The thrust of the proposed work in this project is the investigation of known and potential endocrine genetic mutant mice with growth disorders that may serve as biomedical research models for analogous disorders in man. Individual experiments will be executed to: (1) Characterize established, inherited murine growth disorders and exploit such mutant mice to develop our understanding of normal and abnormal growth processes. (2) Develop therapeutic treatments that will ameliorate the growth disorders in mice and by analogy prove fruitful for treatment of human disorders; (3) Search for and characterize new mutated genes in the mouse causing growth defects, thus providing additional models for investigation of causative factors in such defects; and (4) To make the presently known and future mutated genes of the mouse that affect growth processes known and available to the scientific community.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK017947-13
Application #
3225896
Study Section
Mammalian Genetics Study Section (MGN)
Project Start
1977-09-01
Project End
1988-02-29
Budget Start
1986-09-01
Budget End
1988-02-29
Support Year
13
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Jackson Laboratory
Department
Type
DUNS #
042140483
City
Bar Harbor
State
ME
Country
United States
Zip Code
04609
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Adkison, L R; Taylor, S; Beamer, W G (1990) Mutant gene-induced disorders of structure, function and thyroglobulin synthesis in congenital goitre (cog/cog) in mice. J Endocrinol 126:51-8
Barton, D E; Yang-Feng, T L; Mason, A J et al. (1989) Mapping of genes for inhibin subunits alpha, beta A, and beta B on human and mouse chromosomes and studies of jsd mice. Genomics 5:91-9
Basche, M; Beamer, W G; Schneider, A B (1989) Abnormal properties of thyroglobulin in mice with inherited congenital goiter (cog/cog). Endocrinology 124:1822-9
Beamer, W G; Cunliffe-Beamer, T L; Shultz, K L et al. (1988) Juvenile spermatogonial depletion (jsd): a genetic defect of germ cell proliferation of male mice. Biol Reprod 38:899-908
Jansson, J O; Ekberg, S; Hoath, S B et al. (1988) Growth hormone enhances hepatic epidermal growth factor receptor concentration in mice. J Clin Invest 82:1871-6
Green, R P; Birkenmeier, E H; Beamer, W G et al. (1988) The hypothyroid (hyt/hyt) mouse: a model system for studying the effects of thyroid hormone on developmental changes in gene expression. Proc Natl Acad Sci U S A 85:5592-6