Gould SJ - Search Results

1

Phenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disorders.

Chang CC, Gould SJ. Chang CC, et al. Among authors: gould sj. Am J Hum Genet. 1998 Nov;63(5):1294-306. doi: 10.1086/302103. Am J Hum Genet. 1998. PMID: 9792857 Free PMC article.

2

Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders.

Chang CC, Lee WH, Moser H, Valle D, Gould SJ. Chang CC, et al. Among authors: gould sj. Nat Genet. 1997 Apr;15(4):385-8. doi: 10.1038/ng0497-385. Nat Genet. 1997. PMID: 9090384

3

Metabolic control of peroxisome abundance.

Chang CC, South S, Warren D, Jones J, Moser AB, Moser HW, Gould SJ. Chang CC, et al. Among authors: gould sj. J Cell Sci. 1999 May;112 ( Pt 10):1579-90. doi: 10.1242/jcs.112.10.1579. J Cell Sci. 1999. PMID: 10212151

4

PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import.

Chang CC, Warren DS, Sacksteder KA, Gould SJ. Chang CC, et al. Among authors: gould sj. J Cell Biol. 1999 Nov 15;147(4):761-74. doi: 10.1083/jcb.147.4.761. J Cell Biol. 1999. PMID: 10562279 Free PMC article.

5

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. Among authors: gould sj. Am J Hum Genet. 1998 Aug;63(2):347-59. doi: 10.1086/301963. Am J Hum Genet. 1998. PMID: 9683594 Free PMC article.

6

PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders.

Liu Y, Björkman J, Urquhart A, Wanders RJ, Crane DI, Gould SJ. Liu Y, et al. Among authors: gould sj. Am J Hum Genet. 1999 Sep;65(3):621-34. doi: 10.1086/302534. Am J Hum Genet. 1999. PMID: 10441568 Free PMC article.

7

Peroxisome biogenesis disorders.

Weller S, Gould SJ, Valle D. Weller S, et al. Among authors: gould sj. Annu Rev Genomics Hum Genet. 2003;4:165-211. doi: 10.1146/annurev.genom.4.070802.110424. Annu Rev Genomics Hum Genet. 2003. PMID: 14527301 Review.

8

Alternative splicing suggests extended function of PEX26 in peroxisome biogenesis.

Weller S, Cajigas I, Morrell J, Obie C, Steel G, Gould SJ, Valle D. Weller S, et al. Among authors: gould sj. Am J Hum Genet. 2005 Jun;76(6):987-1007. doi: 10.1086/430637. Epub 2005 Apr 27. Am J Hum Genet. 2005. PMID: 15858711 Free PMC article.

9

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

Warren DS, Wolfe BD, Gould SJ. Warren DS, et al. Among authors: gould sj. 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

10

Disorders of peroxisome biogenesis.

Braverman N, Dodt G, Gould SJ, Valle D. Braverman N, et al. Among authors: gould sj. Hum Mol Genet. 1995;4 Spec No:1791-8. doi: 10.1093/hmg/4.suppl_1.1791. Hum Mol Genet. 1995. PMID: 8541879 Review.

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