ATE166925T1 - Nukleinsäure fragment des x-chromosomen bereichs beteiligt am empfindlichen x-syndrom, nukleotidische sonde und verfahren für die diagnose von geistiger zurückgebliebenheit mit empfindlichem x - Google Patents
Nukleinsäure fragment des x-chromosomen bereichs beteiligt am empfindlichen x-syndrom, nukleotidische sonde und verfahren für die diagnose von geistiger zurückgebliebenheit mit empfindlichem xInfo
- Publication number
- ATE166925T1 ATE166925T1 AT92907135T AT92907135T ATE166925T1 AT E166925 T1 ATE166925 T1 AT E166925T1 AT 92907135 T AT92907135 T AT 92907135T AT 92907135 T AT92907135 T AT 92907135T AT E166925 T1 ATE166925 T1 AT E166925T1
- Authority
- AT
- Austria
- Prior art keywords
- nucleic acid
- acid fragment
- sensitive
- hybridise
- chromosome
- Prior art date
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
- C12Q2600/154—Methylation markers
-
- 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)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9101684A FR2672618B1 (fr) | 1991-02-13 | 1991-02-13 | 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. |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE166925T1 true ATE166925T1 (de) | 1998-06-15 |
Family
ID=9409670
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT92907135T ATE166925T1 (de) | 1991-02-13 | 1992-02-13 | Nukleinsäure fragment des x-chromosomen bereichs beteiligt am empfindlichen x-syndrom, nukleotidische sonde und verfahren für die diagnose von geistiger zurückgebliebenheit mit empfindlichem x |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP0580621B1 (de) |
JP (1) | JPH06507310A (de) |
AT (1) | ATE166925T1 (de) |
AU (1) | AU671418B2 (de) |
CA (1) | CA2104110C (de) |
DE (1) | DE69225797T2 (de) |
ES (1) | ES2118130T3 (de) |
FR (1) | FR2672618B1 (de) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10019058A1 (de) * | 2000-04-06 | 2001-12-20 | Epigenomics Ag | Detektion von Variationen des DNA-Methylierungsprofils |
RU2011142773A (ru) | 2009-03-24 | 2013-04-27 | Эсьюраджен, Инк. | Методы пцр для характеристики 5,-нетранслируемого участка генов fmr1 и fmr2 |
EP2888688B1 (de) | 2012-07-20 | 2019-09-04 | Asuragen, INC. | Umfassende fmr1-genotypisierung |
CN110923305B (zh) * | 2019-11-25 | 2023-12-29 | 广州市达瑞生物技术股份有限公司 | 一种适用于脆性X综合征southern blot印迹杂交检测的DNA分子量标准 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2578847A1 (fr) * | 1985-03-13 | 1986-09-19 | Centre Nat Rech Scient | Sonde adn destinee au diagnostic antenatal de certaines anomalies chromosomiques |
GB8825530D0 (en) * | 1988-11-01 | 1988-12-07 | Medical Res Council | Probe |
GB8928029D0 (en) * | 1989-12-12 | 1990-02-14 | Medical Res Council | Probe |
EP0724646B1 (de) * | 1991-01-04 | 2001-06-27 | Washington University | Mit isoliertem empfindlichem x-syndrom verbundene dns-sequenzen |
-
1991
- 1991-02-13 FR FR9101684A patent/FR2672618B1/fr not_active Expired - Lifetime
-
1992
- 1992-02-13 AT AT92907135T patent/ATE166925T1/de not_active IP Right Cessation
- 1992-02-13 JP JP4506537A patent/JPH06507310A/ja active Pending
- 1992-02-13 DE DE69225797T patent/DE69225797T2/de not_active Expired - Lifetime
- 1992-02-13 ES ES92907135T patent/ES2118130T3/es not_active Expired - Lifetime
- 1992-02-13 AU AU14136/92A patent/AU671418B2/en not_active Expired
- 1992-02-13 EP EP92907135A patent/EP0580621B1/de not_active Expired - Lifetime
- 1992-02-13 CA CA002104110A patent/CA2104110C/fr not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH06507310A (ja) | 1994-08-25 |
DE69225797T2 (de) | 1999-02-04 |
FR2672618A1 (fr) | 1992-08-14 |
DE69225797D1 (de) | 1998-07-09 |
ES2118130T3 (es) | 1998-09-16 |
EP0580621B1 (de) | 1998-06-03 |
CA2104110C (fr) | 2003-12-09 |
CA2104110A1 (fr) | 1992-08-14 |
AU1413692A (en) | 1992-09-15 |
EP0580621A1 (de) | 1994-02-02 |
FR2672618B1 (fr) | 1994-12-02 |
AU671418B2 (en) | 1996-08-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Bell et al. | Functional cooperativity between transcription factors UBF1 and SL1 mediates human ribosomal RNA synthesis | |
Watanabe et al. | Primary and higher order structures of nematode (Ascaris suum) mitochondrial tRNAs lacking either the T or D stem. | |
Ladenburger et al. | Identification of a binding region for human origin recognition complex proteins 1 and 2 that coincides with an origin of DNA replication | |
Schaufele et al. | Overlapping Pit-1 and Sp1 binding sites are both essential to full rat growth hormone gene promoter activity despite mutually exclusive Pit-1 and Sp1 binding. | |
Ridinger et al. | Clustered organization of S100 genes in human and mouse | |
DK1005540T3 (da) | IKK-beta-proteiner, nukleinsyrer og fremgangsmåder | |
DE69133629D1 (de) | nssystem zur Bestimmung von genetischen Krankheiten | |
DE69534733D1 (de) | NEUARTIGE AUF p53 ANSPRECHENDE GENE | |
Sypes et al. | Protein/DNA crosslinking of a TFIID complex reveals novel interactions downstream of the transcription start | |
DE69738804D1 (de) | Blütenorgan-spezifische promotersequenzen | |
Margarit et al. | Identification of conserved potentially regulatory sequences of the SRY gene from 10 different species of mammals | |
Zhou et al. | Mapping of the human RNASEL promoter and expression in cancer and normal cells | |
DE69808743T2 (de) | Netrinrezeptoren | |
Sapp et al. | A newly detected class of mammalian single strand-specific DNA-binding proteins. Effects on DNA polymerase alpha-catalyzed DNA synthesis. | |
Sheng et al. | Structure, sequence, and promoter analysis of human disabled-2 gene (DAB2) | |
ATE166925T1 (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 | |
FR2679253B1 (fr) | Proteines de resistance a la cycloheximide. utilisation comme marqueur de selection par exemple pour controler le transfert d'acides nucleiques. | |
Miller et al. | A transcriptionally active pseudogene in xenopus laevis oocyte 5S DNA | |
Kothary et al. | IS186: an Escherichia coli insertion element isolated from a cDNA library | |
Stanford et al. | DNA sequence of a human Sm autoimmune antigen. The multigene family contains a processed pseudogene. | |
Tee et al. | Temperature gradient gel electrophoresis: detection of a single base substitution in the cattle β‐lactoglobulin gene | |
Roberts et al. | Different active sites of mammalian DNA ligases I and II. | |
Lund et al. | The embryonic and adult mouse U1 snRNA genes map to different chromosomal loci | |
Goldberg et al. | In vitro regulation of DNA-dependent synthesis of Escherichia coli ribosomal protein L12. | |
Gatti et al. | Variation with sex of irradiation-induced chromosome damage in somatic cells of Drosophila melanogaster |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |