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Frontiers in Genetics|June 17, 2022
DNA Methylation Analysis of Turner Syndrome BAVJacob Gutierrez, Brett A Davis, Kimberly A Nevonen, et al.Nature|July 25, 1991
Partial sequence of a candidate gene for the Marfan syndromeC L Maslen, G M Corson, B K Maddox, et al.Communications Chemistry|May 31, 2023
Identification of photocrosslinking peptide ligands by mRNA displayYuteng Wu, M Teresa Bertran, Dhira Joshi, et al.Nature Communications|September 10, 2021
Sequences in the cytoplasmic tail of SARS-CoV-2 Spike facilitate expression at the cell surface and syncytia formationJérôme Cattin-Ortolá, Lawrence G Welch, Sarah L Maslen, et al.Genomics|January 1, 1988
Seven polymorphic loci mapping to human chromosomal region 11q22-qterC L Maslen, C Jones, T Glaser, et al.European Journal of Biochemistry|October 30, 2004
The N-linked oligosaccharides of aminopeptidase N from Manduca sexta: site localization and identification of novel N-glycan structuresElaine Stephens, Jane Sugars, Sarah L Maslen, et al.Gene|August 22, 2006
CRELD2: gene mapping, alternate splicing, and comparative genomic identification of the promoter regionCheryl L Maslen, Darcie Babcock, Jennifer K Redig, et al.Nucleic Acids Research|March 24, 2017
Crystal structure of the N-terminal domain of human Timeless and its interaction with TipinSandro Holzer, Gianluca Degliesposti, Mairi L Kilkenny, et al.Genetic Testing|January 11, 2000
A simple PCR-based assay allows detection of a common mutation, IVS8-1G-->C, in DHCR7 in Smith-Lemli-Opitz syndromeK P Battaile, C L Maslen, C A Wassif, et al.Genetics|April 1, 2016
Penetrance of Congenital Heart Disease in a Mouse Model of Down Syndrome Depends on a Trisomic Potentiator of a Disomic ModifierHuiqing Li, Sarah Edie, Donna Klinedinst, et al.Pageof 13