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Showing 1 - 20 results of 72 for search '(( _ nat ((comp OR com) OR cap) can now ) OR ((( d nair clamp a new ) OR ( j ed conts van ngoc ))))', query time: 1.37s Refine Results
Functional Analysis of the Kv1.1 N255D Mutation Associated with Autosomal Dominant Hypomagnesemia
36th International Symposium on Intensive Care and Emergency Medicine: Brussels, Belgium. 15-18 March 2016

The yeast global transcriptional co-repressor protein Cyc8 can propagate as a prion
Somatic Mutations in the Angiopoietin-Receptor TIE2 Can Cause Both Solitary and Multiple Sporadic Venous Malformations

Glycosylation in health and disease
Three decades of nanopore sequencing

Fine-mapping in the MHC region accounts for 18% additional genetic risk for celiac disease
Quantitative optical trapping on single cellular organelles in cell extract

Differential confounding of rare and common variants in spatially structured populations
Increased proteasomal activity supports photoreceptor survival in inherited retinal degeneration

Advancing the speed, sensitivity and accuracy of biomolecular detection using multi-length-scale engineering
Mechanically axially chiral catenanes and noncanonical mechanically axially chiral rotaxanes

Optogenetic pharmacology for control of native neuronal signaling proteins
Autocatalytic aptazymes enable ligand-dependent exponential amplification of RNA

Measurement of Atom Resolvability in CryoEM Maps with Q-scores
FOXA1 is a critical determinant of Estrogen Receptor function and endocrine response

A photoconvertible fluorescent reporter to track chaperone-mediated autophagy
Phosphorylation switches the general splicing repressor SRp38 to a sequence-specific activator

Phymm and PhymmBL: Metagenomic Phylogenetic Classification with Interpolated Markov Models
Invariant natural killer T cells recognize lipid self-antigen induced by microbial danger signals

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