Search International and National Patent Collections
Some content of this application is unavailable at the moment.
If this situation persists, please contact us atFeedback&Contact
1. (WO2017090915) PNA PROBE FOR DETECTING HEREDITARY HEARING LOSS, AND METHOD FOR DETECTING HEREDITARY HEARING LOSS USING SAME
Latest bibliographic data on file with the International Bureau

Pub. No.: WO/2017/090915 International Application No.: PCT/KR2016/012733
Publication Date: 01.06.2017 International Filing Date: 07.11.2016
IPC:
C12Q 1/68 (2006.01)
C CHEMISTRY; METALLURGY
12
BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
Q
MEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
1
Measuring or testing processes involving enzymes or micro-organisms; Compositions therefor; Processes of preparing such compositions
68
involving nucleic acids
Applicants:
주식회사 시선바이오머티리얼스 SEASUNBIO MATERIALS CO., LTD. [KR/KR]; 대전광역시 유성구 테크노1로 11-3 N517호 #N517, 11-3, Techno 1-ro, Yuseong-gu, Daejeon 34015, KR
Inventors:
송민식 SONG, Minsik; KR
박희경 PARK, Hee Kyung; KR
김경탁 KIM, Kyung Tak; KR
Agent:
특허법인 플러스 PLUS INTERNATIONAL IP LAW FIRM; 대전광역시 서구 한밭대로 809 10층 10F, 809, Hanbat-daero, Seo-gu, Daejeon 35209, KR
Priority Data:
10-2015-016625226.11.2015KR
Title (EN) PNA PROBE FOR DETECTING HEREDITARY HEARING LOSS, AND METHOD FOR DETECTING HEREDITARY HEARING LOSS USING SAME
(FR) SONDE D'ANP POUR DÉTECTER UNE PERTE AUDITIVE HÉRÉDITAIRE ET PROCÉDÉ POUR DÉTECTER DE PERTE AUDITIVE HÉRÉDITAIRE L'UTILISANT
(KO) 유전성 난청 검출용 PNA 프로브 및 이를 이용한 유전성 난청 검출방법
Abstract:
(EN) The present invention relates to a peptide nucleic acid (PNA) probe for detecting hereditary hearing loss, and a method for detecting hereditary hearing loss using the same. It is expected that the PNA probe for detecting hereditary hearing loss and the method for detecting hereditary hearing loss using the same, according to the present invention, would allow genes associated with hearing loss or mutants thereof to be quickly and simply discriminated, and can be used to diagnose hereditary hearing loss at an early stage and diagnose non-syndromic hearing loss and a degree of risk using 11 mutations of GJB2, SLC26A4, 12S rRNA, CDH23 and TMPRSS3 genes which are the main causes of hereditary hearing loss.
(FR) La présente invention concerne une sonde d'acide nucléique peptidique (ANP) pour détecter une perte auditive héréditaire et un procédé pour détecter une perte auditive héréditaire l'utilisant. Selon l'invention, la sonde d'ANP pour détecter une perte auditive héréditaire et le procédé pour détecter une perte auditive héréditaire l'utilisant permettraient la discrimination rapide et simple de gènes associés à la perte auditive ou de leurs mutants et peuvent être utilisés pour diagnostiquer une perte auditive héréditaire à un stade précoce et pour diagnostiquer une perte auditive non syndromique et un degré de risque au moyen de 11 mutations des gènes GJB2, SLC26A4, 12S ARNr, CDH23 and TMPRSS3, qui sont les principales causes d'une perte auditive héréditaire.
(KO) 본 발명은 유전성 난청 검출용 PNA(Peptide Nucleic Acid) 프로브 및 이를 이용한 유전성 난청 검출방법에 관한 것이다. 본 발명에 따른 유전성 난청 검출용 PNA 프로브 및 이를 이용한 유전성 난청 검출방법을 통해 난청과 관련된 유전자 또는 그 변이체를 신속 간단하게 판별할 수 있으며, 유전성 난청의 주요한 원인이 되는 GJB2, SLC26A4, 12S rRNA, CDH23 및 TMPRSS3 유전자의 돌연변이 11개를 이용하여 유전성 난청을 조기에 진단하고 비증후군성 난청 및 위험도를 진단하는데 활용될 수 있을 것으로 기대된다.
front page image
Designated States: AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW
African Regional Intellectual Property Organization (ARIPO) (BW, GH, GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW)
Eurasian Patent Organization (AM, AZ, BY, KG, KZ, RU, TJ, TM)
European Patent Office (AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR)
African Intellectual Property Organization (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, KM, ML, MR, NE, SN, TD, TG)
Publication Language: Korean (KO)
Filing Language: Korean (KO)
Also published as:
CN108291260