Boot RG - Search Results

1

Phenotype diversity in type 1 Gaucher disease: discovering the genetic basis of Gaucher disease/hematologic malignancy phenotype by individual genome analysis.

Lo SM, Choi M, Liu J, Jain D, Boot RG, Kallemeijn WW, Aerts JM, Pashankar F, Kupfer GM, Mane S, Lifton RP, Mistry PK. Lo SM, et al. Among authors: boot rg. Blood. 2012 May 17;119(20):4731-40. doi: 10.1182/blood-2011-10-386862. Epub 2012 Apr 4. Blood. 2012. PMID: 22493294 Free PMC article.

2

Pathogenesis of lysosomal storage disorders as illustrated by Gaucher disease.

Aerts JM, Van Weely S, Boot R, Hollak CE, Tager JM. Aerts JM, et al. J Inherit Metab Dis. 1993;16(2):288-91. doi: 10.1007/BF00710267. J Inherit Metab Dis. 1993. PMID: 8411983 Review. No abstract available.

3

Characterization of glucocerebrosidase in Greek Gaucher disease patients: mutation analysis and biochemical studies.

Michelakakis H, Dimitriou E, Van Weely S, Boot RG, Mavridou I, Verhoek M, Aerts JM. Michelakakis H, et al. Among authors: boot rg. J Inherit Metab Dis. 1995;18(5):609-15. doi: 10.1007/BF02436006. J Inherit Metab Dis. 1995. PMID: 8598642

4

Glucocerebrosidase genotype of Gaucher patients in The Netherlands: limitations in prognostic value.

Boot RG, Hollak CE, Verhoek M, Sloof P, Poorthuis BJ, Kleijer WJ, Wevers RA, van Oers MH, Mannens MM, Aerts JM, van Weely S. Boot RG, et al. Hum Mutat. 1997;10(5):348-58. doi: 10.1002/(SICI)1098-1004(1997)10:5<348::AID-HUMU3>3.0.CO;2-B. Hum Mutat. 1997. PMID: 9375849

5

Biochemistry of glycosphingolipid storage disorders: implications for therapeutic intervention.

Aerts JM, Hollak C, Boot R, Groener A. Aerts JM, et al. Philos Trans R Soc Lond B Biol Sci. 2003 May 29;358(1433):905-14. doi: 10.1098/rstb.2003.1273. Philos Trans R Soc Lond B Biol Sci. 2003. PMID: 12803924 Free PMC article. Review.

6

Transglycosidase activity of chitotriosidase: improved enzymatic assay for the human macrophage chitinase.

Aguilera B, Ghauharali-van der Vlugt K, Helmond MT, Out JM, Donker-Koopman WE, Groener JE, Boot RG, Renkema GH, van der Marel GA, van Boom JH, Overkleeft HS, Aerts JM. Aguilera B, et al. Among authors: boot rg. J Biol Chem. 2003 Oct 17;278(42):40911-6. doi: 10.1074/jbc.M301804200. Epub 2003 Jul 30. J Biol Chem. 2003. PMID: 12890686 Free article.

7

Marked elevation of the chemokine CCL18/PARC in Gaucher disease: a novel surrogate marker for assessing therapeutic intervention.

Boot RG, Verhoek M, de Fost M, Hollak CE, Maas M, Bleijlevens B, van Breemen MJ, van Meurs M, Boven LA, Laman JD, Moran MT, Cox TM, Aerts JM. Boot RG, et al. Blood. 2004 Jan 1;103(1):33-9. doi: 10.1182/blood-2003-05-1612. Epub 2003 Sep 11. Blood. 2004. PMID: 12969956 Free article.

8

Gaucher cells demonstrate a distinct macrophage phenotype and resemble alternatively activated macrophages.

Boven LA, van Meurs M, Boot RG, Mehta A, Boon L, Aerts JM, Laman JD. Boven LA, et al. Among authors: boot rg. Am J Clin Pathol. 2004 Sep;122(3):359-69. doi: 10.1309/BG5V-A8JR-DQH1-M7HN. Am J Clin Pathol. 2004. PMID: 15362365

9

Identification and use of biomarkers in Gaucher disease and other lysosomal storage diseases.

Aerts JM, Hollak CE, van Breemen M, Maas M, Groener JE, Boot RG. Aerts JM, et al. Among authors: boot rg. Acta Paediatr Suppl. 2005 Mar;94(447):43-6; discussion 37-8. doi: 10.1111/j.1651-2227.2005.tb02110.x. Acta Paediatr Suppl. 2005. PMID: 15895711 Review.

10

Human acidic mammalian chitinase erroneously known as eosinophil chemotactic cytokine is not the ortholog of mouse YM1.

Boot RG, Bussink AP, Aerts JM. Boot RG, et al. J Immunol. 2005 Aug 15;175(4):2041-2. doi: 10.4049/jimmunol.175.4.2041-a. J Immunol. 2005. PMID: 16081765 No abstract available.

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