日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Corrigendum: Mutations in genes encoding condensins cause microcephaly through decatenation failure at mitosis

更正:编码凝聚素的基因突变会导致有丝分裂过程中解链失败,从而引起小头畸形。

Martin, Carol-Anne; Murray, Jennie E; Carroll, Paula; Leitch, Andrea; MacKenzie, Karen J; Halachev, Mihail; Fetit, Ahmed E; Keith, Charlotte; Bicknell, Louise S; Fluteau, Adeline; Gautier, Philippe; Hall, Emma A; Joss, Shelagh; Soares, Gabriela; Silva, João; Bober, Michael B; Duker, Angela; Wise, Carol A; Quigley, Alan J; Phadke, Shubha R; Wood, Andrew J; Vagnarelli, Paola; Jackson, Andrew P

A conserved role for Notch signaling in priming the cellular response to Shh through ciliary localisation of the key Shh transducer Smo.

Notch 信号在启动细胞对 Shh 的反应中发挥着保守作用,其机制是通过关键 Shh 转导蛋白 Smo 的纤毛定位

Stasiulewicz Magdalena, Gray Shona D, Mastromina Ioanna, Silva Joana C, Björklund Mia, Seymour Philip A, Booth David, Thompson Calum, Green Richard J, Hall Emma A, Serup Palle, Dale J Kim

Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis

人类和小鼠的WDR35基因突变会导致纤毛发生异常,从而引发短肋多指畸形综合征。

Mill, Pleasantine; Lockhart, Paul J; Fitzpatrick, Elizabeth; Mountford, Hayley S; Hall, Emma A; Reijns, Martin A M; Keighren, Margaret; Bahlo, Melanie; Bromhead, Catherine J; Budd, Peter; Aftimos, Salim; Delatycki, Martin B; Savarirayan, Ravi; Jackson, Ian J; Amor, David J