Ramee Lee

发表

Sortilin is essential for proNGF-induced neuronal cell death

Barbara L. Hempstead, Thomas E. Willnow, P. Madsen, 2004, Nature.

Regulation of Cell Survival by Secreted Proneurotrophins

Barbara L. Hempstead, K. Teng, B. Hempstead, 2001, Science.

Modulation of huntingtin degradation by cAMP-dependent protein kinase A (PKA) phosphorylation of C-HEAT domain Ser2550

M. MacDonald, Ji-Joon Song, Steve Carr, 2022, bioRxiv.

Pro-NGF isolated from the human brain affected by Alzheimer's disease induces neuronal apoptosis mediated by p75NTR.

M. Iglesias, B. Hempstead, I. Ferrer, 2005, The American journal of pathology.

ProNGF Induces p75-Mediated Death of Oligodendrocytes following Spinal Cord Injury

J. Kim, M. Beattie, J. Bresnahan, 2002, Neuron.

Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects.

P. Holmans, T. Gillis, J. Mysore, 2020, American journal of human genetics.

ProBDNF Induces Neuronal Apoptosis via Activation of a Receptor Complex of p75NTR and Sortilin

Barbara L. Hempstead, Ramiro D. Almeida, F. Lee, 2005, The Journal of Neuroscience.

Full sequence of mutant huntingtin 3′-untranslated region and modulation of its gene regulatory activity by endogenous microRNA

M. MacDonald, J. Gusella, I. Seong, 2019, Journal of Human Genetics.

Novel DNA Aptamers that Bind to Mutant Huntingtin and Modify Its Activity

M. MacDonald, Ji-Joon Song, I. Seong, 2018, Molecular therapy. Nucleic acids.

Novel allele-specific quantification methods reveal no effects of adult onset CAG repeats on HTT mRNA and protein levels

T. Gillis, M. MacDonald, J. Gusella, 2017, Human molecular genetics.

Promotion of somatic CAG repeat expansion by Fan1 knock-out in Huntington’s disease knock-in mice is blocked by Mlh1 knock-out

T. Gillis, J. Mysore, M. MacDonald, 2020, Human molecular genetics.

IKBKB reduces huntingtin aggregation by phosphorylating serine 13 via a non-canonical IKK pathway

A. Caricasole, C. Dominguez, Ramee Lee, 2022, Life Science Alliance.

Ultrasensitive quantitative measurement of huntingtin phosphorylation at residue S13.

D. Lavery, A. Caricasole, H. Lashuel, 2020, Biochemical and biophysical research communications.

Mutations causing Lopes-Maciel-Rodan Syndrome are huntingtin hypomorphs.

Ryan L. Collins, T. Gillis, J. Mysore, 2021, Human molecular genetics.

Random Uptake Conditions the Hit-and-run Method High-flux Backbone

P. Madsen, K. Teng, B. Hempstead, 2022 .

Zic2 Regulates Retinal Ganglion Cell Axon Avoidance of ephrinB2 through Inducing Expression of the Guidance Receptor EphB1

C. Mason, Ramee Lee, Timothy J. Petros, 2008, The Journal of Neuroscience.

A Novel p75 Neurotrophin Receptor-Related Protein, NRH2, Regulates Nerve Growth Factor Binding to the TrkA Receptor

B. Hempstead, M. Chao, S. Murray, 2004, The Journal of Neuroscience.

Expression analysis of Huntington disease mouse models reveals robust striatum disease signatures

A. Caricasole, J. Obenauer, Ramee Lee, 2022, bioRxiv.

Human mutant huntingtin disrupts vocal learning in transgenic songbirds

A. Miyanohara, Wan‐chun Liu, M. Marsala, 2015, Nature Neuroscience.

A role for FAN1 in suppressing somatic CAG expansion, combined with the onset-delaying effect of the

T. Gillis, J. Mysore, M. MacDonald, 2020 .

A role for FAN1 in suppressing somatic CAG expansion, combined with the onset-delaying effect of the

T. Gillis, J. Mysore, M. MacDonald, 2022 .