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Dnm1 forms spirals that are structurally tailored to fit mitochondria
Dynamin-related proteins (DRPs) are large self-assembling GTPases whose common function is to regulate membrane dynamics in a variety of cellular processes. Dnm1, which is a yeast DRP (Drp1/Dlp1 inExpand
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Mutation rates at Y chromosome specific microsatellites
A collaborative work was carried out by the Spanish and Portuguese ISFG Working Group (GEP‐ISFG) to estimate Y‐STR mutation rates. Seventeen Y chromosome STR loci (DYS19, DYS385, DYS389I and II,Expand
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High School World History Textbooks: An Analysis of Content Focus and Chronological Approaches
ReSeARCH AbouT SoCiAl STudieS textbooks overwhelmingly supports the conclusion that these books are unpopular and often the subject of intense criticisms. These criticisms concern anything rangingExpand
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World History and Teacher Education: Challenges and Possibilities
This article discusses the role that teacher educators can play in helping their students develop a fuller understanding of world history. Trends such as globalization have led to calls for increasedExpand
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Identification of a Novel Mitochondrial Mutation in Dupuytren’s Disease Using Multiplex DHPLC
Dupuytren’s disease is a familial fibroproliferative disorder of late onset affecting the hands. It is extremely common in individuals of Northern European extraction. Genetic studies have yet toExpand
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Simplified production and concentration of HIV-1-based lentiviral vectors using HYPERFlask vessels and anion exchange membrane chromatography
BackgroundDuring the past twelve years, lentiviral (LV) vectors have emerged as valuable tools for transgene delivery because of their ability to transduce nondividing cells and their capacity toExpand
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From high school to college: changes in women's self-concept and its relationship to eating problems.
A longitudinal panel study of a sample of college women was undertaken to assess changes in women's self-concept from high school to college and during their college years and the relationshipExpand
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Clinical and molecular study in congenital muscular dystrophy with partial laminin α2 (LAMA2) deficiency
Complete laminin α2 (LAMA2) deficiency causes approximately half of congenital muscular dystrophy (CMD) cases. Many loss‐of‐function mutations have been reported in these severe, neonatal‐onsetExpand
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Small- to large-scale production of lentivirus vectors.
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