KR840004944A - 미생물을 이용한 α- 및 β-인터페론의 제조방법 - Google Patents
미생물을 이용한 α- 및 β-인터페론의 제조방법 Download PDFInfo
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- KR840004944A KR840004944A KR1019830002362A KR830002362A KR840004944A KR 840004944 A KR840004944 A KR 840004944A KR 1019830002362 A KR1019830002362 A KR 1019830002362A KR 830002362 A KR830002362 A KR 830002362A KR 840004944 A KR840004944 A KR 840004944A
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- interferon
- cdna
- cells
- rna
- biosynthesis
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
- C12N15/1096—Processes for the isolation, preparation or purification of DNA or RNA cDNA Synthesis; Subtracted cDNA library construction, e.g. RT, RT-PCR
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/52—Cytokines; Lymphokines; Interferons
- C07K14/555—Interferons [IFN]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S930/00—Peptide or protein sequence
- Y10S930/01—Peptide or protein sequence
- Y10S930/14—Lymphokine; related peptides
- Y10S930/142—Interferon
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Genetics & Genomics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Wood Science & Technology (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Plant Pathology (AREA)
- Physics & Mathematics (AREA)
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- Medicinal Chemistry (AREA)
- Bioinformatics & Computational Biology (AREA)
- Toxicology (AREA)
- Gastroenterology & Hepatology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Saccharide Compounds (AREA)
- Peptides Or Proteins (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
제1도는 cDNA클론 뱅크(clone bank)의 제조 공정도.
제2도는 특이 트리데카뉴클레오타이드의 프리머의 사용에 의해 IFN-α 및 IFN-β-특이 DNA서열을 고농도로 함유하는 하이브리드화 샘플인 cDNA의 제조공정도.
Claims (9)
- 매트릭스로 적합한 RNA를 사용하여 합성한 cDNA로부터 클론뱅크를 제조하고, 이 클론뱅크중에서, 목적하는 유전자 생성물의 생합성을 위한 유전 정보를 함유하고 있는 클론을, 프리머로서 유전자 집단중에 저장된 올리고뉴클레오타이드를 사용하여 합성한 cDNA를 하이브리드화 샘플로 사용하거나, 올리고뉴클레오타이드 그 자체를 하이브리드화 샘플로 사용하여 식별하여, 식별된 클론을 배양하고 배양기간 중에 형성된 유전자 생성물을 분리함을 특징으로 하여, 두개 이상의 유전자(서로가 관련되지만 서로가 교차-하이브리드화할 필요는 없다)의 유전자 생성물을 동시에 제조하는 방법.
- 제1항에 있어서, 매트릭스로서 B-임파구 형태의 유도된 인가세포로부터 얻은 RNA를 사용하여 합성된 cDNA로부터 클론 뱅크를 제조하고, 이 클론 뱅크 중에서 α형 또는 β형 니터폐론의 생합성을 위한 유전 정보를 함유하는 클론을, 매트릭스로 인터페론 서열을 함유하는 RNA와 프리머로 인터페론-특이올리고뉴클레오타이드를 사용하여 합성된 cDNA를 하이브리드화 샘플로 사용하거나 올리고뉴클레오타이드 그 자체를 하이브리드화 샘플로 사용하여 식별하여, 식별된 클론을 배양하고 배양기간중에 형성된 유전자 생성물을 분리함을 특징으로 하여, α형 및 β인 터페론을 동시에 제조하는 방버.
- 제2항에 있어서, 트리데카뉴클레오타이드 5'dCCTTCTGGAACTG 3'가 인터폐론-특이 올리고뉴클레오타이드로 사용됨을 특징으로 하는 방법.
- 제2항 또는 3항에 있어서, B-임파구형 인간세포로 세포주 NC-37, 나말와, 아쿠바 또는 RPM1세포를 사용함을 특징으로 하는 방법.
- 제2항 또는 3항에 있어서, B-임파구형 인간세포로 나말와 세포를 사용함을 특징으로 하는 방법.
- 제2항 내지 5항중의 어느 하나에 있어서, α형 인터페론의 생합성을 코드화한 DNA-서열이 다음식의 부분서열을 함유하는 방법.
- 매트릭스로서 B-임파구 형태의 유도된 인간 세포로부터 얻은 RNA를 사용하여 합성한 cDNA로부터 클론 뱅크를 제조하고, 이어서 인터페론 서열을 함유하는 RNA를 매트릭스로 하고 인터페론-특이 올리고뉴클레오타이드를 프리머로 하여 합성한 cDNA를 하이브리드화 샘플로 사용하거나, 올리고뉴클레오타이드 그 자체를 하이브리드화 샘플로 사용하여 α형 또는 β형 인터페론의 생합성을 위한 유전 정보를 함유하는 클론을 식별하여 수득한 DNA-서열 중에 유정 정보를 함유하는 하이브리드 플라스미드를 사용하여 미생물, 바람직하게는에쉐리키아 콜리틀 형질 전환시킴을 특징으로 하여, 상술한 하이브리드 플라스미드 중에 제2항 내지 6항에서 청구한 α형 또는 β형 인터페론의 생합성을 위한 유전정보를 함유하는 미생물을 제조하는 방법.
- 제7항에서 정의한 하이브리드 플리스미드로부터 분리된, α형 또는 β형 인터페론의 아미노산 서열을 코드화하는 cDNA와 플라스미드, 바람직하게는 플라스미드 pBR322를 결합시킴을 특징으로하여, 제7항에서 정의한 하이브리드 플라스미드를 제조하는 방법.
- 인간 세포로부터 RNA를 얻고, 이들로부터 mRNA를 분리하여 이 mRNA를 사용해서 cDNA를 제조함을 특징으로하여, 제7항에서 정의한 하이브리드 플라스미드로부터 분리된, α형 또는 β형 인터페론의 아미노산 서열을 코드화하는 cDNA를 제조하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEP3220116.8 | 1982-05-28 | ||
DE19823220116 DE3220116A1 (de) | 1982-05-28 | 1982-05-28 | Mikrobiologisch hergestellte (alpha)- und ss-interferone, dna-sequenzen, die fuer diese interferone codieren, mikroorganismen, die diese genetische information enthalten, und verfahren zu ihrer herstellung |
DE3220116.8 | 1982-05-28 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR840004944A true KR840004944A (ko) | 1984-10-31 |
KR920006349B1 KR920006349B1 (ko) | 1992-08-03 |
Family
ID=6164725
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019830002362A KR920006349B1 (ko) | 1982-05-28 | 1983-05-28 | 미생물을 이용한 α- 및 β-인터페론의 제조방법 |
Country Status (22)
Country | Link |
---|---|
US (1) | US4820638A (ko) |
EP (1) | EP0095702B1 (ko) |
JP (2) | JPH0774238B2 (ko) |
KR (1) | KR920006349B1 (ko) |
AT (1) | ATE42114T1 (ko) |
AU (1) | AU565479B2 (ko) |
DD (1) | DD211359C4 (ko) |
DE (2) | DE3220116A1 (ko) |
DK (1) | DK164742C (ko) |
ES (2) | ES522762A0 (ko) |
FI (1) | FI82072C (ko) |
GR (1) | GR79236B (ko) |
HK (1) | HK112893A (ko) |
HU (1) | HU196452B (ko) |
IL (1) | IL68790A (ko) |
MX (1) | MX9202815A (ko) |
NO (1) | NO168538C (ko) |
NZ (1) | NZ204384A (ko) |
SG (1) | SG38692G (ko) |
SU (1) | SU1346048A3 (ko) |
UA (1) | UA8037A1 (ko) |
ZA (1) | ZA833845B (ko) |
Families Citing this family (32)
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DE3247922A1 (de) * | 1982-12-24 | 1984-06-28 | Boehringer Ingelheim International GmbH, 6507 Ingelheim | Dna-sequenzen, deren herstellung, diese sequenzen enthaltende plasmide und deren verwendung zur synthese eukaryotischer genprodukte in prokaryoten |
DE3515336C2 (de) * | 1985-04-27 | 1994-01-20 | Boehringer Ingelheim Int | Verfahren zur Herstellung und Reinigung von â-Interferon |
US4709324A (en) * | 1985-11-27 | 1987-11-24 | Motorola, Inc. | Data processor control unit having an interrupt service using instruction prefetch redirection |
CA2025180A1 (en) * | 1989-10-12 | 1991-04-13 | William G. Weisburg | Nucleic acid probes and methods for detecting pathogenic candida yeasts |
US6685933B1 (en) | 1998-07-28 | 2004-02-03 | The United States Of America As Represented By The Department Of Health And Human Services | Interferon α hybrids |
US20020197235A1 (en) * | 2000-11-03 | 2002-12-26 | Moran Stanford Mark | Method for short-term and long-term drug dosimetry |
FR2817559B1 (fr) * | 2000-12-06 | 2003-12-12 | Genodyssee | Procede de determination d'un ou plusieurs polymorphisme(s) fontionnel(s) dans la sequence nucleique d'un gene "candidat" fonctionnel preselectionne et ses applications |
FR2821625B1 (fr) * | 2001-03-01 | 2003-05-16 | Genodyssee | Nouveaux polynucleotides comportant un polymorphisme de type snp fonctionnel dans la sequence nucleotidique du gene ifn-alpha-2 ainsi que de nouveaux polypeptides codes par ces polynucleotides et leurs utilisations therapeutiques |
FR2823220B1 (fr) * | 2001-04-04 | 2003-12-12 | Genodyssee | Nouveaux polynucleotides et polypeptides de l'erythropoietine (epo) |
DE60237721D1 (de) * | 2001-11-09 | 2010-10-28 | Intarcia Therapeutics Inc | Kombinationstherapie mit omega-interferon zur behandlung von hepatitis c virus oder gelbfieber virus infektionen |
US20040063912A1 (en) * | 2002-03-15 | 2004-04-01 | The Brigham And Women's Hospital, Inc. | Central airway administration for systemic delivery of therapeutics |
WO2003099320A1 (en) | 2002-05-24 | 2003-12-04 | Zensun (Shanghai) Sci-Tech.Ltd | Neuregulin based methods and compositions for treating viral myocarditis and dilated cardiomyopathy |
DE60332358D1 (de) * | 2002-09-09 | 2010-06-10 | Hanall Pharmaceutical Co Ltd | Protease-resistente modifizierte interferon alpha polypeptide |
JP4889505B2 (ja) | 2004-02-02 | 2012-03-07 | アンブレツクス・インコーポレイテツド | 被修飾されたヒト成長ホルモンポリペプチドおよびこれらの使用 |
US11246913B2 (en) | 2005-02-03 | 2022-02-15 | Intarcia Therapeutics, Inc. | Suspension formulation comprising an insulinotropic peptide |
WO2006083761A2 (en) | 2005-02-03 | 2006-08-10 | Alza Corporation | Solvent/polymer solutions as suspension vehicles |
ES2351527T3 (es) | 2006-05-30 | 2011-02-07 | Intarcia Therapeutics, Inc | Modulador de flujo en dos piezas con conducto interno para un sistema osmótico de administración. |
EP2359808B1 (en) | 2006-08-09 | 2013-05-22 | Intarcia Therapeutics, Inc | Osmotic delivery systems and piston assemblies |
US20080260820A1 (en) * | 2007-04-19 | 2008-10-23 | Gilles Borrelly | Oral dosage formulations of protease-resistant polypeptides |
EP2157967B1 (en) | 2007-04-23 | 2013-01-16 | Intarcia Therapeutics, Inc | Suspension formulations of insulinotropic peptides and uses thereof |
CA2726861C (en) | 2008-02-13 | 2014-05-27 | Intarcia Therapeutics, Inc. | Devices, formulations, and methods for delivery of multiple beneficial agents |
EP3323423B1 (en) | 2009-09-28 | 2020-06-17 | Intarcia Therapeutics, Inc | Rapid establishment and/or termination of substantial steady-state drug delivery |
US20120208755A1 (en) | 2011-02-16 | 2012-08-16 | Intarcia Therapeutics, Inc. | Compositions, Devices and Methods of Use Thereof for the Treatment of Cancers |
WO2013024158A1 (en) | 2011-08-17 | 2013-02-21 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Combinations of protein kinase inhibitors and interferons or of protein kinase inhibitors and direct acting antivirals for the treatment and the prevention of hcv infection |
WO2013024156A2 (en) | 2011-08-17 | 2013-02-21 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Combinations of anti-hcv-entry factor antibodies and interferons for the treatment and the prevention of hcv infection |
WO2014033266A1 (en) | 2012-08-31 | 2014-03-06 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Anti-sr-bi antibodies for the inhibition of hepatitis c virus infection |
US9889085B1 (en) | 2014-09-30 | 2018-02-13 | Intarcia Therapeutics, Inc. | Therapeutic methods for the treatment of diabetes and related conditions for patients with high baseline HbA1c |
MA44390A (fr) | 2015-06-03 | 2019-01-23 | Intarcia Therapeutics Inc | Systèmes de mise en place et de retrait d'implant |
SG11201810102SA (en) | 2016-05-16 | 2018-12-28 | Intarcia Therapeutics Inc | Glucagon-receptor selective polypeptides and methods of use thereof |
USD860451S1 (en) | 2016-06-02 | 2019-09-17 | Intarcia Therapeutics, Inc. | Implant removal tool |
USD840030S1 (en) | 2016-06-02 | 2019-02-05 | Intarcia Therapeutics, Inc. | Implant placement guide |
CN110225762A (zh) | 2017-01-03 | 2019-09-10 | 因塔西亚制药公司 | 包括glp-1受体激动剂的连续施用和药物的共同施用的方法 |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
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DE2906160A1 (de) * | 1979-02-17 | 1980-09-04 | Thomae Gmbh Dr K | Verbessertes verfahren zur herstellung von humaninterferon |
AU538665B2 (en) * | 1979-10-30 | 1984-08-23 | Juridical Foundation, Japanese Foundation For Cancer Research | Human interferon dna |
IL58765A (en) * | 1979-11-21 | 1986-09-30 | Yeda Res & Dev | Process for the production of essentially pure messenger rna of human fibroblast interferon and process for the production of interferon beta |
US4530901A (en) * | 1980-01-08 | 1985-07-23 | Biogen N.V. | Recombinant DNA molecules and their use in producing human interferon-like polypeptides |
CA1341567C (en) * | 1980-01-08 | 2008-02-19 | Charles Weissmann | Dna sequences, recombinant dna molecules and processes for producing human interferon - like polypeptides |
GB2068970B (en) * | 1980-02-06 | 1983-06-22 | Searle & Co | Recombinant dna technique for the preparation of a protein resembling human interferon |
DE3005897A1 (de) * | 1980-02-16 | 1981-09-03 | Hoechst Ag, 6000 Frankfurt | Genprodukt eines hoeheren organismus aus einem dieses gen enhtaltenden mikroorganismus |
DE3005843A1 (de) * | 1980-02-16 | 1981-09-10 | Hoechst Ag, 6000 Frankfurt | Genprodukt eines hoeheren organismus aus einem dieses gen enthaltenden mikroorganismus |
ES8302778A1 (es) * | 1980-11-10 | 1983-02-01 | Genentech Inc | Un procedimiento para producir un polipeptido antiviral. |
DE3106982A1 (de) * | 1981-02-25 | 1982-09-09 | Dr. Karl Thomae Gmbh, 7950 Biberach | "neues tridecadeoxynukleotid, verfahren zu seiner herstellung und verwendung" |
IL63327A (en) * | 1981-07-16 | 1985-11-29 | Yeda Res & Dev | Production of interferon beta1 and alpha-phage recombinants for its production in host bacteria |
GB2108510B (en) * | 1981-10-03 | 1984-12-12 | Ciba Geigy Ag | Dnas, recombinant dnas, hosts containing them, polypeptides and processes for the production thereof |
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1982
- 1982-05-28 DE DE19823220116 patent/DE3220116A1/de active Granted
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1983
- 1983-05-19 US US06/495,944 patent/US4820638A/en not_active Expired - Fee Related
- 1983-05-23 FI FI831818A patent/FI82072C/fi not_active IP Right Cessation
- 1983-05-24 GR GR71447A patent/GR79236B/el unknown
- 1983-05-24 AT AT83105116T patent/ATE42114T1/de not_active IP Right Cessation
- 1983-05-24 EP EP83105116A patent/EP0095702B1/de not_active Expired
- 1983-05-24 DE DE8383105116T patent/DE3379591D1/de not_active Expired
- 1983-05-26 IL IL68790A patent/IL68790A/xx unknown
- 1983-05-26 DD DD83251287A patent/DD211359C4/de not_active IP Right Cessation
- 1983-05-27 JP JP58093886A patent/JPH0774238B2/ja not_active Expired - Lifetime
- 1983-05-27 ZA ZA833845A patent/ZA833845B/xx unknown
- 1983-05-27 NZ NZ204384A patent/NZ204384A/en unknown
- 1983-05-27 AU AU15044/83A patent/AU565479B2/en not_active Ceased
- 1983-05-27 DK DK239383A patent/DK164742C/da not_active IP Right Cessation
- 1983-05-27 SU SU833598429A patent/SU1346048A3/ru active
- 1983-05-27 NO NO831903A patent/NO168538C/no unknown
- 1983-05-27 UA UA3598429A patent/UA8037A1/uk unknown
- 1983-05-27 HU HU831890A patent/HU196452B/hu not_active IP Right Cessation
- 1983-05-27 ES ES522762A patent/ES522762A0/es active Granted
- 1983-05-28 KR KR1019830002362A patent/KR920006349B1/ko not_active IP Right Cessation
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1984
- 1984-02-01 ES ES529360A patent/ES529360A0/es active Granted
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1992
- 1992-04-07 SG SG386/92A patent/SG38692G/en unknown
- 1992-06-12 MX MX9202815A patent/MX9202815A/es unknown
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1993
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