288 related articles for article (PubMed ID: 12663541)
1. Phenotype-based identification of mouse chromosome instability mutants.
Shima N; Hartford SA; Duffy T; Wilson LA; Schimenti KJ; Schimenti JC
Genetics; 2003 Mar; 163(3):1031-40. PubMed ID: 12663541
[TBL] [Abstract][Full Text] [Related]
2. The mouse genomic instability mutation chaos1 is an allele of Polq that exhibits genetic interaction with Atm.
Shima N; Munroe RJ; Schimenti JC
Mol Cell Biol; 2004 Dec; 24(23):10381-9. PubMed ID: 15542845
[TBL] [Abstract][Full Text] [Related]
3. Identification of novel genetic loci for bone size and mechanosensitivity in an ENU mutant exhibiting decreased bone size.
Srivastava AK; Kapur S; Mohan S; Yu H; Kapur S; Wergedal J; Baylink DJ
J Bone Miner Res; 2005 Jun; 20(6):1041-50. PubMed ID: 15883645
[TBL] [Abstract][Full Text] [Related]
4. 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 EM; Carpenter DA
Genetics; 1999 May; 152(1):373-83. PubMed ID: 10224267
[TBL] [Abstract][Full Text] [Related]
5. Forward genetic screens for meiotic and mitotic recombination-defective mutants in mice.
Reinholdt L; Ashley T; Schimenti J; Shima N
Methods Mol Biol; 2004; 262():87-107. PubMed ID: 14769957
[TBL] [Abstract][Full Text] [Related]
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; 6():164. PubMed ID: 16300676
[TBL] [Abstract][Full Text] [Related]
7. Analysis of breeding and pathology helps refine management practices of a large-scale N'-ethyl-N'-nitrosourea mouse mutagenesis programme.
Smith AP; Polley S; Wells S; Stewart M; Vizor L; Humphreys J; Warren MV; Dear N; Cheeseman MT
Lab Anim; 2009 Jan; 43(1):1-10. PubMed ID: 18987059
[TBL] [Abstract][Full Text] [Related]
8. Genotype-based screen for ENU-induced mutations in mouse embryonic stem cells.
Chen Y; Yee D; Dains K; Chatterjee A; Cavalcoli J; Schneider E; Om J; Woychik RP; Magnuson T
Nat Genet; 2000 Mar; 24(3):314-7. PubMed ID: 10700191
[TBL] [Abstract][Full Text] [Related]
9. An N-ethyl-N-nitrosourea mutagenesis recessive screen identifies two candidate regions for murine cardiomyopathy that map to chromosomes 1 and 15.
Fernandez L; Marchuk DA; Moran JL; Beier DR; Rockman HA
Mamm Genome; 2009 May; 20(5):296-304. PubMed ID: 19387734
[TBL] [Abstract][Full Text] [Related]
10. Identification of three loci affecting HDL-cholesterol levels in a screen for chemically induced recessive mutations in mice.
Juan T; VĂ©niant MM; Helmering J; Babij P; Baker DM; Damore MA; Bass MB; Gyuris T; Chhoa M; Li CM; Ebeling C; Amato J; Carlson GA; Lloyd DJ
J Lipid Res; 2009 Mar; 50(3):534-545. PubMed ID: 18974039
[TBL] [Abstract][Full Text] [Related]
11. Identification of a novel point mutation of mouse proto-oncogene c-kit through N-ethyl-N-nitrosourea mutagenesis.
Ruan HB; Zhang N; Gao X
Genetics; 2005 Feb; 169(2):819-31. PubMed ID: 15731517
[TBL] [Abstract][Full Text] [Related]
12. DNA polymerase POLQ and cellular defense against DNA damage.
Yousefzadeh MJ; Wood RD
DNA Repair (Amst); 2013 Jan; 12(1):1-9. PubMed ID: 23219161
[TBL] [Abstract][Full Text] [Related]
13. Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease.
Caruana G; Farlie PG; Hart AH; Bagheri-Fam S; Wallace MJ; Dobbie MS; Gordon CT; Miller KA; Whittle B; Abud HE; Arkell RM; Cole TJ; Harley VR; Smyth IM; Bertram JF
PLoS One; 2013; 8(3):e55429. PubMed ID: 23469164
[TBL] [Abstract][Full Text] [Related]
14. 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
Proc Natl Acad Sci U S A; 2002 Jan; 99(2):844-9. PubMed ID: 11792855
[TBL] [Abstract][Full Text] [Related]
15. Homology-directed dna repair, mitomycin-c resistance, and chromosome stability is restored with correction of a Brca1 mutation.
Moynahan ME; Cui TY; Jasin M
Cancer Res; 2001 Jun; 61(12):4842-50. PubMed ID: 11406561
[TBL] [Abstract][Full Text] [Related]
16. Implementation of a large-scale ENU mutagenesis program: towards increasing the mouse mutant resource.
Nolan PM; Peters J; Vizor L; Strivens M; Washbourne R; Hough T; Wells C; Glenister P; Thornton C; Martin J; Fisher E; Rogers D; Hagan J; Reavill C; Gray I; Wood J; Spurr N; Browne M; Rastan S; Hunter J; Brown SD
Mamm Genome; 2000 Jul; 11(7):500-6. PubMed ID: 10886012
[TBL] [Abstract][Full Text] [Related]
17. Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1.
Bosman EA; Estabel J; Ismail O; Podrini C; White JK; Steel KP
Mamm Genome; 2013 Feb; 24(1-2):44-53. PubMed ID: 23160729
[TBL] [Abstract][Full Text] [Related]
18. Spectra of gpt mutations in ethylnitrosourea-treated and untreated transgenic mice.
Masumura K; Matsui M; Katoh M; Horiya N; Ueda O; Tanabe H; Yamada M; Suzuki H; Sofuni T; Nohmi T
Environ Mol Mutagen; 1999; 34(1):1-8. PubMed ID: 10462717
[TBL] [Abstract][Full Text] [Related]
19. New variants in the Enpp1 and Ptpn6 genes cause low BMD, crystal-related arthropathy, and vascular calcification.
Babij P; Roudier M; Graves T; Han CY; Chhoa M; Li CM; Juan T; Morony S; Grisanti M; Li X; Yu L; Dwyer D; Lloyd DJ; Bass MB; Richards WG; Ebeling C; Amato J; Carlson G
J Bone Miner Res; 2009 Sep; 24(9):1552-64. PubMed ID: 19419305
[TBL] [Abstract][Full Text] [Related]
20. ENU mutagenesis, a way forward to understand gene function.
Acevedo-Arozena A; Wells S; Potter P; Kelly M; Cox RD; Brown SD
Annu Rev Genomics Hum Genet; 2008; 9():49-69. PubMed ID: 18949851
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]