American literature -- Hispanic American authors; Masculinity
This thesis focuses on how the male-male relationships in contemporary Latino novels by Piri Thomas, Abraham Rodriguez, Jr., Junot Díaz, Arturo Islas, and John Rechy help or hurt the protagonists’ developing masculinity and overall sense of...
Psychic trauma in literature; Holocaust, Jewish (1939-1945), in literature; Gender identity in literature
The project, "The Limits of Language: Gender, Trauma and the Holocaust," contributes a new theoretical reading regarding Holocaust literature. Traditionally, gender studies have provided insight into gendered responses to trauma, but not...
Learning, Psychology of; Child development; Cognition in children
Young children perceive and respond to their environment in a variety of ways based upon their unique combination of approaches to learning. They use a range of intelligences in interacting with their classmates and the classroom setting:...
The frizzy (fr) mutation in Mus musculus affects hair structure and formation. Early studies demonstrated that the gene responsible for frizzy assorts to mouse Chromosome 7 along with pink-eyed dilution (p), chinchilla (cch), and shaker-1 (sh-1). ...
Malory, Thomas, Sir, 15th cent. Morte d'Arthur; Lancelot (Legendary character) -- Romances -- History and criticism
Thomas Malory's Le Morte d'Arthur depicts characters facing problems of identity. Chief among them, Sir Lancelot faces temporary madness when overwhelmed by the incompatible roles he plays in Arthur's court. A useful theoretical lens for...
A study was performed using a convenience sample of 90 students at a northeastern community college to determine gender differences of math anxiety and its effect on math avoidance. Four sections of an introductory English class were given a...
The mouse frizzy (fr) mutation arose on a genetically mixed background and was first described by G.D. Snell of The Jackson Laboratory in 1951. Mice carrying this recessive mutation have curly vibrissae which can be observed as early as one to two...
The recessive male sterility and histoincompatibility mutation (mshi) in the mouse generates pleiotropic effects on graft transplantation and male reproduction. Previous analysis of backcross mice using a large set of microsatellite markers has...
Jaltomata repandidentata, similar to other members of its genus, is known to be self-compatible. The following study identifies J. repandidentata as a species capable of delayed self-pollination and describes the mechanism of delayed selfing...
Minor histocompatibility (H) antigens are typically identified as barriers to transplantation in graft exchange experiments between major histocompatibility complex (MHC)-matched hosts (Bailey 1975; Snell and Bunker 1960). This approach has allowed...
The mouse frizzy (fr) mutation is a Mendelian recessive trait that affects hair structure and formation in mice. The mutation arose in a mouse of mixed origin at the Jackson Lab (Bar Harbor, ME) in 1951. Frizzy is known to be linked to other genes...
Frizzy (fr) is a spontaneous recessive mutation in mice characterized by curly vibrissae, a disheveled coat and short hair (Snell 1951). Previous linkage analysis located the mutant fr allele on Mus musculus Chromosome 7 (Falconer and Snell 1952)....
Receptor-mediated endocytosis as a route of gene delivery shows promise as it is a natural cellular process and allows targeting of ligands to specific cells. A carrier system consisting of two important components: a targetable ligand,...
The male sterility and histoincompatibility mutation (mshi) is an autosomal recessive mutation that produces apparently pleiotropic effects in mice. Mice homozygous for mshi manifest two distinct phenotypes. In both male and female mice, the...
Botany -- Connecticut -- Branford (Town) -- Outer Island
The purpose of this study, on the Outer Island unit of the Stewart B. McKinney National Wildlife Refuge in Branford, CT, from July 1998 to June 1999, was to conduct botanical research and to make an associated collection of plant specimens. All...
Investigation of X-linked histocompatibility may offer an opportunity to find CD and HD minor H haplotype components which are widely separated on the X chromosome. The presence of the HX antigen is detected by placing parental strain grafts onto...
Parental behavior in animals; Rats -- Physiology; Animal mutation
Rats that are hypotrichotic (lacking normal hair) due to the autosomal recessive
shorn (shn) mutation showed a low survival rate in brother by sister matings in a breeding
colony of SU/Csu rats. The majority of rats died before weaning. Subsequent...
Transforming growth factor-alpha (TGFa), a member of the endothelial growth
factor (EGF) family of mitogens, was previously thought to exist solely in neoplastic
cells and the quickly dividing cells of a developing fetus. Since then, TGFa...
Ahearn et al. (J. Heredity 93:210-213) have previously shown that the rat fuzzy and Charles River "hairless" mutations are defects in the same gene on rat Chromosome 1, and are likely orthologues of mouse frizzy (abbreviated fr) on mouse Chromosome...
The pairing and recombination of homologous regions of the X and Y chromosomes, in an area known as the pseudoautosomal region (PAR), has been a phenomenon of interest since its discovery in 1934. Its presence seems to be limited to eutherian...
