Prune1-flox 基因敲除小鼠

1. Gholizadeh, Mehdi Agha, Mohammadi-Sarband, Mina, Fardanesh, Fatemeh, Garshasbi, Masoud. 2022. Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies in a consanguineous Iranian family is associated with a homozygous start loss variant in the PRUNE1 gene. In BMC medical genomics, 15, 78. doi:10.1186/s12920-022-01228-6. https://pubmed.ncbi.nlm.nih.gov/35379233/

2. Wu, Xiaoli, Simard, Louise R, Ding, Hao. 2023. Generation of Conditional Knockout Alleles for PRUNE-1. In Cells, 12, . doi:10.3390/cells12040524. https://pubmed.ncbi.nlm.nih.gov/36831191/

3. Xu, Jiadai, Wang, Yawen, Li, Panpan, Wang, Xiaona, Liu, Peng. 2023. PRUNE1 (located on chromosome 1q21.3) promotes multiple myeloma with 1q21 Gain by enhancing the links between purine and mitochondrion. In British journal of haematology, 203, 599-613. doi:10.1111/bjh.19088. https://pubmed.ncbi.nlm.nih.gov/37666675/

4. Magyar, Christina L, Murdock, David R, Burrage, Lindsay C, Lee, Brendan H, Chao, Hsiao-Tuan. 2022. PRUNE1 c.933G>A synonymous variant induces exon 7 skipping, disrupts the DHHA2 domain, and leads to an atypical NMIHBA syndrome presentation: Case report and review of the literature. In American journal of medical genetics. Part A, 188, 1868-1874. doi:10.1002/ajmg.a.62704. https://pubmed.ncbi.nlm.nih.gov/35194938/