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Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|March 14, 2021
NUTM1-rearranged colorectal sarcoma: a clinicopathologically and genetically distinctive malignant neoplasm with a poor prognosisBenjamin J Van Treeck, Judith Jebastin Thangaiah, Jorge Torres-Mora, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 2004
Mitochondrial localization of estrogen receptor betaShao-Hua Yang, Ran Liu, Evelyn J Perez, et al.
American Journal of Medical Genetics. Part A|March 27, 2013
Fractures in children with neurofibromatosis type 1 from two NF clinicsJaya K George-Abraham, Lisa J Martin, Heidi J Kalkwarf, et al.
Journal of Materials Chemistry. B|October 5, 2018
Elastic serum-albumin based hydrogels: mechanism of formation and application in cardiac tissue engineeringNadav Amdursky, Manuel M Mazo, Michael R Thomas, et al.
The New England Journal of Medicine|April 16, 2015
Apremilast for Behçet's syndrome--a phase 2, placebo-controlled studyGulen Hatemi, Melike Melikoglu, Recep Tunc, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 16, 2015
Assessing the utility of confirmatory studies following identification of large-scale genomic imbalances by microarrayJennifer N Sanmann, Diane L Pickering, Denae M Golden, et al.
Chemistry of Materials : a Publication of the American Chemical Society|September 23, 2016
Electroconductive Hydrogel Based on Functional Poly(Ethylenedioxy Thiophene)Damia Mawad, Arbel Artzy-Schnirman, Joanne Tonkin, et al.
Chest|October 7, 2010
Risk of symptomatic DVT associated with peripherally inserted central cathetersR Scott Evans, Jamie H Sharp, Lorraine H Linford, et al.
ACS Nano|December 8, 2017
Platinum Nanocatalyst Amplification: Redefining the Gold Standard for Lateral Flow Immunoassays with Ultrabroad Dynamic RangeColleen N Loynachan, Michael R Thomas, Eleanor R Gray, et al.
Brain : a Journal of Neurology|March 1, 1997
Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factorN C Fox, A M Kennedy, R J Harvey, et al.
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