Freeze HH - Search Results

1

A mutation map for human glycoside hydrolase genes.

Hansen L, Husein DM, Gericke B, Hansen T, Pedersen O, Tambe MA, Freeze HH, Naim HY, Henrissat B, Wandall HH, Clausen H, Bennett EP. Hansen L, et al. Among authors: freeze hh. Glycobiology. 2020 Jul 16;30(8):500-515. doi: 10.1093/glycob/cwaa010. Glycobiology. 2020. PMID: 32039448 Free PMC article.

2

A new approach to mapping co-localization of multiple glycosyl transferases in functional Golgi preparations.

Etchison JR, Freeze HH. Etchison JR, et al. Among authors: freeze hh. Glycobiology. 1996 Mar;6(2):177-89. doi: 10.1093/glycob/6.2.177. Glycobiology. 1996. PMID: 8727790

3

Update and perspectives on congenital disorders of glycosylation.

Freeze HH. Freeze HH. Glycobiology. 2001 Dec;11(12):129R-143R. Glycobiology. 2001. PMID: 11805072 Review.

4

Hydrophobic Man-1-P derivatives correct abnormal glycosylation in Type I congenital disorder of glycosylation fibroblasts.

Eklund EA, Merbouh N, Ichikawa M, Nishikawa A, Clima JM, Dorman JA, Norberg T, Freeze HH. Eklund EA, et al. Among authors: freeze hh. Glycobiology. 2005 Nov;15(11):1084-93. doi: 10.1093/glycob/cwj006. Epub 2005 Aug 3. Glycobiology. 2005. PMID: 16079417

5

N-glycosylation deficiency reduces ICAM-1 induction and impairs inflammatory response.

He P, Srikrishna G, Freeze HH. He P, et al. Among authors: freeze hh. Glycobiology. 2014 Apr;24(4):392-8. doi: 10.1093/glycob/cwu006. Epub 2014 Jan 28. Glycobiology. 2014. PMID: 24474243 Free PMC article.

6

A glycogene mutation map for discovery of diseases of glycosylation.

Hansen L, Lind-Thomsen A, Joshi HJ, Pedersen NB, Have CT, Kong Y, Wang S, Sparso T, Grarup N, Vester-Christensen MB, Schjoldager K, Freeze HH, Hansen T, Pedersen O, Henrissat B, Mandel U, Clausen H, Wandall HH, Bennett EP. Hansen L, et al. Among authors: freeze hh. Glycobiology. 2015 Feb;25(2):211-24. doi: 10.1093/glycob/cwu104. Epub 2014 Sep 28. Glycobiology. 2015. PMID: 25267602 Free PMC article.

7

A congenital disorder of deglycosylation: Biochemical characterization of N-glycanase 1 deficiency in patient fibroblasts.

He P, Grotzke JE, Ng BG, Gunel M, Jafar-Nejad H, Cresswell P, Enns GM, Freeze HH. He P, et al. Among authors: freeze hh. Glycobiology. 2015 Aug;25(8):836-44. doi: 10.1093/glycob/cwv024. Epub 2015 Apr 21. Glycobiology. 2015. PMID: 25900930 Free PMC article.

8

A "Glyconutrient Sham" and the Jenner Glycobiology and Medicine Symposium.

Schnaar RL, Freeze HH. Schnaar RL, et al. Among authors: freeze hh. Glycobiology. 2017 May 1;27(5):383-384. doi: 10.1093/glycob/cwx024. Glycobiology. 2017. PMID: 28384366 No abstract available.

9

Variant in human POFUT1 reduces enzymatic activity and likely causes a recessive microcephaly, global developmental delay with cardiac and vascular features.

Takeuchi H, Wong D, Schneider M, Freeze HH, Takeuchi M, Berardinelli SJ, Ito A, Lee H, Nelson SF, Haltiwanger RS. Takeuchi H, et al. Among authors: freeze hh. Glycobiology. 2018 May 1;28(5):276-283. doi: 10.1093/glycob/cwy014. Glycobiology. 2018. PMID: 29452367 Free PMC article.

10

Glycosyltransferase genes that cause monogenic congenital disorders of glycosylation are distinct from glycosyltransferase genes associated with complex diseases.

Joshi HJ, Hansen L, Narimatsu Y, Freeze HH, Henrissat B, Bennett E, Wandall HH, Clausen H, Schjoldager KT. Joshi HJ, et al. Among authors: freeze hh. Glycobiology. 2018 May 1;28(5):284-294. doi: 10.1093/glycob/cwy015. Glycobiology. 2018. PMID: 29579191 Free PMC article.

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