PubMed for id: 79705

Year	Number of Results
1994	1
1996	1
2001	1
2002	1
2003	2
2004	2
2005	1
2006	2
2007	6
2008	2
2009	2
2010	2
2011	1
2012	4
2013	2
2014	5
2015	3
2016	3
2017	2
2018	3
2020	2
2021	2
2022	3
2023	1
2024	0

1

Structure and regulation of full-length human leucine-rich repeat kinase 1.

Metcalfe RD, Martinez Fiesco JA, Bonet-Ponce L, Kluss JH, Cookson MR, Zhang P. Metcalfe RD, et al. Nat Commun. 2023 Aug 9;14(1):4797. doi: 10.1038/s41467-023-40532-2. Nat Commun. 2023. PMID: 37558661 Free PMC article.

2

PKC isoforms activate LRRK1 kinase by phosphorylating conserved residues (Ser1064, Ser1074 and Thr1075) within the CORB GTPase domain.

Malik AU, Karapetsas A, Nirujogi RS, Chatterjee D, Phung TK, Wightman M, Gourlay R, Morrice N, Mathea S, Knapp S, Alessi DR. Malik AU, et al. Biochem J. 2022 Sep 30;479(18):1941-1965. doi: 10.1042/BCJ20220308. Biochem J. 2022. PMID: 36040231 Free PMC article.

3

Broadening the phenotype of LRRK1 mutations - Features of malignant osteopetrosis and optic nerve atrophy with intrafamilial variable expressivity.

Chorin O, Chowers G, Agbariah R, Karklinsky S, Barel O, Bar-Joseph I, Reznik-Wolf H, Shamash J, Pode-Shakked B, Jacobson JM, Huna-Baron R, Redler Y, Tirosh I, Vivante A, Raas-Rothschild A. Chorin O, et al. Eur J Med Genet. 2022 Jan;65(1):104383. doi: 10.1016/j.ejmg.2021.104383. Epub 2021 Nov 16. Eur J Med Genet. 2022. PMID: 34798323

4

Identification of a novel LRRK1 mutation in a family with osteosclerotic metaphyseal dysplasia.

Guo L, Girisha KM, Iida A, Hebbar M, Shukla A, Shah H, Nishimura G, Matsumoto N, Nismath S, Miyake N, Ikegawa S. Guo L, et al. J Hum Genet. 2017 Mar;62(3):437-441. doi: 10.1038/jhg.2016.136. Epub 2016 Nov 10. J Hum Genet. 2017. PMID: 27829680

5

Identification of biallelic LRRK1 mutations in osteosclerotic metaphyseal dysplasia and evidence for locus heterogeneity.

Iida A, Xing W, Docx MK, Nakashima T, Wang Z, Kimizuka M, Van Hul W, Rating D, Spranger J, Ohashi H, Miyake N, Matsumoto N, Mohan S, Nishimura G, Mortier G, Ikegawa S. Iida A, et al. J Med Genet. 2016 Aug;53(8):568-74. doi: 10.1136/jmedgenet-2016-103756. Epub 2016 Apr 7. J Med Genet. 2016. PMID: 27055475 Free PMC article.

6

Rare variants in LRRK1 and Parkinson's disease.

Schulte EC, Ellwanger DC, Dihanich S, Manzoni C, Stangl K, Schormair B, Graf E, Eck S, Mollenhauer B, Haubenberger D, Pirker W, Zimprich A, Brücke T, Lichtner P, Peters A, Gieger C, Trenkwalder C, Mewes HW, Meitinger T, Lewis PA, Klünemann HH, Winkelmann J. Schulte EC, et al. Neurogenetics. 2014 Mar;15(1):49-57. doi: 10.1007/s10048-013-0383-8. Epub 2013 Nov 16. Neurogenetics. 2014. PMID: 24241507 Free PMC article.

7

LRRK1 protein kinase activity is stimulated upon binding of GTP to its Roc domain.

Korr D, Toschi L, Donner P, Pohlenz HD, Kreft B, Weiss B. Korr D, et al. Cell Signal. 2006 Jun;18(6):910-20. doi: 10.1016/j.cellsig.2005.08.015. Epub 2005 Oct 21. Cell Signal. 2006. PMID: 16243488

8

Roc, a Ras/GTPase domain in complex proteins.

Bosgraaf L, Van Haastert PJ. Bosgraaf L, et al. Biochim Biophys Acta. 2003 Dec 7;1643(1-3):5-10. doi: 10.1016/j.bbamcr.2003.08.008. Biochim Biophys Acta. 2003. PMID: 14654223 Free article. Review.

9

Genetic Analysis of LRRK1 and LRRK2 Variants in Essential Tremor Patients.

Chen H, Yuan L, Song Z, Deng X, Yang Z, Gong L, Zi X, Deng H. Chen H, et al. Genet Test Mol Biomarkers. 2018 Jun;22(6):398-402. doi: 10.1089/gtmb.2017.0277. Epub 2018 May 29. Genet Test Mol Biomarkers. 2018. PMID: 29812962

10

Human leucine-rich repeat kinase 1 and 2: intersecting or unrelated functions?

Civiero L, Bubacco L. Civiero L, et al. Biochem Soc Trans. 2012 Oct;40(5):1095-101. doi: 10.1042/BST20120123. Biochem Soc Trans. 2012. PMID: 22988872 Review.

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

47 results

Results by year