Similar articles for PMID: 23934451

Year	Number of Results
2004	1
2005	1
2007	1
2008	1
2009	3
2010	1
2012	3
2013	15
2014	17
2015	13
2016	14
2017	15
2018	14
2019	19
2020	11
2021	11
2022	16
2023	5
2024	0

1

Loss of function of Slc20a2 associated with familial idiopathic Basal Ganglia calcification in humans causes brain calcifications in mice.

Jensen N, Schrøder HD, Hejbøl EK, Füchtbauer EM, de Oliveira JR, Pedersen L. Jensen N, et al. J Mol Neurosci. 2013 Nov;51(3):994-9. doi: 10.1007/s12031-013-0085-6. Epub 2013 Aug 10. J Mol Neurosci. 2013. PMID: 23934451 Free PMC article.

2

Analysis of gene expression pattern and neuroanatomical correlates for SLC20A2 (PiT-2) shows a molecular network with potential impact in idiopathic basal ganglia calcification ("Fahr's disease").

da Silva RJ, Pereira IC, Oliveira JR. da Silva RJ, et al. J Mol Neurosci. 2013 Jun;50(2):280-3. doi: 10.1007/s12031-013-0001-0. Epub 2013 Apr 11. J Mol Neurosci. 2013. PMID: 23576097

3

Induced pluripotent stem cells derived from a patient with familial idiopathic basal ganglia calcification (IBGC) caused by a mutation in SLC20A2 gene.

Sekine SI, Kondo T, Murakami N, Imamura K, Enami T, Shibukawa R, Tsukita K, Funayama M, Inden M, Kurita H, Hozumi I, Inoue H. Sekine SI, et al. Stem Cell Res. 2017 Oct;24:40-43. doi: 10.1016/j.scr.2017.07.028. Epub 2017 Jul 29. Stem Cell Res. 2017. PMID: 29034894 Free article.

4

Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcification.

Chen WJ, Yao XP, Zhang QJ, Ni W, He J, Li HF, Liu XY, Zhao GX, Murong SX, Wang N, Wu ZY. Chen WJ, et al. Gene. 2013 Oct 15;529(1):159-62. doi: 10.1016/j.gene.2013.07.071. Epub 2013 Aug 11. Gene. 2013. PMID: 23939468

5

Characteristics and therapeutic potential of sodium-dependent phosphate cotransporters in relation to idiopathic basal ganglia calcification.

Inden M, Kurita H, Hozumi I. Inden M, et al. J Pharmacol Sci. 2022 Jan;148(1):152-155. doi: 10.1016/j.jphs.2021.11.004. Epub 2021 Nov 13. J Pharmacol Sci. 2022. PMID: 34924120 Free article. Review.

6

Familial idiopathic basal ganglia calcification: Histopathologic features of an autopsied patient with an SLC20A2 mutation.

Kimura T, Miura T, Aoki K, Saito S, Hondo H, Konno T, Uchiyama A, Ikeuchi T, Takahashi H, Kakita A. Kimura T, et al. Neuropathology. 2016 Aug;36(4):365-71. doi: 10.1111/neup.12280. Epub 2015 Dec 4. Neuropathology. 2016. PMID: 26635128

7

Association between a novel mutation in SLC20A2 and familial idiopathic basal ganglia calcification.

Zhang Y, Guo X, Wu A. Zhang Y, et al. PLoS One. 2013;8(2):e57060. doi: 10.1371/journal.pone.0057060. Epub 2013 Feb 20. PLoS One. 2013. PMID: 23437308 Free PMC article.

8

Primary Brain Calcification Causal PiT2 Transport-Knockout Variants can Exert Dominant Negative Effects on Wild-Type PiT2 Transport Function in Mammalian Cells.

Larsen FT, Jensen N, Autzen JK, Kongsfelt IB, Pedersen L. Larsen FT, et al. J Mol Neurosci. 2017 Feb;61(2):215-220. doi: 10.1007/s12031-016-0868-7. Epub 2016 Dec 9. J Mol Neurosci. 2017. PMID: 27943094 Free PMC article.

9

SLC20A2 Deficiency in Mice Leads to Elevated Phosphate Levels in Cerbrospinal Fluid and Glymphatic Pathway-Associated Arteriolar Calcification, and Recapitulates Human Idiopathic Basal Ganglia Calcification.

Wallingford MC, Chia JJ, Leaf EM, Borgeia S, Chavkin NW, Sawangmake C, Marro K, Cox TC, Speer MY, Giachelli CM. Wallingford MC, et al. Brain Pathol. 2017 Jan;27(1):64-76. doi: 10.1111/bpa.12362. Epub 2016 May 6. Brain Pathol. 2017. PMID: 26822507 Free PMC article.

10

Fahr's disease linked to a novel SLC20A2 gene mutation manifesting with dynamic aphasia.

Brighina L, Saracchi E, Ferri F, Gagliardi M, Tarantino P, Morzenti S, Musarra M, Patassini M, Annesi G, Ferrarese C. Brighina L, et al. Neurodegener Dis. 2014;14(3):133-8. doi: 10.1159/000365216. Epub 2014 Sep 25. Neurodegener Dis. 2014. PMID: 25348593

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