PubMed for id: 113612

Year	Number of Results
1993	1
2000	1
2002	2
2003	1
2004	4
2010	2
2011	2
2013	1
2014	2
2015	2
2016	4
2017	5
2018	1
2019	1
2020	2
2021	3
2022	2
2023	1
2024	1

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

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.

4

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

5

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

6

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.

7

Spectral and 3D model studies of the interaction of orphan human cytochrome P450 2U1 with substrates and ligands.

Dhers L, Pietrancosta N, Ducassou L, Ramassamy B, Dairou J, Jaouen M, André F, Mansuy D, Boucher JL. Dhers L, et al. Biochim Biophys Acta Gen Subj. 2017 Jan;1861(1 Pt A):3144-3153. doi: 10.1016/j.bbagen.2016.07.018. Epub 2016 Jul 25. Biochim Biophys Acta Gen Subj. 2017. PMID: 27456766

8

CYP2U1 mutations in two Iranian patients with activity induced dystonia, motor regression and spastic paraplegia.

Kariminejad A, Schöls L, Schüle R, Tonekaboni SH, Abolhassani A, Fadaee M, Rosti RO, Gleeson JG. Kariminejad A, et al. Eur J Paediatr Neurol. 2016 Sep;20(5):782-7. doi: 10.1016/j.ejpn.2016.05.013. Epub 2016 Jun 2. Eur J Paediatr Neurol. 2016. PMID: 27292318 Free PMC article.

9

Pigmentary degenerative maculopathy as prominent phenotype in an Italian SPG56/CYP2U1 family.

Leonardi L, Ziccardi L, Marcotulli C, Rubegni A, Longobardi A, Serrao M, Storti E, Pierelli F, Tessa A, Parisi V, Santorelli FM, Carlo C. Leonardi L, et al. J Neurol. 2016 Apr;263(4):781-3. doi: 10.1007/s00415-016-8066-7. Epub 2016 Feb 25. J Neurol. 2016. PMID: 26914923

10

Expression in yeast, new substrates, and construction of a first 3D model of human orphan cytochrome P450 2U1: Interpretation of substrate hydroxylation regioselectivity from docking studies.

Ducassou L, Jonasson G, Dhers L, Pietrancosta N, Ramassamy B, Xu-Li Y, Loriot MA, Beaune P, Bertho G, Lombard M, Mansuy D, André F, Boucher JL. Ducassou L, et al. Biochim Biophys Acta. 2015 Jul;1850(7):1426-37. doi: 10.1016/j.bbagen.2015.03.014. Epub 2015 Apr 7. Biochim Biophys Acta. 2015. PMID: 25857771

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