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Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function.
- Published in:
- EMBO Molecular Medicine, 2019, v. 11, n. 9, p. N.PAG, doi. 10.15252/emmm.201910288
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- Article
Testing of the Storm Water Management Model Low Impact Development Modules.
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- Journal of the American Water Resources Association, 2020, v. 56, n. 2, p. 283, doi. 10.1111/1752-1688.12832
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- Article
A holistic view of mouse enhancer architectures reveals analogous pleiotropic effects and correlation with human disease.
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- BMC Genomics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12864-020-07109-5
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- Article
Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutants.
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- BMC Biology, 2018, v. 16, n. 1, p. 1, doi. 10.1186/s12915-018-0530-7
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- Article
Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features.
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- Journal of Clinical Investigation, 2014, v. 124, n. 4, p. 1468, doi. 10.1172/JCI70372
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- Article
AGAINST A UNIFORM LAW ON THE INCOME TAXATION OF TRUSTS.
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- University of Louisville Law Review, 2023, v. 61, n. 2, p. 317
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- Article
A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways.
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- PLoS Genetics, 2017, v. 13, n. 8, p. 1, doi. 10.1371/journal.pgen.1006969
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- Article
Improving agreement of ASA physical status class between pre-anesthesia screening and day of surgery by adding institutional-specific and ASA-approved examples: a quality improvement project.
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- Perioperative Medicine, 2020, v. 9, n. 1, p. N.PAG, doi. 10.1186/s13741-020-00162-4
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- Article
Capturing sex-specific and hypofertility-linked effects of assisted reproductive technologies on the cord blood DNA methylome.
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- Clinical Epigenetics, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13148-023-01497-7
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- Article
Genetic Factors Regulating Lung Vasculature and Immune Cell Functions Associate with Resistance to Pneumococcal Infection.
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- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0089831
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- Article
Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.
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- PLoS Genetics, 2020, v. 16, n. 12, p. 1, doi. 10.1371/journal.pgen.1009190
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- Article
Application of ATAC-Seq for genomewide analysis of the chromatin state at single myofiber resolution.
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- eLife, 2022, p. 1, doi. 10.7554/eLife.72792
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- Article
Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements.
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- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-09184-z
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- Article
Customized MethylC-Capture Sequencing to Evaluate Variation in the Human Sperm DNA Methylome Representative of Altered Folate Metabolism.
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- Environmental Health Perspectives, 2019, v. 127, n. 8, p. 1, doi. 10.1289/EHP4812
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- Article
Celebrating Thirty Years of the Pace Law Review.
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- Pace Law Review, 2010, v. 30, n. 4, p. 1146, doi. 10.58948/2331-3528.1733
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- Article
Broad-spectrum XX and XY gonadal dysgenesis in patients with a homozygous L193S variant in PPP2R3C.
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- European Journal of Endocrinology, 2022, v. 186, n. 1, p. 65, doi. 10.1530/EJE-21-0910
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- Article
Large-scale analysis of circulating glutamate and adipose gene expression in relation to abdominal obesity.
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- Amino Acids, 2022, v. 54, n. 9, p. 1287, doi. 10.1007/s00726-022-03181-1
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- Article
Cleft palate and minor metabolic disturbances in a mouse global Arl15 gene knockout.
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- FASEB Journal, 2023, v. 37, n. 11, p. 1, doi. 10.1096/fj.202201918R
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- Article
Genic constraint against nonsynonymous variation across the mouse genome.
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- BMC Genomics, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12864-023-09637-2
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- Article
The digital revolution in phenotyping.
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- Briefings in Bioinformatics, 2016, v. 17, n. 5, p. 819, doi. 10.1093/bib/bbv083
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- Article
Increased DNA methylation variability in type 1 diabetes across three immune effector cell types.
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- Nature Communications, 2016, v. 7, n. 11, p. 13555, doi. 10.1038/ncomms13555
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- Article
Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.
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- Nature Communications, 2016, v. 7, n. 8, p. 12444, doi. 10.1038/ncomms12444
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- Article
Erratum: Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants.
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- Nature Communications, 2015, v. 6, n. 7, p. 8016, doi. 10.1038/ncomms9016
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- Article
Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants.
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- Nature Communications, 2015, v. 6, n. 5, p. 7211, doi. 10.1038/ncomms8211
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- Article
Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation.
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- Genome Biology, 2015, v. 16, p. 1, doi. 10.1186/s13059-015-0856-1
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- Article
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains.
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- Genome Biology, 2013, v. 14, n. 7, p. R82, doi. 10.1186/gb-2013-14-7-r82
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- Article
LAW FACULTY EXPERIENCES TEACHING DURING THE PANDEMIC.
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- St. Louis University Law Journal, 2021, v. 65, n. 3, p. 455
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- Article
THE FEDERAL FUTURE OF MEDICATION ABORTION.
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- Indiana Law Review, 2024, v. 57, n. 3, p. 613, doi. 10.18060/28359
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- Article
The Ebola Challenge: West and Central Africa's Containment Strategy.
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- Africa Policy Journal, 2014, v. 10, p. 67
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- Article
A genetic modifier suggests that endurance exercise exacerbates Huntington's disease.
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- Human Molecular Genetics, 2018, v. 27, n. 10, p. 1723, doi. 10.1093/hmg/ddy077
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- Article
A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicity.
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- Human Molecular Genetics, 2015, v. 24, n. 7, p. 1883, doi. 10.1093/hmg/ddu605
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- Article
Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb.
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- Human Molecular Genetics, 2012, v. 21, n. 8, p. 1706, doi. 10.1093/hmg/ddr605
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- Article
A graphical user interface (GUI) for model-based radiation-induced acoustic computed tomography.
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- Journal of Innovative Optical Health Sciences, 2023, v. 16, n. 1, p. 1, doi. 10.1142/S1793545822450043
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- Article
Modifiable Risk Factors for SARS-CoV-2.
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- Integrative Medicine: A Clinician's Journal, 2021, v. 20, n. 5, p. 8
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- Article
Mouse genomic and cellular annotations.
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- Mammalian Genome, 2022, v. 33, n. 1, p. 19, doi. 10.1007/s00335-021-09936-7
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- Article
Current strategies for mutation detection in phenotype-driven screens utilising next generation sequencing.
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- Mammalian Genome, 2015, v. 26, n. 9/10, p. 486, doi. 10.1007/s00335-015-9603-x
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- Article
High throughput sequencing approaches to mutation discovery in the mouse.
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- Mammalian Genome, 2012, v. 23, n. 9/10, p. 499, doi. 10.1007/s00335-012-9424-0
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- Article
Protection Against XY Gonadal Sex Reversal by a Variant Region on Mouse Chromosome 13.
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- Genetics, 2020, v. 214, n. 2, p. 467, doi. 10.1534/genetics.119.302786
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- Article
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.
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- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00595-4
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- Article
Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome.
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- Genome Biology, 2017, v. 18, p. 1, doi. 10.1186/s13059-017-1173-7
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- Article
RELIABLE SCIENCE: OVERCOMING PUBLIC DOUBTS IN THE CLIMATE CHANGE DEBATE.
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- William & Mary Environmental Law & Policy Review, 2012, v. 37, n. 1, p. 219
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- Article
Unlocking the Bottleneck in Forward Genetics Using Whole-Genome Sequencing and Identity by Descent to Isolate Causative Mutations.
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- PLoS Genetics, 2013, v. 9, n. 1, p. 1, doi. 10.1371/journal.pgen.1003219
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- Article
Integrative analysis of vascular endothelial cell genomic features identifies AIDA as a coronary artery disease candidate gene.
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- Genome Biology, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s13059-019-1749-5
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- Publication type:
- Article
Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome.
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- 2019
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- Publication type:
- Correction Notice
Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0273-4
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- Article
Making sense of the linear genome, gene function and TADs.
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- Epigenetics & Chromatin, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s13072-022-00436-9
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- Article
Making sense of the linear genome, gene function and TADs.
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- Epigenetics & Chromatin, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s13072-022-00436-9
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- Article
Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis.
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- Journal of Bone & Mineral Research, 2019, v. 34, n. 7, p. 1324, doi. 10.1002/jbmr.3695
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- Article
An N‐Ethyl‐N‐Nitrosourea (ENU)‐Induced Tyr265Stop Mutation of the DNA Polymerase Accessory Subunit Gamma 2 (Polg2) Is Associated With Renal Calcification in Mice.
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- Journal of Bone & Mineral Research, 2019, v. 34, n. 3, p. 497, doi. 10.1002/jbmr.3624
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- Article
Protein coalitions in a core mammalian biochemical network linked by rapidly evolving proteins.
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- BMC Evolutionary Biology, 2011, v. 11, n. 1, p. 142, doi. 10.1186/1471-2148-11-142
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- Article