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Methods in Molecular Biology (Clifton, N.J.)|September 3, 2013
Optimizing E. coli-based membrane protein production using Lemo21(DE3) and GFP-fusionsAnna Hjelm, Susan Schlegel, Thomas Baumgarten, et al.
European Journal of Endocrinology|June 23, 2026
Universal screening to detect hypothyroidism in pregnant womenStine Linding Andersen, Maja Hjelm Lundgaard, Nanna Maria Uldall Torp, et al.
Pediatric Pulmonology|January 6, 2025
Growth, Body Composition, and Strength of Children With Cystic Fibrosis Treated With Elexacaftor/Tezacaftor/Ivacaftor (ETI)Thomas Boat, Md Monir Hossain, Aisaku Nakamura, et al.
American Journal of Human Genetics|January 23, 1999
Rapid clearance of fetal DNA from maternal plasmaY M Lo, J Zhang, T N Leung, et al.
Cancer Research|August 27, 1999
Quantitative analysis of aberrant p16 methylation using real-time quantitative methylation-specific polymerase chain reactionY M Lo, I H Wong, J Zhang, et al.
Health Informatics Journal|September 1, 2022
Older persons' experience of eHealth services in home health care: A meta-ethnography eHealth services in home health careTerese Lindberg, Boel Sandström, Ewa K Andersson, et al.
Inorganic Chemistry|October 25, 2023
Electrocatalysis of the Oxygen Reduction Reaction by Copper Complexes with Tetradentate Tripodal LigandsMathias L Skavenborg, Mads Sondrup Møller, Christopher J Miller, et al.
The Journal of Pediatrics|January 1, 1996
A prevalent mutation for galactosemia among black AmericansK Lai, S D Langley, R H Singh, et al.
BMC Immunology|January 13, 2011
Shb deficient mice display an augmented TH2 response in peripheral CD4+ T cellsKarin Gustafsson, Gabriela Calounova, Fredrik Hjelm, et al.
The Journal of Molecular Diagnostics : JMD|July 20, 2010
A simple method to confirm and size deletion, duplication, and insertion mutations detected by sequence analysisLawrence N Hjelm, Ephrem L H Chin, Madhuri R Hegde, et al.
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