PubMed for id: 9620

Year	Number of Results
1997	1
1999	2
2000	3
2001	1
2002	1
2003	1
2004	1
2005	2
2009	2
2010	4
2011	4
2012	2
2013	1
2014	3
2015	3
2016	2
2017	4
2018	1
2019	4
2020	3
2021	4
2022	4
2023	5
2024	1

1

CELSR1, a core planar cell polarity protein, features a weakly adhesive and flexible cadherin ectodomain.

Tamilselvan E, Sotomayor M. Tamilselvan E, et al. Structure. 2024 Apr 4;32(4):476-491.e5. doi: 10.1016/j.str.2024.01.003. Epub 2024 Feb 1. Structure. 2024. PMID: 38307021

2

Upregulation of CELSR1 expression promotes ovarian cancer cell proliferation, migration, and invasion.

Zuo J, Zheng A, Wang X, Luo Z, Chen Y, Cheng X, Zhao Y, Zhou X, Tang KF, Du X. Zuo J, et al. Med Oncol. 2023 Dec 9;41(1):10. doi: 10.1007/s12032-023-02232-1. Med Oncol. 2023. PMID: 38070011

3

Lymphedema is associated with CELSR1 in Phelan-McDermid syndrome.

Smith MS, Sarasua SM, Rogers C, Phelan K, Boccuto L. Smith MS, et al. Clin Genet. 2023 Oct;104(4):472-478. doi: 10.1111/cge.14364. Epub 2023 May 26. Clin Genet. 2023. PMID: 37232218

4

Ureteropelvic junction obstruction with primary lymphoedema associated with CELSR1 variants.

Alpaslan M, Mestré-Godin S, Lay A, Giacalone G, Helaers R, Adham S, Kovacsik H, Guillemard S, Mercier E, Boon L, Revencu N, Brouillard P, Quere I, Vikkula M. Alpaslan M, et al. J Med Genet. 2023 Nov 27;60(12):1161-1168. doi: 10.1136/jmg-2023-109171. J Med Genet. 2023. PMID: 37225411

5

CELSR1 variants are associated with partial epilepsy of childhood.

Chen Z, Luo S, Liu ZG, Deng YC, He SL, Liu XR, Yi YH, Wang J, Gao LD, Li BM, Wu ZJ, Ye ZL, Liang DH, Bian WJ, Liao WP; China Epilepsy Gene 1.0 Project. Chen Z, et al. Am J Med Genet B Neuropsychiatr Genet. 2022 Oct;189(7-8):247-256. doi: 10.1002/ajmg.b.32916. Epub 2022 Aug 12. Am J Med Genet B Neuropsychiatr Genet. 2022. PMID: 36453712

6

A CELSR1 variant in a patient with pulmonary arterial hypertension.

Eyries M, Girerd B, Savale L, Soubrier F, Humbert M, Montani D. Eyries M, et al. Clin Genet. 2021 Dec;100(6):771-772. doi: 10.1111/cge.14046. Epub 2021 Aug 25. Clin Genet. 2021. PMID: 34435352 No abstract available.

7

Sex-limited penetrance of lymphedema to females with CELSR1 haploinsufficiency: A second family.

Erickson RP, Lai LW, Mustacich DJ, Bernas MJ, Kuo PH, Witte MH. Erickson RP, et al. Clin Genet. 2019 Nov;96(5):478-482. doi: 10.1111/cge.13622. Epub 2019 Aug 23. Clin Genet. 2019. PMID: 31403174

8

Increasing evidence of hereditary lymphedema caused by CELSR1 loss-of-function variants.

Maltese PE, Michelini S, Ricci M, Maitz S, Fiorentino A, Serrani R, Lazzerotti A, Bruson A, Paolacci S, Benedetti S, Bertelli M. Maltese PE, et al. Am J Med Genet A. 2019 Sep;179(9):1718-1724. doi: 10.1002/ajmg.a.61269. Epub 2019 Jun 18. Am J Med Genet A. 2019. PMID: 31215153

9

Sex-Based Genetic Association Study Identifies CELSR1 as a Possible Chronic Obstructive Pulmonary Disease Risk Locus among Women.

Hardin M, Cho MH, Sharma S, Glass K, Castaldi PJ, McDonald ML, Aschard H, Senter-Sylvia J, Tantisira K, Weiss ST, Hersh CP, Morrow JD, Lomas D, Agusti A, Bakke P, Gulsvik A, O'Connor GT, Dupuis J, Hokanson J, Crapo JD, Beaty TH, Laird N, Silverman EK, DeMeo DL; COPDGene and Evaluation of COPD Longitudinally to Identify Predictive Surrogate End-Points Investigators. Hardin M, et al. Am J Respir Cell Mol Biol. 2017 Mar;56(3):332-341. doi: 10.1165/rcmb.2016-0172OC. Am J Respir Cell Mol Biol. 2017. PMID: 27854507 Free PMC article.

10

CELSR1 Is a Positive Regulator of Endothelial Cell Migration and Angiogenesis.

Zhan YH, Luo QC, Zhang XR, Xiao NA, Lu CX, Yue C, Wang N, Ma QL. Zhan YH, et al. Biochemistry (Mosc). 2016 Jun;81(6):591-9. doi: 10.1134/S0006297916060055. Biochemistry (Mosc). 2016. PMID: 27301287 Free article.

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