Literature DB >> 15318033

An association study of PCQAP polymorphisms and schizophrenia.

Harinder K Sandhu1, Nancy Hollenbeck, Thomas H Wassink, Robert A Philibert.   

Abstract

INTRODUCTION: PCQAP is a member of the mediator family of transcription co-activators that is found in the region of 22q11, which is consistently deleted in DiGeorges/velocranialfacial (VCF) syndrome. As such, it is a gene of interest to behavioral geneticists because VCF is also associated with a high rate of psychosis and because defects in other mediator genes have been linked to psychosis and abnormal neurodevelopmental abnormalities. Recently, DeLuca and colleagues reported that polymorphisms in a trinucleotide repeat in exon 7 of PCQAP were associated with schizophrenia in a case-control study of Italian schizophrenics. OBJECTIVE AND METHODS: To confirm and extend the prior findings, we conducted a case-control association analysis using DNA from 233 schizophrenics and 371 random controls.
RESULTS: Unfortunately, we did not find any significant differences in the distribution of CAG repeat alleles between subjects and controls.
CONCLUSIONS: These findings limit the role of exon 7 PCQAP polymorphisms in the pathogenesis of schizophrenia.

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Year:  2004        PMID: 15318033     DOI: 10.1097/00041444-200409000-00010

Source DB:  PubMed          Journal:  Psychiatr Genet        ISSN: 0955-8829            Impact factor:   2.458


  5 in total

1.  No association between the genetic polymorphisms in the RTN4R gene and schizophrenia in the Chinese population.

Authors:  J Meng; Y Shi; X Zhao; S Guo; H Wang; Y Zheng; R Tang; G Feng; N Gu; H Liu; S Zhu; L He
Journal:  J Neural Transm (Vienna)       Date:  2006-08-10       Impact factor: 3.575

2.  Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios.

Authors:  M Daniele Fallin; Virginia K Lasseter; Dimitrios Avramopoulos; Kristin K Nicodemus; Paula S Wolyniec; John A McGrath; Gary Steel; Gerald Nestadt; Kung-Yee Liang; Richard L Huganir; David Valle; Ann E Pulver
Journal:  Am J Hum Genet       Date:  2005-10-28       Impact factor: 11.025

3.  Promoter Hypermethylation of Tumor-Suppressor Genes p16INK4a, RASSF1A, TIMP3, and PCQAP/MED15 in Salivary DNA as a Quadruple Biomarker Panel for Early Detection of Oral and Oropharyngeal Cancers.

Authors:  Chamikara Liyanage; Asanga Wathupola; Sanjayan Muraleetharan; Kanthi Perera; Chamindie Punyadeera; Preethi Udagama
Journal:  Biomolecules       Date:  2019-04-12

Review 4.  A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review.

Authors:  Luis Fernández; Julián Nevado; Fernando Santos; Damià Heine-Suñer; Victor Martinez-Glez; Sixto García-Miñaur; Rebeca Palomo; Alicia Delicado; Isidora López Pajares; María Palomares; Luis García-Guereta; Eva Valverde; Federico Hawkins; Pablo Lapunzina
Journal:  BMC Med Genet       Date:  2009-06-02       Impact factor: 2.103

5.  Salivary DNA methylation panel to diagnose HPV-positive and HPV-negative head and neck cancers.

Authors:  Yenkai Lim; Yunxia Wan; Dimitrios Vagenas; Dmitry A Ovchinnikov; Chris F L Perry; Melissa J Davis; Chamindie Punyadeera
Journal:  BMC Cancer       Date:  2016-09-23       Impact factor: 4.430

  5 in total

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