PubMed for id: 3689

Year	Number of Results
1968	1
1975	2
1982	1
1984	1
1986	1
1993	2
1997	2
1998	3
1999	6
2000	2
2001	2
2002	1
2003	7
2004	6
2005	8
2006	17
2007	14
2008	17
2009	22
2010	15
2011	21
2012	18
2013	8
2015	1
2024	0

1

Analysis of PITX3 gene in patients with multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration.

Jamrozik Z, Berdynski M, Zekanowski C, Baranczyk-Kuzma A, Sławek J, Kuzma-Kozakiewicz M, Maruszak A, Kwiecinski H. Jamrozik Z, et al. Ann Clin Lab Sci. 2013 Spring;43(2):151-3. Ann Clin Lab Sci. 2013. PMID: 23694789

2

Prenatal ontogeny of the dopamine-dependent neurobehavioral phenotype in Pitx3-deficient mice.

Kleven GA, Joshi P, Voogd M, Ronca AE. Kleven GA, et al. Eur J Neurosci. 2013 May;37(10):1564-72. doi: 10.1111/ejn.12184. Epub 2013 Mar 13. Eur J Neurosci. 2013. PMID: 23489835 Free PMC article.

3

The transcription factor Pitx3 is expressed selectively in midbrain dopaminergic neurons susceptible to neurodegenerative stress.

Luk KC, Rymar VV, van den Munckhof P, Nicolau S, Steriade C, Bifsha P, Drouin J, Sadikot AF. Luk KC, et al. J Neurochem. 2013 Jun;125(6):932-43. doi: 10.1111/jnc.12160. Epub 2013 Mar 6. J Neurochem. 2013. PMID: 23331067 Free article.

4

Meta-analysis of association between PITX3 gene polymorphism and Parkinson's disease.

Tang L, Zhao S, Wang M, Sheth A, Zhao Z, Chen L, Fan X, Chen L. Tang L, et al. J Neurol Sci. 2012 Jun 15;317(1-2):80-6. doi: 10.1016/j.jns.2012.02.025. Epub 2012 Mar 18. J Neurol Sci. 2012. PMID: 22429667

5

A novel synonymous SNP in PITX3 is associated with Parkinson's disease in Chinese population.

Gui Y, Zhao Y, Liu H, Fu J, Xu Z, Hu X. Gui Y, et al. Swiss Med Wkly. 2012 Mar 9;142:w13521. doi: 10.4414/smw.2012.13521. eCollection 2012. Swiss Med Wkly. 2012. PMID: 22411443 Free article.

6

Clinical improvement of the aggressive neurobehavioral phenotype in a patient with a deletion of PITX3 and the absence of L-DOPA in the cerebrospinal fluid.

Derwińska K, Mierzewska H, Goszczańska A, Szczepanik E, Xia Z, Kuśmierska K, Tryfon J, Kutkowska-Kaźmierczak A, Bocian E, Mazurczak T, Obersztyn E, Stankiewicz P. Derwińska K, et al. Am J Med Genet B Neuropsychiatr Genet. 2012 Mar;159B(2):236-42. doi: 10.1002/ajmg.b.32020. Epub 2012 Jan 5. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22223473

7

PITX3 polymorphism is not associated with Parkinson's disease in a Chinese population.

Cai Y, Ding H, Gu Z, Baskys A, Ma J, Chan P. Cai Y, et al. Neurosci Lett. 2011 Nov 21;505(3):260-2. doi: 10.1016/j.neulet.2011.10.034. Epub 2011 Oct 21. Neurosci Lett. 2011. PMID: 22037506

8

Midbrain dopamine neurons associated with reward processing innervate the neurogenic subventricular zone.

Lennington JB, Pope S, Goodheart AE, Drozdowicz L, Daniels SB, Salamone JD, Conover JC. Lennington JB, et al. J Neurosci. 2011 Sep 14;31(37):13078-87. doi: 10.1523/JNEUROSCI.1197-11.2011. J Neurosci. 2011. PMID: 21917791 Free PMC article.

9

A novel 1-bp deletion in PITX3 causing congenital posterior polar cataract.

Berry V, Francis PJ, Prescott Q, Waseem NH, Moore AT, Bhattacharya SS. Berry V, et al. Mol Vis. 2011;17:1249-53. Epub 2011 May 6. Mol Vis. 2011. PMID: 21633712 Free PMC article.

10

Genetic variants of the PITX3 gene are not associated with late-onset sporadic Parkinson's disease in a Chinese population.

Cai Y, Ding H, Gu Z, Ma J, Chan P. Cai Y, et al. Neurosci Lett. 2011 Jul 8;498(2):124-6. doi: 10.1016/j.neulet.2011.04.073. Epub 2011 May 5. Neurosci Lett. 2011. PMID: 21565251

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