118 related articles for article (PubMed ID: 37871882)
21. Novel compound heterozygous mutations in the PEX1 gene in two Chinese newborns with Zellweger syndrome based on whole exome sequencing.
Ge MM; Hu L; Li Z; Cheng G; Yan K; Kong Y; Wang H; Yang L; Zhou W
Clin Chim Acta; 2017 Jul; 470():24-28. PubMed ID: 28432012
[TBL] [Abstract][Full Text] [Related]
22. The peroxisomal AAA-ATPase Pex1/Pex6 unfolds substrates by processive threading.
Gardner BM; Castanzo DT; Chowdhury S; Stjepanovic G; Stefely MS; Hurley JH; Lander GC; Martin A
Nat Commun; 2018 Jan; 9(1):135. PubMed ID: 29321502
[TBL] [Abstract][Full Text] [Related]
23. Peroxisomal monoubiquitinated PEX5 interacts with the AAA ATPases PEX1 and PEX6 and is unfolded during its dislocation into the cytosol.
Pedrosa AG; Francisco T; Bicho D; Dias AF; Barros-Barbosa A; Hagmann V; Dodt G; Rodrigues TA; Azevedo JE
J Biol Chem; 2018 Jul; 293(29):11553-11563. PubMed ID: 29884772
[TBL] [Abstract][Full Text] [Related]
24. Genetic Deciphering of Early-Onset and Severe Retinal Dystrophy Associated with Sensorineural Hearing Loss.
Mechaussier S; Marlin S; Kaplan J; Rozet JM; Perrault I
Adv Exp Med Biol; 2019; 1185():233-238. PubMed ID: 31884617
[TBL] [Abstract][Full Text] [Related]
25. Structure of the peroxisomal Pex1/Pex6 ATPase complex bound to a substrate.
Rüttermann M; Koci M; Lill P; Geladas ED; Kaschani F; Klink BU; Erdmann R; Gatsogiannis C
Nat Commun; 2023 Sep; 14(1):5942. PubMed ID: 37741838
[TBL] [Abstract][Full Text] [Related]
26. Clinical and genetic findings in Hungarian patients with X-linked juvenile retinoschisis.
Lesch B; Szabó V; Kánya M; Somfai GM; Vámos R; Varsányi B; Pámer Z; Knézy K; Salacz G; Janáky M; Ferencz M; Hargitai J; Papp A; Farkas A
Mol Vis; 2008; 14():2321-32. PubMed ID: 19093009
[TBL] [Abstract][Full Text] [Related]
27. Zellweger spectrum disorder patient-derived fibroblasts with the PEX1-Gly843Asp allele recover peroxisome functions in response to flavonoids.
MacLean GE; Argyriou C; Di Pietro E; Sun X; Birjandian S; Saberian P; Hacia JG; Braverman NE
J Cell Biochem; 2019 Mar; 120(3):3243-3258. PubMed ID: 30362618
[TBL] [Abstract][Full Text] [Related]
28. Insights into the Structure and Function of the Pex1/Pex6 AAA-ATPase in Peroxisome Homeostasis.
Judy RM; Sheedy CJ; Gardner BM
Cells; 2022 Jun; 11(13):. PubMed ID: 35805150
[TBL] [Abstract][Full Text] [Related]
29. The PEX1 ATPase Stabilizes PEX6 and Plays Essential Roles in Peroxisome Biology.
Rinaldi MA; Fleming WA; Gonzalez KL; Park J; Ventura MJ; Patel AB; Bartel B
Plant Physiol; 2017 Aug; 174(4):2231-2247. PubMed ID: 28600347
[TBL] [Abstract][Full Text] [Related]
30. Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels.
Walter C; Gootjes J; Mooijer PA; Portsteffen H; Klein C; Waterham HR; Barth PG; Epplen JT; Kunau WH; Wanders RJ; Dodt G
Am J Hum Genet; 2001 Jul; 69(1):35-48. PubMed ID: 11389485
[TBL] [Abstract][Full Text] [Related]
31. New recessive compound heterozygous variants of
Cao WC; Chen QS; Gan R; Huang T; Yan XH
Int J Ophthalmol; 2024; 17(1):107-112. PubMed ID: 38239955
[TBL] [Abstract][Full Text] [Related]
32. Novel PEX1 mutations in fibroblasts from children with Zellweger spectrum disorders exhibit temperature sensitive characteristics.
Liang JS; Hung KL; Lin LJ; Ong WP; Keng WT; Lu JF
Epilepsy Behav; 2023 Aug; 145():109266. PubMed ID: 37385119
[TBL] [Abstract][Full Text] [Related]
33. A newly identified mutation in the
Tanaka AJ; Okumoto K; Tamura S; Abe Y; Hirsch Y; Deng L; Ekstein J; Chung WK; Fujiki Y
Cold Spring Harb Mol Case Stud; 2019 Feb; 5(1):. PubMed ID: 30446579
[TBL] [Abstract][Full Text] [Related]
34. The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes.
Matsumoto N; Tamura S; Fujiki Y
Nat Cell Biol; 2003 May; 5(5):454-60. PubMed ID: 12717447
[TBL] [Abstract][Full Text] [Related]
35. Isoform-specific domain organization determines conformation and function of the peroxisomal biogenesis factor PEX26.
Guder P; Lotz-Havla AS; Woidy M; Reiß DD; Danecka MK; Schatz UA; Becker M; Ensenauer R; Pagel P; Büttner L; Muntau AC; Gersting SW
Biochim Biophys Acta Mol Cell Res; 2019 Mar; 1866(3):518-531. PubMed ID: 30366024
[TBL] [Abstract][Full Text] [Related]
36. Depletion of HNRNPA1 induces peroxisomal autophagy by regulating PEX1 expression.
Park NY; Jo DS; Park SJ; Lee H; Bae JE; Hong Y; Kim JB; Kim YH; Park HJ; Choi JY; Lee HJ; Ryoo ZY; Lee HS; Kim JC; Lee EK; Cho DH
Biochem Biophys Res Commun; 2021 Mar; 545():69-74. PubMed ID: 33545634
[TBL] [Abstract][Full Text] [Related]
37. A patient with X-linked retinoschisis and exudative retinal detachment associated with a pathogenic hemizygous variant c.304c>T in
Tondelli NN; Mencaroni BM; Lemos CMB; Rocha de Sousa J; Sandoval Barbosa GC; Gomes AMV; da Palma MM
Ophthalmic Genet; 2022 Dec; 43(6):871-875. PubMed ID: 36695495
[TBL] [Abstract][Full Text] [Related]
38. Biallelic Mutations in CRB1 Underlie Autosomal Recessive Familial Foveal Retinoschisis.
Vincent A; Ng J; Gerth-Kahlert C; Tavares E; Maynes JT; Wright T; Tiwari A; Tumber A; Li S; Hanson JV; Bahr A; MacDonald H; Bähr L; Westall C; Berger W; Cremers FP; den Hollander AI; Héon E
Invest Ophthalmol Vis Sci; 2016 May; 57(6):2637-46. PubMed ID: 27258436
[TBL] [Abstract][Full Text] [Related]
39. A longitudinal study of retinopathy in the PEX1-Gly844Asp mouse model for mild Zellweger Spectrum Disorder.
Argyriou C; Polosa A; Cecyre B; Hsieh M; Di Pietro E; Cui W; Bouchard JF; Lachapelle P; Braverman N
Exp Eye Res; 2019 Sep; 186():107713. PubMed ID: 31254513
[TBL] [Abstract][Full Text] [Related]
40. Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I.
Tamura S; Okumoto K; Toyama R; Shimozawa N; Tsukamoto T; Suzuki Y; Osumi T; Kondo N; Fujiki Y
Proc Natl Acad Sci U S A; 1998 Apr; 95(8):4350-5. PubMed ID: 9539740
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]