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American Journal of Physiology. Lung Cellular and Molecular Physiology|March 9, 2018
Time-resolved proteome profiling of normal lung developmentAhmed Moghieb, Geremy Clair, Hugh D Mitchell, et al.
ACS Chemical Biology|October 31, 2013
Live cell chemical profiling of temporal redox dynamics in a photoautotrophic cyanobacteriumNatalie C Sadler, Matthew R Melnicki, Margrethe H Serres, et al.
Frontiers in Bioengineering and Biotechnology|February 15, 2021
Multi-Omics Driven Metabolic Network Reconstruction and Analysis of Lignocellulosic Carbon Utilization in Rhodosporidium toruloidesJoonhoon Kim, Samuel T Coradetti, Young-Mo Kim, et al.
Scientific Reports|December 23, 2016
Spatially-Resolved Proteomics: Rapid Quantitative Analysis of Laser Capture Microdissected Alveolar Tissue SamplesGeremy Clair, Paul D Piehowski, Teodora Nicola, et al.
Next Research|January 19, 2026
Persistent urinary metabolic signatures in children with type 1 diabetesErnesto S Nakayasu, Javier E Flores, Lisa M Bramer, et al.
Pharmacology Research & Perspectives|February 23, 2022
Effects of pharmacological inhibition of the sodium-dependent phosphate cotransporter 2b (NPT2b) on intestinal phosphate absorption in mouse and rat modelsXiaojun Wang, Yanping Xu, Xiaohong Yu, et al.
American Journal of Medical Genetics. Part A|February 28, 2012
A phenotype map for 14q32.3 terminal deletionsHartmut Engels, Herdit M Schüler, Alexander M Zink, et al.
American Journal of Human Genetics|March 13, 2012
Haploinsufficiency of ARID1B, a member of the SWI/SNF-a chromatin-remodeling complex, is a frequent cause of intellectual disabilityJuliane Hoyer, Arif B Ekici, Sabine Endele, et al.
Molecular Syndromology|April 10, 2014
Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studiesA M Zink, E Wohlleber, H Engels, et al.
American Journal of Medical Genetics. Part A|November 19, 2016
De novo microdeletions and point mutations affecting SOX2 in three individuals with intellectual disability but without major eye malformationsNicola Dennert, Hartmut Engels, Kirsten Cremer, et al.
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