Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiency.
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Cited by 119 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Epithelial Cell Transformation and Senescence as Indicators of Genome Aging: Current Advances and Unanswered Questions;International Journal of Molecular Sciences;2021-07-14
2. Progressive B Cell Loss in Revertant X-SCID;Journal of Clinical Immunology;2020-07-17
3. Do not let them slip through the net: Catching a case of leaky severe combined immunodeficiency;Journal of Paediatrics and Child Health;2019-11-13
4. A statistical measure for the skewness of X chromosome inactivation based on family trios;BMC Genetics;2018-12
5. Exome sequence identified a c.320A > G ALG13 variant in a female with infantile epileptic encephalopathy with normal glycosylation and random X inactivation: Review of the literature;European Journal of Medical Genetics;2017-10
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