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Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2018, Volume 123, Issue 2, pp. S120 - S121
Journal Article
JFMS open reports, ISSN 2055-1169, 07/2018, Volume 4, Issue 2, p. 2055116918804305
The congenital midline defects of peritoneopericardial diaphragmatic hernia (PPDH) and omphalocele are believed to be related developmental defects, and have... 
Journal Article
Bone, ISSN 8756-3282, 11/2019, Volume 128, p. 115042
Mucopolysaccharidosis (MPS) VII is a lysosomal storage disorder characterized by deficient activity of β-glucuronidase, leading to progressive accumulation of... 
Cartilage | Lysosomal diseases | RNA-Seq | Sly Syndrome | Biomarkers | Mucopolysaccharidosis | Bone | Canine
Journal Article
PLoS Genetics, ISSN 1553-7390, 09/2019, Volume 15, Issue 9
Genomic resources for the domestic dog have improved with the widespread adoption of a 173k SNP array platform and updated reference genome. SNP arrays of this... 
Usage | Dogs | Multiple imputation (Statistics) | Genetic aspects | Nucleotide sequencing | Methods | DNA sequencing
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2015, Volume 10, Issue 9, p. e0138943
Cyclic nucleotide-gated (CNG) ion channels are key mediators underlying signal transduction in retinal and olfactory receptors. Genetic defects in CNGA3 and... 
LEBER CONGENITAL AMAUROSIS | MOLECULAR-DYNAMICS | THERAPY | CHANNEL | STRUCTURAL BASIS | CONE VISION | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | RPE65 MUTATIONS | VOLTAGE-SENSORS | PROTEIN DESIGN | Amino Acid Sequence | Humans | Leucine Zippers | Cyclic Nucleotide-Gated Cation Channels - genetics | Molecular Sequence Data | Color Vision Defects - veterinary | Color Vision Defects - genetics | Molecular Dynamics Simulation | Channelopathies - diagnosis | Channelopathies - genetics | Cyclic Nucleotide-Gated Cation Channels - chemistry | Animals | Dogs | Color Vision Defects - diagnosis | Mutation | Channelopathies - veterinary | Ion Channel Gating | Cyclic Nucleotide-Gated Cation Channels - metabolism | Channelopathies | Care and treatment | Gene mutations | Development and progression | Biosynthesis | Genetic aspects | Research | Color blindness | Veterinary colleges | Animal models | Channelopathy | Genomics | Science | Electrophysiology | Molecular dynamics | Retina | Leucine | Veterinary medicine | Odorant receptors | Acuity | Receptors | CNGA3 gene | Color vision | Cyclic GMP | Evolution | Ion channels | Ion channels (cyclic nucleotide-gated) | Congenital diseases | Computer simulation | Preservation | Channel gating | Visual acuity | Hereditary diseases | Leucine zipper proteins | Blindness | Acetylcholine receptors | Photoreceptors | Transduction | Gene therapy
Journal Article
Journal Article
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, ISSN 0022-3565, 09/2019, Volume 370, Issue 3, pp. 806 - 813
X-linked hypohidrotic ectodermal dysplasia (XLHED) is caused by defects in the EDA gene that inactivate the function of ectodysplasin A1 (EDA1). This leads to... 
MATURATION | PHARMACOLOGY & PHARMACY | DISEASE
Journal Article
Journal Article
Veterinary Dermatology, ISSN 0959-4493, 02/2017, Volume 28, Issue 1, pp. 10 - e3
Journal Article