Rinchik, Eugene M.

A strategy for fine-structure functional analysis of a 6- to 11-centimorgan region of mouse chromosome 7 by high-efficiency mutagenesis.

Rinchik, E. M., Carpenter, D. A., & Selby, P. B. (1990) · Proceedings of the National Academy of Sciences

Plant Genetic and Mutation StudiesCarcinogens and Genotoxicity Assessment

Cited by 118

Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader–Willi syndrome genetic region

Jong, M. T. C., Carey, A. H., Caldwell, K. A., Lau, M. H., Handel, M. A., Driscoll, D. J., Stewart, C. L., Rinchik, E. M., & Nicholls, R. D. (1999) · Human Molecular Genetics

Genetic Syndromes and ImprintingGenomics and Chromatin Dynamics

Cited by 112

N-Ethyl-N-Nitrosourea Mutagenesis of a 6- to 11-cM Subregion of the Fah–Hbb Interval of Mouse Chromosome 7: Completed Testing of 4557 Gametes and Deletion Mapping and Complementation Analysis of 31 Mutations

Rinchik, E. M., & Carpenter, D. A. (1999) · Genetics

Plant Genetic and Mutation StudiesGenetic Mapping and Diversity in Plants and Animals

Cited by 101

Point mutations in the murine fumarylacetoacetate hydrolase gene: Animal models for the human genetic disorder hereditary tyrosinemia type 1

Aponte, J. L., Sega, G. A., Hauser, L. J., Dhar, M. S., Withrow, C. M., Carpenter, D. A., Rinchik, E. M., Culiat, C. T., & Johnson, D. K. (2001) · Proceedings of the National Academy of Sciences

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 68

Murine fumarylacetoacetate hydrolase (Fah) gene is disrupted by a neonatally lethal albino deletion that defines the hepatocyte-specific developmental regulation 1 (hsdr-1) locus.

Klebig, M. L., Russell, L. B., & Rinchik, E. M. (1992) · Proceedings of the National Academy of Sciences

Metabolism and Genetic DisordersGenomic variations and chromosomal abnormalities

Cited by 65

Molecular mapping of albino deletions associated with early embryonic lethality in the mouse

Niswander, L., Kelsey^, G., Schedl, A., Ruppert, S., Sharan, S. K., Holdener-Kenny, B., Rinchik, E. M., Edström, J.-E., & Magnuson, T. (1991) · Genomics

Genomic variations and chromosomal abnormalitiesDevelopmental Biology and Gene Regulation

Cited by 28

Physical mapping of the albino-deletion complex in the mouse to localize alf/hsdr-1, a locus required for neonatal survival

Kelsey, G., Schedl, A., Ruppert, S., Niswander, L., Magnuson, T., Klebig, M. L., Rinchik, E. M., & Schütz, G. (1992) · Genomics

Genomic variations and chromosomal abnormalitiesGenetic Mapping and Diversity in Plants and Animals

Cited by 28

Chromosome jumping from flanking markers defines the minimal region for alf/hsdr-1 within the albino-deletion complex

Schedl, A., Ruppert, S., Kelsey, G., Thies, E., Niswander, L., Magnuson, T., Klebig, M. L., Rinchik, E. M., & Schütz, G. (1992) · Genomics

Genomic variations and chromosomal abnormalitiesMetabolism and Genetic Disorders

Cited by 18

Identification of mutations from phenotype‐driven ENU mutagenesis in mouse chromosome 7

Culiat, C. T., Klebig, M. L., Liu, Z., Monroe, H., Stanford, B., Desai, J., Tandan, S., Hughes, L., Kerley, M. K., Carpenter, D. A., et al. (2005) · Mammalian Genome

Carcinogens and Genotoxicity AssessmentPlant Genetic and Mutation Studies

Cited by 10