PubMed (OMIM) for id: 5192

Year	Number of Results
1995	1
1996	1
1998	2
2000	1
2003	1
2006	2
2008	1
2009	2
2010	2
2012	1
2024	0

1

Genetics and molecular basis of human peroxisome biogenesis disorders.

Waterham HR, Ebberink MS. Waterham HR, et al. Biochim Biophys Acta. 2012 Sep;1822(9):1430-41. doi: 10.1016/j.bbadis.2012.04.006. Epub 2012 Apr 25. Biochim Biophys Acta. 2012. PMID: 22871920 Free article. Review.

2

Mutations in PEX10 are a cause of autosomal recessive ataxia.

Régal L, Ebberink MS, Goemans N, Wanders RJ, De Meirleir L, Jaeken J, Schrooten M, Van Coster R, Waterham HR. Régal L, et al. Ann Neurol. 2010 Aug;68(2):259-63. doi: 10.1002/ana.22035. Ann Neurol. 2010. PMID: 20695019 Review.

3

Drosophila models of peroxisomal biogenesis disorder: peroxins are required for spermatogenesis and very-long-chain fatty acid metabolism.

Chen H, Liu Z, Huang X. Chen H, et al. Hum Mol Genet. 2010 Feb 1;19(3):494-505. doi: 10.1093/hmg/ddp518. Epub 2009 Nov 17. Hum Mol Genet. 2010. PMID: 19933170

4

A PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblasts.

Steinberg SJ, Snowden A, Braverman NE, Chen L, Watkins PA, Clayton PT, Setchell KD, Heubi JE, Raymond GV, Moser AB, Moser HW. Steinberg SJ, et al. J Inherit Metab Dis. 2009 Feb;32(1):109-19. doi: 10.1007/s10545-008-0969-8. Epub 2008 Dec 25. J Inherit Metab Dis. 2009. PMID: 19127411

5

Peroxisome biogenesis disorders.

Steinberg SJ, Dodt G, Raymond GV, Braverman NE, Moser AB, Moser HW. Steinberg SJ, et al. Biochim Biophys Acta. 2006 Dec;1763(12):1733-48. doi: 10.1016/j.bbamcr.2006.09.010. Epub 2006 Sep 14. Biochim Biophys Acta. 2006. PMID: 17055079 Free article. Review.

6

Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients.

Krause C, Rosewich H, Thanos M, Gärtner J. Krause C, et al. Hum Mutat. 2006 Nov;27(11):1157. doi: 10.1002/humu.9462. Hum Mutat. 2006. PMID: 17041890

7

Genetic heterogeneity of peroxisome biogenesis disorders among Japanese patients: evidence for a founder haplotype for the most common PEX10 gene mutation.

Shimozawa N, Nagase T, Takemoto Y, Ohura T, Suzuki Y, Kondo N. Shimozawa N, et al. Am J Med Genet A. 2003 Jul 1;120A(1):40-3. doi: 10.1002/ajmg.a.20030. Am J Med Genet A. 2003. PMID: 12794690

8

Phenotype-genotype relationships in PEX10-deficient peroxisome biogenesis disorder patients.

Warren DS, Wolfe BD, Gould SJ. Warren DS, et al. Hum Mutat. 2000;15(6):509-21. doi: 10.1002/1098-1004(200006)15:6<509::AID-HUMU3>3.0.CO;2-#. Hum Mutat. 2000. PMID: 10862081

9

Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.

Okumoto K, Itoh R, Shimozawa N, Suzuki Y, Tamura S, Kondo N, Fujiki Y. Okumoto K, et al. Hum Mol Genet. 1998 Sep;7(9):1399-405. doi: 10.1093/hmg/7.9.1399. Hum Mol Genet. 1998. PMID: 9700193

10

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. Warren DS, et al. Am J Hum Genet. 1998 Aug;63(2):347-59. doi: 10.1086/301963. Am J Hum Genet. 1998. PMID: 9683594 Free PMC article.

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