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Nature|July 25, 1991
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin geneH C Dietz, G R Cutting, R E Pyeritz, et al.Gene|July 26, 2002
Identification, genomic organization and mRNA expression of CRELD1, the founding member of a unique family of matricellular proteinsPaul A Rupp, Gameil T Fouad, Carley A Egelston, et al.Nature|September 28, 1995
A high-density YAC contig map of human chromosome 22J E Collins, C G Cole, L J Smink, et al.Nature|January 6, 2000
Dominant negative mutations in human PPARgamma associated with severe insulin resistance, diabetes mellitus and hypertensionI Barroso, M Gurnell, V E Crowley, et al.Molecular Cell|November 23, 2016
Mechanism and Regulation of DNA-Protein Crosslink Repair by the DNA-Dependent Metalloprotease SPRTNJulian Stingele, Roberto Bellelli, Ferdinand Alte, et al.Molecular Cell|December 9, 2017
Mechanistic Insights into Autoinhibition of the Oncogenic Chromatin Remodeler ALC1Laura C Lehmann, Graeme Hewitt, Shintaro Aibara, et al.Nature Microbiology|September 19, 2022
Bacterial divisome protein FtsA forms curved antiparallel double filaments when binding to FtsNTim Nierhaus, Stephen H McLaughlin, Frank Bürmann, et al.Molecular Cell|February 28, 2017
PRMT5-Dependent Methylation of the TIP60 Coactivator RUVBL1 Is a Key Regulator of Homologous RecombinationThomas L Clarke, Maria Pilar Sanchez-Bailon, Kelly Chiang, et al.Human Molecular Genetics|June 25, 2016
Cilia gene mutations cause atrioventricular septal defects by multiple mechanismsOzanna Burnicka-Turek, Jeffrey D Steimle, Wenhui Huang, et al.American Journal of Human Genetics|October 9, 2012
An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defectsChristine Ackerman, Adam E Locke, Eleanor Feingold, et al.Pageof 13