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The Journal of Biological Chemistry|April 27, 2012
Proteomic and metabolomic analyses of mitochondrial complex I-deficient mouse model generated by spontaneous B2 short interspersed nuclear element (SINE) insertion into NADH dehydrogenase (ubiquinone) Fe-S protein 4 (Ndufs4) geneDillon W Leong, Jasper C Komen, Chelsee A Hewitt, et al.
Scientific Reports|May 28, 2017
A novel, somatic, transforming mutation in the extracellular domain of Epidermal Growth Factor Receptor identified in myeloproliferative neoplasmD A Casolari, T Nguyen, C M Butcher, et al.
JCI Insight|February 10, 2025
Regulation of lung progenitor plasticity and repair by fatty acid oxidationQuetzalli D Angeles-Lopez, Jhonny Rodriguez-Lopez, Paula Agudelo Garcia, et al.
The European Respiratory Journal|August 11, 2018
Evaluation of the airway microbiome in nontuberculous mycobacteria diseaseImran Sulaiman, Benjamin G Wu, Yonghua Li, et al.
Data in Brief|March 10, 2016
In depth analysis of the Sox4 gene locus that consists of sense and natural antisense transcriptsKing-Hwa Ling, Peter J Brautigan, Sarah Moore, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|February 24, 2001
Lipid-altering efficacy and safety of simvastatin 80 mg/day: worldwide long-term experience in patients with hypercholesterolemiaM H Davidson, E A Stein, D B Hunninghake, et al.
Medrxiv : the Preprint Server for Health Sciences|February 17, 2021
Emergence in late 2020 of multiple lineages of SARS-CoV-2 Spike protein variants affecting amino acid position 677Emma B Hodcroft, Daryl B Domman, Daniel J Snyder, et al.
Blood Cancer Journal|April 11, 2023
TP53 mutation variant allele frequency of ≥10% is associated with poor prognosis in therapy-related myeloid neoplasmsMithun Vinod Shah, Elizabeth Ngoc Hoa Tran, Syed Shah, et al.
JAMA Cardiology|March 29, 2026
Pregnancy-Associated Spontaneous Coronary Artery Dissection: A Report of the iSCAD RegistryAgnes Koczo, Anna Grodzinsky, Esther S H Kim, et al.
Ophthalmology|October 29, 2015
North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13Kent W Small, Adam P DeLuca, S Scott Whitmore, et al.
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