Hudson Freeze
Hudson Freeze
Human Genetics Program
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Cited by
Cited by
Thermus aquaticus gen. n. and sp. n., a Nonsporulating Extreme Thermophile
TD Brock, H Freeze
Journal of bacteriology 98 (1), 289-297, 1969
Symbol nomenclature for graphical representations of glycans
A Varki, RD Cummings, M Aebi, NH Packer, PH Seeberger, JD Esko, ...
Glycobiology 25 (12), 1323-1324, 2015
Lysosomal protease pathways to apoptosis: cleavage of Bid, not pro-caspases, is the most likely route
V Stoka, B Turk, SL Schendel, TH Kim, T Cirman, SJ Snipas, LM Ellerby, ...
Journal of Biological Chemistry 276 (5), 3149-3157, 2001
Proinflammatory S100 proteins regulate the accumulation of myeloid-derived suppressor cells
P Sinha, C Okoro, D Foell, HH Freeze, S Ostrand-Rosenberg, ...
The Journal of Immunology 181 (7), 4666-4675, 2008
Genetic defects in the human glycome
HH Freeze
Nature Reviews Genetics 7 (7), 537-551, 2006
Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy.
R Niehues, M Hasilik, G Alton, C Körner, M Schiebe-Sukumar, HG Koch, ...
The Journal of clinical investigation 101 (7), 1414-1420, 1998
Essentials of glycobiology
P Stanley
(No Title), 2009
Sialic acids
A Varki, R Schauer
Essentials of Glycobiology. 2nd edition, 2009
RAGE, carboxylated glycans and S100A8/A9 play essential roles in colitis-associated carcinogenesis
O Turovskaya, D Foell, P Sinha, T Vogl, R Newlin, J Nayak, M Nguyen, ...
Carcinogenesis 29 (10), 2035-2043, 2008
Endogenous damage-associated molecular pattern molecules at the crossroads of inflammation and cancer
G Srikrishna, HH Freeze
Neoplasia 11 (7), 615-628, 2009
Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder
X Wu, RA Steet, O Bohorov, J Bakker, J Newell, M Krieger, L Spaapen, ...
Nature medicine 10 (5), 518-523, 2004
Correction of leukocyte adhesion deficiency type II with oral fucose
T Marquardt, K Lühn, G Srikrishna, HH Freeze, E Harms, D Vestweber
Blood, The Journal of the American Society of Hematology 94 (12), 3976-3985, 1999
SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder
V Cantagrel, DJ Lefeber, BG Ng, Z Guan, JL Silhavy, SL Bielas, L Lehle, ...
Cell 142 (2), 203-217, 2010
Altered glycan structures: the molecular basis of congenital disorders of glycosylation
HH Freeze, M Aebi
Current opinion in structural biology 15 (5), 490-498, 2005
Solving glycosylation disorders: fundamental approaches reveal complicated pathways
HH Freeze, JX Chong, MJ Bamshad, BG Ng
The American Journal of Human Genetics 94 (2), 161-175, 2014
Multiple phenotypes in phosphoglucomutase 1 deficiency
LC Tegtmeyer, S Rust, M van Scherpenzeel, BG Ng, ME Losfeld, S Timal, ...
New England Journal of Medicine 370 (6), 533-542, 2014
Symbol nomenclature for glycan representation
A Varki, RD Cummings, JD Esko, HH Freeze, P Stanley, JD Marth, ...
Proteomics 9 (24), 5398-5399, 2009
GLUT14, a duplicon of GLUT3, is specifically expressed in testis as alternative splice forms
X Wu, HH Freeze
Genomics 80 (6), 553-557, 2002
Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment
Y Zhang, X Yu, M Ichikawa, JJ Lyons, S Datta, IT Lamborn, H Jing, ES Kim, ...
Journal of Allergy and Clinical Immunology 133 (5), 1400-1409. e5, 2014
Neurological aspects of human glycosylation disorders
HH Freeze, EA Eklund, BG Ng, MC Patterson
Annual review of neuroscience 38, 105-125, 2015
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