PubMed (GeneRIF) for id: 113612

Year	Number of Results
2003	1
2004	1
2010	2
2011	1
2013	1
2014	2
2015	2
2016	4
2017	5
2018	1
2019	1
2020	1
2021	1
2022	2
2024	0

1

Human Orphan Cytochrome P450 2U1 Catalyzes the ω-Hydroxylation of Leukotriene B₄.

Nouri K, Pietrancosta N, Le Corre L, Dansette PM, Mansuy D, Boucher JL. Nouri K, et al. Int J Mol Sci. 2022 Nov 23;23(23):14615. doi: 10.3390/ijms232314615. Int J Mol Sci. 2022. PMID: 36498943 Free PMC article.

2

Generation of iPSC lines from hereditary spastic paraplegia 56 (SPG56) patients and family members carrying CYP2U1 mutations.

Leeson HC, Goh D, Coman D, Wolvetang EJ. Leeson HC, et al. Stem Cell Res. 2022 Oct;64:102917. doi: 10.1016/j.scr.2022.102917. Epub 2022 Sep 14. Stem Cell Res. 2022. PMID: 36166872 Free article.

3

Implication of folate deficiency in CYP2U1 loss of function.

Pujol C, Legrand A, Parodi L, Thomas P, Mochel F, Saracino D, Coarelli G, Croon M, Popovic M, Valet M, Villain N, Elshafie S, Issa M, Zuily S, Renaud M, Marelli-Tosi C, Legendre M, Trimouille A, Kemlin I, Mathieu S, Gleeson JG, Lamari F, Galatolo D, Alkouri R, Tse C, Rodriguez D, Ewenczyk C, Fellmann F, Kuntzer T, Blond E, El Hachimi KH, Darios F, Seyer A, Gazi AD, Giavalisco P, Perin S, Boucher JL, Le Corre L, Santorelli FM, Goizet C, Zaki MS, Picaud S, Mourier A, Steculorum SM, Mignot C, Durr A, Trifunovic A, Stevanin G. Pujol C, et al. J Exp Med. 2021 Nov 1;218(11):e20210846. doi: 10.1084/jem.20210846. Epub 2021 Sep 21. J Exp Med. 2021. PMID: 34546337 Free PMC article.

4

Rare novel CYP2U1 and ZFYVE26 variants identified in two Pakistani families with spastic paraplegia.

Bibi F, Efthymiou S, Bourinaris T, Tariq A, Zafar F, Rana N, Salpietro V, Houlden H, Raja GK; SYNaPS Study Group; Saeed S, Minhas NM. Bibi F, et al. J Neurol Sci. 2020 Apr 15;411:116669. doi: 10.1016/j.jns.2020.116669. Epub 2020 Jan 11. J Neurol Sci. 2020. PMID: 32006740

5

Whole exome sequencing identifies novel variant underlying hereditary spastic paraplegia in consanguineous Pakistani families.

Zulfiqar S, Tariq M, Ali Z, Fatima A, Klar J, Abdullah U, Ali A, Ramzan S, He S, Zhang J, Khan A, Shah S, Khan S, Makhdoom EH, Schuster J, Dahl N, Baig SM. Zulfiqar S, et al. J Clin Neurosci. 2019 Sep;67:19-23. doi: 10.1016/j.jocn.2019.06.039. Epub 2019 Jul 4. J Clin Neurosci. 2019. PMID: 31281085

6

CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56.

Durand CM, Dhers L, Tesson C, Tessa A, Fouillen L, Jacqueré S, Raymond L, Coupry I, Benard G, Darios F, El-Hachimi KH, Astrea G, Rivier F, Banneau G, Pujol C, Lacombe D, Durr A, Babin PJ, Santorelli FM, Pietrancosta N, Boucher JL, Mansuy D, Stevanin G, Goizet C. Durand CM, et al. Hum Mutat. 2018 Jan;39(1):140-151. doi: 10.1002/humu.23359. Epub 2017 Nov 11. Hum Mutat. 2018. PMID: 29034544 Free article.

7

Membrane-bound human orphan cytochrome P450 2U1: Sequence singularities, construction of a full 3D model, and substrate docking.

Ducassou L, Dhers L, Jonasson G, Pietrancosta N, Boucher JL, Mansuy D, André F. Ducassou L, et al. Biochimie. 2017 Sep;140:166-175. doi: 10.1016/j.biochi.2017.07.007. Epub 2017 Jul 23. Biochimie. 2017. PMID: 28743672

8

An atypical case of SPG56/CYP2U1-related spastic paraplegia presenting with delayed myelination.

Minase G, Miyatake S, Nabatame S, Arai H, Koshimizu E, Mizuguchi T, Nakashima M, Miyake N, Saitsu H, Miyamoto T, Sengoku K, Matsumoto N. Minase G, et al. J Hum Genet. 2017 Nov;62(11):997-1000. doi: 10.1038/jhg.2017.77. Epub 2017 Jul 20. J Hum Genet. 2017. PMID: 28725025

9

Cytochrome P450 2U1, a very peculiar member of the human P450s family.

Dhers L, Ducassou L, Boucher JL, Mansuy D. Dhers L, et al. Cell Mol Life Sci. 2017 May;74(10):1859-1869. doi: 10.1007/s00018-016-2443-3. Epub 2017 Jan 12. Cell Mol Life Sci. 2017. PMID: 28083596 Review.

10

SPG46 and SPG56 are rare causes of hereditary spastic paraplegia in China.

Yang YJ, Zhou ZF, Liao XX, Luo YY, Zhan ZX, Huang MF, Zhou L, Tang BS, Shen L, Du J. Yang YJ, et al. J Neurol. 2016 Oct;263(10):2136-8. doi: 10.1007/s00415-016-8256-3. Epub 2016 Aug 23. J Neurol. 2016. PMID: 27553021 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

21 results

Results by year