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Current Protocols|February 17, 2023
Acetylcholinesterase Activity Staining in Freshwater PlanariansChristina Rabeler, TaiXi Gong, Danielle Ireland, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|January 28, 2015
Transparent reporting of a multivariable prediction model for individual prognosis or diagnosis (TRIPOD): the TRIPOD statementG S Collins, J B Reitsma, D G Altman, et al.
The Journal of Craniofacial Surgery|January 8, 2026
Rothwell Classification of AI and Internet Search Results in Blepharoplasty Related QueriesAlexandrea S Collins, Taylor E Kring, Mark Jessup, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 26, 2019
Nebulizer cleaning and disinfection practices in families with cystic fibrosis: The relationship between attitudes, practice and microbe colonizationThomas S Murray, Timothy K O'Rourke, Richard Feinn, et al.
Neurotoxicology and Teratology|April 4, 2019
Screening for neurotoxic potential of 15 flame retardants using freshwater planariansSiqi Zhang, Danielle Ireland, Nisha S Sipes, et al.
Epigenetics & Chromatin|July 17, 2015
Motif signatures in stretch enhancers are enriched for disease-associated genetic variantsDaniel X Quang, Michael R Erdos, Stephen C J Parker, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 23, 1997
Characterization of the CHD family of proteinsT Woodage, M A Basrai, A D Baxevanis, et al.
Mechanisms of Development|April 28, 2009
In vitro hematopoietic differentiation of mouse embryonic stem cells requires the tumor suppressor menin and is mediated by Hoxa9Elizabeth Novotny, Sheila Compton, P Paul Liu, et al.
Surgical Laparoscopy, Endoscopy & Percutaneous Techniques|August 21, 2009
Different perception of surgical risks between physicians and patients undergoing laparoscopic cholecystectomyMassimiliano Tuveri, Giovanni Caocci, Fabio Efficace, et al.
Neuromuscular Disorders : NMD|February 24, 2012
A case of myelopathy, myopathy, peripheral neuropathy and subcortical grey matter degeneration associated with recessive compound heterozygous POLG1 mutationsP McKelvie, R Marotta, D R Thorburn, et al.
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