نتایج جستجو برای: drd2 gene

تعداد نتایج: 1141931  

Journal: :Human molecular genetics 2016
Brian E Cade Daniel J Gottlieb Diane S Lauderdale David A Bennett Aron S Buchman Sarah G Buxbaum Philip L De Jager Daniel S Evans Tibor Fülöp Sina A Gharib W Craig Johnson Hyun Kim Emma K Larkin Seung Ku Lee Andrew S Lim Naresh M Punjabi Chol Shin Katie L Stone Gregory J Tranah Jia Weng Kristine Yaffe Phyllis C Zee Sanjay R Patel Xiaofeng Zhu Susan Redline Richa Saxena

Sleep duration is implicated in the etiologies of chronic diseases and premature mortality. However, the genetic basis for sleep duration is poorly defined. We sought to identify novel genetic components influencing sleep duration in a multi-ethnic sample. Meta-analyses were conducted of genetic associations with self-reported, habitual sleep duration from seven Candidate Gene Association Resou...

Journal: :Psychiatric genetics 2012
Emma S Nyman Anu Loukola Teppo Varilo Anja Taanila Tuula Hurtig Irma Moilanen Sandra Loo James J McGough Marjo-Riitta Järvelin Susan L Smalley Stanley F Nelson Leena Peltonen

Attention-deficit/hyperactivity disorder (ADHD) is a childhood-onset neurodevelopmental disorder with a significant public-health impact. Previously, we described a candidate gene study in a population-based birth cohort that demonstrated an association with ADHD-affected males and the dopamine receptor D2 (DRD2). The current study evaluates potential associations of dopamine receptor genes and...

Journal: :Food & function 2012
Amanda L C Chen Kenneth Blum Thomas J H Chen John Giordano B William Downs David Han Debmalya Barh Eric R Braverman

While there is a considerable body of literature correlating the role of dopaminergic genes and obesity, body mass index, body type, overeating, carbohydrate binging, energy expenditure and low dopamine D2 receptor (D2R) receptor density, there is a paucity of research concerning the dopamine D2 receptor gene (DRD2) variants and percent body fat. We report here the potential association of DRD2...

Journal: :Human molecular genetics 2003
Jubao Duan Mark S Wainwright Josep M Comeron Naruya Saitou Alan R Sanders Joel Gelernter Pablo V Gejman

Although changes in nucleotide sequence affecting the composition and the structure of proteins are well known, functional changes resulting from nucleotide substitutions cannot always be inferred from simple analysis of DNA sequence. Because a strong synonymous codon usage bias in the human DRD2 gene, suggesting selection on synonymous positions, was revealed by the relative independence of th...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1999
C Klein M F Brin P Kramer M Sena-Esteves D de Leon D Doheny S Bressman S Fahn X O Breakefield L J Ozelius

Hereditary autosomal dominant myoclonus dystonia (MD) is a movement disorder characterized by involuntary lightning jerks and dystonic movements and postures alleviated by alcohol. Although various large families with MD have been described, no positive linkage has been found to a chromosomal location. We report a family with eight members with MD. Linkage analysis identified a 23-centimorgan r...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2012
C Savio Chan Jayms D Peterson Tracy S Gertler Kelly E Glajch Ruth E Quintana Qiaoling Cui Luke E Sebel Joshua L Plotkin Weixing Shen Myriam Heiman Nathaniel Heintz Paul Greengard D James Surmeier

Mice carrying bacterial artificial chromosome (BAC) transgenes have become important tools for neuroscientists, providing a powerful means of dissecting complex neural circuits in the brain. Recently, it was reported that one popular line of these mice--mice possessing a BAC transgene with a D(2) dopamine receptor (Drd2) promoter construct coupled to an enhanced green fluorescent protein (eGFP)...

Journal: :Human molecular genetics 2007
Robert Goold Michael Hubank Abigail Hunt Janice Holton Rajesh P Menon Tamas Revesz Massimo Pandolfo Antoni Matilla-Dueñas

Ataxin 1 (Atxn1) is a protein of unknown function associated with spinocerebellar ataxia type 1 (SCA1), a neurodegenerative disease of late onset with variable degrees of cerebellar ataxia, ophthalmoplegia and neuropathy. SCA1 is caused by the toxic effects triggered by an expanded polyglutamine (polyQ) within Atxn1 resulting in neurodegeneration in the cerebellum, brain stem and spinocerebella...

Journal: :Cognitive, affective & behavioral neuroscience 2006
John Fossella Adam E Green Jin Fan

The specificity of genetic effects on brain activation is a central issue in understanding how molecular actions at the synapse relate to anatomic patterns of brain activity. In an effort to understand the basis for the specificity of gene-associated brain activity, we explore a well-studied genetic polymorphism, TaqIA, which lies downstream of the DRD2 gene in the protein-encoding region of a ...

2012
Seungmae Seo Gwen Lomberk Angela Mathison Navtej Buttar Jewel Podratz Ezequiel Calvo Juan Iovanna Stephen Brimijoin Anthony Windebank Raul Urrutia

The importance of Krüppel-like factor (KLF)-mediated transcriptional pathways in the biochemistry of neuronal differentiation has been recognized relatively recently. Elegant studies have revealed that KLF proteins are important regulators of two major molecular and cellular processes critical for neuronal cell differentiation: neurite formation and the expression of neurotransmitter-related ge...

2017
Muhammad Imran Qadeer Ali Amar J. John Mann Shahida Hasnain

Genetic factors contribute to antisocial and criminal behavior. Dopamine transporter DAT-1 (SLC6A3) and DRD2 gene for the dopamine-2 receptor are dopaminergic system genes that regulate dopamine reuptake and signaling, and may be part of the pathogenesis of psychiatric disorders including antisocial behaviors and traits. No previous studies have analyzed DAT-1 and DRD2 polymorphisms in convicte...

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