the endangered species sequentially become extinct, for the plurality of species included in the specific ecosystem based on the probability of extinction of the endangered species; (d) performing an extinction simulation according to the extinction scenario to generate a second food web network for the specific ecosystem; (e) analyzing the first food web network and the second food web network according to certain analysis indicators; (f) based on result values for each of the analysis indicators, quantifying amounts of structural changes in the first food web network and the second food web network to calculate an integrated ecosystem extinction risk index; and (g) evaluating an impact to the ecosystem due to species extinction based on the integrated ecosystem extinction risk index. COPYRIGHT KIPO 2024
2.101200368*CLIMATE CHANGE VULNERABILITY EVALUATION SYSTEM AND A METHOD FOR THE SAME CAPABLE OF VERIFYING FACTORS OF CLIMATE CHANGE VULNERABILITY
KR - 06.11.2012
Int.Class G01W 1/00
GPHYSICS
01MEASURING; TESTING
WMETEOROLOGY
1Meteorology
 Appl.No 1020120044730 Applicant Inventor YU, JEONG AH
PURPOSE: A climate change vulnerability evaluation system and a method for the same are provided to support local governments to set segmented items of climate change adaptation policies. CONSTITUTION: A climate change vulnerability evaluation method includes the following steps: climate change variables are segmented and saved; sensitivity variables, which represent the influence of the climate change variables, are segmented and saved; adaptation capability variables for reducing the influence of the climate change variables and sensitivity variables are segmented and saved; boundary data for administrative districts is saved; respective climate change variables, sensitivity variables, and adaptation capability variables for respective administrative districts are obtained; proxy variables for the respective climate change variables, sensitivity variables, and adaptation capability are saved; weighted values for the respective climate change variables, sensitivity variables, and adaptation capability and for the proxy variables are saved; the proxy variable is standardized; vulnerability is obtained using the standardized proxy value and the weighted values; the vulnerability is standardized; vulnerabilities are compared by administrative district; and the variables, vulnerabilities, and information of the administrative districts are displayed. COPYRIGHT KIPO 2013 null [Reference numerals] (AA) Evaluation item selection(preparation tasks:developing the standardization methodology of vulnerability); (BB) Top-down methodology; (CC) Bottom-top methodology; (EE) Downscaling; (GG) Climate data deduction according to 6 scenarios; (HH) Data establishment for manufacturing proxy variables; (II) Expert interview and reference research; (JJ) Proxy variable selection; (KK) Proxy variable weighed value setting; (LL) Delphi analysis(first time, second time); (MM) Proxy variable standardization and vulnerability index calculation; (NN) Standardization and vulnerability evaluation formula application; (OO) Vulnerability index calculation; (PP) Vulnerability evaluation result mapping(applying to cities in the whole country)
3.1016567440000*ORYZIAS JAVANICUS GENE RESPONSIVE TO EXPOSURE TO TRICLOSAN, AND METHOD FOR DIAGNOSING AQUATIC ENVIRONMENT CONTAMINATION BY USING SAME
KR - 19.09.2016
Int.Class C12Q 1/68
CCHEMISTRY; METALLURGY
12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
1Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
68involving nucleic acids
 Appl.No 1020160024104 Applicant 한국해양과학기술원 Inventor YUM, SEUNG SHIC
The present invention relates to an Oryzias javanicus gene responsive to the exposure to triclosan (TCS), and to a method for diagnosing an aquatic environment contamination by using the same. In particular, Oryzias javanicus is cultured, and is exposed to TCS at a concentration of 6 g/L for 12, 24, 48, and 72 hours. Then, RNA is separated therefrom, and cDNA is synthesized. Also, the cDNA is hybridized by marking the same using Cy3 and Cy5, and an oligo-miroarray is produced for analyzing the cDNA. As a result, it has been confirmed that the expressions are changed in: 93 genes (29 genes increased, 64 genes decreased, refer to Table 1) in a group exposed for 12 hours; 60 genes (19 genes increased, 41 genes decreased, refer to Table 2) in a group exposed for 24 hours; 61 genes (21 genes increased, 40 genes decreased, refer to Table 3) in a group exposed for 48 hours; and 67 genes (22 genes increased, 45 genes decreased, refer to Table 4) in a group exposed for 72 hours. Moreover, by sorting total 183 genes (58 genes increased, 125 genes decreased, refer to Table 5 and Table 6) after excluding overlapping genes, the genes can be useful as biomarkers capable of confirming exposure to TCS. COPYRIGHT KIPO 2016
4.101388629*GENETIC MARKER FOR IDENTIFICATION OF WILD-TYPE OR CULTIVATED-TYPE OF NEOFINETIA FALCATA AND WILD-TYPE OR CULTIVATED-TYPE IDENTIFICATION METHOD USING SAME
KR - 17.04.2014
Int.Class C12Q 1/68
CCHEMISTRY; METALLURGY
12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
1Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
68involving nucleic acids
 Appl.No 1020130113573 Applicant Inventor HAN, JEONG EUN
The present invention relates to a genetic marker for an identification of a wild-type or a cultivated-type of Neofinetia falcate and a wild-type or a cultivated-type identification method using the same, and provides the genetic marker for an identification of a wild-type or a cultivated-type of Neofinetia falcate, which comprises single nucleotide polymorphism (SNP) of a 214^th nucleotide in a C201 genetic fragment of Neofinetia falcate of a sequence number one. In addition, provided is the wild-type or cultivated-type identification method using a single nucleotide polymorphism marker analyzing each SNP genotype (A and G) to genetically predict and judge a classification of a wild-type and a cultivated-type. COPYRIGHT KIPO 2014 [Reference numerals] (AA) Cultivation 1; (BB) Cultivation 2; (CC) Wild-type 1; (DD) Wild-type 2; (EE) G type; (FF) A Type
5.1016567480000*ORYZIAS JAVANICUS GENE RESPONSIVE TO EXPOSURE TO PERFLUOROOCTANE SULFONATE, AND METHOD FOR DIAGNOSING AQUATIC ENVIRONMENT CONTAMINATION BY USING SAME
KR - 19.09.2016
Int.Class C12Q 1/68
CCHEMISTRY; METALLURGY
12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
1Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
68involving nucleic acids
 Appl.No 1020160024110 Applicant 한국해양과학기술원 Inventor YUM, SEUNG SHIC
The present invention relates to an Oryzias javanicus gene responsive to the exposure to perfluorooctane sulfonate (PFOS), and to a method for diagnosing an aquatic environment contamination by using the same. In particular, Oryzias javanicus is cultured, and is exposed to PFOS at a concentration of 90 g/L for 12, 24, 48, and 72 hours. Then, RNA is separated therefrom, and cDNA is synthesized. Also, the cDNA is hybridized by marking the same using Cy3 and Cy5, and an oligo-miroarray is produced for analyzing the cDNA. As a result, it has been confirmed that the expressions are changed in: 35 genes (17 genes increased, 18 genes decreased) in a group exposed for 12 hours; 60 genes (41 genes increased, 19 genes decreased) in a group exposed for 24 hours; 39 genes (17 genes increased, 22 genes decreased) in a group exposed for 48 hours; and 38 genes (17 genes increased, 21 genes decreased) in a group exposed for 72 hours. Moreover, it has been confirmed that total 126 genes (68 genes increased, 58 genes decreased) excluding overlapping genes have changed expression amounts by exposure to PFOS, so the genes can be useful as biomarkers capable of confirming exposure to PFOS. COPYRIGHT KIPO 2016
6.1020210019303LIFE SUPPORT SYSTEM AND METHOD OF OPERATION THEREOF
KR - 22.02.2021
Int.Class A01K 63/00
AHUMAN NECESSITIES
01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
KANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
63Receptacles for live fish, e.g. aquaria; Terraria
 Appl.No 1020190098334 Applicant 국립생태원 Inventor JANG, JI DEOK
The present invention relates to a technical idea of collecting the state of a water tank in real time so as to monitor the state of aquatic life, and monitoring the same in real time from the center. A life support system according to one embodiment comprises: a life support device unit that collects state data on individual equipment installed in a marine exhibition hall using at least one sensor; a network unit that integrates the collected state data and transmits the data to a monitoring server; and a monitoring unit that controls a display device to display the state data transmitted to the monitoring server. COPYRIGHT KIPO 2021
7.101693285*HYDRA GENE RESPONSIVE TO TRICLOSAN EXPOSURE, AND METHOD FOR DIAGNOSING AQUATIC ENVIRONMENTAL CONTAMINATION BY USING SAME
KR - 06.01.2017
Int.Class C12Q 1/68
CCHEMISTRY; METALLURGY
12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
1Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
68involving nucleic acids
 Appl.No 1020160070845 Applicant 한국해양과학기술원 Inventor 염승식
The present invention relates to a Hydra (Hydra magnipapillata) gene responsive to triclosan (TCS) exposure, and to a method for diagnosing aquatic environmental contamination by using the same. In particular, triclosan is exposed at a concentration of 7.35 g/L for 6 hours, 24 hours, and 48 hours by culturing Hydra, and RNA is separated therefrom. Then, cDNA is synthesized, and marking is performed by Cy3 and Cy5, so hybridization is performed. An oligo-microarray is produced, and as a result of analyzing the same, it has been confirmed that an expression amount of 32 genes (20 increases, 12 decreases) is changed in a triclosan 6-hour exposed group by triclosan exposure, 10 genes (9 increases, 1 decrease) in a 24-hour exposed group, and 114 genes (22 increases, 92 decreases) in a 48-hour exposed group. Accordingly, the 156 genes can be useful as biomarkers for confirming triclosan exposure. COPYRIGHT KIPO 2017
8.101695979*FISH TRAP FOR CAPTURING NEUSTON
KR - 13.01.2017
Int.Class A01K 69/00
AHUMAN NECESSITIES
01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
KANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
69Stationary catching devices for fishing
 Appl.No 1020160023872 Applicant 공주대학교 산학협력단 Inventor 유영한
The present invention relates to a fish trap for capturing neuston, which comprises: a first structure including a first frame to which a plurality of supporting bars are connected, a mesh covering an outer side of the first frame, and an attracting object formed on an upper part of the mesh; a triangular frame connected to the attracting object so as to attract neuston; a second structure positioned on an upper part of the triangular frame and including a radial second frame and a light-blocking film covering the second frame. The first structure includes a buoyant body generating buoyancy, so that some portions of the first structure protrude out on the water surface. COPYRIGHT KIPO 2017
9.2003795000000*사물 학습용 카드
KR - 18.03.2005
Int.Class G09B 19/00
GPHYSICS
09EDUCATING; CRYPTOGRAPHY; DISPLAY; ADVERTISING; SEALS
BEDUCATIONAL OR DEMONSTRATION APPLIANCES; APPLIANCES FOR TEACHING, OR COMMUNICATING WITH, THE BLIND, DEAF OR MUTE; MODELS; PLANETARIA; GLOBES; MAPS; DIAGRAMS
19Teaching not covered by other main groups of this subclass
 Appl.No 2020040035522 Applicant Inventor 최희수
본 고안은, 사물 학습용 카드에 관한 것으로서, 전면과 배면 중 일측면에는 사물을 사실적으로 묘사한 실제 이미지가 도시되고, 전면과 배면 중 타측면에는 이미지와 동일한 외곽선을 갖는 실루엣 이미지가 도시된다. 이에 의해, 학습자가 실루엣 이미지를 통해 실제 이미지를 상상하게 되어 학습자의 상상력을 자극하고, 보다 다양한 정보를 다양한 방법으로 제공받으므로, 학습자의 흥미를 지속시킴에 따라, 학습의욕을 고취시켜 학습효과를 향상시킬 수 있다.
10.1020180097756ＣＡＳ9 단백질의 다중-주기 전기천공법에 의한 유전자 조작된 비-사람 포유동물
KR - 31.08.2018
Int.Class C12N 15/87
CCHEMISTRY; METALLURGY
12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
15Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
09Recombinant DNA-technology
87Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
 Appl.No 1020187023409 Applicant 더 잭슨 래보라토리 Inventor 왕, 하오이
본원에 기술된 발명은 Cas9 단백질을 포함하는 CRISPR/Cas9 시스템을 생식세포 또는 착상전 단계 배아(예를 들면, 1개-세포 배아 또는 접합체)내로 다수 주기(예를 들면, 4 내지 10회 주기)의 전기천공법을 통해 도입하여, 동물의 게놈내로 유전적으로 유전되는 변형을 유도함을 통해 유전자도입 동물(예컨대, 비-사람 포유동물)을 생성하기 위한 고 처리량 방법 및 시약을 제공한다.
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