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The Journal of Molecular Diagnostics : JMD|July 20, 2024
Multisite Evaluation and Validation of Optical Genome Mapping for Prenatal Genetic TestingBrynn Levy, Jie Liu, M Anwar Iqbal, et al.
Computational and Structural Biotechnology Journal|March 8, 2021
Biochemical and Structural Characterization of a novel thermophilic esterase EstD11 provide catalytic insights for the HSL familyVega Miguel-Ruano, Ivanna Rivera, Jelena Rajkovic, et al.
The Journal of Clinical Endocrinology and Metabolism|October 31, 2021
Causal and Candidate Gene Variants in a Large Cohort of Women With Primary Ovarian InsufficiencyBushra Gorsi, Edgar Hernandez, Marvin Barry Moore, et al.
Acta Diabetologica|January 30, 2022
Predictive value of admission glycemia in diabetics with pulmonary embolism compared to non-diabetic patientsLjiljana Jovanovic, Milena Rajkovic, Vesna Subota, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 15, 2024
Short-Term Cannabidiol with Δ-9-Tetrahydrocannabinol in Parkinson's Disease: A Randomized TrialYing Liu, Jacquelyn Bainbridge, Stefan Sillau, et al.
American Journal of Hematology|June 4, 2026
Exploring the Burden on Patients Living With and Receiving Treatment for Immune Thrombocytopenia (ITP): Patient and Physician Perceptions From the ITP World Impact Survey (I-WISh) 2.0Nichola Cooper, James Bussel, Waleed Ghanima, et al.
Transplantation Proceedings|January 3, 2006
Human fetal islet transplantation in type 1 diabetics: comparison of immunological effects between multiple implantation regimensP B Djordjevic, N Lalic, V Bumbasirevic, et al.
Archives of Pathology & Laboratory Medicine|November 29, 2022
Copy Number Loss at Chromosome 14q11.2 Correlates With the Proportion of T Cells in Biopsies and Helps Identify T-Cell NeoplasmsArzu Saglam, Kunwar Singh, Jyoti Kumar, et al.
Human Mutation|May 28, 2010
Mutations in SOHLH1 gene associate with nonobstructive azoospermiaYoungsok Choi, Sanghyun Jeon, Mikyung Choi, et al.
Molecular Genetics & Genomic Medicine|March 5, 2021
Deletion of conserved non-coding sequences downstream from NKX2-1: A novel disease-causing mechanism for benign hereditary choreaJun Liao, Keith A Coffman, Joseph Locker, et al.
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