Pages that link to "Q34013921"
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The following pages link to Variant between CPT1B and CHKB associated with susceptibility to narcolepsy (Q34013921):
Displaying 50 items.
- Effects of oral L-carnitine administration in narcolepsy patients: a randomized, double-blind, cross-over and placebo-controlled trial (Q21133761) (← links)
- Polymorphism located between CPT1B and CHKB, and HLA-DRB1*1501-DQB1*0602 haplotype confer susceptibility to CNS hypersomnias (essential hypersomnia) (Q21143792) (← links)
- Abnormally low serum acylcarnitine levels in narcolepsy patients (Q24618853) (← links)
- Genetics of Sleep and Sleep Disorders (Q24619903) (← links)
- Pharmacological validation of candidate causal sleep genes identified in an N2 cross (Q24623267) (← links)
- Control of sleep and wakefulness (Q24634619) (← links)
- Narcolepsy is strongly associated with the T-cell receptor alpha locus (Q24649513) (← links)
- Comparative Transcriptomes and EVO-DEVO Studies Depending on Next Generation Sequencing (Q26778783) (← links)
- An approach based on a genome-wide association study reveals candidate loci for narcolepsy (Q28289535) (← links)
- Identification of the variations in the CPT1B and CHKB genes along with the HLA-DQB1*06:02 allele in Turkish narcolepsy patients and healthy persons (Q28660390) (← links)
- Genome-wide association study of alcohol dependence implicates KIAA0040 on chromosome 1q (Q28943436) (← links)
- Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C (Q29619541) (← links)
- Narcolepsy as an autoimmune disease: the role of H1N1 infection and vaccination. (Q30362783) (← links)
- Inborn errors of metabolism in the biosynthesis and remodelling of phospholipids (Q33417443) (← links)
- Human difference in the genomic era: Facilitating a socially responsible dialogue (Q33588176) (← links)
- Hypocretin/orexin and narcolepsy: new basic and clinical insights (Q33814590) (← links)
- Kinase mutations in human disease: interpreting genotype-phenotype relationships (Q34088851) (← links)
- Highly parallel and short-acting amplification with locus-specific primers to detect single nucleotide polymorphisms by the DigiTag2 assay (Q34130851) (← links)
- Genome-Wide Association Studies of Sleep Disorders (Q34545632) (← links)
- A congenital muscular dystrophy with mitochondrial structural abnormalities caused by defective de novo phosphatidylcholine biosynthesis (Q35040218) (← links)
- Genetic underpinnings of obstructive sleep apnea: are we making progress? (Q35406853) (← links)
- Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population (Q35641758) (← links)
- TCRA, P2RY11, and CPT1B/CHKB associations in Chinese narcolepsy (Q35783354) (← links)
- Follow-up association study of linkage regions reveals multiple candidate genes for carotid plaque in Dominicans. (Q36074782) (← links)
- Central Disorders of Hypersomnolence: Focus on the Narcolepsies and Idiopathic Hypersomnia (Q36411331) (← links)
- Animal models of narcolepsy (Q36764549) (← links)
- NKAIN1-SERINC2 is a functional, replicable and genome-wide significant risk gene region specific for alcohol dependence in subjects of European descent (Q36773254) (← links)
- Evidence for shared genetic risk between methamphetamine-induced psychosis and schizophrenia (Q37103392) (← links)
- Next-generation sequencing in understanding complex neurological disease (Q37331388) (← links)
- Expression quantitative trait loci detected in cell lines are often present in primary tissues (Q37397399) (← links)
- Modeling the genetic basis for human sleep disorders in Drosophila (Q38117145) (← links)
- Hypocretin (orexin) biology and the pathophysiology of narcolepsy with cataplexy (Q38366488) (← links)
- Lessons from Genome-Wide Search for Disease-Related Genes with Special Reference to HLA-Disease Associations (Q38644966) (← links)
- Genome-wide analysis of CNV (copy number variation) and their associations with narcolepsy in a Japanese population (Q39217292) (← links)
- Genome-wide association study of HLA-DQB1*06:02 negative essential hypersomnia (Q40341088) (← links)
- Evaluation of polygenic risks for narcolepsy and essential hypersomnia (Q40519647) (← links)
- Genome-Wide Association Studies in Obstructive Sleep Apnea. Will We Catch a Black Cat in a Dark Room? (Q41631454) (← links)
- Current and Future Treatment Options for Narcolepsy: A Review. (Q41901749) (← links)
- A new Thematic Series: genetics of human lipid diseases (Q42757182) (← links)
- Potentiation of a functional autoantibody in narcolepsy by a cholinesterase inhibitor. (Q43266688) (← links)
- Narcolepsy susceptibility gene CCR3 modulates sleep-wake patterns in mice. (Q47094264) (← links)
- Genome-wide gene expression profiling of human narcolepsy. (Q47397164) (← links)
- Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy (Q48344918) (← links)
- Shiftwork-Mediated Disruptions of Circadian Rhythms and Sleep Homeostasis Cause Serious Health Problems. (Q52690506) (← links)
- Genetics of narcolepsy (Q60916876) (← links)
- Polymorphism located in TCRA locus confers susceptibility to essential hypersomnia with HLA-DRB1*1501-DQB1*0602 haplotype (Q84933891) (← links)
- A missense variant in PER2 is associated with delayed sleep-wake phase disorder in a Japanese population (Q90134177) (← links)
- Association between genetic risk scores and risk of narcolepsy: a case-control study (Q90348238) (← links)
- Recent advances in understanding the genetics of sleep (Q91791910) (← links)
- A variant at 9q34.11 is associated with HLA-DQB1*06:02 negative essential hypersomnia (Q91860704) (← links)