Hudson H. Freeze: search on Z-Library

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1

Congenital Disorders of Glycosylation and the Pediatric Liver

Freeze, Hudson H.

Journal:

Seminars in Liver Disease

Year:

2001

Language:

english

File:

PDF, 291 KB

english, 2001

2

Mutations in GET4 disrupt the transmembrane domain recognition complex pathway

Tambe, Mitali A., Ng, Bobby G., Shimada, Shino, Wolfe, Lynne A., Adams, David R., Gahl, William A., Bamshad, Michael J., Nickerson, Deborah A., Malicdan, May C.V., Freeze, Hudson H.

Journal:

Journal of Inherited Metabolic Disease

Year:

2020

File:

PDF, 2.39 MB

2020

3

Three unreported cases of TMEM199-CDG, a rare genetic liver disease with abnormal glycosylation

Vajro, Pietro, Zielinska, Katarzyna, Ng, Bobby G., Maccarana, Marco, Bengtson, Per, Poeta, Marco, Mandato, Claudia, D’Acunto, Elisa, Freeze, Hudson H., Eklund, Erik A.

Journal:

Orphanet Journal of Rare Diseases

Year:

2018

Language:

english

File:

PDF, 581 KB

english, 2018

4

Handbook of Glycomics || Introduction to Human Glycosylation Disorders

Freeze, Hudson H.

Year:

2010

Language:

english

File:

PDF, 512 KB

english, 2010

5

Intact Golgi synthesize complex branched O-linked chains on glycoside primers: Evidence for the functional continuity of seven glycosyltransferases and three sugar nucleotide transporters

Soohyun Kim, Yoshiaki Miura, James R. Etchison, Hudson H. Freeze

Journal:

Glycoconjugate Journal

Year:

2001

Language:

english

File:

PDF, 200 KB

english, 2001

6

Endogenous Damage-Associated Molecular Pattern Molecules at the Crossroads of Inflammation and Cancer

Srikrishna, Geetha, Freeze, Hudson H.

Journal:

Year:

2009

Language:

english

File:

PDF, 453 KB

english, 2009

7

Using heparin therapy to reverse protein-losing enteropathy in a patient with CDG-Ib

Liem, Ylian S, Bode, Lars, Freeze, Hudson H, Leebeek, Frank WG, Zandbergen, Adrienne AM, Paul Wilson, JH

Journal:

Nature Clinical Practice Gastroenterology & Hepatology

Year:

2008

Language:

english

File:

PDF, 156 KB

english, 2008

8

Urine oligosaccharide screening by MALDI-TOF for the identification of NGLY1 deficiency

Hall, Patricia L., Lam, Christina, Alexander, John J., Asif, Ghazia, Berry, Gerard T., Ferreira, Carlos, Freeze, Hudson H., Gahl, William A., Nickander, Kim K., Sharer, Jon D., Watson, Caroline M., Wo

Journal:

Molecular Genetics and Metabolism

Year:

2018

Language:

english

File:

PDF, 694 KB

english, 2018

9

Modifications of lysosomal enzymes inDictyostelium discoideum

Hudson H. Freeze

Journal:

Molecular and Cellular Biochemistry

Year:

1986

Language:

english

File:

PDF, 1.53 MB

english, 1986

10

Functional significance of PMM2 mutations in mildly affected patients with congenital disorders of glycosylation Ia

Westphal, Vibeke, Peterson, Sandra, Patterson, Marc, Tournay, Anne, Blumenthal, Andrea, Treacy, Eileen P, Freeze, Hudson H

Journal:

Genetics in Medicine

Year:

2001

Language:

english

File:

PDF, 397 KB

english, 2001

11

Congenital Disorder of Glycosylation Id Presenting with Hyperinsulinemic Hypoglycemia and Islet Cell Hyperplasia

Sun, Liangwu, Eklund, Erik A., Chung, Wendy K., Wang, Chao, Cohen, Jason, Freeze, Hudson H.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2005

Language:

english

File:

PDF, 424 KB

english, 2005

12

Biosynthesis of GlcNAc-rich N- and O-glycans in the Golgi apparatus does not require the nucleotide sugar transporter SLC35A3

Szulc, BoÅ¼ena, Sosicka, Paulina, Maszczak-Seneczko, Dorota, Skurska, Edyta, Shauchuk, Auhen, Olczak, Teresa, Freeze, Hudson H., Olczak, Mariusz

Journal:

Journal of Biological Chemistry

Year:

2020

File:

PDF, 6.13 MB

2020

13

Erratum: Carboxylated N-glycans on RAGE promote S100A12 binding and signaling, in Journal of Cellular Biochemistry, by Srikrishna et al.

Geetha Srikrishna, Jonamani Nayak, Bernd Weigle, Achim Temme, Dirk Foell, Larnele Hazelwood, Anna Olsson, Niels Volkmann, Dorit Hanein, Hudson H. Freeze

Journal:

Journal of Cellular Biochemistry

Year:

2010

Language:

english

File:

PDF, 20 KB

english, 2010

14

Altered glycan structures: the molecular basis of congenital disorders of glycosylation

Hudson H Freeze, Markus Aebi

Journal:

Current Opinion in Structural Biology

Year:

2005

Language:

english

File:

PDF, 431 KB

english, 2005

15

Quantitative estimation of bacteriochlorophyll in situ

Gary A. Sojka, Hudson H. Freeze, Howard Gest

Journal:

Archives of Biochemistry and Biophysics

Year:

1970

Language:

english

File:

PDF, 261 KB

english, 1970

16

Metabolic manipulation of glycosylation disorders in humans and animal models

Hudson H. Freeze, Vandana Sharma

Journal:

Seminars in Cell & Developmental Biology

Year:

2010

Language:

english

File:

PDF, 289 KB

english, 2010

17

Structure−Activity Profiles of Complex Biantennary Glycans with Core Fucosylation and with/without Additional α2,3/α2,6 Sialylation: Synthesis of Neoglycoproteins and Their Properties in Lectin Assays, Cell Binding, and Organ Uptake †

Unverzagt, Carlo, André, Sabine, Seifert, Joachim, Kojima, Shuji, Fink, Christian, Srikrishna, Geetha, Freeze, Hudson, Kayser, Klaus, Gabius, Hans-Joachim

Journal:

Journal of Medicinal Chemistry

Year:

2002

Language:

english

File:

PDF, 327 KB

english, 2002

18

The Metabolic Origins of Mannose in Glycoproteins

Ichikawa, Mie, Scott, David A., Losfeld, Marie-Estelle, Freeze, Hudson H.

Journal:

Journal of Biological Chemistry

Year:

2014

Language:

english

File:

PDF, 2.91 MB

english, 2014

19

Achondrogenesis Type 1A — From Mouse to Human

Freeze, Hudson H.

Journal:

Boston Medical and Surgical Journal

Year:

2010

Language:

english

File:

PDF, 76 KB

english, 2010

20

Identification of a frequent variant in ALG6, the cause of Congenital Disorder of Glycosylation-Ic

Vibeke Westphal, Ming Xiao, Pui-Yan Kwok, Hudson H. Freeze

Journal:

Year:

2003

Language:

english

File:

PDF, 59 KB

english, 2003

21

Endo-glycosidase F and peptide N-glycosidase F release the great majority of total cellular N-linked oligosaccharides: Use in demonstrating that sulfated N-linked oligosaccharides are frequently found in cultured cells

Hudson H. Freeze, Ajit Varki

Journal:

Biochemical and Biophysical Research Communications

Year:

1986

Language:

english

File:

PDF, 460 KB

english, 1986

22

Molecular and clinical description of the first US patients with congenital disorder of glycosylation Ig

Erik A. Eklund, John W. Newell, Liangwu Sun, Neung-Seon Seo, Gulay Alper, Jessica Willert, Hudson H. Freeze

Journal:

Molecular Genetics and Metabolism

Year:

2005

Language:

english

File:

PDF, 540 KB

english, 2005

23

Cloning and characterization of glucose transporter 11, a novel sugar transporter that is alternatively spliced in various tissues

Xiaohua Wu, Weizhong Li, Vandana Sharma, Adam Godzik, Hudson H Freeze

Journal:

Molecular Genetics and Metabolism

Year:

2002

Language:

english

File:

PDF, 681 KB

english, 2002

24

Synthesis of β-GlcA-(1→3)-β-Gal and α-GalNAc-(1→4)-β-GleA-(1→3)-β-Gal as Biotinylated 2-Aminoethyl Glycoside and the Streptavidin Complex Formation

Tamura, Jun-ichi, Miura, Yoshiaki, Freeze, Hudson H.

Journal:

Journal of Carbohydrate Chemistry

Year:

1999

Language:

english

File:

PDF, 744 KB

english, 1999

25

Swaiman's Pediatric Neurology || Disorders of Glycosylation

Freeze, Hudson H.

Year:

2017

Language:

english

File:

PDF, 784 KB

english, 2017

26

Mutations in the translocon associated protein complex subunit SSR3 cause a novel Congenital Disorder of Glycosylation.

Ng, Bobby G., Lourenço, Charles Marques, Losfeld, Marie‐Estelle, Buckingham, Kati J., Kircher, Martin, Nickerson, Deborah A., Shendure, Jay, Bamshad, Michael J., Freeze, Hudson H.

Journal:

Journal of Inherited Metabolic Disease

Year:

2019

Language:

english

File:

PDF, 1007 KB

english, 2019

27

Symbol nomenclature for glycan representation

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

Journal:

Year:

2009

Language:

english

File:

PDF, 90 KB

english, 2009

28

The Cysteine Proteinase GenecprGinDictyostelium discoideumHas a Serine-Rich Domain That Contains GlcNAc-1-P

Tonis Ord, Celine Adessi, Liying Wang, Hudson H. Freeze

Journal:

Archives of Biochemistry and Biophysics

Year:

1997

Language:

english

File:

PDF, 396 KB

english, 1997

29

Applied glycoproteomics—approaches to study genetic-environmental collisions causing protein-losing enteropathy

Lars Bode, Hudson H. Freeze

Journal:

Biochimica et Biophysica Acta (BBA) - General Subjects

Year:

2006

Language:

english

File:

PDF, 540 KB

english, 2006

30

Congenital disorder of glycosylation (CDG)-Ih patient with a severe hepato-intestinal phenotype and evolving central nervous system pathology

Erik A. Eklund, Liangwu Sun, Vibeke Westphal, Jennifer L. Northrop, Hudson H. Freeze, Fernando Scaglia

Journal:

The Journal of Pediatrics

Year:

2005

Language:

english

File:

PDF, 116 KB

english, 2005

31

Pubertal development in ALG6 deficiency (congenital disorder of glycosylation type Ic)

Bradley S. Miller, Hudson H. Freeze, Georg F. Hoffmann, Kyriakie Sarafoglou

Journal:

Molecular Genetics and Metabolism

Year:

2011

Language:

english

File:

PDF, 119 KB

english, 2011

32

Leukocyte adhesion deficiency II syndrome, a generalized defect in fucose metabolism

Thorsten Marquardt, Thomas Brune, Kerstin Lühn, Klaus-Peter Zimmer, Christian Körner, Larissa Fabritz, Natascha van der Werft, Josef Vormoor, Hudson H. Freeze, Frank Louwen, Bettina Biermann, Eric Har

Journal:

The Journal of Pediatrics

Year:

1999

Language:

english

File:

PDF, 688 KB

english, 1999

33

Insufficient ER-stress response causes selective mouse cerebellar granule cell degeneration resembling that seen in congenital disorders of glycosylation

Sun, Liangwu, Zhao, Yingjun, Zhou, Kun, Freeze, Hudson H, Zhang, Yun-wu, Xu, Huaxi

Journal:

Molecular Brain

Year:

2013

Language:

english

File:

PDF, 753 KB

english, 2013

34

Solving Glycosylation Disorders: Fundamental Approaches Reveal Complicated Pathways

Freeze, Hudson H., Chong, Jessica X., Bamshad, Michael J., Ng, Bobby G.

Journal:

The American Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 1.67 MB

english, 2014

35

ChemInform Abstract: Synthesis of a Library of β-GlcNAc Glycosides to Screen for Efficient in vivo Glycosyltransferase Acceptors.

Yili Ding, Yoshiaki Miura, James R. Etchison, Hudson H. Freeze, Ole Hindsgaul

Journal:

Year:

1999

File:

PDF, 26 KB

1999

36

Characterization and distribution of multiple antigens on N-linked oligosaccharides of Dictyostelium discoideum proteins

Howard S. Judelson, Hudson H. Freeze, Randall L. Dimond

Journal:

Archives of Biochemistry and Biophysics

Year:

1987

Language:

english

File:

PDF, 1.05 MB

english, 1987

37

ALG11-CDG syndrome: Expanding the phenotype

Haanpää, Maria K., Ng, Bobby G., Gallant, Natalie M., Singh, Kathryn E., Brown, Candida, Kimonis, Virginia, Freeze, Hudson H., Muller, Eric A.

Journal:

American Journal of Medical Genetics Part A

Year:

2019

File:

PDF, 930 KB

2019

38

Carboxylated N-glycans on RAGE promote S100A12 binding and signaling

Geetha Srikrishna, Jonamani Nayak, Bernd Weigle, Achim Temme, Dirk Foell, Larnele Hazelwood, Anna Olsson, Niels Volkmann, Dorit Hanein, Hudson H. Freeze

Journal:

Journal of Cellular Biochemistry

Year:

2010

Language:

english

File:

PDF, 484 KB

english, 2010

39

Glycosylation diseases: Quo vadis?

Harry Schachter, Hudson H. Freeze

Journal:

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Year:

2009

Language:

english

File:

PDF, 160 KB

english, 2009

40

Congenital Disorders of Glycosylation: CDG-I, CDG-II, and Beyond

Journal:

Current Molecular Medicine

Year:

2007

Language:

english

File:

PDF, 456 KB

english, 2007

41

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

He, Ping, Grotzke, Jeff E, Ng, Bobby G, Gunel, Murat, Jafar-Nejad, Hamed, Cresswell, Peter, Enns, Gregory M, Freeze, Hudson H

Journal:

Year:

2015

Language:

english

File:

PDF, 1.06 MB

english, 2015

42

Deficiency of UDP-GlcNAc:Dolichol Phosphate N-Acetylglucosamine-1 Phosphate Transferase (DPAGT1) Causes a Novel Congenital Disorder of Glycosylation Type Ij

Xiaohua Wu, Jeffrey S. Rush, Denise Karaoglu, Donna Krasnewich, Mark S. Lubinsky, Charles J. Waechter, Reid Gilmore, Hudson H. Freeze

Journal:

Year:

2003

Language:

english

File:

PDF, 186 KB

english, 2003

43

Aglycone structure influences α-fucosyltransferase III activity using N-acetyllactosamine glycoside acceptors

Yoshiaki Miura, Soohyun Kim, James R. Etchison, Yili Ding, Ole Hindsgaul, Hudson H. Freeze

Journal:

Glycoconjugate Journal

Year:

1999

Language:

english

File:

PDF, 139 KB

english, 1999

44

Analysis of Multiple Mutations in the hALG6 Gene in a Patient with Congenital Disorder of Glycosylation Ic

Vibeke Westphal, Celine Schottstädt, Thorsten Marquardt, Hudson H Freeze

Journal:

Molecular Genetics and Metabolism

Year:

2000

Language:

english

File:

PDF, 63 KB

english, 2000

45

Towards a therapy for phosphomannomutase 2 deficiency, the defect in CDG-Ia patients

Hudson H. Freeze

Journal:

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Year:

2009

Language:

english

File:

PDF, 368 KB

english, 2009

46

Alpha-Mannosidase-II Deficiency Results in Dyserythropoiesis and Unveils an Alternate Pathway in Oligosaccharide Biosynthesis

Daniel Chui, Masayoshi Oh-Eda, Yung-Feng Liao, Krishnasamy Panneerselvam, Anita Lal, Kurt W Marek, Hudson H Freeze, Kelley W Moremen, Michiko N Fukuda, Jamey D Marth

Journal:

Year:

1997

Language:

english

File:

PDF, 358 KB

english, 1997

47

Human melanoma and Chinese hamster ovary cells galactosylate n-alkyl-β-glucosides using UDP gal:GlcNAc β1,4 galactosyltransferase

Pörtner, Antje, Etchison, James R., Sampath, Deepak, Freeze, Hudson H.

Journal:

Year:

1996

Language:

english

File:

PDF, 750 KB

english, 1996

48

Congenital Disorders of Glycosylation: Glycosylation Defects in Man and Biological Models for Their Study

Marquardt, Thorsten, Freeze, Hudson

Journal:

Biological Chemistry

Year:

2001

Language:

english

File:

PDF, 296 KB

english, 2001

49

Congenital nephrotic syndrome in an infant with ALG1 -congenital disorder of glycosylation

Harshman, Lyndsay A, Ng, Bobby G, Freeze, Hudson H, Trapane, Pamela, Dolezal, Anna, Brophy, Patrick D, Brumbaugh, Jane E

Journal:

Pediatrics International

Year:

2016

Language:

english

File:

PDF, 326 KB

english, 2016

50

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

Joshi, Hiren J, Hansen, Lars, Narimatsu, Yoshiki, Freeze, Hudson H, Henrissat, Bernard, Bennett, Eric, Wandall, Hans H, Clausen, Henrik, Schjoldager, Katrine T

Journal:

Year:

2018

Language:

english

File:

PDF, 812 KB

english, 2018

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