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Items: 15

1.

OCRL localizes to the primary cilium: a new role for cilia in Lowe syndrome.

Luo N, West CC, Murga-Zamalloa CA, Sun L, Anderson RM, Wells CD, Weinreb RN, Travers JB, Khanna H, Sun Y.

Hum Mol Genet. 2012 Aug 1;21(15):3333-44. doi: 10.1093/hmg/dds163. Epub 2012 Apr 27.

2.

Role of Ocrl1 in primary cilia assembly.

Madhivanan K, Ramadesikan S, Aguilar RC.

Int Rev Cell Mol Biol. 2015;317:331-47. doi: 10.1016/bs.ircmb.2015.02.003. Epub 2015 Mar 11. Review.

PMID:
26008789
3.

The 5-phosphatase OCRL in Lowe syndrome and Dent disease 2.

De Matteis MA, Staiano L, Emma F, Devuyst O.

Nat Rev Nephrol. 2017 Aug;13(8):455-470. doi: 10.1038/nrneph.2017.83. Epub 2017 Jul 3. Review.

PMID:
28669993
4.

Structure and function of the Lowe syndrome protein OCRL1.

Lowe M.

Traffic. 2005 Sep;6(9):711-9. Review.

5.

Inositol 5-phosphatases: insights from the Lowe syndrome protein OCRL.

Pirruccello M, De Camilli P.

Trends Biochem Sci. 2012 Apr;37(4):134-43. doi: 10.1016/j.tibs.2012.01.002. Epub 2012 Feb 28. Review.

6.

The cellular and physiological functions of the Lowe syndrome protein OCRL1.

Mehta ZB, Pietka G, Lowe M.

Traffic. 2014 May;15(5):471-87. doi: 10.1111/tra.12160. Epub 2014 Mar 7. Review.

7.

The role of the Lowe syndrome protein OCRL in the endocytic pathway.

Sharma S, Skowronek A, Erdmann KS.

Biol Chem. 2015 Dec;396(12):1293-300. doi: 10.1515/hsz-2015-0180. Review.

PMID:
26351914
8.

The oculocerebrorenal syndrome of Lowe: an update.

Bökenkamp A, Ludwig M.

Pediatr Nephrol. 2016 Dec;31(12):2201-2212. Epub 2016 Mar 24. Review.

9.

[Lowe syndrome(oculocerebrorenal syndrome of Lowe; OCRL)].

Ohno K.

Ryoikibetsu Shokogun Shirizu. 2000;(29 Pt 4):489-90. Review. Japanese. No abstract available.

PMID:
11032004
10.

Crystal structure of the Rab binding domain of OCRL1 in complex with Rab8 and functional implications of the OCRL1/Rab8 module for Lowe syndrome.

Hagemann N, Hou X, Goody RS, Itzen A, Erdmann KS.

Small GTPases. 2012 Apr-Jun;3(2):107-10. doi: 10.4161/sgtp.19380. Review.

PMID:
22790198
11.

Inherited cerebrorenal syndromes.

Schurman SJ, Scheinman SJ.

Nat Rev Nephrol. 2009 Sep;5(9):529-38. doi: 10.1038/nrneph.2009.124. Review.

PMID:
19701229
12.

The inositol polyphosphate 5-phosphatases: traffic controllers, waistline watchers and tumour suppressors?

Astle MV, Horan KA, Ooms LM, Mitchell CA.

Biochem Soc Symp. 2007;(74):161-81. Review.

PMID:
17233589
13.

Inositol polyphosphate 5-phosphatases; new players in the regulation of cilia and ciliopathies.

Conduit SE, Dyson JM, Mitchell CA.

FEBS Lett. 2012 Aug 31;586(18):2846-57. doi: 10.1016/j.febslet.2012.07.037. Epub 2012 Jul 22. Review.

14.

Mendelian disorders of PI metabolizing enzymes.

Staiano L, De Leo MG, Persico M, De Matteis MA.

Biochim Biophys Acta. 2015 Jun;1851(6):867-81. doi: 10.1016/j.bbalip.2014.12.001. Epub 2014 Dec 12. Review.

PMID:
25510381
15.

A Conversation with Scott Lowe.

[No authors listed]

Cold Spring Harb Symp Quant Biol. 2016;81:320-322. doi: 10.1101/sqb.2016.81.031351. Epub 2017 Mar 13. Review. No abstract available.

PMID:
28289162

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