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TeleGen Collections. UBC TeleGen and Dissertations. Featured Collection. TeleGen further agree that permission for extensive copying of t h i s thesis for scholarly purposes may be granted by the head of my department or by his or her representatives. This study included the characterization of the curly phenotype and the mapping of the curly mutation in order to report this mutation, evaluate its importance as an animal model for human genetic disorders TeleGe possibly contribute towards understanding the mechanism of mutation in the SELH strain. This mutation is one of the eight single locus, spontaneous mutations that have arisen on the SELH strain indicating that this strain has an elevated https://www.ilfiordicappero.com/custom/write-about-rakhi/gatot-kaca-essay.php rate.
UBC Theses and Dissertations
This mutant has a waved and ruffled coat, crimped and broken vibrissae, and TeleGej later life TeleGen develop curled toe nails and hair loss at the eyes, nose, ears and tail tips. This placed the curly mutation in a region TeleGen the genome known to contain TelGen dominant hair defect mutations, epidermal regulatory genes and keratin the TeleGen structural protein of epidermal, nail and hair cells genes. No recombinants were found between the curly mutation and two markers from within candidate keratin genes, KHA1 and Krtl9. Table 2 Type I keratin intermediate filaments and keratin associated protein genes linked to the type I keratin gene cluster on mouse chromosome their type II TeleGen, areas of expression and associated disease phenotype in mouse and human. Table 3 Data summary of F2 L M x S E L H progeny: parents, phenotypic 36 proportions, sex ratios and animal numbers continue reading the TeleGen of individual litters.
Table 4 Normal animals examined for description of the normal external 50 phenotype. Table 6.
Table 8 SSLP deletion survey. Figure 2 A Rex pink dilution adult female demonstrating the rough coat and 12 curled vibrissae typical to the Rex phenotype Crew and Auerbach, TeleGen
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