Mutations in STT3A and STT3B cause two congenital disorders of glycosylation von Shrimal, Shiteshu, Ng, Bobby G, Losfeld, Marie-Estelle, Gilmore, Reid, Freeze, Hudson H

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Multiple Phenotypes in Phosphoglucomutase 1 Deficiency von Tegtmeyer, Laura C, Rust, Stephan, van Scherpenzeel, Monique, Ng, Bobby G, Losfeld, Marie-Estelle, Timal, Sharita, Raymond, Kimiyo, He, Ping, Ichikawa, Mie, Veltman, Joris, Huijben, Karin, Shin, Yoon S, Sharma, Vandana, Adamowicz, Maciej, Lammens, Martin, Reunert, Janine, Witten, Anika, Schrapers, Esther, Matthijs, Gert, Jaeken, Jaak, Rymen, Daisy, Stojkovic, Tanya, Laforêt, Pascal, Petit, François, Aumaître, Olivier, Czarnowska, Elzbieta, Piraud, Monique, Podskarbi, Teodor, Stanley, Charles A, Matalon, Reuben, Burda, Patricie, Seyyedi, Soraya, Debus, Volker, Socha, Piotr, Sykut-Cegielska, Jolanta, van Spronsen, Francjan, de Meirleir, Linda, Vajro, Pietro, DeClue, Terry, Ficicioglu, Can, Wada, Yoshinao, Wevers, Ron A, Vanderschaeghe, Dieter, Callewaert, Nico, Fingerhut, Ralph, van Schaftingen, Emile, Freeze, Hudson H, Morava, Eva, Lefeber, Dirk J, Marquardt, Thorsten

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Magnetism in multilayer thin film rings von Ross, C A, Castaño, F J, Jung, W, Ng, B G, Colin, I A, Morecroft, D

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Functional characterization of O‐methyltransferases used to catalyse site‐specific methylation in the post‐tailoring steps of pradimicin biosynthesis von Han, J.W., Ng, B.G., Sohng, J.K., Yoon, Y.J., Choi, G.J., Kim, B.S.

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Electrical observation of asymmetric magnetization configurations in the vortex state of NiFe and Co rings von Nam, Chunghee, Mascaro, M D, Ng, B G, Ross, C A

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Neurology of inherited glycosylation disorders von Freeze, Hudson H, Dr, Prof, Eklund, Erik A, MD, Ng, Bobby G, BS, Patterson, Marc C, Prof

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Magnetoresistance of submicrometre multilayer Wheatstone bridges as a probe of magnetic reversal mechanism von Castaño, F J, Ng, B G, Colin, I A, Morecroft, D, Jung, W, Ross, C A

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Effect of magnetic field direction on the remanent resistance levels and vortex chirality of a multilayered magnetic ring von Nam, Chunghee, Ng, B. G., Castaño, F. J., Ross, C. A.

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ATP6V0A2 mutations present in two Mexican Mestizo children with an autosomal recessive cutis laxa syndrome type IIA von Bahena-Bahena, D, López-Valdez, J, Raymond, K, Salinas-Marín, R, Ortega-García, A, Ng, B G, Freeze, H H, Ruíz-García, M, Martínez-Duncker, I

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Biallelic mutations in CAD, impair de novo pyrimidine biosynthesis and decrease glycosylation precursors von Ng, Bobby G, Wolfe, Lynne A, Ichikawa, Mie, Markello, Thomas, He, Miao, Tifft, Cynthia J, Gahl, William A, Freeze, Hudson H

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Golgi glycosylation and human inherited diseases von Freeze, Hudson H, Ng, Bobby G

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Factor VIII and vWF deficiency in STT3A‐CDG

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Directional alignment of carbon nanotubes in polymer matrices: Contemporary approaches and future advances von Goh, P.S., Ismail, A.F., Ng, B.C.

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Recent advances of inorganic fillers in mixed matrix membrane for gas separation von Goh, P.S., Ismail, A.F., Sanip, S.M., Ng, B.C., Aziz, M.

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A new congenital disorder of glycosylation caused by a mutation in SSR4, the signal sequence receptor 4 protein of the TRAP complex von Losfeld, Marie Estelle, Ng, Bobby G, Kircher, Martin, Buckingham, Kati J, Turner, Emily H, Eroshkin, Alexey, Smith, Joshua D, Shendure, Jay, Nickerson, Deborah A, Bamshad, Michael J, Freeze, Hudson H

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Investigation of submerged membrane photocatalytic reactor (sMPR) operating parameters during oily wastewater treatment process von Ong, C.S., Lau, W.J., Goh, P.S., Ng, B.C., Ismail, A.F.

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Targeted polymerase chain reaction-based enrichment and next generation sequencing for diagnostic testing of congenital disorders of glycosylation von Jones, Melanie A, Bhide, Shruti, Chin, Ephrem, Ng, Bobby G, Rhodenizer, Devin, Zhang, Victor W, Sun, Jessica J, Tanner, Alice, Freeze, Hudson H, Hegde, Madhuri R

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Gas separation performance of polyethersulfone/multi-walled carbon nanotubes mixed matrix membranes von Ismail, A.F., Rahim, N.H., Mustafa, A., Matsuura, T., Ng, B.C., Abdullah, S., Hashemifard, S.A.

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Clinical and biological implications of MYC activation: a common difference between MGUS and newly diagnosed multiple myeloma von Chng, W-J, Huang, G F, Chung, T H, Ng, S B, Gonzalez-Paz, N, Troska-Price, T, Mulligan, G, Chesi, M, Bergsagel, P L, Fonseca, R

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Insulin mimetic peroxovanadium complexes: preparation and structure of potassium oxodiperoxo(pyridine-2-carboxylato)vanadate(V), K2[VO(O2)2(C5H4NCOO)].2H2O, and potassium oxodipero... von Shaver, Alan, Ng, Jesse B, Hall, David A, Lum, Bernadette Soo, Posner, Barry I

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