Publications by authors named "Bregje Christiaenssen"

Article Synopsis
  • * Whole exome sequencing (WES) on family members revealed a specific mutation (c.195del/p.(Thr66ProfsTer55)) that linked with affected individuals, along with two additional variants in SSX1 and USP27X genes.
  • * RNA sequencing showed 14 differentially expressed genes related to neurological disorders in the affected males, reinforcing the connection between the DLG3 mutation and the observed clinical issues in the family.
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GPCRs arguably represent the most effective current therapeutic targets for a plethora of diseases. GPCRs also possess a pivotal role in the regulation of the physiological balance between healthy and pathological conditions; thus, their importance in systems biology cannot be underestimated. The molecular diversity of GPCR signaling systems is likely to be closely associated with disease-associated changes in organismal tissue complexity and compartmentalization, thus enabling a nuanced GPCR-based capacity to interdict multiple disease pathomechanisms at a systemic level.

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