Sweet solution: sugars to the rescue

por Freeze, Hudson H.
Publicado 2002

Modifications of lysosomal enzymes in Dictyostelium discoideum

por Freeze, Hudson H.
Publicado 1986

U.S.-Japan Seminar on Recent Advances in the Understanding of Solar Flares

por Kane, S, Uchida, Y, Tanaka, K, Hudson, H
Publicado 1983

TIME RELATIONS OF GROWTH : II. THE EQUIVALENCE OF AGE IN MAMMALS ESTIMATED ON THE BASIS OF THEIR GROWTH CONSTANTS.

por Brody, Samuel, Sparrow, Chester D., Kibler, Hudson H.
Publicado 1926

GLUT1 is a highly efficient L-fucose transporter

por Ng, Bobby G., Sosicka, Paulina, Xia, Zhijie, Freeze, Hudson H.
Publicado 2022

A Leadership Perspective on the Plastic and Reconstructive Surgery Residency Application Cycle During the COVID-19 Pandemic

por Jain, Abhishek, Brown, Geoffrey, Hudson, H. Todd, Patel, Ashish, Herrera, Fernando A.
Publicado 2022

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

por Sun, Liangwu, Zhao, Yingjun, Zhou, Kun, Freeze, Hudson H, Zhang, Yun-wu, Xu, Huaxi
Publicado 2013

Dissecting Functions of the Conserved Oligomeric Golgi Tethering Complex Using a Cell-Free Assay

por Cottam, Nathanael P, Wilson, Katherine M, Ng, Bobby G, Körner, Christian, Freeze, Hudson H, Ungar, Daniel
Publicado 2014

The Art of Science Communication—A Novel Approach to Science Communication Training

por Greer, Susanna, Alexander, Hannah, Baldwin, Thomas O., Freeze, Hudson H., Thompson, Morgan, Hunt, Geoffrey, Snowflack, Danielle R.
Publicado 2018

A Dominant Heterozygous Mutation in COG4 Causes Saul–Wilson Syndrome, a Primordial Dwarfism, and Disrupts Zebrafish Development via Wnt Signaling

por Xia, Zhi-Jie, Zeng, Xin-Xin I., Tambe, Mitali, Ng, Bobby G., Dong, P. Duc S., Freeze, Hudson H.
Publicado 2021

Uridine monophosphate (UMP)-responsive developmental and epileptic encephalopathy: A case report of two siblings and a review of literature

por Al-Otaibi, Ali, AlAyed, Alaa, Al Madhi, Asma, Saeed, Leena, Ng, Bobby G., Freeze, Hudson H., Almannai, Mohammed
Publicado 2021

Selective inhibition of N-linked glycosylation impairs receptor tyrosine kinase processing

por Klaver, Elsenoor, Zhao, Peng, May, Melanie, Flanagan-Steet, Heather, Freeze, Hudson H., Gilmore, Reid, Wells, Lance, Contessa, Joseph, Steet, Richard
Publicado 2019

Prediction of pre-eclampsia in nulliparous women using routinely collected maternal characteristics: a model development and validation study

por Al-Rubaie, Ziad T. A., Hudson, H. Malcolm, Jenkins, Gregory, Mahmoud, Imad, Ray, Joel G., Askie, Lisa M., Lord, Sarah J.
Publicado 2020

Proteomics reveals signal peptide features determining the client specificity in human TRAP-dependent ER protein import

por Nguyen, Duy, Stutz, Regine, Schorr, Stefan, Lang, Sven, Pfeffer, Stefan, Freeze, Hudson H., Förster, Friedrich, Helms, Volkhard, Dudek, Johanna, Zimmermann, Richard
Publicado 2018

Spontaneous improvement of carbohydrate-deficient transferrin in PMM2-CDG without mannose observed in CDG natural history study

por Witters, Peter, Edmondson, Andrew C., Lam, Christina, Johnsen, Christin, Patterson, Marc C., Raymond, Kimiyo M., He, Miao, Freeze, Hudson H., Morava, Eva
Publicado 2021

Phosphomannose isomerase inhibitors improve N-glycosylation in selected phosphomannomutase-deficient fibroblasts.

por Sharma, Vandana, Ichikawa, Mie, He, Ping, Scott, David A., Bravo, Yalda, Dahl, Russell, Ng, Bobby G., Cosford, Nicholas D. P., Freeze, Hudson H.
Publicado 2011

A zebrafish model of congenital disorders of glycosylation with phosphomannose isomerase deficiency reveals an early opportunity for corrective mannose supplementation

por Chu, Jaime, Mir, Alexander, Gao, Ningguo, Rosa, Sabrina, Monson, Christopher, Sharma, Vandana, Steet, Richard, Freeze, Hudson H., Lehrman, Mark A., Sadler, Kirsten C.
Publicado 2013

MPI‐CDG from a hepatic perspective: Report of two Egyptian cases and review of literature

por Abdel Ghaffar, Tawhida Y., Ng, Bobby G., Elsayed, Solaf M., El Naghi, Suzan, Helmy, Sarah, Mohammed, Nermine, El Hennawy, Ahmed, Freeze, Hudson H.
Publicado 2020

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

por Vajro, Pietro, Zielinska, Katarzyna, Ng, Bobby G., Maccarana, Marco, Bengtson, Per, Poeta, Marco, Mandato, Claudia, D’Acunto, Elisa, Freeze, Hudson H., Eklund, Erik A.
Publicado 2018

COG4 mutation in Saul-Wilson syndrome selectively affects secretion of proteins involved in chondrogenesis in chondrocyte-like cells

por Xia, Zhi-Jie, Mahajan, Sonal, Paul Daniel, Earnest James, Ng, Bobby G., Saraswat, Mayank, Campos, Alexandre Rosa, Murad, Rabi, He, Miao, Freeze, Hudson H.
Publicado 2022