Found: 11
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Prestin-prestin and prestin-GLUT5 interactions in HEK293T cells.
- Published in:
- Developmental Neurobiology (19328451), 2007, v. 67, n. 4, p. 483, doi. 10.1002/dneu.20357
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- Article
The Conserved Tetrameric Subunit Stoichiometry of Slc26 Proteins.
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- Microscopy & Microanalysis, 2013, v. 19, n. 4, p. 799, doi. 10.1017/S1431927613000457
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- Publication type:
- Article
Author Correction: Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system.
- Published in:
- 2024
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- Publication type:
- Correction Notice
Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-023-51137-6
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- Publication type:
- Article
Corrigendum: Loss of LDAH associated with prostate cancer and hearing loss.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 10, p. 1753, doi. 10.1093/hmg/ddz036
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- Publication type:
- Article
Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 9, p. 1474, doi. 10.1093/hmg/ddy436
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- Publication type:
- Article
Loss of LDAH associated with prostate cancer and hearing loss.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 24, p. 4194, doi. 10.1093/hmg/ddy310
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- Publication type:
- Article
Expanding a Wastewater-Based Surveillance Methodology for DNA Isolation from a Workflow Optimized for SARS-CoV-2 RNA Quantification.
- Published in:
- Journal of Biomolecular Techniques, 2023, v. 34, n. 4, p. 1, doi. 10.7171/3fc1f5fe.dfa8d906
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- Publication type:
- Article
A Rapid, Isothermal, and Point-of-Care System for COVID-19 Diagnostics.
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- Journal of Biomolecular Techniques, 2021, v. 32, n. 3, p. 221, doi. 10.7171/jbt.21-3203-019
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- Publication type:
- Article
TAF1 Transcripts and Neurofilament Light Chain as Biomarkers for X‐linked Dystonia‐Parkinsonism.
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- Movement Disorders, 2021, v. 36, n. 1, p. 206, doi. 10.1002/mds.28305
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- Publication type:
- Article
Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome.
- Published in:
- Genome Biology, 2017, v. 18, p. 1, doi. 10.1186/s13059-017-1158-6
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- Publication type:
- Article