Platelet genomics beats the catch-22.
نویسنده
چکیده
advantages such as a larger cargo load ( 14 kb, allowing the inclusion of more genes or larger regulatory elements), different insertion preferences, and the exclusive use of TTAA target sequence.2-4 For some applications, the PB transposition offers an additional advantage: the integrated transposon can be precisely excised by re-expression of PB transposase transiently as shown by several groups in diverse systems. Although the current PB system is inferior for HSPCs to the SB system using the superactive SB100X, I predict that the PB transposase will be improved significantly soon. Together, these transposon systems offer hopes to achieve virusfree, long-term gene transfer and expression in HSPCs and other cell types for various forms of gene therapy. Conflict-of-interest disclosure: The author declares no competing financial interests. ■
منابع مشابه
Detection of 22 q11.2 hemizygous deletion by interphase FISH in a patient with features of CATCH 22 syndrome.
We report an eight years female child with clinical and molecular cytogenetic findings consistent with CATCH 22 syndrome characterized by cardiac defect, typical facial dysmorphism, mental deficiency and chromosome 22 q11.2 deletion. Interphase FISH with 22q 11.2 probe demonstrated hemizygous deletion in 98.5% nuclei. Interphase FISH for diagnosis of CATCH 22 syndrome has not been reported prev...
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CATCH 22 syndrome is characterized by cardiac defects, abnormal facial features, thymic hypoplasia, cleft palate, and hypocalcemia. It is associated with a deletion within chromosome 22q11. This syndrome is not a simple disease. It includes DiGeorge syndrome, conotruncal anomaly face syndrome, and velocardiofacial syndrome. In DiGeorge’s original report, he focused on thymic hypoplasia and hypo...
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ورودعنوان ژورنال:
- Blood
دوره 114 7 شماره
صفحات -
تاریخ انتشار 2009