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American Journal of Medical Genetics. Part A|February 4, 2005
Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated Dutch familiesG M S Mancini, C E Catsman-Berrevoets, I F M de Coo, et al.
Current Rheumatology Reviews|April 14, 2017
Is the Treatment with Biological or Non-biological DMARDS a Modifier of Periodontal Condition in Patients with Rheumatoid Arthritis?Consuelo Romero-Sanchez, C Rodríguez, P Santos-Moreno, et al.
Circulation. Cardiovascular Imaging|January 13, 2025
Abnormal Exercise Electrocardiography With Normal Stress Echocardiography Is Associated With Subclinical Coronary AtherosclerosisJessica M Duran, Peter Shrader, Chuan Hong, et al.
Molecular Genetics and Metabolism|November 9, 2005
Brain abnormalities in a case of malonyl-CoA decarboxylase deficiencyM C Y de Wit, I F M de Coo, E Verbeek, et al.
Cells|October 15, 2025
The GR-LEDGF/p75-HSP27 Axis Contributes to Cross-Resistance Between Enzalutamide and Docetaxel in Prostate CancerPedro T Ochoa, Evelyn S Sanchez-Hernandez, Alfonso M Duran, et al.
American Journal of Human Genetics|October 31, 2000
Molecular characterization of 3-phosphoglycerate dehydrogenase deficiency--a neurometabolic disorder associated with reduced L-serine biosynthesisL W Klomp, T J de Koning, H E Malingré, et al.
Biochemistry|August 5, 2016
Protocols for Molecular Modeling with Rosetta3 and RosettaScriptsBrian J Bender, Alberto Cisneros, Amanda M Duran, et al.
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