Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients

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The 5-HT3B subunit is a major determinant of serotonin-receptor function

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Increased efficiency of mRNA 3′ end formation: a new genetic mechanism contributing to hereditary thrombophilia

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Are Schizophrenic and Bipolar Disorders Related? A Review of Family and Molecular Studies

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Variations in the 5-Hydroxytryptamine Type 3B Receptor Gene as Predictors of the Efficacy of Antiemetic Treatment in Cancer Patients

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Association between the 5′ UTR variant C178T of the serotonin receptor gene HTR3A and bipolar affective disorder

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Polymorphism in the 3'-untranslated region of TNFalpha mRNA impairs binding of the post-transcriptional regulatory protein HuR to TNFalpha mRNA

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Systematic screening for mutations in the promoter and the coding region of the 5‐HT_1A gene

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Characterization of disease-associated mutations affecting an exonic splicing enhancer and two cryptic splice sites in exon 13 of the cystic fibrosis transmembrane conductance regulator gene

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Serotonin receptor gene HTR3A variants in schizophrenic and bipolar affective patients.

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Linkage results on 11Q21‐22 in Eastern Quebec pedigrees densely affected by schizophrenia

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Novel mutations in 5-HT3A and 5-HT3B receptor genes not associated with clozapine response

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The human serotonin 7 (5-HT7) receptor gene: genomic organization and systematic mutation screening in schizophrenia and bipolar affective disorder.

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A NON-ITERATIVE ACCURATE ASYMPTOTIC CONFIDENCE INTERVAL FOR THE DIFFERENCE BETWEEN TWO PROPORTIONS

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A novel deletion of the <scp>l</scp>‐ferritin iron‐responsive element responsible for severe hereditary hyperferritinaemia–cataract syndrome

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Lack of genetically determined structural variants of the human serotonin-1E (5-HT1E) receptor protein points to its evolutionary conservation

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Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia

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Human 5-HT5AReceptor Gene: Systematic Screening for DNA Sequence Variation and Linkage Mapping on Chromosome 7q34–q36 Using a Polymorphism in the 5′ Untranslated Region

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