FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Hudson Freeze

Research Profile

Disorders

Phenomena

Glycosylation

Chemicals & Drugs

Physiology

Mutation

Concepts & Ideas

Molecular Sequence Data

Anatomy

Living Beings

Genes & Molecular Sequences

Carbohydrate Sequence

Co-author Network

Publications

TOP 3
Bobby G Ng; Deborah A Nickerson; Marc C Patterson; Kimiyo Raymond; Jay Shendure; Joshua D Smith; Marta Szybowska; Emily H Turner; Michael J Bamshad; Kati J Buckingham; Jessica X Chong; Alexey Eroshkin; Rodney David Gilbert; Miao He; Martin Kircher; Mariya Kozenko; Chumei Li; Marie E Losfeld; Hudson H Freeze
Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation.
Hudson H Freeze
Understanding human glycosylation disorders: biochemistry leads the charge.
Jaime Chu; Hudson H Freeze; Ningguo Gao; Mark A Lehrman; Alexander Mir; Christopher Monson; Sabrina Rosa; Vandana Sharma; Richard Steet; Kirsten C Sadler
A zebrafish model of congenital disorders of glycosylation with phosphomannose isomerase deficiency reveals an early opportunity for corrective mannose supplementation.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Hudson Freeze (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Bobby G Ng; Deborah A Nickerson; Marc C Patterson; Kimiyo Raymond; Jay Shendure; Joshua D Smith; Marta Szybowska; Emily H Turner; Michael J Bamshad; Kati J Buckingham; Jessica X Chong; Alexey Eroshkin; Rodney David Gilbert; Miao He; Martin Kircher; Mariya Kozenko; Chumei Li; Marie E Losfeld; Hudson H Freeze
Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation.
American journal of human genetics 2013;92(4):632-6.
2013: Hudson H Freeze
Understanding human glycosylation disorders: biochemistry leads the charge.
The Journal of biological chemistry 2013;288(10):6936-45.
2013: Jaime Chu; Hudson H Freeze; Ningguo Gao; Mark A Lehrman; Alexander Mir; Christopher Monson; Sabrina Rosa; Vandana Sharma; Richard Steet; Kirsten C Sadler
A zebrafish model of congenital disorders of glycosylation with phosphomannose isomerase deficiency reveals an early opportunity for corrective mannose supplementation.
Disease models & mechanisms 2013;6(1):95-105.
2012: Abigail Cline; Heather Flanagan-Steet; Hudson H Freeze; Ningguo Gao; Mark A Lehrman; Sabrina Rosa; Kirsten C Sadler; Vandana Sharma; Roberto Sonon; Parastoo Azadi; Richard Steet
A zebrafish model of PMM2-CDG reveals altered neurogenesis and a substrate-accumulation mechanism for N-linked glycosylation deficiency.
Molecular biology of the cell 2012;23(21):4175-87.
2012: Marie-Estelle Losfeld; Bobby G Ng; Ilyas Singec; Francesca Soncin; Hudson H Freeze
A sensitive green fluorescent protein biomarker of N-glycosylation site occupancy.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2012;26(10):4210-7.
2012: François Foulquier; Hudson H Freeze; Nathalie Guffon; Jaak Jaeken; Dominique Legrand; Mustapha Amyere; Willem ANNAERT; Riet Bammens; Neil Buist; David Cheillan; Didier Demaegd; Willy Morelle; Pierre Morsomme; Valérie Race; Claire Rosnoblet; Els Schollen; Emile Van Schaftingen; Miikka Vikkula; Renate Zeevaert; Gert Matthijs
TMEM165 deficiency causes a congenital disorder of glycosylation.
American journal of human genetics 2012;91(1):15-26.
2012: Ping He; Marie-Estelle Losfeld; Bobby G Ng; Wenhong Zhu; Hudson H Freeze
Identification of intercellular cell adhesion molecule 1 (ICAM-1) as a hypoglycosylation marker in congenital disorders of glycosylation cells.
The Journal of biological chemistry 2012;287(22):18210-7.
2012: Hudson H Freeze; Bobby G Ng; Erik A Eklund; Marc C Patterson
Neurology of inherited glycosylation disorders.
Lancet neurology 2012;11(5):453-66.
2012: Bobby G Ng; Amy S Paller; Rhonda E Schnur; Sigrid Tinschert; Roy Wiliams; Janice Zunich; Shruti Bhide; Vincent Cantagrel; Alexey M Eroshkin; Joseph G Gleeson; Karl Hackmann; Ping He; Madhuri R Hegde; Melanie A Jones; Hudson H Freeze
Mutations in the glycosylphosphatidylinositol gene PIGL cause CHIME syndrome.
American journal of human genetics 2012;90(4):685-8.
2012: Melanie A Jones; Marie-Estelle Losfeld; Bobby G Ng; Kimiyo Raymond; Devin Rhodenizer; Gerard Berry; Shruti Bhide; Ephrem Chin; Hudson H Freeze; Miao He; Ping He; Madhuri R Hegde
DDOST mutations identified by whole-exome sequencing are implicated in congenital disorders of glycosylation.
American journal of human genetics 2012;90(2):363-8.
2011: Vandana Sharma; David A Scott; Ping He; Mie Ichikawa; Bobby G Ng; Yalda Bravo; Nicholas D P Cosford; Russell Dahl; Hudson H Freeze
Phosphomannose isomerase inhibitors improve N-glycosylation in selected phosphomannomutase-deficient fibroblasts.
The Journal of biological chemistry 2011;286(45):39431-8.
2011: Melanie A Jones; Bobby G Ng; Devin Rhodenizer; Jessica J Sun; Alice Tanner; Victor W Zhang; Shruti Bhide; Ephrem Chin; Hudson H Freeze; Madhuri R Hegde
Targeted polymerase chain reaction-based enrichment and next generation sequencing for diagnostic testing of congenital disorders of glycosylation.
Genetics in medicine : official journal of the American College of Medical Genetics 2011;13(11):921-32.
2011: Hudson H Freeze; Bobby G Ng
Golgi glycosylation and human inherited diseases.
Cold Spring Harbor perspectives in biology 2011;3(9):a005371.
2011: Russell Dahl; Yalda Bravo; Vandana Sharma; Mie Ichikawa; Raveendra-Panickar Dhanya; Michael Hedrick; Brock Brown; Justin Rascon; Michael Vicchiarelli; Arianna Mangravita-Novo; Li Yang; Derek Stonich; Ying Su; Layton H Smith; Eduard Sergienko; Hudson H Freeze; Nicholas D P Cosford
Potent, selective, and orally available benzoisothiazolone phosphomannose isomerase inhibitors as probes for congenital disorder of glycosylation Ia.
Journal of medicinal chemistry 2011;54(10):3661-8.
2011: Bradley S Miller; Hudson H Freeze; Georg F Hoffmann; Kyriakie Sarafoglou
Pubertal development in ALG6 deficiency (congenital disorder of glycosylation type Ic).
Molecular genetics and metabolism 2011;103(1):101-3.
2011: Vandana Sharma; Hudson H Freeze
Mannose efflux from the cells: a potential source of mannose in blood.
The Journal of biological chemistry 2011;286(12):10193-200.
2011: Bobby G Ng; Vandana Sharma; Liangwu Sun; Eva Loh; Wanjin Hong; Stacey K H Tay; Hudson H Freeze
Identification of the first COG-CDG patient of Indian origin.
Molecular genetics and metabolism 2011;102(3):364-7.
2010: Hudson H Freeze; Christian Kranz
Endoglycosidase and glycoamidase release of N-linked glycans.
Current protocols in protein science / editorial board, John E. Coligan ... [et al.] 2010;Chapter 12():Unit12.4.
2010: Fei Ying Cheong; Vandana Sharma; Anastasia Blagoveshchenskaya; Viola M J Oorschot; Ben Brankatschk; Judith Klumperman; Hudson H Freeze; Peter Mayinger
Spatial regulation of Golgi phosphatidylinositol-4-phosphate is required for enzyme localization and glycosylation fidelity.
Traffic (Copenhagen, Denmark) 2010;11(9):1180-90.
2010: Hudson H Freeze; Vandana Sharma
Metabolic manipulation of glycosylation disorders in humans and animal models.
Seminars in cell & developmental biology 2010;21(6):655-62.
2010: Vincent Cantagrel; Dirk J Lefeber; Bobby G Ng; Ziqiang Guan; Jennifer L Silhavy; Stephanie L Bielas; Ludwig Lehle; Hans Hombauer; Maciej Adamowicz; Ewa Swiezewska; Arjan P De Brouwer; Peter Blümel; Jolanta Sykut-Cegielska; Scott Houliston; Dominika Swistun; bassam rushdi ali; William B Dobyns; Dusica Babovic-Vuksanovic; Hans van Bokhoven; Ron A Wevers; Christian R H Raetz; Hudson H Freeze; Eva Morava; Lihadh Al-Gazali; Joseph G Gleeson
SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder.
Cell 2010;142(2):203-17.
2010: Joseph N Contessa; Mahaveer S Bhojani; Hudson H Freeze; Brian D Ross; Alnawaz Rehemtulla; Theodore S Lawrence
Molecular imaging of N-linked glycosylation suggests glycan biosynthesis is a novel target for cancer therapy.
Clinical cancer research : an official journal of the American Association for Cancer Research 2010;16(12):3205-14.
2010: Geetha Srikrishna; Jonamani Nayak; Bernd Weigle; Achim Temme; Dirk Foell; Larnele Hazelwood; Anna Olsson; Niels Volkmann; Dorit Hanein; Hudson H Freeze
Carboxylated N-glycans on RAGE promote S100A12 binding and signaling.
Journal of cellular biochemistry 2010;110(3):645-59.
2010: Hudson H Freeze; Christian Kranz
Endoglycosidase and glycoamidase release of N-linked glycans.
Current protocols in immunology / edited by John E. Coligan ... [et al.] 2010;Chapter 8():Unit 8.15.1-25.
2010: Hudson H Freeze
Achondrogenesis type 1A--from mouse to human.
The New England journal of medicine 2010;362(3):266-7.
2010: Hudson H Freeze; Christian Kranz
Endoglycosidase and glycoamidase release of N-linked glycans.
Current protocols in molecular biology / edited by Frederick M. Ausubel ... [et al.] 2010;Chapter 17():Unit 17.13A.
2009: Ajit Varki; Richard D Cummings; Jeffrey D Esko; Hudson H Freeze; Pamela Stanley; Jamey D Marth; Carolyn R Bertozzi; Gerald W Hart; Marilynn E Etzler
Symbol nomenclature for glycan representation.
Proteomics 2009;9(24):5398-9.
2009: Wendy Vleugels; Micha A Haeuptle; Bobby G Ng; Jean-Claude Michalski; Roberta Battini; Carlo Dionisi Vici; Mark D Ludman; Jaak Jaeken; François Foulquier; Hudson H Freeze; Gert Matthijs; Thierry Hennet
RFT1 deficiency in three novel CDG patients.
Human mutation 2009;30(10):1428-34.
2009: Jaak Jaeken; Thierry Hennet; Gert Matthijs; Hudson H Freeze
CDG nomenclature: time for a change!
Biochimica et biophysica acta 2009;1792(9):825-6.
2009: Hudson H Freeze
Towards a therapy for phosphomannomutase 2 deficiency, the defect in CDG-Ia patients.
Biochimica et biophysica acta 2009;1792(9):835-40.
2009: Harry Schachter; Hudson H Freeze
Glycosylation diseases: quo vadis?
Biochimica et biophysica acta 2009;1792(9):925-30.
2009: Ajit Varki; Hudson H Freeze; Adriana E Manzi
Overview of glycoconjugate analysis.
Current protocols in protein science / editorial board, John E. Coligan ... [et al.] 2009;Chapter 12():Unit 12.1 12.1.1-8.
2009: Geetha Srikrishna; Hudson H Freeze
Endogenous damage-associated molecular pattern molecules at the crossroads of inflammation and cancer.
Neoplasia (New York, N.Y.) 2009;11(7):615-28.
2009: Aya Higashidani; Lars Bode; Atsushi Nishikawa; Hudson H Freeze
Exogenous mannose does not raise steady state mannose-6-phosphate pools of normal or N-glycosylation-deficient human fibroblasts.
Molecular genetics and metabolism 2009;96(4):268-72.
2009: Beatrice Amadi; Andrew O Fagbemi; Paul Kelly; Mwiya Mwiya; Franco Torrente; Camilla Salvestrini; Richard Day; Michael H Golden; Erik A Eklund; Hudson H Freeze; Simon H Murch
Reduced production of sulfated glycosaminoglycans occurs in Zambian children with kwashiorkor but not marasmus.
The American journal of clinical nutrition 2009;89(2):592-600.
2008: Hudson H Freeze; Christian Kranz
Endoglycosidase and glycoamidase release of N-linked glycans.
Current protocols in immunology / edited by John E. Coligan ... [et al.] 2008;Chapter 8():Unit 8.15.
2008: Pratima Sinha; Chinonyerem Okoro; Dirk Foell; Hudson H Freeze; Suzanne Ostrand-Rosenberg; Geetha Srikrishna
Proinflammatory S100 proteins regulate the accumulation of myeloid-derived suppressor cells.
Journal of immunology (Baltimore, Md. : 1950) 2008;181(7):4666-75.
2008: Olga Turovskaya; Dirk Foell; Pratima Sinha; Thomas Vogl; Robbin Newlin; Jonamani Nayak; Mien Nguyen; Anna Olsson; Peter P Nawroth; Angelika Bierhaus; Nissi Varki; Mitchell Kronenberg; Hudson H Freeze; Geetha Srikrishna
RAGE, carboxylated glycans and S100A8/A9 play essential roles in colitis-associated carcinogenesis.
Carcinogenesis 2008;29(10):2035-43.
2008: Ronald Schnaar; Hudson H Freeze
A "glyconutrient sham".
Glycobiology 2008;18(9):652-7; discussion 658-63.
2008: Joseph N Contessa; Mahaveer S Bhojani; Hudson H Freeze; Alnawaz Rehemtulla; Theodore S Lawrence
Inhibition of N-linked glycosylation disrupts receptor tyrosine kinase signaling in tumor cells.
Cancer research 2008;68(10):3803-9.
2008: Ylian S Liem; Lars Bode; Hudson H Freeze; Frank W G Leebeek; Adrienne Am Zandbergen; Jh Paul Wilson
Using heparin therapy to reverse protein-losing enteropathy in a patient with CDG-Ib.
Nature clinical practice. Gastroenterology & hepatology 2008;5(4):220-4.
2008: Naonobu Fujita; Ayako Tamura; Aya Higashidani; Takashi Tonozuka; Hudson H Freeze; Atsushi Nishikawa
The relative contribution of mannose salvage pathways to glycosylation in PMI-deficient mouse embryonic fibroblast cells.
The FEBS journal 2008;275(4):788-98.
2008: Lars Bode; Camilla Salvestrini; Pyong Woo Park; Jin-Ping Li; Jeffrey D Esko; Yu Yamaguchi; Simon H Murch; Hudson H Freeze
Heparan sulfate and syndecan-1 are essential in maintaining murine and human intestinal epithelial barrier function.
The Journal of clinical investigation 2008;118(1):229-38.
2007: Kylie T Greig; Jennifer Antonchuk; Donald Metcalf; Phillip O Morgan; Danielle L Krebs; Jian-Guo Zhang; Douglas F Hacking; Lars Bode; Lorraine Robb; Christian Kranz; Carolyn de Graaf; Melanie Bahlo; Nicos A Nicola; Stephen L Nutt; Hudson H Freeze; Warren S Alexander; Douglas J Hilton; Benjamin T Kile
Agm1/Pgm3-mediated sugar nucleotide synthesis is essential for hematopoiesis and development.
Molecular and cellular biology 2007;27(16):5849-59.
2007: Christian Kranz; Liangwu Sun; Erik A Eklund; Donna Krasnewich; Janet R Casey; Hudson H Freeze
CDG-Id in two siblings with partially different phenotypes.
American journal of medical genetics. Part A 2007;143A(13):1414-20.
2007: Christian Kranz; Alice A Basinger; Müge Güçsavaş-Calikoğlu; Liangwu Sun; CM Powell; Frederick W Henderson; Arthur S Aylsworth; Hudson H Freeze
Expanding spectrum of congenital disorder of glycosylation Ig (CDG-Ig): sibs with a unique skeletal dysplasia, hypogammaglobulinemia, cardiomyopathy, genital malformations, and early lethality.
American journal of medical genetics. Part A 2007;143A(12):1371-8.
2007: Hudson H Freeze
Congenital Disorders of Glycosylation: CDG-I, CDG-II, and beyond.
Current molecular medicine 2007;7(4):389-96.
2007: Hudson H Freeze
Novel perspectives on glycosylation and human disease.
Current molecular medicine 2007;7(4):387.
2007: Bobby G Ng; Christian Kranz; E E O Hagebeuk; M Duran; N G G M Abeling; B Wuyts; Daniel Ungar; Vladimir Lupashin; C M Hartdorff; Bwee Tien Poll-The; Hudson H Freeze
Molecular and clinical characterization of a Moroccan Cog7 deficient patient.
Molecular genetics and metabolism 2007;91(2):201-4.
2007: Christian Kranz; Bobby G Ng; Liangwu Sun; Vandana Sharma; Erik A Eklund; Yoshiaki Miura; Daniel Ungar; Vladimir Lupashin; R Dennis Winkel; John F Cipollo; Catherine E Costello; Eva Loh; Wanjin Hong; Hudson H Freeze
COG8 deficiency causes new congenital disorder of glycosylation type IIh.
Human molecular genetics 2007;16(7):731-41.
2006: Hudson H Freeze; Christian Kranz
Endoglycosidase and glycoamidase release of N-linked oligosaccharides.
Current protocols in protein science / editorial board, John E. Coligan ... [et al.] 2006;Chapter 12():Unit 12.4.
2006: Ronald D Cohn; Erik Eklund; Amanda L Bergner; James F Casella; S Lee Woods; Janyne E Althaus; Karin J Blakemore; Harold E Fox; Julie E Hoover-Fong; Ada Hamosh; Nancy Braverman; Hudson H Freeze; Simeon Boyd
Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylation.
Pediatrics 2006;118(2):e514-21.
2006: Hudson H Freeze
Genetic defects in the human glycome.
Nature reviews. Genetics 2006;7(7):537-51.
2006: Marilisa Leone; Hudson H Freeze; Chui Sien Chan; Surya De
The Nuclear Overhauser Effect in the lead identification process.
Current drug discovery technologies 2006;3(2):91-100.
2006: Erik A Eklund; Hudson H Freeze
The congenital disorders of glycosylation: a multifaceted group of syndromes.
NeuroRx : the journal of the American Society for Experimental NeuroTherapeutics 2006;3(2):254-63.
2006: Lars Bode; Hudson H Freeze
Applied glycoproteomics--approaches to study genetic-environmental collisions causing protein-losing enteropathy.
Biochimica et biophysica acta 2006;1760(4):547-59.
2006: Lars Bode; Simon H Murch; Hudson H Freeze
Heparan sulfate plays a central role in a dynamic in vitro model of protein-losing enteropathy.
The Journal of biological chemistry 2006;281(12):7809-15.
2006: Charles DeRossi; Lars Bode; Erik A Eklund; Fangrong Zhang; Joseph A Davis; Vibeke Westphal; Ling Wang; Alexander D Borowsky; Hudson H Freeze
Ablation of mouse phosphomannose isomerase (Mpi) causes mannose 6-phosphate accumulation, toxicity, and embryonic lethality.
The Journal of biological chemistry 2006;281(9):5916-27.
2006: Claudia Mandato; Lars Brive; Yoshiaki Miura; Joseph Alex Davis; Nicolina Di Cosmo; Stefania Lucariello; Severo Pagliardini; Neungseon Seo; Giancarlo Parenti; Raffaella Vecchione; Hudson H Freeze; Pietro Vajro
Cryptogenic liver disease in four children: a novel congenital disorder of glycosylation.
Pediatric research 2006;59(2):293-8.
2006: Erik A Eklund; Liangwu Sun; Samuel P Yang; Romela M Pasion; Erik C Thorland; Hudson H Freeze
Congenital disorder of glycosylation Ic due to a de novo deletion and an hALG-6 mutation.
Biochemical and biophysical research communications 2006;339(3):755-60.
2005: Yoshiaki Miura; Stacey K H Tay; Marion M Aw; Erik A Eklund; Hudson H Freeze
Clinical and biochemical characterization of a patient with congenital disorder of glycosylation (CDG) IIx.
The Journal of pediatrics 2005;147(6):851-3.
2005: Erik A Eklund; Liangwu Sun; Vibeke Westphal; Jennifer Northrop; Hudson H Freeze; Fernando Scaglia
Congenital disorder of glycosylation (CDG)-Ih patient with a severe hepato-intestinal phenotype and evolving central nervous system pathology.
The Journal of pediatrics 2005;147(6):847-50.
2005: Erik A Eklund; Nabyl Merbouh; Mie Ichikawa; Atsushi Nishikawa; Jessica M Clima; James A Dorman; Thomas Norberg; Hudson H Freeze
Hydrophobic Man-1-P derivatives correct abnormal glycosylation in Type I congenital disorder of glycosylation fibroblasts.
Glycobiology 2005;15(11):1084-93.
2005: Geetha Srikrishna; Olga Turovskaya; Raziya B Shaikh; Robbin Newlin; Dirk Foell; Simon H Murch; Mitchell Kronenberg; Hudson H Freeze
Carboxylated glycans mediate colitis through activation of NF-kappa B.
Journal of immunology (Baltimore, Md. : 1950) 2005;175(8):5412-22.
2005: Hudson H Freeze; Markus Aebi
Altered glycan structures: the molecular basis of congenital disorders of glycosylation.
Current opinion in structural biology 2005;15(5):490-8.
2005: Erik A Eklund; Hudson H Freeze
Essentials of glycosylation.
Seminars in pediatric neurology 2005;12(3):134-43.
2005: Liangwu Sun; Erik A Eklund; Johan L K Van Hove; Hudson H Freeze; Janet A Thomas
Clinical and molecular characterization of the first adult congenital disorder of glycosylation (CDG) type Ic patient.
American journal of medical genetics. Part A 2005;137(1):22-6.
2005: Geetha Srikrishna; Lars Brive; Hudson H Freeze
Novel carboxylated N-glycans contain oligosaccharide-linked glutamic acid.
Biochemical and biophysical research communications 2005;332(4):1020-7.
2005: Liangwu Sun; Erik A Eklund; Wendy Chung; Chao Wang; Jason Cohen; Hudson H Freeze
Congenital disorder of glycosylation id presenting with hyperinsulinemic hypoglycemia and islet cell hyperplasia.
The Journal of clinical endocrinology and metabolism 2005;90(7):4371-5.
2005: Lars Bode; Erik A Eklund; Simon H Murch; Hudson H Freeze
Heparan sulfate depletion amplifies TNF-alpha-induced protein leakage in an in vitro model of protein-losing enteropathy.
American journal of physiology. Gastrointestinal and liver physiology 2005;288(5):G1015-23.
2005: Erik A Eklund; John W Newell; Liangwu Sun; Neungseon Seo; Gulay Alper; Jessica Willert; Hudson H Freeze
Molecular and clinical description of the first US patients with congenital disorder of glycosylation Ig.
Molecular genetics and metabolism 2005;84(1):25-31.
2004: Kai-Lin Chu; Yin-Hsiu Chien; Chen-En Tsai; Hudson H Freeze; Erik Eklund; Wuh-Liang Hwu
Carbohydrate deficient glycoprotein syndrome type Ia.
Journal of the Formosan Medical Association = Taiwan yi zhi 2004;103(9):721-3.
2004: Xiaohua Wu; Richard Steet; Ognian Bohorov; Jaap Bakker; John Newell; Monty Krieger; L J M Spaapen; Stuart Kornfeld; Hudson H Freeze
Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorder.
Nature medicine 2004;10(5):518-23.
2004: Anders Helander; Jonas Bergström; Hudson H Freeze
Testing for congenital disorders of glycosylation by HPLC measurement of serum transferrin glycoforms.
Clinical chemistry 2004;50(5):954-8.
2003: Vibeke Westphal; Ming Xiao; Pui-Yan Kwok; Hudson H Freeze
Identification of a frequent variant in ALG6, the cause of Congenital Disorder of Glycosylation-Ic.
Human mutation 2003;22(5):420-1.
2003: Xiaohua Wu; Jeffrey S Rush; Denise Karaoglu; Donna Krasnewich; Mark S Lubinsky; Charles J Waechter; Reid Gilmore; Hudson H Freeze
Deficiency of UDP-GlcNAc:Dolichol Phosphate N-Acetylglucosamine-1 Phosphate Transferase (DPAGT1) causes a novel congenital disorder of Glycosylation Type Ij.
Human mutation 2003;22(2):144-50.
2003: Paul T Martin; Hudson H Freeze
Glycobiology of neuromuscular disorders.
Glycobiology 2003;13(8):67R-75R.
2003: J W Newell; Neungseon Seo; Gregory M Enns; M McCraken; J F Mantovani; Hudson H Freeze
Congenital disorder of glycosylation Ic in patients of Indian origin.
Molecular genetics and metabolism 2003;79(3):221-8.
2003: Bradley S Miller; Hudson H Freeze
New disorders in carbohydrate metabolism: congenital disorders of glycosylation and their impact on the endocrine system.
Reviews in endocrine & metabolic disorders 2003;4(1):103-13.
2003: Yijun Li; Yuko Ogata; Hudson H Freeze; C Ronald Scott; Frantisek Turecek; Michael H Gelb
Affinity capture and elution/electrospray ionization mass spectrometry assay of phosphomannomutase and phosphomannose isomerase for the multiplex analysis of congenital disorders of glycosylation types Ia and Ib.
Analytical chemistry 2003;75(1):42-8.
2002: Hudson H Freeze
Human disorders in N-glycosylation and animal models.
Biochimica et biophysica acta 2002;1573(3):388-93.
2002: Xiaohua Wu; Hudson H Freeze
GLUT14, a duplicon of GLUT3, is specifically expressed in testis as alternative splice forms.
Genomics 2002;80(6):553-7.
2002: Gregory M Enns; Robert D Steiner; Neil Buist; Charles Cowan; Kathleen A Leppig; Marjorie F McCracken; Vibeke Westphal; Hudson H Freeze; John F O'brien; Jaak Jaeken; Gert Matthijs; Sarina Behera; Louanne Hudgins
Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 sialotransferrin pattern and diverse ethnic origins.
The Journal of pediatrics 2002;141(5):695-700.
2002: Hudson H Freeze
Sweet solution: sugars to the rescue.
The Journal of cell biology 2002;158(4):615-6.
2002: Joseph A Davis; Xiao-Hua Wu; Ling Wang; Charles DeRossi; Vibeke Westphal; Rongrong Wu; Gordon Alton; Geetha Srikrishna; Hudson H Freeze
Molecular cloning, gene organization, and expression of mouse Mpi encoding phosphomannose isomerase.
Glycobiology 2002;12(7):435-42.
2002: Xiaohua Wu; Weizhong Li; Vandana Sharma; Adam Godzik; Hudson H Freeze
Cloning and characterization of glucose transporter 11, a novel sugar transporter that is alternatively spliced in various tissues.
Molecular genetics and metabolism 2002;76(1):37-45.
2002: Geetha Srikrishna; Henri Huttunen; Lena Johansson; Bernd Weigle; Yu Yamaguchi; Heikki Rauvala; Hudson H Freeze
N -Glycans on the receptor for advanced glycation end products influence amphoterin binding and neurite outgrowth.
Journal of neurochemistry 2002;80(6):998-1008.
2002: Vibeke Westphal; Susanne Kjaergaard; Els Schollen; Kevin Martens; Stephanie Grunewald; Marianne Schwartz; Gert Matthijs; Hudson H Freeze
A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiency.
Human molecular genetics 2002;11(5):599-604.
2001: Hudson H Freeze
Update and perspectives on congenital disorders of glycosylation.
Glycobiology 2001;11(12):129R-143R.
2001: Christian Kranz; Jonas Denecke; M A Lehrman; S Ray; P Kienz; G Kreissel; D Sagi; Jasna Peter-Katalinic; Hudson H Freeze; T Schmid; S Jackowski-Dohrmann; Erik Harms; Thorsten Marquardt
A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If).
The Journal of clinical investigation 2001;108(11):1613-9.
2001: Vibeke Westphal; S Peterson; M Patterson; A Tournay; A Blumenthal; E P Treacy; Hudson H Freeze
Functional significance of PMM2 mutations in mildly affected patients with congenital disorders of glycosylation Ia.
Genetics in medicine : official journal of the American College of Medical Genetics 2001;3(6):393-8.
2001: Joseph A Davis; Hudson H Freeze
Studies of mannose metabolism and effects of long-term mannose ingestion in the mouse.
Biochimica et biophysica acta 2001;1528(2-3):116-26.
2001: S Kim; Y Miura; JR Etchison; Hudson H Freeze
Intact Golgi synthesize complex branched O-linked chains on glycoside primers: evidence for the functional continuity of seven glycosyltransferases and three sugar nucleotide transporters.
Glycoconjugate journal 2001;18(8):623-33.
2001: Hudson H Freeze; Vibeke Westphal
Balancing N-linked glycosylation to avoid disease.
Biochimie 2001;83(8):791-9.
2001: L D Powell; Ajit Varki; Hudson H Freeze
Release of saccharides from glycoconjugates.
Current protocols in immunology / edited by John E. Coligan ... [et al.] 2001;Chapter 8():Unit 8.15.
2001: Hudson H Freeze
Lectin affinity chromatography.
Current protocols in protein science / editorial board, John E. Coligan ... [et al.] 2001;Chapter 9():Unit 9.1.
2001: Ajit Varki; Hudson H Freeze; A E Manzi
Overview of glycoconjugate analysis.
Current protocols in protein science / editorial board, John E. Coligan ... [et al.] 2001;Chapter 12():Unit 12.1.
2001: Hudson H Freeze
Endoglycosidase and glycoamidase release of N-linked oligosaccharides.
Current protocols in molecular biology / edited by Frederick M. Ausubel ... [et al.] 2001;Chapter 17():Unit17.13A.
2001: Vibeke Westphal; Susanne Kjaergaard; Joseph A Davis; S M Peterson; Flemming Skovby; Hudson H Freeze
Genetic and metabolic analysis of the first adult with congenital disorder of glycosylation type Ib: long-term outcome and effects of mannose supplementation.
Molecular genetics and metabolism 2001;73(1):77-85.
2001: Vibeke Westphal; Gregory M Enns; M F McCracken; Hudson H Freeze
Functional analysis of novel mutations in a congenital disorder of glycosylation Ia patient with mixed Asian ancestry.
Molecular genetics and metabolism 2001;73(1):71-6.
2001: Geetha Srikrishna; K Panneerselvam; Vibeke Westphal; V Abraham; Ajit Varki; Hudson H Freeze
Two proteins modulating transendothelial migration of leukocytes recognize novel carboxylated glycans on endothelial cells.
Journal of immunology (Baltimore, Md. : 1950) 2001;166(7):4678-88.
2001: Veronika Stoka; Boris Turk; SL Schendel; T H Kim; Tina Cirman; Scott J Snipas; Lisa M Ellerby; Dale E Bredesen; Hudson H Freeze; M Abrahamson; D Bromme; Stan Krajewski; John C Reed; X M Yin; Vito Turk; Guy S Salvesen
Lysosomal protease pathways to apoptosis. Cleavage of bid, not pro-caspases, is the most likely route.
The Journal of biological chemistry 2001;276(5):3149-57.
2001: Thorsten Marquardt; Hudson H Freeze
Congenital disorders of glycosylation: glycosylation defects in man and biological models for their study.
Biological chemistry 2001;382(2):161-77.
2001: Geetha Srikrishna; D K Toomre; A Manzi; K Panneerselvam; Hudson H Freeze; Ajit Varki; N M Varki
A novel anionic modification of N-glycans on mammalian endothelial cells is recognized by activated neutrophils and modulates acute inflammatory responses.
Journal of immunology (Baltimore, Md. : 1950) 2001;166(1):624-32.
2000: Vibeke Westphal; Simon H Murch; S Kim; Geetha Srikrishna; Bryan Winchester; Richard Day; Hudson H Freeze
Reduced heparan sulfate accumulation in enterocytes contributes to protein-losing enteropathy in a congenital disorder of glycosylation.
The American journal of pathology 2000;157(6):1917-25.
2000: Vibeke Westphal; Geetha Srikrishna; Hudson H Freeze
Congenital disorders of glycosylation: have you encountered them?
Genetics in medicine : official journal of the American College of Medical Genetics 2000;2(6):329-37.
2000: Gert Matthijs; Els Schollen; Cecilia Bjursell; Anna Erlandson; Hudson H Freeze; F Imtiaz; Susanne Kjaergaard; Tommy Martinsson; Marianne Schwartz; Nathalie Seta; Sandrine Vuillaumier-Barrot; Vibeke Westphal; Bryan Winchester
Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia).
Human mutation 2000;16(5):386-94.
2000: Els Schollen; Lambertus Dorland; Tom J de Koning; Otto P van Diggelen; Jan G M Huijmans; T Marquardt; D Babovic-Vuksanovic; M Patterson; F Imtiaz; Bryan Winchester; Maciej Adamowicz; Ewa Pronicka; Hudson H Freeze; Gert Matthijs
Genomic organization of the human phosphomannose isomerase (MPI) gene and mutation analysis in patients with congenital disorders of glycosylation type Ib (CDG-Ib).
Human mutation 2000;16(3):247-52.
2000: Jeffrey S Rush; K Panneerselvam; Charles J Waechter; Hudson H Freeze
Mannose supplementation corrects GDP-mannose deficiency in cultured fibroblasts from some patients with Congenital Disorders of Glycosylation (CDG).
Glycobiology 2000;10(8):829-35.
2000: Vibeke Westphal; C Schottstädt; T Marquardt; Hudson H Freeze
Analysis of multiple mutations in the hALG6 gene in a patient with congenital disorder of glycosylation Ic.
Molecular genetics and metabolism 2000;70(3):219-23.
2000: S Kim; Vibeke Westphal; Geetha Srikrishna; DP Mehta; S Peterson; J Filiano; Pamela S Karnes; Marc C Patterson; Hudson H Freeze
Dolichol phosphate mannose synthase (DPM1) mutations define congenital disorder of glycosylation Ie (CDG-Ie)
The Journal of clinical investigation 2000;105(2):191-8.
1999: Thorsten Marquardt; Kerstin Lühn; Geetha Srikrishna; Hudson H Freeze; Erik Harms; Dietmar Vestweber
Correction of leukocyte adhesion deficiency type II with oral fucose.
Blood 1999;94(12):3976-85.
1999: Dusica Babovic-Vuksanovic; Marc C Patterson; W Frederick Schwenk; John F O'brien; Jerry Vockley; Hudson H Freeze; DP Mehta; Virginia V Michels
Severe hypoglycemia as a presenting symptom of carbohydrate-deficient glycoprotein syndrome.
The Journal of pediatrics 1999;135(6):775-81.
1999: Y Miura; S Kim; JR Etchison; Y Ding; O Hindsgaul; Hudson H Freeze
Aglycone structure influences alpha-fucosyltransferase III activity using N-acetyllactosamine glycoside acceptors.
Glycoconjugate journal 1999;16(11):725-30.
1999: Hudson H Freeze; M Aebi
Molecular basis of carbohydrate-deficient glycoprotein syndromes type I with normal phosphomannomutase activity.
Biochimica et biophysica acta 1999;1455(2-3):167-78.
1999: Y Miura; Y Ding; A Manzi; O Hindsgaul; Hudson H Freeze
Characterization of mammalian UDP-GalNAc:glucuronide alpha 1-4-N-acetylgalactosaminyltransferase.
Glycobiology 1999;9(10):1053-60.
1999: Hudson H Freeze
New diagnosis and treatment of congenital hepatic fibrosis.
Journal of pediatric gastroenterology and nutrition 1999;29(1):104-6.
1999: Thorsten Marquardt; Thomas Brune; Kerstin Lühn; K P Zimmer; C Körner; L Fabritz; N van der Werft; Josef Vormoor; Hudson H Freeze; Frank Louwen; B Biermann; Erik Harms; K von Figura; Dietmar Vestweber; Hans Georg Koch
Leukocyte adhesion deficiency II syndrome, a generalized defect in fucose metabolism.
The Journal of pediatrics 1999;134(6):681-8.
1999: Hudson H Freeze
Human glycosylation disorders and sugar supplement therapy.
Biochemical and biophysical research communications 1999;255(2):189-93.
1998: Susanne Kjaergaard; Bengt Kristiansson; Helena Stibler; Hudson H Freeze; Marianne Schwartz; Tommy Martinsson; Flemming Skovby
Failure of short-term mannose therapy of patients with carbohydrate-deficient glycoprotein syndrome type 1A.
Acta paediatrica (Oslo, Norway : 1992) 1998;87(8):884-8.
1998: Y Miura; Hudson H Freeze
alpha-N-acetylgalactosamine-capping of chondroitin sulfate core region oligosaccharides primed on xylosides.
Glycobiology 1998;8(8):813-9.
1998: Geetha Srikrishna; Ling Wang; Hudson H Freeze
Fucosebeta-1-P-Ser is a new type of glycosylation: using antibodies to identify a novel structure in Dictyostelium discoideum and study multiple types of fucosylation during growth and development.
Glycobiology 1998;8(8):799-811.
1998: Ralf Niehues; Martin Hasilik; Gordon Alton; Christian Körner; M Schiebe-Sukumar; H G Koch; K P Zimmer; R Wu; E Harms; Karin Reiter; Kurt von Figura; Hudson H Freeze; Hinrich Karsten Harms; Thorsten Marquardt
Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy.
The Journal of clinical investigation 1998;101(7):1414-20.
1998: Gordon Alton; Martin Hasilik; Ralf Niehues; K Panneerselvam; JR Etchison; F Fana; Hudson H Freeze
Direct utilization of mannose for mammalian glycoprotein biosynthesis.
Glycobiology 1998;8(3):285-95.
1997: DP Mehta; JR Etchison; R Wu; Hudson H Freeze
UDP-GlcNAc:Ser-protein N-acetylglucosamine-1-phosphotransferase from Dictyostelium discoideum recognizes serine-containing peptides and eukaryotic cysteine proteinases.
The Journal of biological chemistry 1997;272(45):28638-45.
1997: Geetha Srikrishna; N M Varki; P C Newell; Ajit Varki; Hudson H Freeze
An IgG monoclonal antibody against Dictyostelium discoideum glycoproteins specifically recognizes Fucalpha1,6GlcNAcbeta in the core of N-linked glycans. Localized expression of core-fucosylated glycoconjugates in human tissues.
The Journal of biological chemistry 1997;272(41):25743-52.
1997: K Panneerselvam; JR Etchison; Hudson H Freeze
Human fibroblasts prefer mannose over glucose as a source of mannose for N-glycosylation. Evidence for the functional importance of transported mannose.
The Journal of biological chemistry 1997;272(37):23123-9.
1997: G M Souza; DP Mehta; M Lammertz; JM Rodriguez-Paris; R Wu; James A Cardelli; Hudson H Freeze
Dictyostelium lysosomal proteins with different sugar modifications sort to functionally distinct compartments.
Journal of cell science 1997;110 ( Pt 18)():2239-48.
1997: K Panneerselvam; JR Etchison; Flemming Skovby; Hudson H Freeze
Abnormal metabolism of mannose in families with carbohydrate-deficient glycoprotein syndrome type 1.
Biochemical and molecular medicine 1997;61(2):161-7.
1997: Gordon Alton; Susanne Kjaergaard; JR Etchison; Flemming Skovby; Hudson H Freeze
Oral ingestion of mannose elevates blood mannose levels: a first step toward a potential therapy for carbohydrate-deficient glycoprotein syndrome type I.
Biochemical and molecular medicine 1997;60(2):127-33.
1997: JR Etchison; Hudson H Freeze
Enzymatic assay of D-mannose in serum.
Clinical chemistry 1997;43(3):533-8.
1997: T Ord; C Adessi; L Wang; Hudson H Freeze
The cysteine proteinase gene cprG in Dictyostelium discoideum has a serine-rich domain that contains GlcNAc-1-P.
Archives of biochemistry and biophysics 1997;339(1):64-72.
1997: Hudson H Freeze; M Lammertz; Negin Iranfar; Danny Fuller; K Panneerselvam; William F Loomis
Consequences of disrupting the gene that encodes alpha-glucosidase II in the N-linked oligosaccharide biosynthesis pathway of Dictyostelium discoideum.
Developmental genetics 1997;21(3):177-86.
1996: DP Mehta; M Ichikawa; P V Salimath; JR Etchison; R Haak; A Manzi; Hudson H Freeze
A lysosomal cysteine proteinase from Dictyostelium discoideum contains N-acetylglucosamine-1-phosphate bound to serine but not mannose-6-phosphate on N-linked oligosaccharides.
The Journal of biological chemistry 1996;271(18):10897-903.
1996: K Panneerselvam; Hudson H Freeze
Mannose enters mammalian cells using a specific transporter that is insensitive to glucose.
The Journal of biological chemistry 1996;271(16):9417-21.
1996: K Panneerselvam; Hudson H Freeze
Mannose corrects altered N-glycosylation in carbohydrate-deficient glycoprotein syndrome fibroblasts.
The Journal of clinical investigation 1996;97(6):1478-87.
1996: JR Etchison; Hudson H Freeze
A new approach to mapping co-localization of multiple glycosyl transferases in functional Golgi preparations.
Glycobiology 1996;6(2):177-89.
1996: A Pörtner; JR Etchison; D Sampath; Hudson H Freeze
Human melanoma and Chinese hamster ovary cells galactosylate n-alkyl-beta-glucosides using UDP gal:GlcNAc beta 1,4 galactosyltransferase.
Glycobiology 1996;6(1):7-13.
1995: G M Souza; J Hirai; DP Mehta; Hudson H Freeze
Identification of two novel Dictyostelium discoideum cysteine proteinases that carry N-acetylglucosamine-1-P-modification.
The Journal of biological chemistry 1995;270(48):28938-45.
1995: K E Norgard-Sumnicht; L Roux; D K Toomre; A Manzi; Hudson H Freeze; Ajit Varki
Unusual anionic N-linked oligosaccharides from bovine lung.
The Journal of biological chemistry 1995;270(46):27634-45.
1995: DP Mehta; JR Etchison; Hudson H Freeze
Characterization, subcellular localization, and developmental regulation of a cysteine proteinase from Dictyostelium discoideum.
Archives of biochemistry and biophysics 1995;321(1):191-8.
1995: P V Salimath; R C Spiro; Hudson H Freeze
Identification of a novel glycosaminoglycan core-like molecule. II. Alpha-GalNAc-capped xylosides can be made by many cell types.
The Journal of biological chemistry 1995;270(16):9164-8.
1995: A Manzi; P V Salimath; R C Spiro; P A Keifer; Hudson H Freeze
Identification of a novel glycosaminoglycan core-like molecule. I. 500 MHz 1H NMR analysis using a nano-NMR probe indicates the presence of a terminal alpha-GalNAc residue capping 4-methylumbelliferyl-beta-D-xylosides.
The Journal of biological chemistry 1995;270(16):9154-63.
1995: K Panneerselvam; Hudson H Freeze
Enzymes involved in the synthesis of mannose-6-phosphate from glucose are normal in carbohydrate deficient glycoprotein syndrome fibroblasts.
Biochemical and biophysical research communications 1995;208(2):517-22.
1995: Hudson H Freeze; M Ichikawa
Identification of N-acetylglucosamine-alpha-1-phosphate transferase activity in Dictyostelium discoideum: an enzyme that initiates phosphoglycosylation.
Biochemical and biophysical research communications 1995;208(1):384-9.
1995: JR Etchison; Geetha Srikrishna; Hudson H Freeze
A novel method to co-localize glycosaminoglycan-core oligosaccharide glycosyltransferases in rat liver Golgi. Co-localization of galactosyltransferase I with a sialyltransferase.
The Journal of biological chemistry 1995;270(2):756-64.
1994: L D Powell; K Paneerselvam; R Vij; S Diaz; A Manzi; N Buist; Hudson H Freeze; Ajit Varki
Carbohydrate-deficient glycoprotein syndrome: not an N-linked oligosaccharide processing defect, but an abnormality in lipid-linked oligosaccharide biosynthesis?
The Journal of clinical investigation 1994;94(5):1901-9.
1993: B K Hayes; Hudson H Freeze; Ajit Varki
Biosynthesis of oligosaccharides in intact Golgi preparations from rat liver. Analysis of N-linked glycans labeled by UDP-[6-3H]N-acetylglucosamine.
The Journal of biological chemistry 1993;268(22):16139-54.
1993: Hudson H Freeze; D Sampath; A Varki
Alpha- and beta-xylosides alter glycolipid synthesis in human melanoma and Chinese hamster ovary cells.
The Journal of biological chemistry 1993;268(3):1618-27.
1992: D Sampath; A Varki; Hudson H Freeze
The spectrum of incomplete N-linked oligosaccharides synthesized by endothelial cells in the presence of brefeldin A.
The Journal of biological chemistry 1992;267(7):4440-55.
1992: Hudson H Freeze; O Hindsgaul; M Ichikawa
A novel pathway for phosphorylated oligosaccharide biosynthesis. Identification of an oligosaccharide-specific phosphate methyltransferase in dictyostelium discoideum.
The Journal of biological chemistry 1992;267(7):4431-9.
1991: R C Spiro; Hudson H Freeze; D Sampath; J A Garcia
Uncoupling of chondroitin sulfate glycosaminoglycan synthesis by brefeldin A.
The Journal of cell biology 1991;115(5):1463-73.
1990: James A Cardelli; J M Bush; D Ebert; Hudson H Freeze
Sulfated N-linked oligosaccharides affect secretion but are not essential for the transport, proteolytic processing, and sorting of lysosomal enzymes in Dictyostelium discoideum.
The Journal of biological chemistry 1990;265(15):8847-53.
1990: Hudson H Freeze; P Koza-Taylor; Jeffrey Jones; William F Loomis
Cell-free N-glycosylation in Dictyostelium discoideum: analysis of wild-type and mutants defective in lipid-linked oligosaccharide biosynthesis.
Journal of cellular biochemistry 1990;43(1):27-42.
1990: James A Cardelli; J Schatzle; J M Bush; J Richardson; D Ebert; Hudson H Freeze
Biochemical and genetic analysis of the biosynthesis, sorting, and secretion of Dictyostelium lysosomal enzymes.
Developmental genetics 1990;11(5-6):454-62.
1990: Hudson H Freeze; J M Bush; James A Cardelli
Biochemical and genetic analysis of an antigenic determinant found on N-linked oligosaccharides in Dictyostelium.
Developmental genetics 1990;11(5-6):463-72.
1989: Hudson H Freeze; P Koza-Taylor; A Saunders; James A Cardelli
The effects of altered N-linked oligosaccharide structures on maturation and targeting of lysosomal enzymes in Dictyostelium discoideum.
The Journal of biological chemistry 1989;264(32):19278-86.
1989: D L Ebert; Hudson H Freeze; J Richardson; Randall Dimond; James A Cardelli
A Dictyostelium discoideum mutant that missorts and oversecretes lysosomal enzyme precursors is defective in endocytosis.
The Journal of cell biology 1989;109(4 Pt 1):1445-56.
1989: Hudson H Freeze; L Willies; S Hamilton; P Koza-Taylor
Two mutants of Dictyostelium discoideum that lack a sulfated carbohydrate antigenic determinant synthesize a truncated lipid-linked precursor of N-linked oligosaccharides.
The Journal of biological chemistry 1989;264(10):5653-9.
1988: G Sundblad; S Kajiji; V Quaranta; Hudson H Freeze; Ajit Varki
Sulfated N-linked oligosaccharides in mammalian cells. III. Characterization of a pancreatic carcinoma cell surface glycoprotein with N- and O-sulfate esters on asparagine-linked glycans.
The Journal of biological chemistry 1988;263(18):8897-903.
1988: G Sundblad; S Holojda; L Roux; Ajit Varki; Hudson H Freeze
Sulfated N-linked oligosaccharides in mammalian cells. II. Identification of glycosaminoglycan-like chains attached to complex-type glycans.
The Journal of biological chemistry 1988;263(18):8890-6.
1988: L Roux; S Holojda; G Sundblad; Hudson H Freeze; Ajit Varki
Sulfated N-linked oligosaccharides in mammalian cells. I. Complex-type chains with sialic acids and O-sulfate esters.
The Journal of biological chemistry 1988;263(18):8879-89.
1987: H S Judelson; Hudson H Freeze; Randall Dimond
Characterization and distribution of multiple antigens on N-linked oligosaccharides of Dictyostelium discoideum proteins.
Archives of biochemistry and biophysics 1987;253(2):305-14.
1984: Hudson H Freeze; R C Mierendorf; R Wunderlich; Randall Dimond
Sulfated oligosaccharides block antibodies to many Dictyostelium discoideum acid hydrolases.
The Journal of biological chemistry 1984;259(16):10641-3.
1984: Hudson H Freeze; JR Etchison
Presence of a nonlysosomal endo-beta-N-acetylglucosaminidase in the cellular slime mold Dictyostelium discoideum.
Archives of biochemistry and biophysics 1984;232(1):414-21.