Rinchik EM - Search Results

1

A sensitized screen of N-ethyl-N-nitrosourea-mutagenized mice identifies dominant mutants predisposed to diabetic nephropathy.

Tchekneva EE, Rinchik EM, Polosukhina D, Davis LS, Kadkina V, Mohamed Y, Dunn SR, Sharma K, Qi Z, Fogo AB, Breyer MD. Tchekneva EE, et al. Among authors: rinchik em. J Am Soc Nephrol. 2007 Jan;18(1):103-12. doi: 10.1681/ASN.2006020164. Epub 2006 Dec 6. J Am Soc Nephrol. 2007. PMID: 17151334

2

Single amino acid substitution in aquaporin 11 causes renal failure.

Tchekneva EE, Khuchua Z, Davis LS, Kadkina V, Dunn SR, Bachman S, Ishibashi K, Rinchik EM, Harris RC, Dikov MM, Breyer MD. Tchekneva EE, et al. Among authors: rinchik em. J Am Soc Nephrol. 2008 Oct;19(10):1955-64. doi: 10.1681/ASN.2008030296. Epub 2008 Aug 13. J Am Soc Nephrol. 2008. PMID: 18701606 Free PMC article.

3

The Tennessee Mouse Genome Consortium: identification of ocular mutants.

Jablonski MM, Wang X, Lu L, Miller DR, Rinchik EM, Williams RW, Goldowitz D. Jablonski MM, et al. Among authors: rinchik em. Vis Neurosci. 2005 Sep-Oct;22(5):595-604. doi: 10.1017/S0952523805225087. Vis Neurosci. 2005. PMID: 16332270

4

Pleiotropy in microdeletion syndromes: neurologic and spermatogenic abnormalities in mice homozygous for the p6H deletion are likely due to dysfunction of a single gene.

Rinchik EM, Carpenter DA, Handel MA. Rinchik EM, et al. Proc Natl Acad Sci U S A. 1995 Jul 3;92(14):6394-8. doi: 10.1073/pnas.92.14.6394. Proc Natl Acad Sci U S A. 1995. PMID: 7604002 Free PMC article.

5

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

Michaud EJ, Culiat CT, Klebig ML, Barker PE, Cain KT, Carpenter DJ, Easter LL, Foster CM, Gardner AW, Guo ZY, Houser KJ, Hughes LA, Kerley MK, Liu Z, Olszewski RE, Pinn I, Shaw GD, Shinpock SG, Wymore AM, Rinchik EM, Johnson DK. Michaud EJ, et al. Among authors: rinchik em. BMC Genomics. 2005 Nov 21;6:164. doi: 10.1186/1471-2164-6-164. BMC Genomics. 2005. PMID: 16300676 Free PMC article.

6

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

Aponte JL, Sega GA, Hauser LJ, Dhar MS, Withrow CM, Carpenter DA, Rinchik EM, Culiat CT, Johnson DK. Aponte JL, et al. Among authors: rinchik em. Proc Natl Acad Sci U S A. 2001 Jan 16;98(2):641-5. doi: 10.1073/pnas.98.2.641. Proc Natl Acad Sci U S A. 2001. PMID: 11209059 Free PMC article.

7

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 to human chromosome 11p14-p15.

Rinchik EM, Carpenter DA, Johnson DK. Rinchik EM, et al. Proc Natl Acad Sci U S A. 2002 Jan 22;99(2):844-9. doi: 10.1073/pnas.022628199. Epub 2002 Jan 15. Proc Natl Acad Sci U S A. 2002. PMID: 11792855 Free PMC article.

8

An ENU-induced mutation in Rs1h causes disruption of retinal structure and function.

Jablonski MM, Dalke C, Wang X, Lu L, Manly KF, Pretsch W, Favor J, Pardue MT, Rinchik EM, Williams RW, Goldowitz D, Graw J. Jablonski MM, et al. Among authors: rinchik em. Mol Vis. 2005 Jul 27;11:569-81. Mol Vis. 2005. PMID: 16088326 Free article.

9

Effects of ENU dosage on mouse strains.

Justice MJ, Carpenter DA, Favor J, Neuhauser-Klaus A, Hrabé de Angelis M, Soewarto D, Moser A, Cordes S, Miller D, Chapman V, Weber JS, Rinchik EM, Hunsicker PR, Russell WL, Bode VC. Justice MJ, et al. Among authors: rinchik em. Mamm Genome. 2000 Jul;11(7):484-8. doi: 10.1007/s003350010094. Mamm Genome. 2000. PMID: 10886010

10

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

Rinchik EM, Carpenter DA, Selby PB. Rinchik EM, et al. Proc Natl Acad Sci U S A. 1990 Feb;87(3):896-900. doi: 10.1073/pnas.87.3.896. Proc Natl Acad Sci U S A. 1990. PMID: 2300582 Free PMC article.

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