Moser HW - Search Results

1

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

2

Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome.

Gärtner J, Moser H, Valle D. Gärtner J, et al. Nat Genet. 1992 Apr;1(1):16-23. doi: 10.1038/ng0492-16. Nat Genet. 1992. PMID: 1301993

3

Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata.

Braverman N, Steel G, Obie C, Moser A, Moser H, Gould SJ, Valle D. Braverman N, et al. Nat Genet. 1997 Apr;15(4):369-76. doi: 10.1038/ng0497-369. Nat Genet. 1997. PMID: 9090381

4

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. Nat Genet. 1997 Apr;15(4):385-8. doi: 10.1038/ng0497-385. Nat Genet. 1997. PMID: 9090384

5

Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders.

Slawecki ML, Dodt G, Steinberg S, Moser AB, Moser HW, Gould SJ. Slawecki ML, et al. Among authors: moser hw, moser ab. J Cell Sci. 1995 May;108 ( Pt 5):1817-29. doi: 10.1242/jcs.108.5.1817. J Cell Sci. 1995. PMID: 7544797

6

Altered expression of ALDP in X-linked adrenoleukodystrophy.

Watkins PA, Gould SJ, Smith MA, Braiterman LT, Wei HM, Kok F, Moser AB, Moser HW, Smith KD. Watkins PA, et al. Among authors: moser hw, moser ab. Am J Hum Genet. 1995 Aug;57(2):292-301. Am J Hum Genet. 1995. PMID: 7668254 Free PMC article.

7

Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders.

Dodt G, Braverman N, Wong C, Moser A, Moser HW, Watkins P, Valle D, Gould SJ. Dodt G, et al. Among authors: moser hw, moser a. Nat Genet. 1995 Feb;9(2):115-25. doi: 10.1038/ng0295-115. Nat Genet. 1995. PMID: 7719337

8

The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor.

Yahraus T, Braverman N, Dodt G, Kalish JE, Morrell JC, Moser HW, Valle D, Gould SJ. Yahraus T, et al. Among authors: moser hw. EMBO J. 1996 Jun 17;15(12):2914-23. EMBO J. 1996. PMID: 8670792 Free PMC article.

9

Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders.

Reuber BE, Germain-Lee E, Collins CS, Morrell JC, Ameritunga R, Moser HW, Valle D, Gould SJ. Reuber BE, et al. Among authors: moser hw. Nat Genet. 1997 Dec;17(4):445-8. doi: 10.1038/ng1297-445. Nat Genet. 1997. PMID: 9398847

10

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: moser hw, moser ab. J Cell Sci. 1999 May;112 ( Pt 10):1579-90. doi: 10.1242/jcs.112.10.1579. J Cell Sci. 1999. PMID: 10212151

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