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Items: 1 to 50 of 86

1.

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

Mentzer SE, Sundberg JP, Awgulewitsch A, Chao HH, Carpenter DA, Zhang WD, Rinchik EM, You Y.

Vet Dermatol. 2008 Dec;19(6):358-67. doi: 10.1111/j.1365-3164.2008.00709.x. Epub 2008 Nov 14.

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.

J Am Soc Nephrol. 2008 Oct;19(10):1955-64. doi: 10.1681/ASN.2008030296. Epub 2008 Aug 13.

3.

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.

J Am Soc Nephrol. 2007 Jan;18(1):103-12. Epub 2006 Dec 6.

4.

Nell1-deficient mice have reduced expression of extracellular matrix proteins causing cranial and vertebral defects.

Desai J, Shannon ME, Johnson MD, Ruff DW, Hughes LA, Kerley MK, Carpenter DA, Johnson DK, Rinchik EM, Culiat CT.

Hum Mol Genet. 2006 Apr 15;15(8):1329-41. Epub 2006 Mar 14.

PMID:
16537572
5.

The Tennessee Mouse Genome Consortium: identification of ocular mutants.

Jablonski MM, Wang X, Lu L, Miller DR, Rinchik EM, Williams RW, Goldowitz D.

Vis Neurosci. 2005 Sep-Oct;22(5):595-604.

PMID:
16332270
6.

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.

BMC Genomics. 2005 Nov 21;6:164.

7.

X-ray-induced deletion complexes in embryonic stem cells on mouse chromosome 15.

Chick WS, Mentzer SE, Carpenter DA, Rinchik EM, Johnson D, You Y.

Mamm Genome. 2005 Sep;16(9):661-71. Epub 2005 Oct 20.

PMID:
16245023
8.

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

Culiat CT, Klebig ML, Liu Z, Monroe H, Stanford B, Desai J, Tandan S, Hughes L, Kerley MK, Carpenter DA, Johnson DK, Rinchik EM, Li Q.

Mamm Genome. 2005 Aug;16(8):555-66.

PMID:
16180137
9.

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.

Mol Vis. 2005 Jul 27;11:569-81.

10.

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

Johnson DK, Rinchik EM, Moustaid-Moussa N, Miller DR, Williams RW, Michaud EJ, Jablonski MM, Elberger A, Hamre K, Smeyne R, Chesler E, Goldowitz D.

Age (Dordr). 2005 Mar;27(1):75-90. doi: 10.1007/s11357-005-4131-3. Epub 2005 May 2.

11.

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

Chick WS, Mentzer SE, Carpenter DA, Rinchik EM, You Y.

Genetics. 2004 Jun;167(2):889-95.

12.

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

Klebig ML, Wall MD, Potter MD, Rowe EL, Carpenter DA, Rinchik EM.

Proc Natl Acad Sci U S A. 2003 Jul 8;100(14):8360-5. Epub 2003 Jun 27.

13.

The Polycomb-group gene eed regulates thymocyte differentiation and suppresses the development of carcinogen-induced T-cell lymphomas.

Richie ER, Schumacher A, Angel JM, Holloway M, Rinchik EM, Magnuson T.

Oncogene. 2002 Jan 10;21(2):299-306.

15.

Sequence interpretation. Functional annotation of mouse genome sequences.

Nadeau JH, Balling R, Barsh G, Beier D, Brown SD, Bucan M, Camper S, Carlson G, Copeland N, Eppig J, Fletcher C, Frankel WN, Ganten D, Goldowitz D, Goodnow C, Guenet JL, Hicks G, Hrabe de Angelis M, Jackson I, Jacob HJ, Jenkins N, Johnson D, Justice M, Kay S, Kingsley D, Lehrach H, Magnuson T, Meisler M, Poustka A, Rinchik EM, Rossant J, Russell LB, Schimenti J, Shiroishi T, Skarnes WC, Soriano P, Stanford W, Takahashi JS, Wurst W, Zimmer A; International Mouse Mutagenesis Consortium.

Science. 2001 Feb 16;291(5507):1251-5. No abstract available.

PMID:
11233449
16.

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.

Proc Natl Acad Sci U S A. 2001 Jan 16;98(2):641-5.

17.
18.
19.

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.

Mamm Genome. 2000 Jul;11(7):484-8.

PMID:
10886010
20.

Molecular characterization of radiation- and chemically induced mutations associated with neuromuscular tremors, runting, juvenile lethality, and sperm defects in jdf2 mice.

Walkowicz M, Ji Y, Ren X, Horsthemke B, Russell LB, Johnson D, Rinchik EM, Nicholls RD, Stubbs L.

Mamm Genome. 1999 Sep;10(9):870-8.

PMID:
10441737
22.

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

Jong MT, Carey AH, Caldwell KA, Lau MH, Handel MA, Driscoll DJ, Stewart CL, Rinchik EM, Nicholls RD.

Hum Mol Genet. 1999 May;8(5):795-803.

PMID:
10196368
23.
24.

Mutations in the murine fitness 1 gene result in defective hematopoiesis.

Potter MD, Shinpock SG, Popp RA, Godfrey V, Carpenter DA, Bernstein A, Johnson DK, Rinchik EM.

Blood. 1997 Sep 1;90(5):1850-7.

25.

Induced mouse chromosomal rearrangements as tools for identifying critical developmental genes and pathways.

Culiat CT, Carver EA, Walkowicz M, Rinchik EM, Cacheiro NL, Russell LB, Generoso WM, Stubbs L.

Reprod Toxicol. 1997 Mar-Jun;11(2-3):345-51. Review.

PMID:
9100310
26.

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

Wu M, Rinchik EM, Wilkinson E, Johnson DK.

Proc Natl Acad Sci U S A. 1997 Feb 4;94(3):890-4.

27.

Mapping of the ARIX homeodomain gene to mouse chromosome 7 and human chromosome 11q13.

Johnson KR, Smith L, Johnson DK, Rhodes J, Rinchik EM, Thayer M, Lewis EJ.

Genomics. 1996 May 1;33(3):527-31.

PMID:
8661014
28.

Tlag1, a novel murine tumor susceptibility gene that regulates MNU-induced thymic lymphoma development.

Richie ER, Angel JM, Rinchik EM.

Prog Clin Biol Res. 1996;395:23-32. Review. No abstract available.

PMID:
8895981
29.

Mutagenesis and behavioral screening for altered circadian activity identifies the mouse mutant, Wheels.

Pickard GE, Sollars PJ, Rinchik EM, Nolan PM, Bucan M.

Brain Res. 1995 Dec 24;705(1-2):255-66.

PMID:
8821757
30.

Molecular analysis of 36 mutations at the mouse pink-eyed dilution (p) locus.

Johnson DK, Stubbs LJ, Culiat CT, Montgomery CS, Russell LB, Rinchik EM.

Genetics. 1995 Dec;141(4):1563-71.

31.

Deficiency of the beta 3 subunit of the type A gamma-aminobutyric acid receptor causes cleft palate in mice.

Culiat CT, Stubbs LJ, Woychik RP, Russell LB, Johnson DK, Rinchik EM.

Nat Genet. 1995 Nov;11(3):344-6.

PMID:
7581464
33.

Phenotypic and physical analysis of a chemically induced mutation disrupting anterior axial development in the mouse.

Holdener BC, Rinchik EM, Magnuson T.

Mamm Genome. 1995 Jul;6(7):474-5. No abstract available.

PMID:
7579891
34.

Physical localization of eed: a region of mouse chromosome 7 required for gastrulation.

Holdener BC, Thomas JW, Schumacher A, Potter MD, Rinchik EM, Sharan SK, Magnuson T.

Genomics. 1995 Jun 10;27(3):447-56.

PMID:
7558026
35.

A high-resolution map of the brown (b, Tyrp1) deletion complex of mouse chromosome 4.

Bell JA, Rinchik EM, Raymond S, Suffolk R, Jackson IJ.

Mamm Genome. 1995 Jun;6(6):389-95.

PMID:
7647459
36.

Genetic and physical mapping of the fitness 1 (fit1) locus within the Fes-Hbb region of mouse chromosome 7.

Potter MD, Klebig ML, Carpenter DA, Rinchik EM.

Mamm Genome. 1995 Feb;6(2):70-5.

PMID:
7767008
37.

Clustering of six human 11p15 gene homologs within a 500-kb interval of proximal mouse chromosome 7.

Stubbs L, Rinchik EM, Goldberg E, Rudy B, Handel MA, Johnson D.

Genomics. 1994 Nov 15;24(2):324-32.

PMID:
7698755
38.

The mouse scurfy (sf) mutation is tightly linked to Gata1 and Tfe3 on the proximal X chromosome.

Blair PJ, Carpenter DA, Godfrey VL, Russell LB, Wilkinson JE, Rinchik EM.

Mamm Genome. 1994 Oct;5(10):652-4. No abstract available.

PMID:
7849405
40.
41.

Phenotypic consequences of deletion of the gamma 3, alpha 5, or beta 3 subunit of the type A gamma-aminobutyric acid receptor in mice.

Culiat CT, Stubbs LJ, Montgomery CS, Russell LB, Rinchik EM.

Proc Natl Acad Sci U S A. 1994 Mar 29;91(7):2815-8.

42.

Fine structure mapping and deletion analysis of the murine piebald locus.

Metallinos DL, Oppenheimer AJ, Rinchik EM, Russell LB, Dietrich W, Tilghman SM.

Genetics. 1994 Jan;136(1):217-23.

44.
45.

High-frequency induction of chromosomal rearrangements in mouse germ cells by the chemotherapeutic agent chlorambucil.

Rinchik EM, Flaherty L, Russell LB.

Bioessays. 1993 Dec;15(12):831-6. Review.

PMID:
8141802
47.

Concordance between isolated cleft palate in mice and alterations within a region including the gene encoding the beta 3 subunit of the type A gamma-aminobutyric acid receptor.

Culiat CT, Stubbs L, Nicholls RD, Montgomery CS, Russell LB, Johnson DK, Rinchik EM.

Proc Natl Acad Sci U S A. 1993 Jun 1;90(11):5105-9.

48.

Overexpression of cyclin D1 in mouse skin carcinogenesis.

Bianchi AB, Fischer SM, Robles AI, Rinchik EM, Conti CJ.

Oncogene. 1993 May;8(5):1127-33.

PMID:
8479737
49.

Molecular analysis of viable spontaneous and radiation-induced albino (c)-locus mutations in the mouse.

Rinchik EM, Stoye JP, Frankel WN, Coffin J, Kwon BS, Russell LB.

Mutat Res. 1993 Apr;286(2):199-207.

PMID:
7681531
50.

Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse.

Nicholls RD, Gottlieb W, Russell LB, Davda M, Horsthemke B, Rinchik EM.

Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):2050-4.

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