AU2016225033B2 - Methods and reagents for predicting predisposition to refractive error - Google Patents

Methods and reagents for predicting predisposition to refractive error Download PDF

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Publication number
AU2016225033B2
AU2016225033B2 AU2016225033A AU2016225033A AU2016225033B2 AU 2016225033 B2 AU2016225033 B2 AU 2016225033B2 AU 2016225033 A AU2016225033 A AU 2016225033A AU 2016225033 A AU2016225033 A AU 2016225033A AU 2016225033 B2 AU2016225033 B2 AU 2016225033B2
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Australia
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exon
opsin gene
opsin
mrna
amplification products
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AU2016225033A
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AU2016225033A1 (en
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Jay Neitz
Maureen Neitz
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University of Washington
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University of Washington
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • 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
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • 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
    • C12Q2600/118Prognosis of disease development
    • 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

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Genetics & Genomics (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Biomedical Technology (AREA)
  • Biophysics (AREA)
  • Biotechnology (AREA)
  • Physics & Mathematics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Microbiology (AREA)
  • Biochemistry (AREA)
  • Pathology (AREA)
  • Immunology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Medical Informatics (AREA)
  • Surgery (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Plant Pathology (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Other Investigation Or Analysis Of Materials By Electrical Means (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
AU2016225033A 2015-02-27 2016-02-29 Methods and reagents for predicting predisposition to refractive error Ceased AU2016225033B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201562126284P 2015-02-27 2015-02-27
US62/126,284 2015-02-27
PCT/US2016/020033 WO2016138512A1 (en) 2015-02-27 2016-02-29 Methods and reagents for predicting predisposition to refractive error

Publications (2)

Publication Number Publication Date
AU2016225033A1 AU2016225033A1 (en) 2017-10-12
AU2016225033B2 true AU2016225033B2 (en) 2021-11-11

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ID=56789879

Family Applications (1)

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AU2016225033A Ceased AU2016225033B2 (en) 2015-02-27 2016-02-29 Methods and reagents for predicting predisposition to refractive error

Country Status (9)

Country Link
US (1) US10787707B2 (enExample)
EP (1) EP3261525B1 (enExample)
JP (1) JP7240097B2 (enExample)
KR (1) KR102551638B1 (enExample)
CN (1) CN107529987B (enExample)
AU (1) AU2016225033B2 (enExample)
CA (1) CA2977808A1 (enExample)
SG (2) SG11201706933TA (enExample)
WO (1) WO2016138512A1 (enExample)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2017306044B2 (en) 2016-08-01 2022-07-14 University Of Washington Ophthalmic lenses for treating myopia
JP7222981B2 (ja) 2017-05-08 2023-02-15 サイトグラス・ヴィジョン・インコーポレイテッド 近視を軽減するためのコンタクトレンズおよびその製造方法
US10884264B2 (en) 2018-01-30 2021-01-05 Sightglass Vision, Inc. Ophthalmic lenses with light scattering for treating myopia
AU2019302757B2 (en) 2018-07-12 2022-09-01 Sightglass Vision, Inc. Methods and devices for reducing myopia in children
US12416818B2 (en) 2019-03-01 2025-09-16 Sightglass Vision, Inc. Ophthalmic lenses for reducing myopic progression and methods of making the same
CA3137950A1 (en) 2019-04-23 2020-10-29 Sightglass Vision, Inc. Ophthalmic lenses with dynamic optical properties for reducing development of myopia

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5800992A (en) 1989-06-07 1998-09-01 Fodor; Stephen P.A. Method of detecting nucleic acids
US6582908B2 (en) 1990-12-06 2003-06-24 Affymetrix, Inc. Oligonucleotides
US6706867B1 (en) 2000-12-19 2004-03-16 The United States Of America As Represented By The Department Of Health And Human Services DNA array sequence selection
EP1256632A3 (en) 2001-05-07 2004-01-02 Smithkline Beecham Corporation High throughput polymorphism screening
US20040110179A1 (en) 2002-03-15 2004-06-10 Shuber Anthony P. Method for alteration detection
DE60300792T2 (de) 2002-05-09 2005-12-01 Matsushita Electric Industrial Co., Ltd., Kadoma Inline-Elektronenkanone und Farbbildröhre mit selbiger
US20050208555A1 (en) 2004-03-16 2005-09-22 Affymetrix, Inc. Methods of genotyping
ITRM20050325A1 (it) 2005-06-23 2006-12-24 Univ Roma Isoforma di splicing alternativo del gene codificante per la proteina lox-1, usi e metodi relativi.
US7906289B2 (en) 2008-07-28 2011-03-15 Kaohsiung Medical University Using genetic polymorphisms of the BICD1 gene as a method for diagnosing and treating myopia
WO2010075319A2 (en) 2008-12-22 2010-07-01 The Medical College Of Wisconsin, Inc. Method and apparatus for limiting growth of eye length
US20120172419A1 (en) * 2009-09-15 2012-07-05 Medical College Of Wisconsin Research Foundation Inc. Reagents and methods for modulating cone photoreceptor activity
JP5901046B2 (ja) 2010-02-19 2016-04-06 国立大学法人 千葉大学 OATP1B3mRNAの新規な選択的スプライシングバリアント
JP6141193B2 (ja) 2011-01-14 2017-06-07 ザ ユニバーシティ オブ ワシントン スルー イッツ センター フォー コマーシャライゼーションThe University Of Washington Through Its Center For Commercialization 患者の近視になる可能性又は眼軸長関連障害への罹りやすさを決定する方法
WO2012116248A1 (en) 2011-02-24 2012-08-30 Massachusetts Institute Of Technology ALTERNATIVELY SPLICED mRNA ISOFORMS AS PROGNOSTIC INDICATORS FOR METASTATIC CANCER

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
McClements, M. et al., "Variations in opsin coding sequences cause X-linked cone dysfunction syndrome with myopia and dichromacy," Investigative ophthalmology & visual science, 2013, 54(2), pp.1361-1369. *

Also Published As

Publication number Publication date
JP2018512121A (ja) 2018-05-17
SG10202102575SA (en) 2021-04-29
US20180112268A1 (en) 2018-04-26
EP3261525A4 (en) 2018-07-18
EP3261525B1 (en) 2021-09-29
WO2016138512A1 (en) 2016-09-01
JP7240097B2 (ja) 2023-03-15
CN107529987A (zh) 2018-01-02
AU2016225033A1 (en) 2017-10-12
EP3261525A1 (en) 2018-01-03
KR20170122212A (ko) 2017-11-03
US10787707B2 (en) 2020-09-29
HK1248498A1 (zh) 2018-10-19
SG11201706933TA (en) 2017-09-28
CA2977808A1 (en) 2016-09-01
CN107529987B (zh) 2021-04-20
KR102551638B1 (ko) 2023-07-05

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