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Carme Fuster

Researcher at Autonomous University of Barcelona

Publications -  44
Citations -  1469

Carme Fuster is an academic researcher from Autonomous University of Barcelona. The author has contributed to research in topics: Aneuploidy & X chromosome. The author has an hindex of 18, co-authored 44 publications receiving 1413 citations.

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Biodistribution, long-term survival, and safety of human adipose tissue-derived mesenchymal stem cells transplanted in nude mice by high sensitivity non-invasive bioluminescence imaging.

TL;DR: It would appear that hAMSCs, contrary to their murine correlatives, could be safe candidates for autologous cell therapy procedures since in the authors' experiments they show undetectable predisposition to oncogenic transformation after cultivation in vitro and implantation in mice.
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Clinical application of multiplex quantitative fluorescent polymerase chain reaction (QF-PCR) for the rapid prenatal detection of common chromosome aneuploidies

TL;DR: The assay proved to be so efficient and reliable that in most aneuploidy cases, in which ultrasound findings were in agreement with the molecular result, therapeutical interventions were possible without waiting for the result of cytogenetic analysis.
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Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR, results of 9 years of clinical experience

TL;DR: Despite being deliberately targeted to common chromosome aneuploidies, the rapid quantitative fluorescent polymerase chain reaction (QF‐PCR) tests can detect the majority of chromosome abnormalities in prenatal diagnosis.
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Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR. Assessment on 18 000 consecutive clinical samples

TL;DR: QF-PCR proved to be efficient and reliable in detecting major numerical chromosome disorders and relieves anxiety of most parents within 24 h from sampling and accelerates therapeutic interventions in the case of an abnormal result.
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Cytogenetic effects of radiotherapy. Breakpoint distribution in induced chromosome aberrations.

TL;DR: The results show that chromosomes 1, 3, and 7 were significantly more affected than other chromosomes by ionizing radiation in vivo, and some bands also showed a special sensitivity to radiation, and band 1q32 was the most affected.