Show simple item record

dc.contributor.advisorSmith, David I.
dc.contributor.advisorLiu, Wanguo
dc.contributor.authorPandhi, Nikhil
dc.date.accessioned2011-10-19T18:57:41Z
dc.date.available2011-10-19T18:57:41Z
dc.date.issued1997
dc.identifier.urihttp://hdl.handle.net/10920/23683
dc.descriptionvi, 36 p.en_US
dc.description.abstractMicrofibrils are the major constituents of connective tissues, providing structural integrity and serving as the scaffolding for deposition of tropoelastin to form elastic fibers. A variety of proteins compose the structure of microfibrils, the most prominent of which is fibrillin-1 encoded by FBN 1 on human chromosome ISq21. Fibrillin-1 monomers contain large numbers of calcium binding epidermal growth factor-like motifs (EGFcb), which play an important role in the elasticity and strength of connective tissues. Mutations in FBN1 cause Marfan syndrome (MFS), an autosomal dominant connective tissue disorder with prominent manifestations in the skeleton, eye and cardiovascular system. A number of conditions related to MFS are also due to FBN 1 mutations and are referred to as Marfan-like disorders. The most life threatening of the Marfan-like disorders are ascending aortic aneurysms (AAA). AAA develop due to high blood pressure in the aorta, leading to eventual rupture or dissection of the tissue. In this study, the FBN1 genomes of individuals with AAA were studied using polymerase chain reaction as well as a novel, but powerful technique known as denaturing high performance liquid chromatography (DHPLC). DHPLC makes the technical challenge of searching a large gene such as FBN 1 (110 kb) for mutations much easier and accurate than in the past. Four de novo mutations were discovered in four unrelated individuals with aortic aneurysms in this study, with each mutation residing in EGFcb-like coding regions of FBN 1. This study investigates the relationship between the four FBN 1 mutations and the loss of aortic tissue strength, loss of aortic tissue elasticity, and abnormally high blood pressure, with respect to the development of aortic aneurysms.en_US
dc.description.sponsorshipGene Discovery Lab. Mayo Clinic. Rochester, Minnesota.
dc.description.sponsorshipThe Comprehensive Cancer Center and Molecular Cancer Genetics. Mayo Clinic. Rochester, Minnesota.
dc.format.mimetypeapplication/pdf
dc.language.isoen_USen_US
dc.publisherKalamazoo Collegeen_US
dc.relation.ispartofKalamazoo College Biology Senior Individualized Projects Collection
dc.relation.ispartofseriesSenior Individualized Projects. Biology;
dc.rightsU.S. copyright laws protect this material. Commercial use or distribution of this material is not permitted without prior written permission of the copyright holder.
dc.titleMutations in FBN1 Sequences Coding for EGFcb Motifs in Individuals with Ascending Aortic Aneurysmsen_US
dc.typeThesisen_US
KCollege.Access.ContactIf you are not a current Kalamazoo College student, faculty, or staff member, email dspace@kzoo.edu to request access to this thesis.


Files in this item

Thumbnail

This item appears in the following Collection(s)

  • Biology Senior Individualized Projects [1520]
    This collection includes Senior Individualized Projects (SIP's) completed in the Biology Department. Abstracts are generally available to the public, but PDF files are available only to current Kalamazoo College students, faculty, and staff.

Show simple item record