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6. "Lowe syndrome: A particularly severe phenotype without clinical kidney involvement". Abdalla E; El-Beheiry A; Dieterich K; Thevenon J; Fauré J; Rendu J Am J Med Genet A; 2018 Feb; 176(2):460-464. PubMed ID: 29226564 [TBL] [Abstract][Full Text] [Related]
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8. Oculocerebrorenal syndrome of Lowe: Survey of ophthalmic presentations and management. Ma X; Ning K; Jabbehdari S; Prosseda PP; Hu Y; Shue A; Lambert SR; Sun Y Eur J Ophthalmol; 2020 Sep; 30(5):966-973. PubMed ID: 32340490 [TBL] [Abstract][Full Text] [Related]
9. 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. PubMed ID: 28669993 [TBL] [Abstract][Full Text] [Related]
10. The 5-phosphatase OCRL mediates retrograde transport of the mannose 6-phosphate receptor by regulating a Rac1-cofilin signalling module. van Rahden VA; Brand K; Najm J; Heeren J; Pfeffer SR; Braulke T; Kutsche K Hum Mol Genet; 2012 Dec; 21(23):5019-38. PubMed ID: 22907655 [TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 26351914 [TBL] [Abstract][Full Text] [Related]
12. The oculocerebrorenal syndrome of Lowe: an update. Bökenkamp A; Ludwig M Pediatr Nephrol; 2016 Dec; 31(12):2201-2212. PubMed ID: 27011217 [TBL] [Abstract][Full Text] [Related]
13. Lowe syndrome - Old and new evidence of secondary mitochondrial dysfunction. Dumic KK; Anticevic D; Petrinovic-Doresic J; Zigman T; Zarković K; Rokic F; Vugrek O Eur J Med Genet; 2020 Oct; 63(10):104022. PubMed ID: 32712215 [TBL] [Abstract][Full Text] [Related]
14. Decreased urinary excretion of the ectodomain form of megalin (A-megalin) in children with OCRL gene mutations. Suruda C; Tsuji S; Yamanouchi S; Kimata T; Huan NT; Kurosawa H; Hirayama Y; Tsukaguchi H; Saito A; Kaneko K Pediatr Nephrol; 2017 Apr; 32(4):621-625. PubMed ID: 27766457 [TBL] [Abstract][Full Text] [Related]
15. 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; 21(15):3333-44. PubMed ID: 22543976 [TBL] [Abstract][Full Text] [Related]
16. Complete oculocerebrorenal phenotype of Lowe syndrome in a female patient with half reduction of inositol polyphosphate 5-phosphatase. Yamamoto K; Hasegawa Y; Ohata Y; Satomura K; Mizoguchi Y; Shimotsuji T; Yamamoto T CEN Case Rep; 2020 May; 9(2):95-100. PubMed ID: 31707643 [TBL] [Abstract][Full Text] [Related]
17. Lowe syndrome - Case report with a novel mutation in the oculocerebrorenal gene. Sethi S; Sethi N; Mehta S; Kaur S; Makkar V; Sohal PM Saudi J Kidney Dis Transpl; 2020; 31(1):285-288. PubMed ID: 32129227 [TBL] [Abstract][Full Text] [Related]
18. Ocular Pathology of Oculocerebrorenal Syndrome of Lowe: Novel Mutations and Genotype-Phenotype Analysis. Song E; Luo N; Alvarado JA; Lim M; Walnuss C; Neely D; Spandau D; Ghaffarieh A; Sun Y Sci Rep; 2017 May; 7(1):1442. PubMed ID: 28473699 [TBL] [Abstract][Full Text] [Related]
19. Establishment of patient-specific induced pluripotent stem cell line SDUBMSi009-A from a patient with X-linked Lowe syndrome. Liu X; Liu Y; Ma Y; Gong Y; Liu Q; Sun W; Guo H Stem Cell Res; 2021 Mar; 51():102171. PubMed ID: 33540283 [TBL] [Abstract][Full Text] [Related]
20. A role of OCRL in clathrin-coated pit dynamics and uncoating revealed by studies of Lowe syndrome cells. Nández R; Balkin DM; Messa M; Liang L; Paradise S; Czapla H; Hein MY; Duncan JS; Mann M; De Camilli P Elife; 2014 Aug; 3():e02975. PubMed ID: 25107275 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]