ATE186074T1 - Verfahren für die in-vitro-diagnose von mit charcot-marie-tooth-krankheit vom typ-1a zusammenhängenden chromosomenanomalien - Google Patents

Verfahren für die in-vitro-diagnose von mit charcot-marie-tooth-krankheit vom typ-1a zusammenhängenden chromosomenanomalien

Info

Publication number
ATE186074T1
ATE186074T1 AT92909895T AT92909895T ATE186074T1 AT E186074 T1 ATE186074 T1 AT E186074T1 AT 92909895 T AT92909895 T AT 92909895T AT 92909895 T AT92909895 T AT 92909895T AT E186074 T1 ATE186074 T1 AT E186074T1
Authority
AT
Austria
Prior art keywords
probes
vitro diagnosis
chromosome
anomals
charcot
Prior art date
Application number
AT92909895T
Other languages
English (en)
Inventor
Broeckhoven Christine Van
Peter Raeymaekers
Jonghe Peter De
Jean-Jacques Martin
Original Assignee
Innogenetics Nv
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Innogenetics Nv filed Critical Innogenetics Nv
Application granted granted Critical
Publication of ATE186074T1 publication Critical patent/ATE186074T1/de

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
    • 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
    • C12Q2600/172—Haplotypes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Organic Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • Zoology (AREA)
  • Analytical Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • Molecular Biology (AREA)
  • Biophysics (AREA)
  • Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Immunology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Dental Tools And Instruments Or Auxiliary Dental Instruments (AREA)
AT92909895T 1991-05-07 1992-05-06 Verfahren für die in-vitro-diagnose von mit charcot-marie-tooth-krankheit vom typ-1a zusammenhängenden chromosomenanomalien ATE186074T1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP91401220A EP0512181A1 (de) 1991-05-07 1991-05-07 Verfahren zum in vitro Nachweis von Chromosomenanomalien, korrelierend mit der CMT1A-Krankheit

Publications (1)

Publication Number Publication Date
ATE186074T1 true ATE186074T1 (de) 1999-11-15

Family

ID=8208565

Family Applications (1)

Application Number Title Priority Date Filing Date
AT92909895T ATE186074T1 (de) 1991-05-07 1992-05-06 Verfahren für die in-vitro-diagnose von mit charcot-marie-tooth-krankheit vom typ-1a zusammenhängenden chromosomenanomalien

Country Status (10)

Country Link
US (1) US6110670A (de)
EP (2) EP0512181A1 (de)
AT (1) ATE186074T1 (de)
AU (1) AU1683192A (de)
CA (1) CA2102300A1 (de)
DE (1) DE69230221T2 (de)
DK (1) DK0584145T3 (de)
ES (1) ES2139596T3 (de)
GR (1) GR3032235T3 (de)
WO (1) WO1992019770A2 (de)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6225057B1 (en) * 1998-07-23 2001-05-01 Palleja, Zavier Estivell Duplications of human chromosome 15q24-25 and anxiety disorders, diagnostic methods for their detection
FR2808276B1 (fr) * 2000-04-26 2004-04-02 Renaud Nalin Procede d'extraction indirecte de l'adn d'organismes non cultivables et adn susceptible d'etre obtenu par ledit procede
US7273698B2 (en) 2000-12-13 2007-09-25 Baylor College Of Medicine Defects in periaxin associated with myelinopathies
US10337054B2 (en) 2004-02-02 2019-07-02 Quantum-Si Incorporated Enrichment of nucleic acid targets
US8529744B2 (en) 2004-02-02 2013-09-10 Boreal Genomics Corp. Enrichment of nucleic acid targets
US9186685B2 (en) 2012-01-13 2015-11-17 The University Of British Columbia Multiple arm apparatus and methods for separation of particles
EP1720636A4 (de) 2004-02-02 2012-06-20 Univ British Columbia Scodaphorese und verfahren und vorrichtungen zum bewegen und aufkonzentrieren von teilchen
KR100613038B1 (ko) 2004-07-07 2006-08-16 공주대학교 산학협력단 염색체 17ｐ11.2-ｐ12 지역의 중복을 제외한 유전자돌연변이를 발병 원인으로 하는 ＣＭＴ 질환의 진단방법및 진단키트
KR100642421B1 (ko) * 2004-07-07 2006-11-03 공주대학교 산학협력단 염색체 17ｐ11.2-ｐ12 지역의 중복 및 결실로 발병하는유전성 신경질환의 진단방법 및 진단키트
CA2496294A1 (en) 2005-02-07 2006-08-07 The University Of British Columbia Apparatus and methods for concentrating and separating particles such as molecules
US8475641B2 (en) 2008-02-01 2013-07-02 The University Of British Columbia Methods and apparatus for particle introduction and recovery
US8877028B2 (en) 2009-04-21 2014-11-04 The University Of British Columbia System and methods for detection of particles
CA2742327A1 (en) 2011-05-20 2012-11-20 The University Of British Columiba Systems and methods for enhanced scoda
WO2013166444A2 (en) 2012-05-04 2013-11-07 Boreal Genomics Corp. Biomarker analysis using scodaphoresis
US9340835B2 (en) 2013-03-15 2016-05-17 Boreal Genomics Corp. Method for separating homoduplexed and heteroduplexed nucleic acids
WO2016185284A1 (en) 2015-05-20 2016-11-24 Boreal Genomics, Inc. Method for isolating target nucleic acid using heteroduplex binding proteins
US12011716B2 (en) 2019-10-29 2024-06-18 Quantum-Si Incorporated Peristaltic pumping of fluids and associated methods, systems, and devices

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5306616A (en) * 1991-06-06 1994-04-26 Baylor College Of Medicine Molecular diagnosis of autosomal dominant charcot-marie-tooth disease
AU2226592A (en) * 1991-06-06 1993-01-08 Baylor College Of Medicine Molecular diagnosis of autosomal dominant charcot-marie-tooth disease

Also Published As

Publication number Publication date
DK0584145T3 (da) 2000-04-25
CA2102300A1 (en) 1992-11-08
DE69230221D1 (de) 1999-12-02
AU1683192A (en) 1992-12-21
ES2139596T3 (es) 2000-02-16
EP0584145A1 (de) 1994-03-02
EP0584145B1 (de) 1999-10-27
WO1992019770A2 (en) 1992-11-12
EP0512181A1 (de) 1992-11-11
US6110670A (en) 2000-08-29
WO1992019770A3 (en) 1993-01-07
DE69230221T2 (de) 2000-05-31
GR3032235T3 (en) 2000-04-27

Similar Documents

Publication Publication Date Title
ATE186074T1 (de) Verfahren für die in-vitro-diagnose von mit charcot-marie-tooth-krankheit vom typ-1a zusammenhängenden chromosomenanomalien
Amler et al. Amplified N-myc in human neuroblastoma cells is often arranged as clustered tandem repeats of differently recombined DNA
Gerdes et al. Dynamic changes in the higher-level chromatin organization of specific sequences revealed by in situ hybridization to nuclear halos.
DE69416692T2 (de) Mittels nukleinsäureanalogs induzierte transkription von doppelsträngiger dna
DE3834636C2 (de)
Porter et al. Evidence on primate phylogeny from ε-globin gene sequences and flanking regions
ATE185912T1 (de) Verfahren und gerät zur automatischen bestimmung von gewebe
FR2710075B1 (fr) Réactif et procédé pour la détection d'une séquence nucléotidique avec amplification de signal.
ATE330009T1 (de) Zusammensetzung und methoden bezogen auf dna fehlpaarungsreparaturgene
DE3220116A1 (de) Mikrobiologisch hergestellte (alpha)- und ss-interferone, dna-sequenzen, die fuer diese interferone codieren, mikroorganismen, die diese genetische information enthalten, und verfahren zu ihrer herstellung
Drumheller et al. Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.
Smith et al. Molecular genetic delineation of a deletion of chromosome 13q12→ q13 in a patient with autism and auditory processing deficits
DE69510336D1 (de) Verfahren zur diagnose von praeklampsie
Lin et al. A suggestion for the nomenclature of the fluorescent banding patterns in human metaphase chromosomes
PT82405B (pt) Processo de hibridizacao de duas cadeias de oligonucleotidos complementares e sondas para a sua realizacao
Farace et al. No detectable reiteration of genes coding for mouse MOPC 41 immunoglobulin light-chain mRNA.
DE69705936D1 (de) Teil der intronsequenz des von hippel-lindau(vhl)-gens und seine verwendung zur krankheitsdiagnose
ATE261497T1 (de) Diagnostisches verfahren und gerät
Patil et al. A high resolution physical map of 2.5 Mbp of the Down syndrome region on chromosome 21
DE69022362D1 (de) Nukleinsäuresonden für die detektion von neisseria gonorrhoeae.
Jacob et al. Acceleration of axonal outgrowth in motor axons from mature and old F344 rats after a conditioning lesion
Roses et al. Recombinant DNA strategies in genetic neurological diseases
SULKAVA et al. No elevated sister chromatid exchange in Alzheimer's disease
Chand et al. Long-range organization of reiterated sequences, including the SSX1 cDNA, at the OATL1 cluster in Xp11. 23
Suto et al. Visual Demonstration of the Organization of the Human Complement C4 and 21-Hydroxylase Genes by High-Resolution Fluorescencein SituHybridization

Legal Events

Date Code Title Description
REN Ceased due to non-payment of the annual fee