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Items: 4

1.
Large deletion of the peroxisomal acyl-CoA oxidase gene in pseudoneonatal adrenoleukodystrophy.
B Fournier, J M Saudubray, B Benichou, S Lyonnet, A Munnich, H Clevers, B T Poll-The
J Clin Invest. 1994 Aug; 94(2): 526–531. doi: 10.1172/JCI117365
PMCID:
PMC296126
SummaryPage BrowsePDF–1.2M
2.
Impaired dendritic-cell function in ectodermal dysplasia with immune deficiency is linked to defective NEMO ubiquitination
Stephane T. Temmerman, Chi A. Ma, Louis Borges, Marek Kubin, Shuying Liu, Jonathan M. J. Derry, Ashish Jain
Blood. 2006 Oct 1; 108(7): 2324–2331. Prepublished online 2006 Jun 22. doi: 10.1182/blood-2006-04-017210
PMCID:
PMC1895566
AbstractArticle
3.
Impact on Genetic Networks in Human Macrophages by a CCR5 Strain of Human Immunodeficiency Virus Type 1
Carter R. Coberley, James J. Kohler, Joseph N. Brown, Joseph T. Oshier, Henry V. Baker, Michael P. Popp, John W. Sleasman, Maureen M. Goodenow
J Virol. 2004 Nov; 78(21): 11477–11486. doi: 10.1128/JVI.78.21.11477-11486.2004
PMCID:
PMC523249
AbstractArticlePDF–283K
4.
Molecular characterization of the human peroxisomal branchedchain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome
Eveline Baumgart, Johannes C. T. Vanhooren, Mark Fransen, Peter Marynen, Magda Puype, Joël Vandekerckhove, Jack A. M. Leunissen, H. Dariush Fahimi, Guy P. Mannaerts, Paul P. Van Veldhoven
Proc Natl Acad Sci U S A. 1996 Nov 26; 93(24): 13748–13753. doi: 10.1073/pnas.93.24.13748
PMCID:
PMC19413
AbstractArticlePDF–465K

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