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Results: 16

Related Articles by Review for PubMed (Select 14506246)

1.

Misfolding, degradation, and aggregation of variant proteins. The molecular pathogenesis of short chain acyl-CoA dehydrogenase (SCAD) deficiency.

Pedersen CB, Bross P, Winter VS, Corydon TJ, Bolund L, Bartlett K, Vockley J, Gregersen N.

J Biol Chem. 2003 Nov 28;278(48):47449-58. Epub 2003 Sep 23.

2.

Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiency.

Shirao K, Okada S, Tajima G, Tsumura M, Hara K, Yasunaga S, Ohtsubo M, Hata I, Sakura N, Shigematsu Y, Takihara Y, Kobayashi M.

Hum Genet. 2010 Jun;127(6):619-28. doi: 10.1007/s00439-010-0822-7. Epub 2010 Apr 8. Review.

PMID:
20376488
3.

Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship.

Gregersen N, Andresen BS, Corydon MJ, Corydon TJ, Olsen RK, Bolund L, Bross P.

Hum Mutat. 2001 Sep;18(3):169-89. Review.

PMID:
11524729
4.

Genetic and cellular modifiers of oxidative stress: what can we learn from fatty acid oxidation defects?

Olsen RK, Cornelius N, Gregersen N.

Mol Genet Metab. 2013;110 Suppl:S31-9. doi: 10.1016/j.ymgme.2013.10.007. Epub 2013 Oct 12. Review.

PMID:
24206932
5.
6.

Protein misfolding and degradation in genetic diseases.

Bross P, Corydon TJ, Andresen BS, Jørgensen MM, Bolund L, Gregersen N.

Hum Mutat. 1999;14(3):186-98. Review.

PMID:
10477427
7.

Impaired folding and subunit assembly as disease mechanism: the example of medium-chain acyl-CoA dehydrogenase deficiency.

Bross P, Andresen BS, Gregersen N.

Prog Nucleic Acid Res Mol Biol. 1998;58:301-37. Review.

PMID:
9308370
8.

The role of chaperone-assisted folding and quality control in inborn errors of metabolism: protein folding disorders.

Gregersen N, Bross P, Andrese BS, Pedersen CB, Corydon TJ, Bolund L.

J Inherit Metab Dis. 2001 Apr;24(2):189-212. Review.

PMID:
11405340
9.

[Short-chain acyl-CoA dehydrogenase (SCAD) deficiency].

Inoue M, Yamaguchi S.

Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):417-9. Review. Japanese. No abstract available.

PMID:
9590088
10.

Protein misfolding, aggregation, and degradation in disease.

Gregersen N, Bolund L, Bross P.

Mol Biotechnol. 2005 Oct;31(2):141-50. Review.

PMID:
16170215
11.

Protein misfolding in conformational disorders: rescue of folding defects and chemical chaperoning.

Leandro P, Gomes CM.

Mini Rev Med Chem. 2008 Aug;8(9):901-11. Review.

PMID:
18691147
12.

Converging concepts of protein folding in vitro and in vivo.

Hartl FU, Hayer-Hartl M.

Nat Struct Mol Biol. 2009 Jun;16(6):574-81. doi: 10.1038/nsmb.1591. Review.

PMID:
19491934
13.

Molecular chaperone disorders: defective Hsp60 in neurodegeneration.

Bross P, Magnoni R, Bie AS.

Curr Top Med Chem. 2012;12(22):2491-503. Review.

PMID:
23339303
14.

A model for PKC involvement in the pathogenesis of inborn errors of metabolism.

Boneh A.

Trends Mol Med. 2002 Nov;8(11):524-31. Review.

PMID:
12421686
15.

Protein misfolding and human disease.

Gregersen N, Bross P, Vang S, Christensen JH.

Annu Rev Genomics Hum Genet. 2006;7:103-24. Review.

PMID:
16722804
16.

Protein misfolding, aggregation, and degradation in disease.

Gregersen N, Bolund L, Bross P.

Methods Mol Biol. 2003;232:3-16. Review. No abstract available.

PMID:
12840535
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