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Science (New York, N.Y.)|June 16, 2001
Loss of huntingtin-mediated BDNF gene transcription in Huntington's diseaseC Zuccato, A Ciammola, D Rigamonti, et al.
Human Molecular Genetics|March 1, 1993
The isolation of cDNAs within the Huntington disease region by hybridisation of yeast artificial chromosomes to a cDNA libraryR G Snell, L A Doucette-Stamm, K M Gillespie, et al.
Neuro-Oncology Advances|June 16, 2023
The prognostic impact of subclonal IDH1 mutation in grade 2-4 astrocytomasMeenakshi Vij, Raquel T Yokoda, Omid Rashidipour, et al.
Neurology|August 28, 2002
Clinical and genetic heterogeneity in benign hereditary choreaG J Breedveld, A K Percy, M E MacDonald, et al.
American Journal of Physiology. Heart and Circulatory Physiology|October 21, 2022
Smad3 promotes adverse cardiovascular remodeling and dysfunction in doxorubicin-treated heartsMelissa S Cobb, Shixin Tao, Katherine Shortt, et al.
Immunity|March 17, 2007
Ikaros DNA-binding proteins as integral components of B cell developmental-stage-specific regulatory circuitsElizabeth C Thompson, Bradley S Cobb, Pierangela Sabbattini, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 2008
T cell receptor signaling controls Foxp3 expression via PI3K, Akt, and mTORStephan Sauer, Ludovica Bruno, Arnulf Hertweck, et al.
Annals of Neurology|February 24, 2001
Quantitative neuropathological changes in presymptomatic Huntington's diseaseE Gómez-Tortosa, M E MacDonald, J C Friend, et al.
The Journal of Experimental Medicine|October 21, 2009
Runx proteins regulate Foxp3 expressionLudovica Bruno, Luca Mazzarella, Maarten Hoogenkamp, et al.
Somatic Cell and Molecular Genetics|July 14, 1998
Exon trapping and sequence-based methods of gene finding in transcript mapping of human 4p16.3I Pribill, G T Barnes, J Chen, et al.
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