261 related articles for article (PubMed ID: 3294860)
1. The influenza hemagglutinin insertion signal is not cleaved and does not halt translocation when presented to the endoplasmic reticulum membrane as part of a translocating polypeptide.
Finidori J; Rizzolo L; Gonzalez A; Kreibich G; Adesnik M; Sabatini DD
J Cell Biol; 1987 Jun; 104(6):1705-14. PubMed ID: 3294860
[TBL] [Abstract][Full Text] [Related]
2. Biosynthesis and intracellular sorting of growth hormone-viral envelope glycoprotein hybrids.
Rizzolo LJ; Finidori J; Gonzalez A; Arpin M; Ivanov IE; Adesnik M; Sabatini DD
J Cell Biol; 1985 Oct; 101(4):1351-62. PubMed ID: 2995406
[TBL] [Abstract][Full Text] [Related]
3. Signals for the incorporation and orientation of cytochrome P450 in the endoplasmic reticulum membrane.
Monier S; Van Luc P; Kreibich G; Sabatini DD; Adesnik M
J Cell Biol; 1988 Aug; 107(2):457-70. PubMed ID: 3047140
[TBL] [Abstract][Full Text] [Related]
4. Integration of membrane proteins into the endoplasmic reticulum requires GTP.
Wilson C; Connolly T; Morrison T; Gilmore R
J Cell Biol; 1988 Jul; 107(1):69-77. PubMed ID: 2839521
[TBL] [Abstract][Full Text] [Related]
5. Signal peptidase can cleave inside a polytopic membrane protein.
Beltzer JP; Wessels HP; Spiess M
FEBS Lett; 1989 Aug; 253(1-2):93-8. PubMed ID: 2668036
[TBL] [Abstract][Full Text] [Related]
6. Positive charges at the NH2 terminus convert the membrane-anchor signal peptide of cytochrome P-450 to a secretory signal peptide.
Szczesna-Skorupa E; Browne N; Mead D; Kemper B
Proc Natl Acad Sci U S A; 1988 Feb; 85(3):738-42. PubMed ID: 3422456
[TBL] [Abstract][Full Text] [Related]
7. Transposition of domains between the M2 and HN viral membrane proteins results in polypeptides which can adopt more than one membrane orientation.
Parks GD; Hull JD; Lamb RA
J Cell Biol; 1989 Nov; 109(5):2023-32. PubMed ID: 2553741
[TBL] [Abstract][Full Text] [Related]
8. Targeting of the hepatitis B virus precore protein to the endoplasmic reticulum membrane: after signal peptide cleavage translocation can be aborted and the product released into the cytoplasm.
Garcia PD; Ou JH; Rutter WJ; Walter P
J Cell Biol; 1988 Apr; 106(4):1093-104. PubMed ID: 3283145
[TBL] [Abstract][Full Text] [Related]
9. Posttranslational translocation of influenza virus hemagglutinin across microsomal membranes.
Chao CC; Bird P; Gething MJ; Sambrook J
Mol Cell Biol; 1987 Oct; 7(10):3842-5. PubMed ID: 3683400
[TBL] [Abstract][Full Text] [Related]
10. A short amino-terminal segment of microsomal cytochrome P-450 functions both as an insertion signal and as a stop-transfer sequence.
Sakaguchi M; Mihara K; Sato R
EMBO J; 1987 Aug; 6(8):2425-31. PubMed ID: 2822391
[TBL] [Abstract][Full Text] [Related]
11. Isolation and characterization of cDNA clones for rat ribophorin I: complete coding sequence and in vitro synthesis and insertion of the encoded product into endoplasmic reticulum membranes.
Harnik-Ort V; Prakash K; Marcantonio E; Colman DR; Rosenfeld MG; Adesnik M; Sabatini DD; Kreibich G
J Cell Biol; 1987 Apr; 104(4):855-63. PubMed ID: 3031084
[TBL] [Abstract][Full Text] [Related]
12. Evidence for the loop model of signal-sequence insertion into the endoplasmic reticulum.
Shaw AS; Rottier PJ; Rose JK
Proc Natl Acad Sci U S A; 1988 Oct; 85(20):7592-6. PubMed ID: 2845415
[TBL] [Abstract][Full Text] [Related]
13. A tripartite structure of the signals that determine protein insertion into the endoplasmic reticulum membrane.
Haeuptle MT; Flint N; Gough NM; Dobberstein B
J Cell Biol; 1989 Apr; 108(4):1227-36. PubMed ID: 2784443
[TBL] [Abstract][Full Text] [Related]
14. Mitochondrial porin can be translocated across both endoplasmic reticulum and mitochondrial membranes.
Sakaguchi M; Hachiya N; Mihara K; Omura T
J Biochem; 1992 Aug; 112(2):243-8. PubMed ID: 1328170
[TBL] [Abstract][Full Text] [Related]
15. A sorting signal for the basolateral delivery of the vesicular stomatitis virus (VSV) G protein lies in its luminal domain: analysis of the targeting of VSV G-influenza hemagglutinin chimeras.
Compton T; Ivanov IE; Gottlieb T; Rindler M; Adesnik M; Sabatini DD
Proc Natl Acad Sci U S A; 1989 Jun; 86(11):4112-6. PubMed ID: 2542964
[TBL] [Abstract][Full Text] [Related]
16. Analysis of progressive deletions of the transmembrane and cytoplasmic domains of influenza hemagglutinin.
Doyle C; Sambrook J; Gething MJ
J Cell Biol; 1986 Oct; 103(4):1193-204. PubMed ID: 3771631
[TBL] [Abstract][Full Text] [Related]
17. Truncations of a secretory protein define minimum lengths required for binding to signal recognition particle and translocation across the endoplasmic reticulum membrane.
Okun MM; Eskridge EM; Shields D
J Biol Chem; 1990 May; 265(13):7478-84. PubMed ID: 2185250
[TBL] [Abstract][Full Text] [Related]
18. Functions of signal and signal-anchor sequences are determined by the balance between the hydrophobic segment and the N-terminal charge.
Sakaguchi M; Tomiyoshi R; Kuroiwa T; Mihara K; Omura T
Proc Natl Acad Sci U S A; 1992 Jan; 89(1):16-9. PubMed ID: 1729684
[TBL] [Abstract][Full Text] [Related]
19. A chimeric avian retrovirus containing the influenza virus hemagglutinin gene has an expanded host range.
Dong J; Roth MG; Hunter E
J Virol; 1992 Dec; 66(12):7374-82. PubMed ID: 1331528
[TBL] [Abstract][Full Text] [Related]
20. Na(+)/H(+) exchanger NHE3 has 11 membrane spanning domains and a cleaved signal peptide: topology analysis using in vitro transcription/translation.
Zizak M; Cavet ME; Bayle D; Tse CM; Hallen S; Sachs G; Donowitz M
Biochemistry; 2000 Jul; 39(27):8102-12. PubMed ID: 10891093
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
