Literature for DOID 12858: Huntington's disease
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Denotes literature images)
Introduction to nucleocytoplasmic transport: molecules and mechanisms.,
Peters R,
Methods Mol Biol. January 1, 2006; 322:1940-6029.
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Simple sequence in brain and nervous system specific proteins.,
Huntley MA,Mahmood S,Golding GB,
Genome. April 1, 2005; 48(2):0831-2796.
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Expanded CTG triplet blocks from the myotonic dystrophy gene create the strongest known natural nucleosome positioning elements.,
Wang YH,Griffith J,
Genomics. January 20, 1995; 25(2):1089-8646.
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Huntingtin is required for ciliogenesis and neurogenesis during early Xenopus development.,
Haremaki T,Deglincerti A,Brivanlou AH,
Dev Biol. December 15, 2015; 408(2):1095-564X.
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Using Xenopus to understand human disease and developmental disorders.,
Sater AK,Moody SA,
Genesis. January 1, 2017; 55(1-2):1526-968X.
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Xenopus leads the way: Frogs as a pioneering model to understand the human brain.,
Exner CRT,Willsey HR,
Genesis. February 1, 2021; 59(1-2):1526-968X.
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Influence of Sox protein SUMOylation on neural development and regeneration.,
Chang KC,
Neural Regen Res. March 1, 2022; 17(3):1673-5374.
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Huntingtin CAG expansion impairs germ layer patterning in synthetic human 2D gastruloids through polarity defects.,
Galgoczi S,Ruzo A,Markopoulos C,Yoney A,Phan-Everson T,Li S,Haremaki T,Metzger JJ,Etoc F,Brivanlou AH,
Development. October 1, 2021; 148(19):1477-9129.
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