JP2014530004A5 - - Google Patents

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JP2014530004A5
JP2014530004A5 JP2014531947A JP2014531947A JP2014530004A5 JP 2014530004 A5 JP2014530004 A5 JP 2014530004A5 JP 2014531947 A JP2014531947 A JP 2014531947A JP 2014531947 A JP2014531947 A JP 2014531947A JP 2014530004 A5 JP2014530004 A5 JP 2014530004A5
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Japan
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compound
wing segment
modified
modified oligonucleotide
seq
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JP2014531947A
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Japanese (ja)
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JP2014530004A (ja
JP6092226B2 (ja
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Priority claimed from PCT/US2012/056249 external-priority patent/WO2013043817A1/en
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JP2014531947A 2011-09-20 2012-09-20 Ｇｃｇｒ発現のアンチセンス調整 Active JP6092226B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161537007P 2011-09-20 2011-09-20
US61/537,007 2011-09-20
PCT/US2012/056249 WO2013043817A1 (en) 2011-09-20 2012-09-20 Antisense modulation of gcgr expression

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2017020906A Division JP6538736B2 (ja) 2011-09-20 2017-02-08 Ｇｃｇｒ発現のアンチセンス調整

Publications (3)

Publication Number Publication Date
JP2014530004A JP2014530004A (ja) 2014-11-17
JP2014530004A5 true JP2014530004A5 (OSRAM) 2015-02-05
JP6092226B2 JP6092226B2 (ja) 2017-03-08

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JP2014531947A Active JP6092226B2 (ja) 2011-09-20 2012-09-20 Ｇｃｇｒ発現のアンチセンス調整
JP2017020906A Active JP6538736B2 (ja) 2011-09-20 2017-02-08 Ｇｃｇｒ発現のアンチセンス調整

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JP2017020906A Active JP6538736B2 (ja) 2011-09-20 2017-02-08 Ｇｃｇｒ発現のアンチセンス調整

Country Status (16)

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US (2) US8865674B2 (OSRAM)
EP (2) EP3401401B1 (OSRAM)
JP (2) JP6092226B2 (OSRAM)
KR (1) KR101840512B1 (OSRAM)
CN (2) CN108410868A (OSRAM)
AU (2) AU2012312433B2 (OSRAM)
BR (1) BR112014006587B1 (OSRAM)
CA (1) CA2849273C (OSRAM)
DK (1) DK2758533T3 (OSRAM)
ES (2) ES2673721T3 (OSRAM)
IL (1) IL231560B (OSRAM)
IN (1) IN2014CN02736A (OSRAM)
MX (1) MX353322B (OSRAM)
NO (1) NO2925947T3 (OSRAM)
RU (1) RU2598709C2 (OSRAM)
WO (1) WO2013043817A1 (OSRAM)

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CN108026529A (zh) * 2015-09-30 2018-05-11 Ionis制药公司 组合疗法
MA46089A (fr) 2016-08-30 2019-07-10 Regeneron Pharma Procédés de traitement de la résistance à l'insuline grave par interférence avec la signalisation du récepteur du glucagon
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