Triggs-Raine B - Search Results

1

A complete deficiency of Hyaluronoglucosaminidase 1 (HYAL1) presenting as familial juvenile idiopathic arthritis.

Imundo L, Leduc CA, Guha S, Brown M, Perino G, Gushulak L, Triggs-Raine B, Chung WK. Imundo L, et al. J Inherit Metab Dis. 2011 Oct;34(5):1013-22. doi: 10.1007/s10545-011-9343-3. Epub 2011 May 11. J Inherit Metab Dis. 2011. PMID: 21559944

2

Hyal-1 but not Hyal-3 deficiency has an impact on ovarian folliculogenesis and female fertility by altering the follistatin/activin/Smad3 pathway and the apoptotic process.

Dumaresq-Doiron K, Edjekouane L, Orimoto AM, Yoffou PH, Gushulak L, Triggs-Raine B, Carmona E. Dumaresq-Doiron K, et al. J Cell Physiol. 2012 May;227(5):1911-22. doi: 10.1002/jcp.22919. J Cell Physiol. 2012. PMID: 21732362

3

Hyaluronidase 1 and β-hexosaminidase have redundant functions in hyaluronan and chondroitin sulfate degradation.

Gushulak L, Hemming R, Martin D, Seyrantepe V, Pshezhetsky A, Triggs-Raine B. Gushulak L, et al. J Biol Chem. 2012 May 11;287(20):16689-97. doi: 10.1074/jbc.M112.350447. Epub 2012 Mar 26. J Biol Chem. 2012. PMID: 22451654 Free PMC article.

4

The adult polyglucosan body disease mutation GBE1 c.1076A>C occurs at high frequency in persons of Ashkenazi Jewish background.

Hussain A, Armistead J, Gushulak L, Kruck C, Pind S, Triggs-Raine B, Natowicz MR. Hussain A, et al. Biochem Biophys Res Commun. 2012 Sep 21;426(2):286-8. doi: 10.1016/j.bbrc.2012.08.089. Epub 2012 Aug 25. Biochem Biophys Res Commun. 2012. PMID: 22943850

5

Mutations in HYAL1, a member of a tandemly distributed multigene family encoding disparate hyaluronidase activities, cause a newly described lysosomal disorder, mucopolysaccharidosis IX.

Triggs-Raine B, Salo TJ, Zhang H, Wicklow BA, Natowicz MR. Triggs-Raine B, et al. Proc Natl Acad Sci U S A. 1999 May 25;96(11):6296-300. doi: 10.1073/pnas.96.11.6296. Proc Natl Acad Sci U S A. 1999. PMID: 10339581 Free PMC article.

6

Benign HEXA mutations, C739T(R247W) and C745T(R249W), cause beta-hexosaminidase A pseudodeficiency by reducing the alpha-subunit protein levels.

Cao Z, Petroulakis E, Salo T, Triggs-Raine B. Cao Z, et al. J Biol Chem. 1997 Jun 6;272(23):14975-82. doi: 10.1074/jbc.272.23.14975. J Biol Chem. 1997. PMID: 9169471 Free article.

7

Structural and functional characterization of Streptomyces plicatus beta-N-acetylhexosaminidase by comparative molecular modeling and site-directed mutagenesis.

Mark BL, Wasney GA, Salo TJ, Khan AR, Cao Z, Robbins PW, James MN, Triggs-Raine BL. Mark BL, et al. J Biol Chem. 1998 Jul 31;273(31):19618-24. doi: 10.1074/jbc.273.31.19618. J Biol Chem. 1998. PMID: 9677388 Free article.

8

Human growth factor receptor bound 14 binds the activated insulin receptor and alters the insulin-stimulated tyrosine phosphorylation levels of multiple proteins.

Hemming R, Agatep R, Badiani K, Wyant K, Arthur G, Gietz RD, Triggs-Raine B. Hemming R, et al. Biochem Cell Biol. 2001;79(1):21-32. Biochem Cell Biol. 2001. PMID: 11235915

9

Characterization of the murine hyaluronidase gene region reveals complex organization and cotranscription of Hyal1 with downstream genes, Fus2 and Hyal3.

Shuttleworth TL, Wilson MD, Wicklow BA, Wilkins JA, Triggs-Raine BL. Shuttleworth TL, et al. J Biol Chem. 2002 Jun 21;277(25):23008-18. doi: 10.1074/jbc.M108991200. Epub 2002 Apr 2. J Biol Chem. 2002. PMID: 11929860 Free article.

10

Evaluation of the risk for Tay-Sachs disease in individuals of French Canadian ancestry living in new England.

Martin DC, Mark BL, Triggs-Raine BL, Natowicz MR. Martin DC, et al. Clin Chem. 2007 Mar;53(3):392-8. doi: 10.1373/clinchem.2006.082727. Epub 2007 Jan 26. Clin Chem. 2007. PMID: 17259242

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