18th International Mouse Genome Conference
17-22 October 2004, Seattle, USA
Plenary Presentations * Oral
Presentations * Poster
Abstracts * Photos
Verne Chapman Memorial Lecture * Table
of Contents * Attendees * Awards
ORAL PRESENTERS ABSTRACTS
Session 10 – Models of Human Diseases
Chair: Maja Bucan
Genetics of Atherosclerosis: Integrating
Genetic and Gene Expression Data
Aldons Lusis
Professor,
University of California, Los Angeles, United States
Models of Human Diseases Papers
Jenna
: A novel ENU Hyperactive Mouse Mutant with an Enhanced Acoustic Startle Response
Keays DA 1, Nolan P 2, Oliver P 3, Tian G 4,
Fullerton J 1, Rees M 5, Harvey RJ 6, Cowan NJ 4, Davies KE 3, Flint J 1
1 Wellcome Trust Centre for Human Genetics, Oxford University,
Oxford, United Kingdom,
2 MRC Mammalian Genetics Unit,
Harwell, Didcot, United Kingdom, 3 Department of Human Anatomy
and Genetics, Oxford University, Oxford, United Kingdom, 4 Department
of Biochemistry, New York University Medical Center, New York, United States,
5 Swansea Clinical School, University of Wales Swansea, Singleton
Park, Swansea, United Kingdom, 6 Department of Pharmacology,
The School of Pharmacy, London, United Kingdom
Estimating the Contribution of Genetic, Diet
and Gender Effects to the Phenotypic Variation Observed in Metabolic Syndrome-Related
Traits between A/J and C57BL/6J Mice
Sinasac DS, Nadeau
JH
Case Western Reserve University, Cleveland, United States
Mutant Analysis Reveals Whirlin as a Dynamic
Organiser in the Growing Hair Cell Stereocilium
Kikkawa Y 1, Mburu P 1, Morse S 1,
Kominami R 2, Townsend S 1, Brown S 1
1 MRC, Harwell, United Kingdom, 2 Tokyo Metropolitan
Institute of Medical Science (Rinshoken), Tokyo, Japan
Discovery of a Gene Causing Human Congenital
Diaphragmatic Defect and Pulmonary Hypoplasia by Characterization of an ENU-Induced
Mouse Model
Ackerman KG 1, Vargas SO 2, Beier DR 1
1 Brigham and Women's Hospital/Harvard Med Sch, Boston,
United States, 2 Children's Hospital/Harvard Med Sch, Boston,
United States
ENU-induced Mouse Enamelin (Enam) Mutants
as Models for Different Clinical Subtypes of Human Amelogenesis Imperfecta (AI)
Masuya H 1, Shimizu K 2, Sezutsu
H 1, Sakuraba Y 1, Nagano J 1,
Shimizu A 1, Fijimoto N 1, Ishijima J 1,
Kaneda H 1, Kobayashi K 1, Maeda T 2,
Gondo Y 1, Noda T 1, Wakana S 1,
Shiroishi T 1
1 RIKEN GSC, Tsukuba, Japan,
2 Nihon University, Matsudo, Japan