Hoogeveen-Westerveld M - Search Results

1

Characterization of the human lysosomal alpha-glucosidase gene.

Hoefsloot LH, Hoogeveen-Westerveld M, Reuser AJ, Oostra BA. Hoefsloot LH, et al. Biochem J. 1990 Dec 1;272(2):493-7. doi: 10.1042/bj2720493. Biochem J. 1990. PMID: 2268276 Free PMC article.

2

An XbaI restriction site polymorphism in the acid alpha-glucosidase gene (GAA).

Hoefsloot LH, Hoogeveen-Westerveld M, Oostra BA, Reuser AJ. Hoefsloot LH, et al. Nucleic Acids Res. 1991 Feb 11;19(3):682. doi: 10.1093/nar/19.3.682-a. Nucleic Acids Res. 1991. PMID: 1672755 Free PMC article.

3

HindIII/EcoRI polymorphism in the GAA gene.

Hoefsloot LH, Hoogeveen-Westerveld M, Sakuraba H, Suzuki Y, Oostra BA, Reuser AJ. Hoefsloot LH, et al. Nucleic Acids Res. 1990 Oct 11;18(19):5921. doi: 10.1093/nar/18.19.5921. Nucleic Acids Res. 1990. PMID: 1977144 Free PMC article.

4

Expression and routeing of human lysosomal alpha-glucosidase in transiently transfected mammalian cells.

Hoefsloot LH, Willemsen R, Kroos MA, Hoogeveen-Westerveld M, Hermans MM, Van der Ploeg AT, Oostra BA, Reuser AJ. Hoefsloot LH, et al. Biochem J. 1990 Dec 1;272(2):485-92. doi: 10.1042/bj2720485. Biochem J. 1990. PMID: 2268275 Free PMC article.

5

Adult and infantile glycogenosis type II in one family, explained by allelic diversity.

Hoefsloot LH, van der Ploeg AT, Kroos MA, Hoogeveen-Westerveld M, Oostra BA, Reuser AJ. Hoefsloot LH, et al. Am J Hum Genet. 1990 Jan;46(1):45-52. Am J Hum Genet. 1990. PMID: 2403755 Free PMC article.

6

Glycogenosis type II: protein and DNA analysis in five South African families from various ethnic origins.

Van der Ploeg AT, Hoefsloot LH, Hoogeveen-Westerveld M, Petersen EM, Reuser AJ. Van der Ploeg AT, et al. Am J Hum Genet. 1989 Jun;44(6):787-93. Am J Hum Genet. 1989. PMID: 2658562 Free PMC article.

7

Primary structure and processing of lysosomal alpha-glucosidase; homology with the intestinal sucrase-isomaltase complex.

Hoefsloot LH, Hoogeveen-Westerveld M, Kroos MA, van Beeumen J, Reuser AJ, Oostra BA. Hoefsloot LH, et al. EMBO J. 1988 Jun;7(6):1697-704. doi: 10.1002/j.1460-2075.1988.tb02998.x. EMBO J. 1988. PMID: 3049072 Free PMC article.

8

The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome.

Willemsen R, Hoogeveen-Westerveld M, Reis S, Holstege J, Severijnen LA, Nieuwenhuizen IM, Schrier M, van Unen L, Tassone F, Hoogeveen AT, Hagerman PJ, Mientjes EJ, Oostra BA. Willemsen R, et al. Hum Mol Genet. 2003 May 1;12(9):949-59. doi: 10.1093/hmg/ddg114. Hum Mol Genet. 2003. PMID: 12700164 Free article.

9

Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivo.

Mientjes EJ, Willemsen R, Kirkpatrick LL, Nieuwenhuizen IM, Hoogeveen-Westerveld M, Verweij M, Reis S, Bardoni B, Hoogeveen AT, Oostra BA, Nelson DL. Mientjes EJ, et al. Hum Mol Genet. 2004 Jul 1;13(13):1291-302. doi: 10.1093/hmg/ddh150. Epub 2004 May 5. Hum Mol Genet. 2004. PMID: 15128702

10

The generation of a conditional Fmr1 knock out mouse model to study Fmrp function in vivo.

Mientjes EJ, Nieuwenhuizen I, Kirkpatrick L, Zu T, Hoogeveen-Westerveld M, Severijnen L, Rifé M, Willemsen R, Nelson DL, Oostra BA. Mientjes EJ, et al. Neurobiol Dis. 2006 Mar;21(3):549-55. doi: 10.1016/j.nbd.2005.08.019. Epub 2005 Oct 26. Neurobiol Dis. 2006. PMID: 16257225

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