Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 457

1.

Defective endoplasmic reticulum-resident membrane protein CLN6 affects lysosomal degradation of endocytosed arylsulfatase A.

Heine C, Koch B, Storch S, Kohlschütter A, Palmer DN, Braulke T.

J Biol Chem. 2004 May 21;279(21):22347-52. Epub 2004 Mar 9.

PMID:
15010453
[PubMed - indexed for MEDLINE]
Free Article
2.

Topology and endoplasmic reticulum retention signals of the lysosomal storage disease-related membrane protein CLN6.

Heine C, Quitsch A, Storch S, Martin Y, Lonka L, Lehesjoki AE, Mole SE, Braulke T.

Mol Membr Biol. 2007 Jan-Feb;24(1):74-87.

PMID:
17453415
[PubMed - indexed for MEDLINE]
3.

CLN6, which is associated with a lysosomal storage disease, is an endoplasmic reticulum protein.

Mole SE, Michaux G, Codlin S, Wheeler RB, Sharp JD, Cutler DF.

Exp Cell Res. 2004 Aug 15;298(2):399-406.

PMID:
15265688
[PubMed - indexed for MEDLINE]
4.

The neuronal ceroid lipofuscinosis CLN8 membrane protein is a resident of the endoplasmic reticulum.

Lonka L, Kyttälä A, Ranta S, Jalanko A, Lehesjoki AE.

Hum Mol Genet. 2000 Jul 1;9(11):1691-7.

PMID:
10861296
[PubMed - indexed for MEDLINE]
Free Article
5.

Pathogenic mutations cause rapid degradation of lysosomal storage disease-related membrane protein CLN6.

Kurze AK, Galliciotti G, Heine C, Mole SE, Quitsch A, Braulke T.

Hum Mutat. 2010 Feb;31(2):E1163-74. doi: 10.1002/humu.21184.

PMID:
20020536
[PubMed - indexed for MEDLINE]
6.

Biosynthesis, glycosylation, and enzymatic processing in vivo of human tripeptidyl-peptidase I.

Golabek AA, Kida E, Walus M, Wujek P, Mehta P, Wisniewski KE.

J Biol Chem. 2003 Feb 28;278(9):7135-45. Epub 2002 Dec 17.

PMID:
12488460
[PubMed - indexed for MEDLINE]
Free Article
8.

N-glycosylation is crucial for folding, trafficking, and stability of human tripeptidyl-peptidase I.

Wujek P, Kida E, Walus M, Wisniewski KE, Golabek AA.

J Biol Chem. 2004 Mar 26;279(13):12827-39. Epub 2003 Dec 31.

PMID:
14702339
[PubMed - indexed for MEDLINE]
Free Article
9.

Disruption of the autophagy-lysosome pathway is involved in neuropathology of the nclf mouse model of neuronal ceroid lipofuscinosis.

Thelen M, Damme M, Schweizer M, Hagel C, Wong AM, Cooper JD, Braulke T, Galliciotti G.

PLoS One. 2012;7(4):e35493. doi: 10.1371/journal.pone.0035493. Epub 2012 Apr 20. Erratum in: PLoS One. 2012;7(5): doi/10.1371/annotation/a4b06d46-8eb9-4d15-a15a-41bf4b5ccb8b. Daμμe, Markus [corrected to Damme, Markus]..

PMID:
22536393
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Misfolded endoplasmic reticulum retained subunits cause degradation of wild-type subunits of arylsulfatase A heteromers.

Poeppel P, Abouzied MM, Völker C, Gieselmann V.

FEBS J. 2010 Aug;277(16):3404-14. doi: 10.1111/j.1742-4658.2010.07745.x. Epub 2010 Jul 14.

PMID:
20646068
[PubMed - indexed for MEDLINE]
11.
12.

Sec34 is implicated in traffic from the endoplasmic reticulum to the Golgi and exists in a complex with GTC-90 and ldlBp.

Loh E, Hong W.

J Biol Chem. 2002 Jun 14;277(24):21955-61. Epub 2002 Apr 2.

PMID:
11929878
[PubMed - indexed for MEDLINE]
Free Article
13.

Targeting of the dual oxidase 2 N-terminal region to the plasma membrane.

Morand S, Agnandji D, Noel-Hudson MS, Nicolas V, Buisson S, Macon-Lemaitre L, Gnidehou S, Kaniewski J, Ohayon R, Virion A, Dupuy C.

J Biol Chem. 2004 Jul 16;279(29):30244-51. Epub 2004 May 18.

PMID:
15150274
[PubMed - indexed for MEDLINE]
Free Article
14.

Atrophic macular degeneration mutations in ELOVL4 result in the intracellular misrouting of the protein.

Ambasudhan R, Wang X, Jablonski MM, Thompson DA, Lagali PS, Wong PW, Sieving PA, Ayyagari R.

Genomics. 2004 Apr;83(4):615-25.

PMID:
15028284
[PubMed - indexed for MEDLINE]
15.

Missense mutations as a cause of metachromatic leukodystrophy. Degradation of arylsulfatase A in the endoplasmic reticulum.

Poeppel P, Habetha M, Marcão A, Büssow H, Berna L, Gieselmann V.

FEBS J. 2005 Mar;272(5):1179-88.

PMID:
15720392
[PubMed - indexed for MEDLINE]
Free Article
16.

Biosynthesis and intracellular post-translational processing of normal and mutant platelet glycoprotein GPIb-IX.

Ulsemer P, Strassel C, Baas MJ, Salamero J, Chasserot-Golaz S, Cazenave JP, De La Salle C, Lanza F.

Biochem J. 2001 Sep 1;358(Pt 2):295-303.

PMID:
11513727
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Proteomics of endoplasmic reticulum-Golgi intermediate compartment (ERGIC) membranes from brefeldin A-treated HepG2 cells identifies ERGIC-32, a new cycling protein that interacts with human Erv46.

Breuza L, Halbeisen R, Jenö P, Otte S, Barlowe C, Hong W, Hauri HP.

J Biol Chem. 2004 Nov 5;279(45):47242-53. Epub 2004 Aug 11.

PMID:
15308636
[PubMed - indexed for MEDLINE]
Free Article
18.
19.

Apical transport and folding of prostate-specific membrane antigen occurs independent of glycan processing.

Castelletti D, Fracasso G, Alfalah M, Cingarlini S, Colombatti M, Naim HY.

J Biol Chem. 2006 Feb 10;281(6):3505-12. Epub 2005 Oct 12.

PMID:
16221666
[PubMed - indexed for MEDLINE]
Free Article
20.

Intracellular transport and sorting of the oligodendrocyte transmembrane proteolipid protein.

Gow A, Friedrich VL Jr, Lazzarini RA.

J Neurosci Res. 1994 Apr 1;37(5):563-73.

PMID:
7518005
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk