JP2008504837A5 - - Google Patents

Download PDF

Info

Publication number
JP2008504837A5
JP2008504837A5 JP2007519914A JP2007519914A JP2008504837A5 JP 2008504837 A5 JP2008504837 A5 JP 2008504837A5 JP 2007519914 A JP2007519914 A JP 2007519914A JP 2007519914 A JP2007519914 A JP 2007519914A JP 2008504837 A5 JP2008504837 A5 JP 2008504837A5
Authority
JP
Japan
Prior art keywords
autism
pitx1
subject
spectrum disorder
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.)
Granted
Application number
JP2007519914A
Other languages
English (en)
Japanese (ja)
Other versions
JP4949240B2 (ja
JP2008504837A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/IB2005/002319 external-priority patent/WO2006003520A2/en
Publication of JP2008504837A publication Critical patent/JP2008504837A/ja
Publication of JP2008504837A5 publication Critical patent/JP2008504837A5/ja
Application granted granted Critical
Publication of JP4949240B2 publication Critical patent/JP4949240B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

JP2007519914A 2004-07-01 2005-06-30 転写因子をコードするヒト自閉症素因遺伝子及びその使用 Expired - Fee Related JP4949240B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US58413004P 2004-07-01 2004-07-01
US60/584,130 2004-07-01
PCT/IB2005/002319 WO2006003520A2 (en) 2004-07-01 2005-06-30 Human autism predisposition gene encoding a transcription factor and uses thereof

Publications (3)

Publication Number Publication Date
JP2008504837A JP2008504837A (ja) 2008-02-21
JP2008504837A5 true JP2008504837A5 (https=) 2008-07-24
JP4949240B2 JP4949240B2 (ja) 2012-06-06

Family

ID=35432082

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007519914A Expired - Fee Related JP4949240B2 (ja) 2004-07-01 2005-06-30 転写因子をコードするヒト自閉症素因遺伝子及びその使用

Country Status (10)

Country Link
US (1) US20070218068A1 (https=)
EP (1) EP1761649B1 (https=)
JP (1) JP4949240B2 (https=)
AT (1) ATE382101T1 (https=)
AU (1) AU2005258838B2 (https=)
CA (1) CA2571365A1 (https=)
DE (1) DE602005004026T2 (https=)
ES (1) ES2299059T3 (https=)
IL (1) IL179751A (https=)
WO (1) WO2006003520A2 (https=)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110118135A1 (en) * 2008-01-09 2011-05-19 State Matthew W Mutations in Contaction Associated Protein 2 (CNTNAP2) are Associated with Increased Risk for Ideopathic Autism
WO2009150221A1 (en) * 2008-06-12 2009-12-17 Integragen A method for autism prediction
EP2963129A3 (en) * 2008-11-12 2016-05-11 University of Utah Research Foundation Autism associated genetic markers
WO2011067296A1 (en) 2009-12-01 2011-06-09 Integragen A combination of eight risk alleles associated with autism
KR101167942B1 (ko) 2010-02-12 2012-07-23 차의과학대학교 산학협력단 Alg12 유전자로부터 유래된 단일염기다형을 포함하는 폴리뉴클레오티드, 이를 포함하는 마이크로어레이 및 진단키트, 및 이를 이용한 자폐 스펙트럼 장애 분석방법
CA2797319A1 (en) 2010-05-04 2011-11-10 Integragen A new combination of eight risk alleles associated with autism
EP2860265B1 (en) 2011-02-24 2016-10-26 The Chinese University of Hong Kong Determining fetal DNA percentage for twins
CN111808943B (zh) * 2020-06-18 2021-07-20 重庆浦洛通基因医学研究院有限公司 一种精神类个体化用药基因检测方法

Similar Documents

Publication Publication Date Title
Chen et al. Adding genetic risk score to family history identifies twice as many high‐risk men for prostate cancer: results from the prostate cancer prevention trial
Froehlich et al. Clinical importance of risk variants in the dihydropyrimidine dehydrogenase gene for the prediction of early‐onset fluoropyrimidine toxicity
Knight et al. Conditional analysis identifies three novel major histocompatibility complex loci associated with psoriasis
Parnell et al. The autoimmune disease-associated transcription factors EOMES and TBX21 are dysregulated in multiple sclerosis and define a molecular subtype of disease
Hanson et al. Genetic Variants in ERAP 1 and ERAP 2 Associated With Immune‐Mediated Diseases Influence Protein Expression and the Isoform Profile
Shi et al. Association between single nucleotide polymorphisms in deoxycytidine kinase and treatment response among acute myeloid leukaemia patients
Medina et al. RHOA is a modulator of the cholesterol-lowering effects of statin
do Rego Borges et al. Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Brazilian population with high African ancestry
JP2012503985A5 (https=)
EP2730663B1 (en) Genetic factors associated with inhibitor development in hemophilia A
Lu et al. Single nucleotide polymorphisms within interferon signaling pathway genes are associated with colorectal cancer susceptibility and survival
Duan et al. DTNBP1 (Dystrobrevin binding protein 1) and schizophrenia: association evidence in the 3′ end of the gene
Onrat et al. Prevalence of myocardial infarction polymorphisms in Afyonkarahisar, Western Turkey
JP2008504837A5 (https=)
Radwan et al. Comprehensive evaluation of the association of APOE genetic variation with plasma lipoprotein traits in US whites and African blacks
Wang et al. Polymorphisms of ST 2‐IL 18R1‐IL 18 RAP gene cluster: a new risk for autoimmune thyroid diseases
Li et al. Analysis of ADAM17 polymorphisms and susceptibility to sporadic abdominal aortic aneurysm
Shrif et al. Evaluation of the effects of VKORC1 polymorphisms and haplotypes, CYP2C9 genotypes, and clinical factors on warfarin response in Sudanese patients
Ramsey et al. Genetics of pleiotropic effects of dexamethasone
Umamaheswaran et al. Genetic analysis of OCT1 gene polymorphisms in an Indian population
Hannula-Jouppi et al. Genetic susceptibility to non-necrotizing erysipelas/cellulitis
Maekawa et al. Development of a rapid and inexpensive assay for detecting a surrogate genetic polymorphism of HLA-B* 58: 01: a partially predictive but useful biomarker for allopurinol-related Stevens-Johnson syndrome/toxic epidermal necrolysis in Japanese
Kawasaki et al. Association of TNFAIP3 polymorphism with susceptibility to systemic lupus erythematosus in a Japanese population
Masoodi et al. Computational analysis of breast cancer GWAS loci identifies the putative deleterious effect of STXBP4 and ZNF404 gene variants
JP2008532499A5 (https=)