ITRM20020130A1 - Mezzi diagnostici e terapeutici per la sindrome da ritardo mentale legata al cromosoma x. - Google Patents
Mezzi diagnostici e terapeutici per la sindrome da ritardo mentale legata al cromosoma x.Info
- Publication number
- ITRM20020130A1 ITRM20020130A1 IT2002RM000130A ITRM20020130A ITRM20020130A1 IT RM20020130 A1 ITRM20020130 A1 IT RM20020130A1 IT 2002RM000130 A IT2002RM000130 A IT 2002RM000130A IT RM20020130 A ITRM20020130 A IT RM20020130A IT RM20020130 A1 ITRM20020130 A1 IT RM20020130A1
- Authority
- IT
- Italy
- Prior art keywords
- chromosome
- diagnostic
- therapeutic means
- delay syndrome
- syndrome linked
- 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
- C12Q2600/156—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)
- Peptides Or Proteins (AREA)
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT2002RM000130A ITRM20020130A1 (it) | 2002-03-08 | 2002-03-08 | Mezzi diagnostici e terapeutici per la sindrome da ritardo mentale legata al cromosoma x. |
EP03712654A EP1483412A2 (en) | 2002-03-08 | 2003-03-06 | Facl4 and mutation thereof in x-linked mental retardation syndrome |
AU2003217466A AU2003217466A1 (en) | 2002-03-08 | 2003-03-06 | Facl4 and mutation thereof on x-linkend mental retardation syndrome |
PCT/IT2003/000134 WO2003076659A2 (en) | 2002-03-08 | 2003-03-06 | Facl4 and mutation thereof on x-linkend mental retardation syndrome |
US10/507,145 US20050130162A1 (en) | 2002-03-08 | 2003-03-06 | Diagnostic and therapeutic tools for the x-linked mental retardation syndrome |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT2002RM000130A ITRM20020130A1 (it) | 2002-03-08 | 2002-03-08 | Mezzi diagnostici e terapeutici per la sindrome da ritardo mentale legata al cromosoma x. |
Publications (2)
Publication Number | Publication Date |
---|---|
ITRM20020130A0 ITRM20020130A0 (it) | 2002-03-08 |
ITRM20020130A1 true ITRM20020130A1 (it) | 2003-09-08 |
Family
ID=11456160
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IT2002RM000130A ITRM20020130A1 (it) | 2002-03-08 | 2002-03-08 | Mezzi diagnostici e terapeutici per la sindrome da ritardo mentale legata al cromosoma x. |
Country Status (5)
Country | Link |
---|---|
US (1) | US20050130162A1 (it) |
EP (1) | EP1483412A2 (it) |
AU (1) | AU2003217466A1 (it) |
IT (1) | ITRM20020130A1 (it) |
WO (1) | WO2003076659A2 (it) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN117487817B (zh) * | 2023-12-29 | 2024-04-23 | 湖南家辉生物技术有限公司 | Il1rapl1基因突变体、突变体蛋白、试剂、试剂盒及应用 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1311660A4 (en) * | 2000-08-21 | 2004-07-28 | Univ Utah Res Found | METHOD FOR SCREENING INHIBITORS OF HUMAN FATTY ACID COA LIGASE 4 |
-
2002
- 2002-03-08 IT IT2002RM000130A patent/ITRM20020130A1/it unknown
-
2003
- 2003-03-06 US US10/507,145 patent/US20050130162A1/en not_active Abandoned
- 2003-03-06 AU AU2003217466A patent/AU2003217466A1/en not_active Abandoned
- 2003-03-06 WO PCT/IT2003/000134 patent/WO2003076659A2/en not_active Application Discontinuation
- 2003-03-06 EP EP03712654A patent/EP1483412A2/en not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
WO2003076659A2 (en) | 2003-09-18 |
AU2003217466A1 (en) | 2003-09-22 |
AU2003217466A8 (en) | 2003-09-22 |
US20050130162A1 (en) | 2005-06-16 |
WO2003076659A3 (en) | 2003-12-31 |
EP1483412A2 (en) | 2004-12-08 |
ITRM20020130A0 (it) | 2002-03-08 |
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