Associated Papers
Actionable perturbations of damage responses by TCL1/ATM and epigenetic lesions form the basis of T-PLL.
Schrader A et al.
Nature Communications, 2018
29449575 (PubMed )
Supplement: 41467_2017_2688_MOESM20_ESM.xlsx › c__Freq_TP092
Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP.
Coll M et al.
Plos One, 2017
Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.
Ryu GM et al.
Nucleic Acids Research, 2009
19139070 (PubMed )
Supplement: gkn1008_nar-01723-s-2008-File009.xls › TypeII_
Characterization of the effects of four HTR3B polymorphisms on human 5-HT3AB receptor expression and signalling.
Krzywkowski K et al.
Pharmacogenetics and Genomics, 2008
Naturally occurring variants in the HTR3B gene significantly alter properties of human heteromeric 5-hydroxytryptamine-3A/B receptors.
Walstab J et al.
Pharmacogenetics and Genomics, 2008
Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients.
Frank B et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2004
Mutational analysis of serotonin receptor genes: HTR3A and HTR3B in fibromyalgia patients.
Frank B et al.
Clinical Rheumatology, 2004
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