Found: 15
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Magnetic Resonance Acoustic Radiation Force Imaging (MR-ARFI) for the monitoring of High Intensity Focused Ultrasound (HIFU) ablation in anisotropic tissue.
- Published in:
- MAGMA: Magnetic Resonance Materials in Physics, Biology & Medicine, 2023, v. 36, n. 5, p. 737, doi. 10.1007/s10334-023-01062-6
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- Publication type:
- Article
Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy.
- Published in:
- Movement Disorders Clinical Practice, 2020, v. 7, n. 8, p. 940, doi. 10.1002/mdc3.13086
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- Publication type:
- Article
Impact of changes to policy for Mexican risk travel on Canadian blood donor deferrals.
- Published in:
- Blood Transfusion (17232007), 2013, v. 11, n. 4, p. 580, doi. 10.2450/2013.0261-12
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- Publication type:
- Article
Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportion.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Autosomal recessive cerebellar ataxia caused by a homozygous mutation in PMPCA.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
A pseudouridine synthase module is essential for mitochondrial protein synthesis and cell viability.
- Published in:
- EMBO Reports, 2017, v. 18, n. 1, p. 28, doi. 10.15252/embr.201643391
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- Publication type:
- Article
The leukodystrophy mutation Polr3b R103H causes homozygote mouse embryonic lethality and impairs RNA polymerase III biogenesis.
- Published in:
- Molecular Brain, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13041-019-0479-7
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- Publication type:
- Article
Sacs R272C missense homozygous mice develop an ataxia phenotype.
- Published in:
- Molecular Brain, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13041-019-0438-3
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- Publication type:
- Article
Absence of neurological abnormalities in mice homozygous for the Polr3a G672E hypomyelinating leukodystrophy mutation.
- Published in:
- Molecular Brain, 2017, v. 10, p. 1, doi. 10.1186/s13041-017-0294-y
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- Publication type:
- Article
Live single-cell laser tag.
- Published in:
- Nature Communications, 2016, v. 7, n. 5, p. 11636, doi. 10.1038/ncomms11636
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- Publication type:
- Article
Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III.
- Published in:
- Nature Communications, 2015, v. 6, n. 7, p. 7623, doi. 10.1038/ncomms8623
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- Publication type:
- Article
Intronic small nucleolar RNAs regulate host gene splicing through base pairing with their adjacent intronic sequences.
- Published in:
- Genome Biology, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s13059-023-03002-y
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- Publication type:
- Article
Revealing nascent RNA processing dynamics with nano-COP.
- Published in:
- Nature Protocols, 2021, v. 16, n. 3, p. 1343, doi. 10.1038/s41596-020-00469-y
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- Publication type:
- Article
Mutations in GALC cause late-onset Krabbe disease with predominant cerebellar ataxia.
- Published in:
- Neurogenetics, 2016, v. 17, n. 2, p. 137, doi. 10.1007/s10048-016-0476-2
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- Publication type:
- Article
A novel frameshift mutation in FGF14 causes an autosomal dominant episodic ataxia.
- Published in:
- Neurogenetics, 2015, v. 16, n. 3, p. 233, doi. 10.1007/s10048-014-0436-7
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- Publication type:
- Article