Deletion of the SELENOP gene leads to CNS atrophy with cerebellar ataxia in dogs

Genetic ataxias: update on classification and diagnostic approaches

(2021) Natalie Witek et al.   Current Neurology and Neuroscience Reports

Selenium at the Neural Barriers: AReview

(2021) Nikolay Solovyev et al.   Frontiers in Neuroscience

YARS2 Missense Variant in Belgian Shepherd Dogs with Cardiomyopathy and Juvenile Mortality

(2020) Corinne Gurtner et al.   Genes

Natural history and epidemiology of the spinocerebellar ataxias: Insights from the first description to nowadays

(2020) Stephanie Suzanne de Oliveira Scott et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

The Classification of Autosomal Recessive Cerebellar Ataxias: a Consensus Statement from the Society for Research on the Cerebellum and Ataxias Task Force

(2019) Marie Beaudin et al.   CEREBELLUM

A comprehensive biomedical variant catalogue based on whole genome sequences of 582 dogs and eight wolves

(2019) V. Jagannathan et al.   ANIMAL GENETICS

Selenocysteine β-Lyase: Biochemistry, Regulation and Physiological Role of the Selenocysteine Decomposition Enzyme

(2019) Lucia A. Seale   Antioxidants

A SINE Insertion in ATP1B2 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA2)

(2017) Nico Mauri et al.   G3-Genes Genomes Genetics

The novel homozygous KCNJ10 c.986T>C (p.(Leu329Pro)) variant is pathogenic for the SeSAME/EAST homologue in Malinois dogs

(2016) Mario Van Poucke et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Classifications of neurogenetic diseases: An increasingly complex problem

(2016) J.-M. Vallat et al.   REVUE NEUROLOGIQUE

A Missense Variant in KCNJ10 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA1)

(2016) Nico Mauri et al.   G3-Genes Genomes Genetics

Regulation of Selenium Metabolism and Transport

(2015) Raymond F. Burk et al.   Annual Review of Nutrition

Importance of selenium and selenoprotein for brain function: From antioxidant protection to neuronal signalling

(2015) Nikolay D. Solovyev   JOURNAL OF INORGANIC BIOCHEMISTRY

Ataxia

(2015) Umar Akbar et al.   NEUROLOGIC CLINICS

Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactate

(2015) Anna-Kaisa Anttonen et al.   NEUROLOGY

Cerebellar Hypoplasia in Mice Lacking Selenoprotein Biosynthesis in Neurons

(2014) Eva K. Wirth et al.   BIOLOGICAL TRACE ELEMENT RESEARCH

Selenoprotein P and apolipoprotein E receptor-2 interact at the blood-brain barrier and also within the brain to maintain an essential selenium pool that protects against neurodegeneration

(2014) Raymond F. Burk et al.   FASEB JOURNAL

DoGSD: the dog and wolf genome SNP database

(2014) Bing Bai et al.   NUCLEIC ACIDS RESEARCH

Canine Hereditary Ataxia

(2014) Ganokon Urkasemsin et al.   VETERINARY CLINICS OF NORTH AMERICA-SMALL ANIMAL PRACTICE

A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff

(2012) Pablo Cingolani et al.   FLY

Progression of neurodegeneration and morphologic changes in the brains of juvenile mice with selenoprotein P deleted

(2011) Samuel W. Caito et al.   BRAIN RESEARCH

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

(2010) A. McKenna et al.   GENOME RESEARCH

Neurodegeneration in Mice Resulting From Loss of Functional Selenoprotein P or Its Receptor Apolipoprotein E Receptor 2

(2008) William M. Valentine et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY