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Items: 7

1.

The oculocerebrorenal syndrome of Lowe: an update.

Bökenkamp A, Ludwig M.

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

2.

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. Review.

3.

Compensatory Role of Inositol 5-Phosphatase INPP5B to OCRL in Primary Cilia Formation in Oculocerebrorenal Syndrome of Lowe.

Luo N, Kumar A, Conwell M, Weinreb RN, Anderson R, Sun Y.

PLoS One. 2013 Jun 21;8(6):e66727. doi: 10.1371/journal.pone.0066727.

4.

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. Review.

5.

Impaired neural development in a zebrafish model for Lowe syndrome.

Ramirez IB, Pietka G, Jones DR, Divecha N, Alia A, Baraban SC, Hurlstone AF, Lowe M.

Hum Mol Genet. 2012 Apr 15;21(8):1744-59. doi: 10.1093/hmg/ddr608.

6.

Recognition of the F&H motif by the Lowe syndrome protein OCRL.

Pirruccello M, Swan LE, Folta-Stogniew E, De Camilli P.

Nat Struct Mol Biol. 2011 Jun 12;18(7):789-95. doi: 10.1038/nsmb.2071.

7.

Mouse model for Lowe syndrome/Dent Disease 2 renal tubulopathy.

Bothwell SP, Chan E, Bernardini IM, Kuo YM, Gahl WA, Nussbaum RL.

J Am Soc Nephrol. 2011 Mar;22(3):443-8. doi: 10.1681/ASN.2010050565.

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