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Items: 26

1.
2.

Higher-order oligomerization targets plasma membrane proteins and HIV gag to exosomes.

Fang Y, Wu N, Gan X, Yan W, Morrell JC, Gould SJ.

PLoS Biol. 2007 Jun;5(6):e158.

3.

Detecting patterns of protein distribution and gene expression in silico.

Bassett D, Morrell JC, Gatto GJ Jr, Bai J, Geisbrecht BV, Hieter P, Gould SJ.

Proc Natl Acad Sci U S A. 2005 Jan 11;102(2):516. No abstract available.

4.

PEX3 functions as a PEX19 docking factor in the import of class I peroxisomal membrane proteins.

Fang Y, Morrell JC, Jones JM, Gould SJ.

J Cell Biol. 2004 Mar 15;164(6):863-75. Epub 2004 Mar 8.

5.
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PEX11 beta deficiency is lethal and impairs neuronal migration but does not abrogate peroxisome function.

Li X, Baumgart E, Morrell JC, Jimenez-Sanchez G, Valle D, Gould SJ.

Mol Cell Biol. 2002 Jun;22(12):4358-65.

8.

Multiple distinct targeting signals in integral peroxisomal membrane proteins.

Jones JM, Morrell JC, Gould SJ.

J Cell Biol. 2001 Jun 11;153(6):1141-50.

9.

The peroxisome biogenesis factors pex4p, pex22p, pex1p, and pex6p act in the terminal steps of peroxisomal matrix protein import.

Collins CS, Kalish JE, Morrell JC, McCaffery JM, Gould SJ.

Mol Cell Biol. 2000 Oct;20(20):7516-26.

10.
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Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia.

Sacksteder KA, Biery BJ, Morrell JC, Goodman BK, Geisbrecht BV, Cox RP, Gould SJ, Geraghty MT.

Am J Hum Genet. 2000 Jun;66(6):1736-43. Epub 2000 Apr 20.

12.

The mouse gene PDCR encodes a peroxisomal delta(2), delta(4)-dienoyl-CoA reductase.

Geisbrecht BV, Liang X, Morrell JC, Schulz H, Gould SJ.

J Biol Chem. 1999 Sep 3;274(36):25814-20.

13.

MCD encodes peroxisomal and cytoplasmic forms of malonyl-CoA decarboxylase and is mutated in malonyl-CoA decarboxylase deficiency.

Sacksteder KA, Morrell JC, Wanders RJ, Matalon R, Gould SJ.

J Biol Chem. 1999 Aug 27;274(35):24461-8.

14.

Detecting patterns of protein distribution and gene expression in silico.

Geraghty MT, Bassett D, Morrell JC, Gatto GJ Jr, Bai J, Geisbrecht BV, Hieter P, Gould SJ.

Proc Natl Acad Sci U S A. 1999 Mar 16;96(6):2937-42. Retraction in: Bassett D, Morrell JC, Gatto GJ Jr, Bai J, Geisbrecht BV, Hieter P, Gould SJ. Proc Natl Acad Sci U S A. 2005 Jan 11;102(2):516.

15.

Molecular characterization of Saccharomyces cerevisiae Delta3, Delta2-enoyl-CoA isomerase.

Geisbrecht BV, Zhu D, Schulz K, Nau K, Morrell JC, Geraghty M, Schulz H, Erdmann R, Gould SJ.

J Biol Chem. 1998 Dec 11;273(50):33184-91. Erratum in: J Biol Chem. 2005 Apr 1;280(13):13203.

16.

Expression of PEX11beta mediates peroxisome proliferation in the absence of extracellular stimuli.

Schrader M, Reuber BE, Morrell JC, Jimenez-Sanchez G, Obie C, Stroh TA, Valle D, Schroer TA, Gould SJ.

J Biol Chem. 1998 Nov 6;273(45):29607-14.

17.

Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.

Warren DS, Morrell JC, Moser HW, Valle D, Gould SJ.

Am J Hum Genet. 1998 Aug;63(2):347-59.

18.

Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders.

Reuber BE, Germain-Lee E, Collins CS, Morrell JC, Ameritunga R, Moser HW, Valle D, Gould SJ.

Nat Genet. 1997 Dec;17(4):445-8.

PMID:
9398847
19.

Identification of PAHX, a Refsum disease gene.

Mihalik SJ, Morrell JC, Kim D, Sacksteder KA, Watkins PA, Gould SJ.

Nat Genet. 1997 Oct;17(2):185-9.

PMID:
9326939
20.

Pex13p is an SH3 protein of the peroxisome membrane and a docking factor for the predominantly cytoplasmic PTs1 receptor.

Gould SJ, Kalish JE, Morrell JC, Bjorkman J, Urquhart AJ, Crane DI.

J Cell Biol. 1996 Oct;135(1):85-95.

21.

Characterization of a novel component of the peroxisomal protein import apparatus using fluorescent peroxisomal proteins.

Kalish JE, Keller GA, Morrell JC, Mihalik SJ, Smith B, Cregg JM, Gould SJ.

EMBO J. 1996 Jul 1;15(13):3275-85.

22.

The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor.

Yahraus T, Braverman N, Dodt G, Kalish JE, Morrell JC, Moser HW, Valle D, Gould SJ.

EMBO J. 1996 Jun 17;15(12):2914-23.

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Chromosomal rearrangement segregating with adrenoleukodystrophy: a molecular analysis.

Sack GH Jr, Alpern M, Webster T, Feil RP, Morrell JC, Chen G, Chen W, Caskey CT, Moser HW.

Proc Natl Acad Sci U S A. 1993 Oct 15;90(20):9489-93.

25.

Visual pigment gene changes in adrenoleukodystrophy.

Sack GH Jr, Morrell JC.

Invest Ophthalmol Vis Sci. 1993 Aug;34(9):2634-7.

PMID:
8344786
26.

Adrenoleukodystrophy: overlapping deletions point to a gene location in Xq28.

Sack GH Jr, Morrell JC.

Biochem Biophys Res Commun. 1993 Mar 31;191(3):955-60.

PMID:
8466536

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