PubMed (Bookshelf cited) for id: 442869

Year	Number of Results
1999	2
2009	1
2010	1
2011	2
2012	1
2013	2
2014	1
2015	4
2016	2
2017	3
2018	4
2024	0

1

AP-4 vesicles contribute to spatial control of autophagy via RUSC-dependent peripheral delivery of ATG9A.

Davies AK, Itzhak DN, Edgar JR, Archuleta TL, Hirst J, Jackson LP, Robinson MS, Borner GHH. Davies AK, et al. Nat Commun. 2018 Sep 27;9(1):3958. doi: 10.1038/s41467-018-06172-7. Nat Commun. 2018. PMID: 30262884 Free PMC article.

2

Altered distribution of ATG9A and accumulation of axonal aggregates in neurons from a mouse model of AP-4 deficiency syndrome.

De Pace R, Skirzewski M, Damme M, Mattera R, Mercurio J, Foster AM, Cuitino L, Jarnik M, Hoffmann V, Morris HD, Han TU, Mancini GMS, Buonanno A, Bonifacino JS. De Pace R, et al. PLoS Genet. 2018 Apr 26;14(4):e1007363. doi: 10.1371/journal.pgen.1007363. eCollection 2018 Apr. PLoS Genet. 2018. PMID: 29698489 Free PMC article.

3

AP4 deficiency: A novel form of neurodegeneration with brain iron accumulation?

Roubertie A, Hieu N, Roux CJ, Leboucq N, Manes G, Charif M, Echenne B, Goizet C, Guissart C, Meyer P, Marelli C, Rivier F, Burglen L, Horvath R, Hamel CP, Lenaers G. Roubertie A, et al. Neurol Genet. 2018 Jan 24;4(1):e217. doi: 10.1212/NXG.0000000000000217. eCollection 2018 Feb. Neurol Genet. 2018. PMID: 29473051 Free PMC article.

4

Clinical and genetic characterization of AP4B1-associated SPG47.

Ebrahimi-Fakhari D, Cheng C, Dies K, Diplock A, Pier DB, Ryan CS, Lanpher BC, Hirst J, Chung WK, Sahin M, Rosser E, Darras B, Bennett JT; CureSPG47. Ebrahimi-Fakhari D, et al. Am J Med Genet A. 2018 Feb;176(2):311-318. doi: 10.1002/ajmg.a.38561. Epub 2017 Nov 28. Am J Med Genet A. 2018. PMID: 29193663

5

AP-4 mediates export of ATG9A from the trans-Golgi network to promote autophagosome formation.

Mattera R, Park SY, De Pace R, Guardia CM, Bonifacino JS. Mattera R, et al. Proc Natl Acad Sci U S A. 2017 Dec 12;114(50):E10697-E10706. doi: 10.1073/pnas.1717327114. Epub 2017 Nov 27. Proc Natl Acad Sci U S A. 2017. PMID: 29180427 Free PMC article.

6

A homozygous splice variant in AP4S1 mimicking neurodegeneration with brain iron accumulation.

Vill K, Müller-Felber W, Alhaddad B, Strom TM, Teusch V, Weigand H, Blaschek A, Meitinger T, Haack TB. Vill K, et al. Mov Disord. 2017 May;32(5):797-799. doi: 10.1002/mds.26922. Epub 2017 Feb 2. Mov Disord. 2017. PMID: 28150420 No abstract available.

7

Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force.

Marras C, Lang A, van de Warrenburg BP, Sue CM, Tabrizi SJ, Bertram L, Mercimek-Mahmutoglu S, Ebrahimi-Fakhari D, Warner TT, Durr A, Assmann B, Lohmann K, Kostic V, Klein C. Marras C, et al. Mov Disord. 2016 Apr;31(4):436-57. doi: 10.1002/mds.26527. Mov Disord. 2016. PMID: 27079681 Review.

8

Molecular Basis for the Interaction Between AP4 β4 and its Accessory Protein, Tepsin.

Frazier MN, Davies AK, Voehler M, Kendall AK, Borner GH, Chazin WJ, Robinson MS, Jackson LP. Frazier MN, et al. Traffic. 2016 Apr;17(4):400-15. doi: 10.1111/tra.12375. Epub 2016 Mar 4. Traffic. 2016. PMID: 26756312 Free PMC article.

9

Association between Rare Variants in AP4E1, a Component of Intracellular Trafficking, and Persistent Stuttering.

Raza MH, Mattera R, Morell R, Sainz E, Rahn R, Gutierrez J, Paris E, Root J, Solomon B, Brewer C, Basra MA, Khan S, Riazuddin S, Braun A, Bonifacino JS, Drayna D. Raza MH, et al. Am J Hum Genet. 2015 Nov 5;97(5):715-25. doi: 10.1016/j.ajhg.2015.10.007. Am J Hum Genet. 2015. PMID: 26544806 Free PMC article.

10

Bivalent Motif-Ear Interactions Mediate the Association of the Accessory Protein Tepsin with the AP-4 Adaptor Complex.

Mattera R, Guardia CM, Sidhu SS, Bonifacino JS. Mattera R, et al. J Biol Chem. 2015 Dec 25;290(52):30736-49. doi: 10.1074/jbc.M115.683409. Epub 2015 Nov 5. J Biol Chem. 2015. PMID: 26542808 Free PMC article.

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