Literature DB >> 10854099

Positional cloning and characterisation of the human DLGAP2 gene and its exclusion in progressive epilepsy with mental retardation.

S Ranta1, Y Zhang, B Ross, E Takkunen, A Hirvasniemi, A de la Chapelle, T C Gilliam, A E Lehesjoki.   

Abstract

In search of the gene for progressive epilepsy with mental retardation (EPMR) we identified DLGAP2, the human homolog of the gene encoding the rat PSD-95/SAP90-associated protein-2 (Dlgap2). We extended the transcript in both the 5' and 3' directions and characterised the genomic structure of the approximately 10 kb gene. Sequence comparisons of human DLGAP2 cDNA sequences obtained from human testis and brain cDNA libraries with homologous rat genes suggest alternative splicing in the 5' end of the gene. The 5' coding sequence of the testis cDNA is complete, whereas based on homology with the rat gene 103 bp of coding sequence may still be missing in the 5' end of the DLGAP2 brain transcript. DLGAP2 was excluded as the gene responsible for EPMR.

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Year:  2000        PMID: 10854099     DOI: 10.1038/sj.ejhg.5200440

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  13 in total

1.  Genetic variation in imprinted genes is associated with risk of late-onset Alzheimer's disease.

Authors:  Mamoonah Chaudhry; Xingbin Wang; Mikhil N Bamne; Shahida Hasnain; F Yesim Demirci; Oscar L Lopez; M Ilyas Kamboh
Journal:  J Alzheimers Dis       Date:  2015       Impact factor: 4.472

2.  Computational and experimental identification of novel human imprinted genes.

Authors:  Philippe P Luedi; Fred S Dietrich; Jennifer R Weidman; Jason M Bosko; Randy L Jirtle; Alexander J Hartemink
Journal:  Genome Res       Date:  2007-11-30       Impact factor: 9.043

3.  Genetic variability in scaffolding proteins and risk for schizophrenia and autism-spectrum disorders: a systematic review.

Authors:  Jordi Soler; Lourdes Fañanás; Mara Parellada; Marie-Odile Krebs; Guy A Rouleau; Mar Fatjó-Vilas
Journal:  J Psychiatry Neurosci       Date:  2018-05-28       Impact factor: 6.186

4.  Genetic variability in scaffolding proteins and risk for schizophrenia and autism-spectrum disorders: a systematic review.

Authors:  Jordi Soler; Lourdes Fañanás; Mara Parellada; Marie-Odile Krebs; Guy A Rouleau; Mar Fatjó-Vilas
Journal:  J Psychiatry Neurosci       Date:  2018-07       Impact factor: 6.186

5.  Multiomic analysis of mice epilepsy models suggest that miR-21a expression modulates mRNA and protein levels related to seizure deterioration.

Authors:  Xiaoxiao Hu; Xin Fu; A O Jiang; Xukui Yang; Xiaodong Fang; Guohua Gong; Chengxi Wei
Journal:  Genet Res (Camb)       Date:  2015-12-22       Impact factor: 1.588

6.  Transcriptome profiling of the ventral pallidum reveals a role for pallido-thalamic neurons in cocaine reward.

Authors:  Michel Engeln; Megan E Fox; Ramesh Chandra; Eric Y Choi; Hyungwoo Nam; Houman Qadir; Shavin S Thomas; Victoria M Rhodes; Makeda D Turner; Rae J Herman; Cali A Calarco; Mary Kay Lobo
Journal:  Mol Psychiatry       Date:  2022-06-28       Impact factor: 13.437

Review 7.  Insight from animal models of environmentally driven epigenetic changes in the developing and adult brain.

Authors:  Tiffany S Doherty; Tania L Roth
Journal:  Dev Psychopathol       Date:  2016-09-30

8.  Inherited unbalanced translocation (4p16.3p15.32 duplication/8p23.3p23.2deletion) in the four generation pedigree with intellectual disability/developmental delay.

Authors:  Dongmei Hao; Yajuan Li; Lisha Chen; Xiliang Wang; Mengxing Wang; Yuexin Yu
Journal:  Mol Cytogenet       Date:  2021-07-08       Impact factor: 2.009

9.  DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis.

Authors:  Bonnie R Joubert; Janine F Felix; Paul Yousefi; Kelly M Bakulski; Allan C Just; Carrie Breton; Sarah E Reese; Christina A Markunas; Rebecca C Richmond; Cheng-Jian Xu; Leanne K Küpers; Sam S Oh; Cathrine Hoyo; Olena Gruzieva; Cilla Söderhäll; Lucas A Salas; Nour Baïz; Hongmei Zhang; Johanna Lepeule; Carlos Ruiz; Symen Ligthart; Tianyuan Wang; Jack A Taylor; Liesbeth Duijts; Gemma C Sharp; Soesma A Jankipersadsing; Roy M Nilsen; Ahmad Vaez; M Daniele Fallin; Donglei Hu; Augusto A Litonjua; Bernard F Fuemmeler; Karen Huen; Juha Kere; Inger Kull; Monica Cheng Munthe-Kaas; Ulrike Gehring; Mariona Bustamante; Marie José Saurel-Coubizolles; Bilal M Quraishi; Jie Ren; Jörg Tost; Juan R Gonzalez; Marjolein J Peters; Siri E Håberg; Zongli Xu; Joyce B van Meurs; Tom R Gaunt; Marjan Kerkhof; Eva Corpeleijn; Andrew P Feinberg; Celeste Eng; Andrea A Baccarelli; Sara E Benjamin Neelon; Asa Bradman; Simon Kebede Merid; Anna Bergström; Zdenko Herceg; Hector Hernandez-Vargas; Bert Brunekreef; Mariona Pinart; Barbara Heude; Susan Ewart; Jin Yao; Nathanaël Lemonnier; Oscar H Franco; Michael C Wu; Albert Hofman; Wendy McArdle; Pieter Van der Vlies; Fahimeh Falahi; Matthew W Gillman; Lisa F Barcellos; Ashish Kumar; Magnus Wickman; Stefano Guerra; Marie-Aline Charles; John Holloway; Charles Auffray; Henning W Tiemeier; George Davey Smith; Dirkje Postma; Marie-France Hivert; Brenda Eskenazi; Martine Vrijheid; Hasan Arshad; Josep M Antó; Abbas Dehghan; Wilfried Karmaus; Isabella Annesi-Maesano; Jordi Sunyer; Akram Ghantous; Göran Pershagen; Nina Holland; Susan K Murphy; Dawn L DeMeo; Esteban G Burchard; Christine Ladd-Acosta; Harold Snieder; Wenche Nystad; Gerard H Koppelman; Caroline L Relton; Vincent W V Jaddoe; Allen Wilcox; Erik Melén; Stephanie J London
Journal:  Am J Hum Genet       Date:  2016-03-31       Impact factor: 11.043

10.  Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disorders.

Authors:  Wei-Hsien Chien; Susan Shur-Fen Gau; Hsiao-Mei Liao; Yen-Nan Chiu; Yu-Yu Wu; Yu-Shu Huang; Wen-Che Tsai; Ho-Min Tsai; Chia-Hsiang Chen
Journal:  Mol Autism       Date:  2013-08-01       Impact factor: 7.509

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