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Lab on a Chip|January 28, 2015
An integrated optofluidic device for single-cell sorting driven by mechanical propertiesT Yang, P Paiè, G Nava, et al.
Biomacromolecules|February 19, 2015
Tough coating proteins: subtle sequence variation modulates cohesionSaurabh Das, Dusty R Miller, Yair Kaufman, et al.
ACS Bio & Med Chem Au|August 26, 2024
Mass Spectrometry-Based Protein Footprinting Defines the Binding Pocket of Crotonylated H3K14 in the PHD1 Domain of BAF45D within the BAF Chromatin Remodeling ComplexMarissa R Martinez, Janna Kiselar, Benlian Wang, et al.
World Neurosurgery|May 12, 2026
Venous sinus stenting in idiopathic intracranial hypertension: a systematic review of an emerging intervention with favorable outcomes but unresolved standardizationJose A Figueroa-Sanchez, Francisco A Luna-Rangel, Hector R Martinez, et al.
Archives of General Psychiatry|August 1, 1987
The Spanish Diagnostic Interview Schedule. Reliability and concordance with clinical diagnoses in Puerto RicoG J Canino, H R Bird, P E Shrout, et al.
The American Journal of Tropical Medicine and Hygiene|October 1, 1995
Biochemical systematics and population genetic structure of Anopheles pseudopunctipennis, vector of malaria in Central and South AmericaS Manguin, D R Roberts, E L Peyton, et al.
The Journal of Surgical Research|January 10, 2013
Nomograms to predict risk of in-hospital and post-discharge venous thromboembolism after abdominal and thoracic surgery: an American College of Surgeons National Surgical Quality Improvement Program analysisDhruvil R Shah, Hui Wang, Richard J Bold, et al.
The Journal of Infectious Diseases|August 8, 2013
Staphylococcal Enterotoxin B-specific monoclonal antibody 20B1 successfully treats diverse Staphylococcus aureus infectionsAvanish K Varshney, Xiaobo Wang, Matthew D Scharff, et al.
Journal of Instrumentation : an IOP and SISSA Journal|June 11, 2013
Energy and coincidence time resolution measurements of CdTe detectors for PETG Ariño, M Chmeissani, G De Lorenzo, et al.
Genes, Brain, and Behavior|October 15, 2013
Identification and biochemical characterization of the novel mutation m.8839G>C in the mitochondrial ATP6 gene associated with NARP syndromeA Blanco-Grau, I Bonaventura-Ibars, J Coll-Cantí, et al.
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