JPH04501357A - フラジルx症候群を検出するためのプローブ - Google Patents
フラジルx症候群を検出するためのプローブInfo
- Publication number
- JPH04501357A JPH04501357A JP1511190A JP51119089A JPH04501357A JP H04501357 A JPH04501357 A JP H04501357A JP 1511190 A JP1511190 A JP 1511190A JP 51119089 A JP51119089 A JP 51119089A JP H04501357 A JPH04501357 A JP H04501357A
- Authority
- JP
- Japan
- Prior art keywords
- dna
- flagyl
- iai
- human
- nucleic acid
- 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.)
- Pending
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6893—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids related to diseases not provided for elsewhere
- G01N33/6896—Neurological disorders, e.g. Alzheimer's disease
-
- 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
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
-
- 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
- C12Q1/6813—Hybridisation assays
- C12Q1/6827—Hybridisation assays for detection of mutation or polymorphism
-
- 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
- C12Q1/6813—Hybridisation assays
- C12Q1/6827—Hybridisation assays for detection of mutation or polymorphism
- C12Q1/683—Hybridisation assays for detection of mutation or polymorphism involving restriction enzymes, e.g. restriction fragment length polymorphism [RFLP]
-
- 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)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Zoology (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Immunology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Analytical Chemistry (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Physics & Mathematics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Pathology (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Cell Biology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Gastroenterology & Hepatology (AREA)
- Toxicology (AREA)
- Food Science & Technology (AREA)
- General Physics & Mathematics (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB888825530A GB8825530D0 (en) | 1988-11-01 | 1988-11-01 | Probe |
| GB8825530.2 | 1988-11-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH04501357A true JPH04501357A (ja) | 1992-03-12 |
Family
ID=10646112
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1511190A Pending JPH04501357A (ja) | 1988-11-01 | 1989-11-01 | フラジルx症候群を検出するためのプローブ |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0441821A1 (de) |
| JP (1) | JPH04501357A (de) |
| AU (1) | AU4487189A (de) |
| GB (1) | GB8825530D0 (de) |
| WO (1) | WO1990005194A1 (de) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8928029D0 (en) * | 1989-12-12 | 1990-02-14 | Medical Res Council | Probe |
| CA2094938A1 (en) * | 1991-01-04 | 1992-07-05 | Grant R. Sutherland | Dna sequences related to isolated fragile x syndrome |
| WO1992014840A1 (fr) * | 1991-02-13 | 1992-09-03 | Institut National De La Sante Et De La Recherche Medicale | Fragment d'acide nucleique de la region du chromosome x implique dans le syndrome x fragile, sonde nucleotidique et procede pour le diagnostic du retard mental avec x fragile |
| FR2672618B1 (fr) * | 1991-02-13 | 1994-12-02 | Centre Nat Rech Scient | Fragment d'acide nucleique de la region du chromosome x implique dans le syndrome x fragile, sonde nucleotidique et procede pour le diagnostic du retard mental avec x fragile. |
| US6180337B1 (en) * | 1991-05-24 | 2001-01-30 | Baylor College Of Medicine | Diagnosis of the fragile X syndrome |
| US5876949A (en) * | 1995-05-31 | 1999-03-02 | The Trustees Of The University Of Pennsylvania | Antibodies specific for fragile X related proteins and method of using the same |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8627123D0 (en) * | 1986-11-13 | 1986-12-10 | Amersham Int Plc | Dna sequence |
-
1988
- 1988-11-01 GB GB888825530A patent/GB8825530D0/en active Pending
-
1989
- 1989-11-01 JP JP1511190A patent/JPH04501357A/ja active Pending
- 1989-11-01 AU AU44871/89A patent/AU4487189A/en not_active Abandoned
- 1989-11-01 WO PCT/GB1989/001303 patent/WO1990005194A1/en not_active Ceased
- 1989-11-01 EP EP89912003A patent/EP0441821A1/de not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| AU4487189A (en) | 1990-05-28 |
| GB8825530D0 (en) | 1988-12-07 |
| EP0441821A1 (de) | 1991-08-21 |
| WO1990005194A1 (en) | 1990-05-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Carrier et al. | Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11 | |
| Severini et al. | A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14 | |
| Barton et al. | The myosin alkali light chains of mouse ventricular and slow skeletal muscle are indistinguishable and are encoded by the same gene. | |
| Bhattacharya et al. | Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1. 28 | |
| JP2750228B2 (ja) | 遺伝的特性決定用ポリヌクレオチド | |
| Pereira et al. | Novel viruses in human faeces | |
| Ranum et al. | Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p | |
| Georges et al. | Characterization of a set of variable number of tandem repeat markers conserved in Bovidae | |
| US5654148A (en) | Multicolor in situ hybridization methods for genetic testing | |
| Flomen et al. | Construction and Analysis of a Sequence-Ready Map in 4q25: Rieger Syndrome Can Be Caused by Haploinsufficiency ofRIEG, but Also by Chromosome Breaks≈ 90 kb Upstream of This Gene | |
| Rich et al. | Spinocerebellar ataxia: localization of an autosomal dominant locus between two markers on human chromosome 6 | |
| Wainscoat et al. | The molecular basis for the clinical diversity of β thalassaemia in Cypriots | |
| Darras et al. | Normal human genomic restriction-fragment patterns and polymorphisms revealed by hybridization with the entire dystrophin cDNA | |
| US5723293A (en) | Diagnostic method and kit for determining Rh blood group genotype | |
| Overhauser et al. | Identification of 28 DNA fragments that detect RFLPs in 13 distinct physical regions of the short arm of chromosome 5 | |
| JPH04501357A (ja) | フラジルx症候群を検出するためのプローブ | |
| JP4130125B2 (ja) | 牛における複合脊椎奇形キャリアーを同定するための遺伝試験 | |
| US5262529A (en) | Diagnosis of hereditary retinal degenerative diseases | |
| Wakui et al. | Familial 14-Mb deletion at 21q11. 2–q21. 3 and variable phenotypic expression | |
| Bettecken et al. | Identification of a 220-kb insertion into the Duchenne gene in a family with an atypical course of muscular dystrophy | |
| Diehl et al. | A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) gene | |
| DE69225797T2 (de) | Nukleinsäure fragment des x-chromosomen bereichs beteiligt am empfindlichen x-syndrom, nukleotidische sonde und verfahren für die diagnose von geistiger zurückgebliebenheit mit empfindlichem x | |
| Connor et al. | Application of an intragenic genomic probe to genetic counselling for haemophilia B in the west of Scotland. | |
| Bird et al. | The use of apolipoprotein CII as a genetic marker for myotonic dystrophy | |
| CA2116628A1 (en) | Method for the diagnosis of cadasil |