The MicrobeThe CRISPR-Cas systems, initially identified as bacterial defense mechanisms, have become innovative tools for genetic research and translational therapeutics. These systems are made up of clustered regularly interspaced short palindromic repeats (CRISPR)
Kamran Saeed +3 more
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Oculomotor Apraxia as an Early Presenting Sign of Juvenile‐Onset Huntington's Disease [PDF]
, 2023 Emily A. Innes +4 more
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Lentiviral Vector-Mediated Gene Transfer and RNA Silencing Technology in Neuronal Dysfunctions [PDF]
, 2018 Lentiviral-mediated gene transfer in vivo or in cultured mammalian neurons can be used to address a wide variety of biological questions, to design animals models for specific neurodegenerative pathologies, or to test potential therapeutic approaches in ...
Dreyer, Jean-Luc
core
The impact of molecular biology on clinical neurology. [PDF]
, 2001 Advances in molecular biology have increased our understanding of both inherited and sporadic forms of neurological disease. In this review, the impact of these advances is discussed in relation to specific neurological conditions.
Ho, SL, Mak, W
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Juvenile‐Onset Huntington's Disease in Peru: A Case Series of 32 Patients
, 2022 Anastasia Vishnevetsky +7 more
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A-49Early Identification of Neurocognitive Deficits and Symptom Manifestation Associated with Juvenile Huntington's Disease (JHD) in a Preschooler: A Pediatric Case Study [PDF]
, 2017 Charles Cederberg +2 more
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Developing Stem Cell Therapies for Juvenile and Adult-Onset Huntington's Disease
, 2015 Kyle D. Fink +9 more
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Wheel running from a juvenile age delays onset of specific motor deficits but does not alter protein aggregate density in a mouse model of Huntington's disease [PDF]
, 2008 Anton van Dellen +4 more
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SPATIAL MEMORY IN HUNTINGTON'S DISEASE: A COMPARATIVE REVIEW OF HUMAN AND ANIMAL DATA [PDF]
, 2016 Fink, Kyle D +4 more
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