Functional annotation of mammalian genomic DNA sequence by chemical mutagenesis: A fine-structure genetic mutation map of a 1- to 2-cM segment of mouse chromosome 7 corresponding t...

Por Rinchik, Eugene M., Carpenter, Donald A., Johnson, Dabney K.
Publicado em 2002

Inherited somatic mosaicism caused by an intracisternal A particle insertion in the mouse tyrosinase gene

Por Wu, Min, Rinchik, Eugene M., Wilkinson, Erby, Johnson, Dabney K.
Publicado em 1997

Molecular Genetic Analysis of the DILUTE-SHORT EAR ( d-se) Region of the Mouse

Por Rinchik, Eugene M., Russell, Liane B., Copeland, Neal G., Jenkins, Nancy A.
Publicado em 1986

Modification of an existing chromosomal inversion to engineer a balancer for mouse chromosome 15.

Por Chick, Wallace S H, Mentzer, Sarah E, Carpenter, Donald A, Rinchik, Eugene M, You, Yun
Publicado em 2004

Mutations in the clathrin-assembly gene Picalm are responsible for the hematopoietic and iron metabolism abnormalities in fit1 mice

Por Klebig, Mitchell L., Wall, Melissa D., Potter, Mark D., Rowe, Erica L., Carpenter, Donald A., Rinchik, Eugene M.
Publicado em 2003

The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered Hoxc gene expression in the ears

Por Mentzer, Sarah E., Sundberg, John P., Awgulewitsch, Alexander, Chao, Hanna HJ., Carpenter, Donald A., Zhang, Wei-Dong, Rinchik, Eugene M., You, Yun
Publicado em 2008

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

Por Aponte, Jennifer L., Sega, Gary A., Hauser, Loren J., Dhar, Madhu S., Withrow, Catherine M., Carpenter, Donald A., Rinchik, Eugene M., Culiat, Cymbeline T., Johnson, Dabney K.
Publicado em 2001

Single Amino Acid Substitution in Aquaporin 11 Causes Renal Failure

Por Tchekneva, Elena E., Khuchua, Zaza, Davis, Linda S., Kadkina, Veronika, Dunn, Stephen R., Bachman, Sebastian, Ishibashi, Kenichi, Rinchik, Eugene M., Harris, Raymond C., Dikov, Mikhail M., Breyer, Matthew D.
Publicado em 2008

Phenotype screening for genetically determined age-onset disorders and increased longevity in ENU-mutagenized mice

Por Johnson, Dabney K., Rinchik, Eugene M., Moustaid-Moussa, Naima, Miller, Darla R., Williams, Robert W., Michaud, Edward J., Jablonski, Monica M., Elberger, Andrea, Hamre, Kristen, Smeyne, Richard, Chesler, Elissa, Goldowitz, Daniel
Publicado em 2005

Efficient gene-driven germ-line point mutagenesis of C57BL/6J mice

Por Michaud, Edward J, Culiat, Cymbeline T, Klebig, Mitchell L, Barker, Paul E, Cain, KT, Carpenter, Debra J, Easter, Lori L, Foster, Carmen M, Gardner, Alysyn W, Guo, ZY, Houser, Kay J, Hughes, Lori A, Kerley, Marilyn K, Liu, Zhaowei, Olszewski, Robert E, Pinn, Irina, Shaw, Ginger D, Shinpock, Sarah G, Wymore, Ann M, Rinchik, Eugene M, Johnson, Dabney K
Publicado em 2005