JP2010508029A5 - - Google Patents

Download PDF

Info

Publication number
JP2010508029A5
JP2010508029A5 JP2009534893A JP2009534893A JP2010508029A5 JP 2010508029 A5 JP2010508029 A5 JP 2010508029A5 JP 2009534893 A JP2009534893 A JP 2009534893A JP 2009534893 A JP2009534893 A JP 2009534893A JP 2010508029 A5 JP2010508029 A5 JP 2010508029A5
Authority
JP
Japan
Prior art keywords
seq
intron
polymorphism
genotype
gene
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
JP2009534893A
Other languages
English (en)
Japanese (ja)
Other versions
JP2010508029A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2007/082683 external-priority patent/WO2008052167A2/en
Publication of JP2010508029A publication Critical patent/JP2010508029A/ja
Publication of JP2010508029A5 publication Critical patent/JP2010508029A5/ja
Withdrawn legal-status Critical Current

Links

JP2009534893A 2006-10-27 2007-10-26 抗うつ薬による治療時に有害事象を発現する危険性のある患者の識別方法 Withdrawn JP2010508029A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US85497806P 2006-10-27 2006-10-27
PCT/US2007/082683 WO2008052167A2 (en) 2006-10-27 2007-10-26 Methods to identify patients at risk of developing adverse events during treatment with antidepressant medication

Publications (2)

Publication Number Publication Date
JP2010508029A JP2010508029A (ja) 2010-03-18
JP2010508029A5 true JP2010508029A5 (https=) 2010-12-16

Family

ID=39276298

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009534893A Withdrawn JP2010508029A (ja) 2006-10-27 2007-10-26 抗うつ薬による治療時に有害事象を発現する危険性のある患者の識別方法

Country Status (5)

Country Link
US (2) US7906283B2 (https=)
EP (1) EP2087136A2 (https=)
JP (1) JP2010508029A (https=)
CA (1) CA2667812A1 (https=)
WO (1) WO2008052167A2 (https=)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2166112B1 (en) 2008-09-18 2013-06-05 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Means and methods for diagnosing predisposition for treatment emergent suicidal ideation
CA2736936A1 (en) 2008-09-18 2010-03-25 Andreas Menke Means and methods for diagnosing predisposition for treatment emergent suicidal ideation (tesi)
CA2918054C (en) * 2013-07-11 2022-12-13 The Johns Hopkins University A dna methylation and genotype specific biomarker of suicide attempt and/or suicide ideation
US11122997B2 (en) 2015-04-17 2021-09-21 Mayo Foundation For Medical Education And Research Modulating the aryl hydrocarbon receptor system to treat major depressive disorder
CA2891830A1 (en) 2015-05-15 2016-11-15 Centre For Addiction And Mental Health Genetic markers for suicide risk and related methods

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1410036A2 (en) 2001-01-19 2004-04-21 Mindsense Biosystems Ltd. Methods and compositions for diagnosing and treating a subject having depression
US7083921B2 (en) 2001-08-29 2006-08-01 The Board Of Trustees Of The Leland Stanford Junior University Method to determine the risk for side effects of an SSRI treatment in a person
JP5348840B2 (ja) 2003-02-20 2013-11-20 メイヨ・ファウンデーション・フォー・メディカル・エデュケーション・アンド・リサーチ 薬物を選択する方法
WO2004103394A2 (en) * 2003-05-15 2004-12-02 University Of Chicago Method and compositions for nerve regeneration
US20050069936A1 (en) 2003-09-26 2005-03-31 Cornelius Diamond Diagnostic markers of depression treatment and methods of use thereof
US20060160119A1 (en) 2005-01-14 2006-07-20 Barbara Turner Genetic screening for improving treatment of patients diagnosed with depression
US20080299125A1 (en) 2006-06-05 2008-12-04 Perlegen Sciences, Inc. Genetic basis of treatment response in depression patients

Similar Documents

Publication Publication Date Title
Lin et al. High-resolution melting analyses for genetic variants in ARID5B and IKZF1 with childhood acute lymphoblastic leukemia susceptibility loci in Taiwan
JP2012503985A5 (https=)
WO2008048120A2 (en) Methods and compositions for assessment of pulmonary function and disorders
JP2012040029A (ja) 変異の検出方法およびそれに用いるキット
JP2013081450A (ja) 多型検出用プローブ、多型検出方法、薬効判定方法及び多型検出用試薬キット
JP2010508029A5 (https=)
CN103492570B (zh) 一种强直性脊柱炎相关特异性单核苷酸多态性的检测方法及其试剂盒
Gilje et al. High-fidelity DNA polymerase enhances the sensitivity of a peptide nucleic acid clamp PCR assay for K-ras mutations
JP2013074888A (ja) IL28B(rs8099917)とITPA(rs1127354)の変異を検出する方法
CN102808030A (zh) 单核苷多态性rs3888188在检测结核病易感性中的应用
WO2006123955A2 (en) Methods for the assesssment of risk of developing lung cancer using analysis of genetic polymorphisms
US20160076104A1 (en) Methods and compositions for assessment of pulmonary function and disorders
EP2443258A1 (en) Methods and compositions for assessment of pulmonary function and disorders
CN103502469B (zh) 强直性脊柱炎易感性单核苷酸多态性的检测方法、试剂盒及其应用
JP2023515665A5 (https=)
US20100144776A1 (en) Use of snps for the diagnosis of a pain protective haplotype in the gtp cyclohydrolase 1 gene (gch1)
WO2021066038A1 (ja) 膀胱癌治療におけるbcg膀胱内注入療法の治療効果を予測するためのバイオマーカー、方法、キット及びアレイ
US20130281319A1 (en) Methods and compositions for assessment of pulmonary function and disorders
Paradis et al. Quantitative assay for the detection of the V617F variant in the Janus kinase 2 (JAK2) gene using the Luminex xMAP technology
CN104404044B (zh) 与心肌梗死易感相关的anril基因外显子区单核苷酸多态位点的检测方法及其应用
Wang et al. Correlation between OPN gene polymorphisms and the risk of nasopharyngeal carcinoma
CN103502451B (zh) 强直性脊柱炎相关特异性单核苷酸多态性的检测方法及其试剂盒
CN110904215A (zh) 用于同步检测slco1b1基因的两个snp位点的基因多态性的方法
CN103525839B (zh) 包括74g>a突变的cyp2d6基因片段、所编码的蛋白质片段及其应用
Schneider et al. Rapid analysis of XRCC1 polymorphisms using real-time polymerase chain reaction