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Molecular Genetics & Genomic Medicine|May 4, 2021
A novel essential splice site variant in SPTB in a large hereditary spherocytosis familyTaina T Nieminen, Sandya Liyanarachchi, Daniel F Comiskey, et al.
Biosensors|November 26, 2025
Correction: He et al. A Novel Optical Fiber Terahertz Biosensor Based on Anti-Resonance for the Rapid and Nondestructive Detection of Tumor Cells. <i>Biosensors</i> 2023, <i>13</i>, 947Zhe He, Yueping Luo, Guorong Huang, et al.
Biosensors|October 27, 2023
A Novel Optical Fiber Terahertz Biosensor Based on Anti-Resonance for The Rapid and Nondestructive Detection of Tumor CellsZhe He, Yueping Luo, Guorong Huang, et al.
Biosensors & Bioelectronics|May 24, 2021
Streptavidin-functionalized terahertz metamaterials for attomolar exosomal microRNA assay in pancreatic cancer based on duplex-specific nuclease-triggered rolling circle amplificationXinyu Zhan, Sha Yang, Guorong Huang, et al.
Journal of Neural Transmission. General Section|January 1, 1991
Plasma amine oxidase activities in Norrie disease patients with an X-chromosomal deletion affecting monoamine oxidaseD L Murphy, K B Sims, F Karoum, et al.
American Journal of Human Genetics|April 1, 1997
Assignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysisK Avela, M Lipsanen-Nyman, J Perheentupa, et al.
Sports Medicine (Auckland, N.Z.)|November 1, 1993
Gender verification in competitive sportsJ L Simpson, A Ljungqvist, A de la Chapelle, et al.
International Journal of Cancer|March 17, 2000
Predictive genetic testing for hereditary non-polyposis colorectal cancer: uptake and long-term satisfactionK Aktan-Collan, J P Mecklin, H Järvinen, et al.
Mikrochimica Acta|January 15, 2019
Surface-enhanced Raman scattering method for the identification of methicillin-resistant Staphylococcus aureus using positively charged silver nanoparticlesXueping Chen, Meiqiong Tang, Yu Liu, et al.
Applied and Theoretical Electrophoresis : the Official Journal of the International Electrophoresis Society|January 1, 1991
Abnormal protein in the cerebrospinal fluid of patients with a submicroscopic X-chromosomal deletion associated with Norrie disease: preliminary reportJ E Joy, R Poglod, D L Murphy, et al.
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