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CA2370884A1 - Polymorphismes de nucleotides simples dans des genes mitochondriaux qui segregent avec la maladie d'alzheimer - Google Patents

Polymorphismes de nucleotides simples dans des genes mitochondriaux qui segregent avec la maladie d'alzheimer Download PDF

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Publication number
CA2370884A1
CA2370884A1 CA002370884A CA2370884A CA2370884A1 CA 2370884 A1 CA2370884 A1 CA 2370884A1 CA 002370884 A CA002370884 A CA 002370884A CA 2370884 A CA2370884 A CA 2370884A CA 2370884 A1 CA2370884 A1 CA 2370884A1
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Canada
Prior art keywords
mitochondrial
disease
single nucleotide
alzheimer
gene
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Abandoned
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CA002370884A
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English (en)
Inventor
Corinna Herrnstadt
Robert E. Davis
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Migenix Corp
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Individual
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Publication of CA2370884A1 publication Critical patent/CA2370884A1/fr
Abandoned legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING 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
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6813Hybridisation assays
    • C12Q1/6834Enzymatic or biochemical coupling of nucleic acids to a solid phase
    • C12Q1/6837Enzymatic or biochemical coupling of nucleic acids to a solid phase using probe arrays or probe chips
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING 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
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6883Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING 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
    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/156Polymorphic or mutational markers
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING 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
    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/172Haplotypes

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • General Health & Medical Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • Immunology (AREA)
  • Molecular Biology (AREA)
  • Physics & Mathematics (AREA)
  • Microbiology (AREA)
  • Neurology (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • General Engineering & Computer Science (AREA)
  • Biophysics (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Pathology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La présente invention porte sur des compositions et des méthodes fondées sur la détermination de polymorphismes de nucléotides simples dans l'ADN mt ou dans des mutations homoplasmiques d'ADN mt, utilisées pour détecter la présence de la maladie d'Alzheimer (AD) ou le risque de l'avoir, et pour identifier des agents appropriés pour traiter cette maladie.
CA002370884A 1999-04-20 2000-04-19 Polymorphismes de nucleotides simples dans des genes mitochondriaux qui segregent avec la maladie d'alzheimer Abandoned CA2370884A1 (fr)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US13044799P 1999-04-20 1999-04-20
US60/130,447 1999-04-20
US16090199P 1999-10-22 1999-10-22
US60/160,901 1999-10-22
PCT/US2000/010906 WO2000063441A2 (fr) 1999-04-20 2000-04-19 Polymorphismes de nucleotides simples dans des genes mitochondriaux qui segregent avec la maladie d'alzheimer

Publications (1)

Publication Number Publication Date
CA2370884A1 true CA2370884A1 (fr) 2000-10-26

Family

ID=26828492

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002370884A Abandoned CA2370884A1 (fr) 1999-04-20 2000-04-19 Polymorphismes de nucleotides simples dans des genes mitochondriaux qui segregent avec la maladie d'alzheimer

Country Status (5)

Country Link
EP (1) EP1208225A2 (fr)
JP (1) JP2003521879A (fr)
AU (1) AU4368300A (fr)
CA (1) CA2370884A1 (fr)
WO (1) WO2000063441A2 (fr)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20040034582A (ko) * 2000-12-04 2004-04-28 프리마겐 홀딩 비.브이. 내공생체 세포소기관의 시험 및 그것에 의해 동정할 수있는 화합물
WO2005056573A1 (fr) * 2002-06-10 2005-06-23 1304854 Ontario Ltd. Sequences completes du genome mitochondrial utilisees comme outil de diagnostic pour des sciences de la sante
GB2380194B (en) * 2001-10-01 2005-06-22 Roger Michael Marchbanks A mitochondrial mutation associated with schizophrenia and increased oxidative stress
US6897025B2 (en) * 2002-01-07 2005-05-24 Perlegen Sciences, Inc. Genetic analysis systems and methods
CA2513191A1 (fr) * 2003-01-30 2004-08-12 Research Development Foundation Procedes et compositions d'analyse de l'expression genique liee a la mitochondrie
BRPI0410789B8 (pt) 2003-05-21 2021-05-25 Andes Biotechnologies Global Inc composição farmacêutica, uso de um ou mais oligonucleotídeos, e, método de detecção
KR101363032B1 (ko) 2005-04-18 2014-02-13 미토믹스 인크. 일광 노출, 전립선암 및 다른 암의 검출용 진단 도구로서미토콘드리아 돌연변이 및 전위
US20130022979A1 (en) 2005-04-18 2013-01-24 Genesis Genomics Inc. 3.4kb MITOCHONDRIAL DNA DELETION FOR USE IN THE DETECTION OF CANCER
EP2557421A3 (fr) * 2007-03-23 2013-06-05 King's College London Activité mitochondriale altérée dans les maladies liées au stress oxydant
EP2593787B1 (fr) * 2010-07-16 2018-07-04 Stichting VUmc Méthode d'analyser une prise de sang d'un sujet pour la présence d'un marqueur de la maladie
JP5934726B2 (ja) * 2011-03-18 2016-06-15 フェレニヒング フォール クリステリック ホーヘル オンデルウィス,ウェテンシャペリク オンデルツォーケン パティエンテンツォルフ 疾患マーカーの存在を被験者の血液サンプルで分析する方法
ES2482866B1 (es) * 2012-11-22 2015-05-12 Consejo Superior De Investigaciones Científicas (Csic) Método de diagnóstico y/o pronóstico de enfermedades neurodegenerativas.
ES2546743B1 (es) * 2014-03-28 2016-07-07 Institut D'investigació Biomèdica De Bellvitge (Idibell) Marcadores mitocondriales de enfermedades neurodegenerativas
GB2566516A (en) 2017-09-15 2019-03-20 Univ Oxford Innovation Ltd Electrochemical recognition and quantification of cytochrome c oxidase expression in bacteria
TW202033760A (zh) * 2018-11-28 2020-09-16 國立大學法人千葉大學 多因素遺傳疾病的基因檢測法、及檢測套件
CN113862346B (zh) * 2021-09-26 2023-07-07 北京大学 长链非编码rna在治疗阿尔茨海默病中的应用

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5494794A (en) * 1992-10-20 1996-02-27 Emory University Detection of mitochondrial DNA mutations associated with Alzheimer's disease and Parkinson's disease
US5976798A (en) * 1994-03-30 1999-11-02 Mitokor Methods for detecting mitochondrial mutations diagnostic for Alzheimer's disease and methods for determining heteroplasmy of mitochondrial nucleic acid
US5565323A (en) * 1994-03-30 1996-10-15 Mitokor Cytochrome oxidase mutations aiding diagnosis of sporadic alzheimer's disease
US6027883A (en) * 1994-03-30 2000-02-22 Mitokor Optimal procedure for isolation of mutant mitochondrial alleles
JPH1099085A (ja) * 1996-05-16 1998-04-21 Affymetrix Inc ヒトミトコンドリアdnaの多形性

Also Published As

Publication number Publication date
WO2000063441A3 (fr) 2002-03-14
AU4368300A (en) 2000-11-02
EP1208225A2 (fr) 2002-05-29
JP2003521879A (ja) 2003-07-22
WO2000063441A2 (fr) 2000-10-26

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