Klomp LW - Search Results

1

The ubiquitously expressed MURR1 protein is absent in canine copper toxicosis.

Klomp AE, van de Sluis B, Klomp LW, Wijmenga C. Klomp AE, et al. Among authors: klomp lw. J Hepatol. 2003 Nov;39(5):703-9. doi: 10.1016/s0168-8278(03)00380-5. J Hepatol. 2003. PMID: 14568250

2

The gene product Murr1 restricts HIV-1 replication in resting CD4+ lymphocytes.

Ganesh L, Burstein E, Guha-Niyogi A, Louder MK, Mascola JR, Klomp LW, Wijmenga C, Duckett CS, Nabel GJ. Ganesh L, et al. Among authors: klomp lw. Nature. 2003 Dec 18;426(6968):853-7. doi: 10.1038/nature02171. Nature. 2003. PMID: 14685242

3

A novel role for XIAP in copper homeostasis through regulation of MURR1.

Burstein E, Ganesh L, Dick RD, van De Sluis B, Wilkinson JC, Klomp LW, Wijmenga C, Brewer GJ, Nabel GJ, Duckett CS. Burstein E, et al. Among authors: klomp lw. EMBO J. 2004 Jan 14;23(1):244-54. doi: 10.1038/sj.emboj.7600031. Epub 2003 Dec 18. EMBO J. 2004. PMID: 14685266 Free PMC article.

4

ATOX1: a novel copper-responsive transcription factor in mammals?

Muller PA, Klomp LW. Muller PA, et al. Among authors: klomp lw. Int J Biochem Cell Biol. 2009 Jun;41(6):1233-6. doi: 10.1016/j.biocel.2008.08.001. Epub 2008 Aug 7. Int J Biochem Cell Biol. 2009. PMID: 18761103 Review.

5

The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a meta-analysis.

Stapelbroek JM, Bollen CW, van Amstel JK, van Erpecum KJ, van Hattum J, van den Berg LH, Klomp LW, Houwen RH. Stapelbroek JM, et al. Among authors: klomp lw. J Hepatol. 2004 Nov;41(5):758-63. doi: 10.1016/j.jhep.2004.07.017. J Hepatol. 2004. PMID: 15519648

6

The copper toxicosis gene product Murr1 directly interacts with the Wilson disease protein.

Tao TY, Liu F, Klomp L, Wijmenga C, Gitlin JD. Tao TY, et al. J Biol Chem. 2003 Oct 24;278(43):41593-6. doi: 10.1074/jbc.C300391200. Epub 2003 Sep 10. J Biol Chem. 2003. PMID: 12968035

7

Progressive familial intrahepatic cholestasis type 1 and extrahepatic features: no catch-up of stature growth, exacerbation of diarrhea, and appearance of liver steatosis after liver transplantation.

Lykavieris P, van Mil S, Cresteil D, Fabre M, Hadchouel M, Klomp L, Bernard O, Jacquemin E. Lykavieris P, et al. J Hepatol. 2003 Sep;39(3):447-52. doi: 10.1016/s0168-8278(03)00286-1. J Hepatol. 2003. PMID: 12927934

8

FIC1, the protein affected in two forms of hereditary cholestasis, is localized in the cholangiocyte and the canalicular membrane of the hepatocyte.

Eppens EF, van Mil SW, de Vree JM, Mok KS, Juijn JA, Oude Elferink RP, Berger R, Houwen RH, Klomp LW. Eppens EF, et al. Among authors: klomp lw. J Hepatol. 2001 Oct;35(4):436-43. doi: 10.1016/s0168-8278(01)00158-1. J Hepatol. 2001. PMID: 11682026

9

[From gene to disease; Wilson disease: copper storage due to mutations in ATP7B].

Stapelbroek JM, Ploos van Amstel JK, van Hattum J, van den Berg LH, Klomp LW, Houwen RH. Stapelbroek JM, et al. Among authors: klomp lw. Ned Tijdschr Geneeskd. 2003 Mar 29;147(13):603-5. Ned Tijdschr Geneeskd. 2003. PMID: 12701394 Review. Dutch.

10

Genetics of familial intrahepatic cholestasis syndromes.

van Mil SW, Houwen RH, Klomp LW. van Mil SW, et al. Among authors: klomp lw. J Med Genet. 2005 Jun;42(6):449-63. doi: 10.1136/jmg.2004.026187. J Med Genet. 2005. PMID: 15937079 Free PMC article. Review.

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