Transcriptomic Approach to Lesch-Nyhan Disease (original) (raw)
2014, Nucleosides, Nucleotides and Nucleic Acids
visibility
…
description
12 pages
link
1 file
Sign up to get access to over 50M papers
Sign up for access to the world's latest research
Related papers
Attenuated variants of Lesch-Nyhan disease
Brain, 2010
Genome studies and molecular genetics
Current Opinion in Plant Biology, 2003
Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015)
BMC Genomics, 2016
Genetic approaches to studying complex human disease
2013
Clinical Validation of Targeted Next-Generation Sequencing for Inherited Disorders
Archives of Pathology & Laboratory Medicine, 2015
The differential disease regulome
2011
Cell Line and DNA Biobank From Patients Affected by Genetic Diseases
Open Journal of Bioresources, 2014
Mechanisms of RNA-mediated Disease
Journal of Biological Chemistry, 2009
Framework for the Integration of Genomics, Epigenomics and Transcriptomics in Complex Diseases
Human Heredity, 2015
Molecular genetics of Dravet syndrome
Developmental Medicine & Child Neurology, 2011
Loading Preview
Sorry, preview is currently unavailable. You can download the paper by clicking the button above.
Related papers
Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants
New England Journal of Medicine, 2012
Identification of the genetic causes of orphan diseases
2013
Basic concepts of medical genetics, pathogenetics, part 3
Egyptian Journal of Medical Human Genetics, 2013
Genetic Mapping and Exome Sequencing Identify Variants Associated with Five Novel Diseases
PLoS ONE, 2012
Leshin et al RNA Biology 2010.pdf
HPRT-APRT-deficient mice are not a model for lesch-nyhan syndrome
Human Molecular Genetics, 1996
Genome Stability and Human Diseases
Subcellular Biochemistry, 2010
Clinical utility gene card for: Lesch–Nyhan syndrome
European Journal of Human Genetics, 2011
Basic concepts of medical genetics, pathogenetics: Part 1
Egyptian Journal of Medical Human Genetics, 2012
Whole genome analysis of a Vietnamese trio
Journal of Biosciences, 2015
Rare single gene disorders: estimating baseline prevalence and outcomes worldwide
Journal of Community Genetics, 2018
Molecular genetics of Usher syndrome
Cellular and Molecular Life Sciences (CMLS), 1999
Systems Analysis of Human Multigene Disorders
Springer eBooks, 2014
Genome biology, 2004
Manual of Genebank Operations and Procedures
Application of genomic technologies
Nutrition, 2004
Identification of novel candidate disease genes from de novo exonic copy number variants
Genome Medicine, 2017
Neural Wiskott–Aldrich Syndrome Protein
Springer eBooks, 2012
Genetic Neuromuscular Disorders
2014
The Journal of Headache and Pain, 2015
Functional Genomics of Lung Disease
American Journal of Respiratory Cell and Molecular Biology, 2004
Analysis of disease-associated objects at the Rat Genome Database
Database, 2013
Complete Genomic Screen in Parkinson Disease
JAMA, 2001
Related topics
BiologyMedicineGene ontologyBiochemistry and cell biologyGene expression profilingfibroblasts