PubMed for id: 56521

Year	Number of Results
2000	1
2002	1
2004	2
2005	1
2006	3
2007	1
2011	2
2012	1
2014	1
2015	2
2017	5
2018	3
2019	2
2020	1
2021	4
2022	1
2023	3
2024	2

1

DNAJC12 causes breast cancer chemotherapy resistance by repressing doxorubicin-induced ferroptosis and apoptosis via activation of AKT.

Shen M, Cao S, Long X, Xiao L, Yang L, Zhang P, Li L, Chen F, Lei T, Gao H, Ye F, Bu H. Shen M, et al. Redox Biol. 2024 Apr;70:103035. doi: 10.1016/j.redox.2024.103035. Epub 2024 Jan 24. Redox Biol. 2024. PMID: 38306757 Free PMC article.

2

DNAJC12 in Monoamine Metabolism, Neurodevelopment, and Neurodegeneration.

Deng IB, Follett J, Bu M, Farrer MJ. Deng IB, et al. Mov Disord. 2024 Feb;39(2):249-258. doi: 10.1002/mds.29677. Epub 2023 Nov 28. Mov Disord. 2024. PMID: 38014588 Review.

3

A rare cause of hyperphenylalaninemia: four cases from a single family with DNAJC12 deficiency.

Gunes D, Senturk L. Gunes D, et al. J Pediatr Endocrinol Metab. 2023 Jun 7;36(8):791-797. doi: 10.1515/jpem-2023-0049. Print 2023 Aug 28. J Pediatr Endocrinol Metab. 2023. PMID: 37283250

4

Restless legs syndrome in DNAJC12 deficiency.

Porta F, Neirotti A, Spada M. Porta F, et al. Neurol Sci. 2023 Jun;44(6):2167-2172. doi: 10.1007/s10072-023-06733-9. Epub 2023 Mar 10. Neurol Sci. 2023. PMID: 36897462

5

DNACJ12 deficiency in patients with unexplained hyperphenylalaninemia: two new patients and a novel variant.

Çıkı K, Yıldız Y, Yücel Yılmaz D, Pektaş E, Tokatlı A, Özgül RK, Sivri HS, Dursun A. Çıkı K, et al. Metab Brain Dis. 2021 Aug;36(6):1405-1410. doi: 10.1007/s11011-021-00753-0. Epub 2021 May 20. Metab Brain Dis. 2021. PMID: 34014443

6

Pathogenic variants of DNAJC12 and evaluation of the encoded cochaperone as a genetic modifier of hyperphenylalaninemia.

Gallego D, Leal F, Gámez A, Castro M, Navarrete R, Sanchez-Lijarcio O, Vitoria I, Bueno-Delgado M, Belanger-Quintana A, Morais A, Pedrón-Giner C, García I, Campistol J, Artuch R, Alcaide C, Cornejo V, Gil D, Yahyaoui R, Desviat LR, Ugarte M, Martínez A, Pérez B. Gallego D, et al. Hum Mutat. 2020 Jul;41(7):1329-1338. doi: 10.1002/humu.24026. Epub 2020 Apr 30. Hum Mutat. 2020. PMID: 32333439 Free article.

7

Phenylalanine hydroxylase variants interact with the co-chaperone DNAJC12.

Jung-Kc K, Himmelreich N, Prestegård KS, Shi TS, Scherer T, Ying M, Jorge-Finnigan A, Thöny B, Blau N, Martinez A. Jung-Kc K, et al. Hum Mutat. 2019 Apr;40(4):483-494. doi: 10.1002/humu.23712. Epub 2019 Feb 6. Hum Mutat. 2019. PMID: 30667134

8

Increased Expression of DNAJC12 is Associated with Aggressive Phenotype of Gastric Cancer.

Uno Y, Kanda M, Miwa T, Umeda S, Tanaka H, Tanaka C, Kobayashi D, Suenaga M, Hattori N, Hayashi M, Yamada S, Nakayama G, Fujiwara M, Kodera Y. Uno Y, et al. Ann Surg Oncol. 2019 Mar;26(3):836-844. doi: 10.1245/s10434-018-07149-y. Epub 2019 Jan 7. Ann Surg Oncol. 2019. PMID: 30617870

9

DNAJC12-associated developmental delay, movement disorder, and mild hyperphenylalaninemia identified by whole-exome sequencing re-analysis.

Veenma D, Cordeiro D, Sondheimer N, Mercimek-Andrews S. Veenma D, et al. Eur J Hum Genet. 2018 Dec;26(12):1867-1870. doi: 10.1038/s41431-018-0237-9. Epub 2018 Aug 23. Eur J Hum Genet. 2018. PMID: 30139987 Free PMC article.

10

DNAJC12 mutation is rare in Chinese Han population with Parkinson's disease.

Fan Y, Yang ZH, Li F, Hu XC, Yue YW, Yang J, Liu YT, Liu H, Wang YL, Shi CH, Xu YM. Fan Y, et al. Neurobiol Aging. 2018 Aug;68:159.e1-159.e2. doi: 10.1016/j.neurobiolaging.2018.04.012. Epub 2018 May 2. Neurobiol Aging. 2018. PMID: 29801756

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

33 results

Results by year