Haltiwanger RS - Search Results

1

Hydrocephalus in mouse B3glct mutants is likely caused by defects in multiple B3GLCT substrates in ependymal cells and subcommissural organ.

Neupane S, Goto J, Berardinelli SJ, Ito A, Haltiwanger RS, Holdener BC. Neupane S, et al. Among authors: haltiwanger rs. Glycobiology. 2021 Sep 9;31(8):988-1004. doi: 10.1093/glycob/cwab033. Glycobiology. 2021. PMID: 33909046 Free PMC article.

2

The O-linked fucose glycosylation pathway: identification and characterization of a uridine diphosphoglucose: fucose-beta1,3-glucosyltransferase activity from Chinese hamster ovary cells.

Moloney DJ, Haltiwanger RS. Moloney DJ, et al. Among authors: haltiwanger rs. Glycobiology. 1999 Jul;9(7):679-87. doi: 10.1093/glycob/9.7.679. Glycobiology. 1999. PMID: 10362837

3

O-glycosylation of EGF repeats: identification and initial characterization of a UDP-glucose: protein O-glucosyltransferase.

Shao L, Luo Y, Moloney DJ, Haltiwanger R. Shao L, et al. Glycobiology. 2002 Nov;12(11):763-70. doi: 10.1093/glycob/cwf085. Glycobiology. 2002. PMID: 12460944

4

O-fucosylation of thrombospondin type 1 repeats restricts epithelial to mesenchymal transition (EMT) and maintains epiblast pluripotency during mouse gastrulation.

Du J, Takeuchi H, Leonhard-Melief C, Shroyer KR, Dlugosz M, Haltiwanger RS, Holdener BC. Du J, et al. Among authors: haltiwanger rs. Dev Biol. 2010 Oct 1;346(1):25-38. doi: 10.1016/j.ydbio.2010.07.008. Epub 2010 Jul 14. Dev Biol. 2010. PMID: 20637190 Free PMC article.

5

6-alkynyl fucose is a bioorthogonal analog for O-fucosylation of epidermal growth factor-like repeats and thrombospondin type-1 repeats by protein O-fucosyltransferases 1 and 2.

Al-Shareffi E, Chaubard JL, Leonhard-Melief C, Wang SK, Wong CH, Haltiwanger RS. Al-Shareffi E, et al. Among authors: haltiwanger rs. Glycobiology. 2013 Feb;23(2):188-98. doi: 10.1093/glycob/cws140. Epub 2012 Oct 8. Glycobiology. 2013. PMID: 23045360 Free PMC article.

6

Peters plus syndrome mutations disrupt a noncanonical ER quality-control mechanism.

Vasudevan D, Takeuchi H, Johar SS, Majerus E, Haltiwanger RS. Vasudevan D, et al. Among authors: haltiwanger rs. Curr Biol. 2015 Feb 2;25(3):286-295. doi: 10.1016/j.cub.2014.11.049. Epub 2014 Dec 24. Curr Biol. 2015. PMID: 25544610 Free PMC article.

7

Genetic and biochemical evidence that gastrulation defects in Pofut2 mutants result from defects in ADAMTS9 secretion.

Benz BA, Nandadasa S, Takeuchi M, Grady RC, Takeuchi H, LoPilato RK, Kakuda S, Somerville RPT, Apte SS, Haltiwanger RS, Holdener BC. Benz BA, et al. Among authors: haltiwanger rs. Dev Biol. 2016 Aug 1;416(1):111-122. doi: 10.1016/j.ydbio.2016.05.038. Epub 2016 Jun 10. Dev Biol. 2016. PMID: 27297885 Free PMC article.

8

Unusual life cycle and impact on microfibril assembly of ADAMTS17, a secreted metalloprotease mutated in genetic eye disease.

Hubmacher D, Schneider M, Berardinelli SJ, Takeuchi H, Willard B, Reinhardt DP, Haltiwanger RS, Apte SS. Hubmacher D, et al. Among authors: haltiwanger rs. Sci Rep. 2017 Feb 8;7:41871. doi: 10.1038/srep41871. Sci Rep. 2017. PMID: 28176809 Free PMC article.

9

Rapid screening of sugar-nucleotide donor specificities of putative glycosyltransferases.

Sheikh MO, Halmo SM, Patel S, Middleton D, Takeuchi H, Schafer CM, West CM, Haltiwanger RS, Avci FY, Moremen KW, Wells L. Sheikh MO, et al. Among authors: haltiwanger rs. Glycobiology. 2017 Mar 1;27(3):206-212. doi: 10.1093/glycob/cww114. Glycobiology. 2017. PMID: 28177478 Free PMC article.

10

Biological functions of fucose in mammals.

Schneider M, Al-Shareffi E, Haltiwanger RS. Schneider M, et al. Among authors: haltiwanger rs. Glycobiology. 2017 Jul 1;27(7):601-618. doi: 10.1093/glycob/cwx034. Glycobiology. 2017. PMID: 28430973 Free PMC article. Review.

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