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Cell|February 21, 1992
Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family memberJ D Brook, M E McCurrach, H G Harley, et al.Genomics|February 1, 1994
YAC contigs for 4q35 in the region of the facioscapulohumeral muscular dystrophy (FSHD) geneB Weiffenbach, J Dubois, S Manning, et al.Proceedings of the National Academy of Sciences of the United States of America|November 26, 2020
Tolerogenic nanoparticles suppress central nervous system inflammationJessica E Kenison, Aditi Jhaveri, Zhaorong Li, et al.Journal of Dentistry|April 16, 2013
Streptococcus mutans biofilm disruption by κ-casein glycopeptideStuart G Dashper, Sze-Wei Liu, Katrina A Walsh, et al.The Journal of Clinical Psychiatry|July 1, 1996
Factors associated with pharmacologic noncompliance in patients with maniaP E Keck, S L McElroy, S M Strakowski, et al.Annals of Internal Medicine|January 15, 1993
Clinical and genetic studies of renal cell carcinomas in a family with a constitutional chromosome 3;8 translocation. Genetics of familial renal carcinomaF P Li, H J Decker, B Zbar, et al.Scientific Reports|February 6, 2019
Self-assembly of dental surface nanofilaments and remineralisation by SnF<sub>2</sub> and CPP-ACP nanocomplexesJames R Fernando, Peiyan Shen, Christina P C Sim, et al.Clinical Colorectal Cancer|March 18, 2004
Dihydropyrimidine dehydrogenase and thymidylate synthase polymorphisms and their association with 5-fluorouracil/leucovorin chemotherapy in colorectal cancerAndrew X Zhu, Thomas A Puchalski, Vincent P Stanton, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 27, 2023
Coxa Vara Deformity in Fibrous Dysplasia/McCune-Albright Syndrome: Prevalence, Natural History and Risk Factors: A Two-Center StudyMaartje E Meier, Natasha M Appelman-Dijkstra, Michael T Collins, et al.Nature Genetics|June 11, 1992
The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1AL J Valentijn, P A Bolhuis, I Zorn, et al.Pageof 20