David Housman

Affiliations: 
Massachusetts Institute of Technology, Cambridge, MA, United States 
Area:
Human Genetics, Huntington's disease, Myotonic dystrophy, Fragile-X syndrome
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"David Housman"
Mean distance: 14.54 (cluster 11)
 

Parents

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Harvey  F. Lodish post-doc (Cell Biology Tree)

Children

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J. Michael Andresen research assistant UMN
James (Jim) F. Gusella grad student
Robert Levenson grad student MIT
Heather L. Hinds grad student 1991-1993 MIT
Jill R. Crittenden post-doc MIT
Daniel A. Haber post-doc MIT (Cell Biology Tree)
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Publications

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Crittenden JR, Tillberg PW, Riad MH, et al. (2016) Striosome-dendron bouquets highlight a unique striatonigral circuit targeting dopamine-containing neurons. Proceedings of the National Academy of Sciences of the United States of America
Ouyang Q, Nakayama T, Baytas O, et al. (2016) Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features. Proceedings of the National Academy of Sciences of the United States of America
Ochaba J, Lukacsovich T, Csikos G, et al. (2014) Potential function for the Huntingtin protein as a scaffold for selective autophagy. Proceedings of the National Academy of Sciences of the United States of America. 111: 16889-94
Bugiardini E, Meola G, Alvarez C, et al. (2014) Consensus on cerebral involvement in myotonic dystrophy. Workshop report: May 24-27, 2013, Ferrere (AT), Italy Neuromuscular Disorders. 24: 445-452
Gipson TA, Neueder A, Wexler NS, et al. (2013) Aberrantly spliced HTT, a new player in Huntington's disease pathogenesis. Rna Biology. 10: 1647-52
Boissonneault KR, Henningsen BM, Bates SS, et al. (2013) Gene expression studies for the analysis of domoic acid production in the marine diatom Pseudo-nitzschia multiseries. Bmc Molecular Biology. 14: 25
Vashishtha M, Ng CW, Yildirim F, et al. (2013) Targeting H3K4 trimethylation in Huntington disease. Proceedings of the National Academy of Sciences of the United States of America. 110: E3027-36
Sontag EM, Joachimiak LA, Tan Z, et al. (2013) Exogenous delivery of chaperonin subunit fragment ApiCCT1 modulates mutant Huntingtin cellular phenotypes. Proceedings of the National Academy of Sciences of the United States of America. 110: 3077-82
Ng CW, Yildirim F, Yap YS, et al. (2013) Extensive changes in DNA methylation are associated with expression of mutant huntingtin. Proceedings of the National Academy of Sciences of the United States of America. 110: 2354-9
Sathasivam K, Neueder A, Gipson TA, et al. (2013) Aberrant splicing of HTT generates the pathogenic exon 1 protein in Huntington disease. Proceedings of the National Academy of Sciences of the United States of America. 110: 2366-70
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