Pages that link to "Q28588491"

The following pages link to Restless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon (Q28588491):

Displaying 41 items.

• Meis homeobox 1 (Q21495981) (← links)
• Restless Legs Syndrome: Current Concepts about Disease Pathophysiology (Q26740533) (← links)
• Genomic Views of Transcriptional Enhancers: Essential Determinants of Cellular Identity and Activity-Dependent Responses in the CNS (Q26782959) (← links)
• Nuclear organization and 3D chromatin architecture in cognition and neuropsychiatric disorders (Q28077403) (← links)
• MEIS1 variant as a determinant of autonomic imbalance in Restless Legs Syndrome. (Q30846389) (← links)
• Allele-specific quantitative proteomics unravels molecular mechanisms modulated by cis-regulatory PPARG locus variation (Q33558410) (← links)
• Mechanisms of iron metabolism in Caenorhabditis elegans (Q33658871) (← links)
• Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome (Q33685725) (← links)
• Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits (Q33855009) (← links)
• Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome (Q33858791) (← links)
• Enhancer variants: evaluating functions in common disease (Q34624842) (← links)
• Path from schizophrenia genomics to biology: gene regulation and perturbation in neurons derived from induced pluripotent stem cells and genome editing (Q35095120) (← links)
• Non-coding genetic variants in human disease (Q36065325) (← links)
• Common variation in atrial fibrillation: navigating the path from genetic association to mechanism (Q36650580) (← links)
• Sensitive detection of chromatin-altering polymorphisms reveals autoimmune disease mechanisms (Q38896272) (← links)
• Animal models of RLS phenotypes (Q39007031) (← links)
• Retinoic Acid Receptor β Controls Development of Striatonigral Projection Neurons through FGF-Dependent and Meis1-Dependent Mechanisms (Q40382542) (← links)
• Modeling disease risk through analysis of physical interactions between genetic variants within chromatin regulatory circuitry (Q40513382) (← links)
• Meis1: effects on motor phenotypes and the sensorimotor system in mice (Q41440563) (← links)
• Topologically associating domains are ancient features that coincide with Metazoan clusters of extreme noncoding conservation (Q41620969) (← links)
• Intragenic CpG islands play important roles in bivalent chromatin assembly of developmental genes (Q41989052) (← links)
• Two new targeted alleles for the comprehensive analysis of Meis1 functions in the mouse. (Q42182352) (← links)
• Association of Restless Legs Syndrome With Incident Parkinson's Disease (Q46768619) (← links)
• Conserved non-coding elements: developmental gene regulation meets genome organization (Q47112088) (← links)
• Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis (Q47243963) (← links)
• Sleep disturbance by pramipexole is modified by Meis1 in mice (Q47711250) (← links)
• A screen for deeply conserved non-coding GWAS SNPs uncovers a MIR-9-2 functional mutation associated to retinal vasculature defects in human (Q50420340) (← links)
• Lack of Association Between Shape and Volume of Subcortical Brain Structures and Restless Legs Syndrome. (Q55038904) (← links)
• Restless Legs Syndrome and Other Movement Disorders of Sleep-Treatment Update (Q58563261) (← links)
• Differential Dopamine D1 and D3 Receptor Modulation and Expression in the Spinal Cord of Two Mouse Models of Restless Legs Syndrome (Q58764775) (← links)
• Genomic Enhancers in Brain Health and Disease (Q61818064) (← links)
• Genetics of Restless Legs Syndrome (RLS) (Q61980338) (← links)
• Iron in Restless Legs Syndrome (Q61980376) (← links)
• Serum Ferritin Levels in Parkinson's Disease Patients with and without Restless Legs Syndrome. (Q64928536) (← links)
• MEIS1 and Restless Legs Syndrome: A Comprehensive Review (Q90265009) (← links)
• A novel measure of non-coding genome conservation identifies genomic regulatory blocks within primates (Q90390258) (← links)
• Comorbidities, treatment, and pathophysiology in restless legs syndrome (Q91661113) (← links)
• Evolutionary Loss of Genomic Proximity to Conserved Noncoding Elements Impacted the Gene Expression Dynamics During Mammalian Brain Development (Q91842299) (← links)
• The Role of BTBD9 in Striatum and Restless Legs Syndrome (Q92831388) (← links)
• Gene Regulatory Networks in Peripheral Mononuclear Cells Reveals Critical Regulatory Modules and Regulators of Multiple Sclerosis (Q93106633) (← links)
• SKOR1 has a transcriptional regulatory role on genes involved in pathways related to restless legs syndrome (Q96641016) (← links)