Publications by authors named "M Nakhoul"

Article Synopsis
  • Xp11 translocation renal cell carcinoma (tRCC) is a rare cancer that mostly affects females and is caused by a fusion of the TFE3 gene on chromosome X with other genes.
  • The study explores how TFE3 fusions occur through rearrangements and whether these fusions arise from the active or inactive X chromosomes, shedding light on tRCC's female predominance.
  • Findings show that TFE3 fusions are typically due to reciprocal translocations and that specific translocations involving the inactive X chromosome contribute to the higher incidence of tRCC in females, revealing important insights into cancer genetics and sex differences.
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Pyrene and acene derivatives are an important source of materials for optoelectronic device applications both as emitters and organic semiconductors. The mobility of major charge carriers is correlated with the coupling constants of the respective major charge carrier as well as the relaxation energies. Herein, we have applied range-separated density functionals for the estimation of said values.

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Background: Global tuberculosis (TB) drug resistance (DR) surveillance focuses on rifampicin. We examined the potential of public and surveillance () whole-genome sequencing (WGS) data, to generate expanded country-level resistance prevalence estimates (antibiograms) using in silico resistance prediction.

Methods: We curated and quality-controlled WGS data.

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Background: Organ donation shortage and in particular organ procurement is an international concern as the gap between the number of donors and recipients is steadily growing. Organ procurement is a chain of steps with donor identification and referral (ID&R) as the very first link in this chain. Failure of this step hinders the progress in the organ transplantation program.

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Article Synopsis
  • Xp11 translocation renal cell carcinoma (tRCC) is a type of kidney cancer that mostly affects females, caused by genetic rearrangements on the X chromosome.
  • The study investigates how these genetic fusions occur, focusing on whether they emerge from active or inactive X chromosomes in females and their link to the female predominance in this cancer.
  • The findings reveal a significant 2:1 ratio of female to male fusions resulting from X:autosomal translocations, suggesting that inactive X chromosomes contribute to this female bias in tRCC and highlight the unique role of sex chromosomes in cancer development.
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