Found: 9
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CRISPR/Cas9-mediated gene editing ameliorates neurotoxicity in mouse model of Huntington's disease.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Virtual clinicopathologic correlation rounds for inpatient consult skin biopsies during the COVID‐19 pandemic: A quality improvement study.
- Published in:
- Journal of Cutaneous Pathology, 2022, v. 49, n. 1, p. 107, doi. 10.1111/cup.14133
- By:
- Publication type:
- Article
Targeted Histone Peptides: Insights into the Spatial Regulation of the Methyltransferase PRC2 by using a Surrogate of Heterotypic Chromatin.
- Published in:
- Angewandte Chemie International Edition, 2015, v. 54, n. 22, p. 6457, doi. 10.1002/anie.201500085
- By:
- Publication type:
- Article
Targeted Histone Peptides: Insights into the Spatial Regulation of the Methyltransferase PRC2 by using a Surrogate of Heterotypic Chromatin.
- Published in:
- Angewandte Chemie, 2015, v. 127, n. 22, p. 6557, doi. 10.1002/ange.201500085
- By:
- Publication type:
- Article
Fragile X-Associated Tremor/Ataxia Syndrome: From Molecular Pathogenesis to Development of Therapeutics.
- Published in:
- Frontiers in Cellular Neuroscience, 2017, v. 11, p. 1, doi. 10.3389/fncel.2017.00128
- By:
- Publication type:
- Article
Tools to study the severity of itch in 8‐ to 17‐year‐old children: Validation of TweenItchyQoL and ItchyQuant.
- Published in:
- Pediatric Dermatology, 2021, v. 38, n. 5, p. 1118, doi. 10.1111/pde.14662
- By:
- Publication type:
- Article
Pruritus assessment tools for 6 to 7‐year‐old children: KidsItchyQoL and ItchyQuant.
- Published in:
- Pediatric Dermatology, 2021, v. 38, n. 3, p. 591, doi. 10.1111/pde.14563
- By:
- Publication type:
- Article
Cell type-specific DNA methylome signatures reveal epigenetic mechanisms for neuronal diversity and neurodevelopmental disorder.
- Published in:
- Human Molecular Genetics, 2023, v. 32, n. 2, p. 218, doi. 10.1093/hmg/ddac189
- By:
- Publication type:
- Article
Metabolic pathways modulate the neuronal toxicity associated with fragile X-associated tremor/ataxia syndrome.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 6, p. 980, doi. 10.1093/hmg/ddy410
- By:
- Publication type:
- Article