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Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78). [electronic resource] by
- Estrada-Cuzcano, Alejandro
- Martin, Shaun
- Chamova, Teodora
- Synofzik, Matthis
- Timmann, Dagmar
- Holemans, Tine
- Andreeva, Albena
- Reichbauer, Jennifer
- De Rycke, Riet
- Chang, Dae-In
- van Veen, Sarah
- Samuel, Jean
- Schöls, Ludger
- Pöppel, Thorsten
- Mollerup Sørensen, Danny
- Asselbergh, Bob
- Klein, Christine
- Zuchner, Stephan
- Jordanova, Albena
- Vangheluwe, Peter
- Tournev, Ivailo
- Schüle, Rebecca
Producer: 20170512
In:
Brain : a journal of neurology vol. 140
Availability: No items available.
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2718.
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DNA methylation modifier LSH inhibits p53 ubiquitination and transactivates p53 to promote lipid metabolism. [electronic resource] by
- Chen, Ling
- Shi, Ying
- Liu, Na
- Wang, Zuli
- Yang, Rui
- Yan, Bin
- Liu, Xiaoli
- Lai, Weiwei
- Liu, Yating
- Xiao, Desheng
- Zhou, Hu
- Cheng, Yan
- Cao, Ya
- Liu, Shuang
- Xia, Zanxian
- Tao, Yongguang
Producer: 20200526
In:
Epigenetics & chromatin vol. 12
Availability: No items available.
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2719.
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