AUPQ882600A0 - Mutations in ion channels - Google Patents
Mutations in ion channelsInfo
- Publication number
- AUPQ882600A0 AUPQ882600A0 AUPQ8826A AUPQ882600A AUPQ882600A0 AU PQ882600 A0 AUPQ882600 A0 AU PQ882600A0 AU PQ8826 A AUPQ8826 A AU PQ8826A AU PQ882600 A AUPQ882600 A AU PQ882600A AU PQ882600 A0 AUPQ882600 A0 AU PQ882600A0
- Authority
- AU
- Australia
- Prior art keywords
- mutations
- ion channels
- channels
- ion
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING 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
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING 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
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/156—Polymorphic or mutational markers
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Analytical Chemistry (AREA)
- Zoology (AREA)
- Genetics & Genomics (AREA)
- Engineering & Computer Science (AREA)
- Pathology (AREA)
- Immunology (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Biophysics (AREA)
- Physics & Mathematics (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AUPQ8826A AUPQ882600A0 (en) | 2000-07-18 | 2000-07-18 | Mutations in ion channels |
AU2001272218A AU2001272218A1 (en) | 2000-07-18 | 2001-07-18 | Identification of two principal mutations in ion channels associated with idiopathic generalised epilepsies |
PCT/AU2001/000872 WO2002006521A1 (en) | 2000-07-18 | 2001-07-18 | Identification of two principal mutations in ion channels associated with idiopathic generalised epilepsies |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AUPQ8826A AUPQ882600A0 (en) | 2000-07-18 | 2000-07-18 | Mutations in ion channels |
Publications (1)
Publication Number | Publication Date |
---|---|
AUPQ882600A0 true AUPQ882600A0 (en) | 2000-08-10 |
Family
ID=3822889
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AUPQ8826A Abandoned AUPQ882600A0 (en) | 2000-07-18 | 2000-07-18 | Mutations in ion channels |
Country Status (2)
Country | Link |
---|---|
AU (1) | AUPQ882600A0 (en) |
WO (1) | WO2002006521A1 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1407013B1 (en) | 2001-07-18 | 2007-09-12 | Bionomics Limited | Mutations in ion channels |
AU2003904154A0 (en) * | 2003-08-07 | 2003-08-21 | Bionomics Limited | Mutations in ion channels |
AU2003901425A0 (en) | 2003-03-27 | 2003-04-10 | Bionomics Limited | A diagnostic method for epilepsy |
NZ564892A (en) * | 2005-06-16 | 2011-10-28 | Bionomics Ltd | Methods of treatment, and diagnosis of epilepsy by detecting a D674G mutation in the SCN1A gene |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU701228B2 (en) * | 1995-06-28 | 1999-01-21 | University Of Bonn | Diagnostic and treatment methods relating to Autosomal Dominant Nocturnal Frontal Lobe Epilepsy (ADNFLE) |
-
2000
- 2000-07-18 AU AUPQ8826A patent/AUPQ882600A0/en not_active Abandoned
-
2001
- 2001-07-18 WO PCT/AU2001/000872 patent/WO2002006521A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
WO2002006521A1 (en) | 2002-01-24 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
NAA1 | Application designating australia and claiming priority from australian document |
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