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Matthew P Wilson

5PUBLICATIONS

14CO-AUTHORS

Molecular targetsMolecular medicineGene and molecular therapyEpigenetics (incl. genome methylation and epigenomics)Medical biochemistry - proteins and peptides (incl. medical proteomics)

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Publications (5)

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|Jul 01, 2024

The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene.

Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore

|Aug 04, 2023

Beyond genetics: Deciphering the impact of missense variants in CAD deficiency.

Francisco Del Caño-Ochoa, Bobby G Ng, Antonio Rubio-Del-Campo

|Mar 09, 2022

CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane trafficking.

Matthew P Wilson, Zoé Durin, Özlem Unal

|Mar 17, 2021

SLC37A4-CDG: Second patient.

Matthew P Wilson, Dulce Quelhas, Elisa Leão-Teles

|Aug 08, 2017

An LC-MS/MS-Based Method for the Quantification of Pyridox(am)ine 5'-Phosphate Oxidase Activity in Dried Blood Spots from Patients with Epilepsy.

Matthew P Wilson, Emma J Footitt, Apostolos Papandreou

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Frequent Collaborators

1 joint publications

Kevin A Mills

1 joint publications

Francisco Del Caño-Ochoa

1 joint publications

Bobby G Ng

1 joint publications

Antonio Rubio-Del-Campo

1 joint publications

Sonal Mahajan

1 joint publications

Marçal Vilar

1 joint publications

Daisy Rymen

1 joint publications

Paula Sánchez-Pintos

1 joint publications

Joanna Kenny

1 joint publications

Myriam Ley Martos

Frequent Collaborators

1 joint publications

Kevin A Mills

1 joint publications

Francisco Del Caño-Ochoa

1 joint publications

Bobby G Ng

1 joint publications

Antonio Rubio-Del-Campo

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