Genomic analyses of glycine decarboxylase neurogenic mutations yield a large-scale prediction model for prenatal disease

Large scale analyses of genotype-phenotype relationships of glycine decarboxylase mutations and neurological disease severity

(2020) Joseph Farris et al.   PLoS Computational Biology

Glycine decarboxylase regulates the maintenance and induction of pluripotency via metabolic control

(2019) Phil Jun Kang et al.   METABOLIC ENGINEERING

Identification of a new GLDC gene alternative splicing variant and its protumorigenic roles in lung cancer

(2019) Yingli Yuan et al.   Future Oncology

SWISS-MODEL: homology modelling of protein structures and complexes

(2018) Andrew Waterhouse et al.   NUCLEIC ACIDS RESEARCH

Movement Disorders and Neurometabolic Diseases

(2018) Celanie K. Christensen et al.   Seminars in Pediatric Neurology

Identification and characterization of GLDC as host susceptibility gene to severe influenza

(2018) Jie Zhou et al.   EMBO Molecular Medicine

Analysis of Large-Scale Mutagenesis Data To Assess the Impact of Single Amino Acid Substitutions

(2017) Vanessa E. Gray et al.   GENETICS

Nonketotic hyperglycinemia: Functional assessment of missense variants in GLDC to understand phenotypes of the disease

(2017) Irene Bravo-Alonso et al.   HUMAN MUTATION

Direct visualization of critical hydrogen atoms in a pyridoxal 5′-phosphate enzyme

(2017) Steven Dajnowicz et al.   Nature Communications

Analysis of Large-Scale Mutagenesis Data To Assess the Impact of Single Amino Acid Substitutions

(2017) Vanessa E. Gray et al.   GENETICS

The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT

(2016) Curtis R. Coughlin et al.   GENETICS IN MEDICINE

Neurodevelopmental Outcome and Treatment Efficacy of Benzoate and Dextromethorphan in Siblings with Attenuated Nonketotic Hyperglycinemia

(2016) Kendra J. Bjoraker et al.   JOURNAL OF PEDIATRICS

ConSurf 2016: an improved methodology to estimate and visualize evolutionary conservation in macromolecules

(2016) Haim Ashkenazy et al.   NUCLEIC ACIDS RESEARCH

The SWISS-MODEL Repository—new features and functionality

(2016) Stefan Bienert et al.   NUCLEIC ACIDS RESEARCH

Chronic administration of an HDAC inhibitor treats both neurological and systemic Niemann-Pick type C disease in a mouse model

(2016) Md. Suhail Alam et al.   Science Translational Medicine

Biochemical and molecular predictors for prognosis in nonketotic hyperglycinemia

(2015) Michael A. Swanson et al.   ANNALS OF NEUROLOGY

SHMT2 drives glioma cell survival in ischaemia but imposes a dependence on glycine clearance

(2015) Dohoon Kim et al.   NATURE

GtRNAdb 2.0: an expanded database of transfer RNA genes identified in complete and draft genomes

(2015) Patricia P. Chan et al.   NUCLEIC ACIDS RESEARCH

Glycine decarboxylase deficiency causes neural tube defects and features of non-ketotic hyperglycinemia in mice

(2015) Yun Jin Pai et al.   Nature Communications

Structure of the Homodimeric Glycine Decarboxylase P-protein fromSynechocystissp. PCC 6803 Suggests a Mechanism for Redox Regulation

(2013) Dirk Hasse et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Glycine Decarboxylase Activity Drives Non-Small Cell Lung Cancer Tumor-Initiating Cells and Tumorigenesis

(2012) Wen Cai Zhang et al.   CELL

A novel mouse model of Niemann–Pick type C disease carrying a D1005G-Npc1 mutation comparable to commonly observed human mutations

(2011) Robert A. Maue et al.   HUMAN MOLECULAR GENETICS

Prediction of long-term outcome in glycine encephalopathy: a clinical survey

(2011) Julia B. Hennermann et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Automated comparative protein structure modeling with SWISS-MODEL and Swiss-PdbViewer: A historical perspective

(2010) Nicolas Guex et al.   ELECTROPHORESIS

Nonketotic Hyperglycinemia and Acquired Hydrocephalus

(2009) Uluc Yis et al.   PEDIATRIC NEUROLOGY