User profiles for Nathan R. Wilson
 | Nathan R. WilsonCo-Founder and CTO, Nara Logics, Inc. Verified email at mit.edu Cited by 4096 |
[HTML][HTML] Regulation of dendritic spine morphology and synaptic function by Shank and Homer
The Shank family of proteins interacts with NMDA receptor and metabotropic glutamate
receptor complexes in the postsynaptic density (PSD). Targeted to the PSD by a PDZ-dependent …
receptor complexes in the postsynaptic density (PSD). Targeted to the PSD by a PDZ-dependent …
Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice
Rett Syndrome (RTT) is a severe form of X-linked mental retardation caused by mutations in
the gene coding for methyl CpG-binding protein 2 (MECP2). Mice deficient in MeCP2 have a …
the gene coding for methyl CpG-binding protein 2 (MECP2). Mice deficient in MeCP2 have a …
Division and subtraction by distinct cortical inhibitory networks in vivo
Brain circuits process information through specialized neuronal subclasses interacting
within a network. Revealing their interplay requires activating specific cells while monitoring …
within a network. Revealing their interplay requires activating specific cells while monitoring …
Presynaptic regulation of quantal size by the vesicular glutamate transporter VGLUT1
A fundamental question in synaptic physiology is whether the unitary strength of a synapse
can be regulated by presynaptic characteristics and, if so, what those characteristics might be…
can be regulated by presynaptic characteristics and, if so, what those characteristics might be…
[PDF][PDF] Response features of parvalbumin-expressing interneurons suggest precise roles for subtypes of inhibition in visual cortex
Inhibitory interneurons in the cerebral cortex include a vast array of subtypes, varying in
their molecular signatures, electrophysiological properties, and connectivity patterns. This …
their molecular signatures, electrophysiological properties, and connectivity patterns. This …
Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive aplastic anemia
…, SK Rafi, AJ Olm-Shipman, NR Wilson… - Blood, The Journal …, 2013 - ashpublications.org
We recently identified 2 siblings afflicted with idiopathic, autosomal recessive aplastic
anemia. Whole-exome sequencing identified a novel homozygous missense mutation in …
anemia. Whole-exome sequencing identified a novel homozygous missense mutation in …
[HTML][HTML] SPECC1L deficiency results in increased adherens junction stability and reduced cranial neural crest cell delamination
NR Wilson, AJ Olm-Shipman, DS Acevedo… - Scientific reports, 2016 - nature.com
Cranial neural crest cells (CNCCs) delaminate from embryonic neural folds and migrate to
pharyngeal arches, which give rise to most mid-facial structures. CNCC dysfunction plays a …
pharyngeal arches, which give rise to most mid-facial structures. CNCC dysfunction plays a …
Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB …
… Nathan R Wilson4, … Stewart R … Durbin R …
Central nervous system involvement in blastic plasmacytoid dendritic cell neoplasm
N Pemmaraju, NR Wilson, JD Khoury… - Blood, The Journal …, 2021 - ashpublications.org
… Nathaniel R. Wilson … Clinical profile of IMGN632, a novel CD123-targeting antibody-drug
conjugate (ADC), in patients with relapsed/refractory (R/R) blastic plasmacytoid dendritic cell …
conjugate (ADC), in patients with relapsed/refractory (R/R) blastic plasmacytoid dendritic cell …
Novel therapeutic approaches in blastic plasmacytoid dendritic cell neoplasm (BPDCN): era of targeted therapy
NR Wilson, M Konopleva, JD Khoury… - … Lymphoma Myeloma and …, 2021 - Elsevier
Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare hematologic malignancy
arising from the aberrant transformation of plasmacytoid dendritic cells (pDCs) and involving …
arising from the aberrant transformation of plasmacytoid dendritic cells (pDCs) and involving …