153 related articles for article (PubMed ID: 10886015)
1. Saturation mutagenesis for dominant eye morphological defects in the mouse Mus musculus.
Favor J; Neuhäuser-Klaus A
Mamm Genome; 2000 Jul; 11(7):520-5. PubMed ID: 10886015
[TBL] [Abstract][Full Text] [Related]
2. Enzyme-activity mutants in Mus musculus. I. Phenotypic description and genetic characterization of ethylnitrosourea-induced mutations.
Pretsch W
Mamm Genome; 2000 Jul; 11(7):537-42. PubMed ID: 10886019
[TBL] [Abstract][Full Text] [Related]
3. 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]
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. Inducing mutations in the mouse genome with the chemical mutagen ethylnitrosourea.
Massironi SM; Reis BL; Carneiro JG; Barbosa LB; Ariza CB; Santos GC; Guénet JL; Godard AL
Braz J Med Biol Res; 2006 Sep; 39(9):1217-26. PubMed ID: 16972005
[TBL] [Abstract][Full Text] [Related]
6. Screening for dysmorphological abnormalities--a powerful tool to isolate new mouse mutants.
Fuchs H; Schughart K; Wolf E; Balling R; Hrabé de Angelis M
Mamm Genome; 2000 Jul; 11(7):528-30. PubMed ID: 10886017
[No Abstract] [Full Text] [Related]
7. Establishing an ENU mutagenesis screen for the piebald region of mouse Chromosome 14.
Hagge-Greenberg A; Snow P; O'Brien TP
Mamm Genome; 2001 Dec; 12(12):938-41. PubMed ID: 11707782
[No Abstract] [Full Text] [Related]
8. The frequency of dominant cataract and recessive specific-locus mutations in mice derived from 80 or 160 mg ethylnitrosourea per kg body weight treated spermatogonia.
Favor J
Mutat Res; 1986 Aug; 162(1):69-80. PubMed ID: 3724777
[TBL] [Abstract][Full Text] [Related]
9. A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.
Nolan PM; Peters J; Strivens M; Rogers D; Hagan J; Spurr N; Gray IC; Vizor L; Brooker D; Whitehill E; Washbourne R; Hough T; Greenaway S; Hewitt M; Liu X; McCormack S; Pickford K; Selley R; Wells C; Tymowska-Lalanne Z; Roby P; Glenister P; Thornton C; Thaung C; Stevenson JA; Arkell R; Mburu P; Hardisty R; Kiernan A; Erven A; Steel KP; Voegeling S; Guenet JL; Nickols C; Sadri R; Nasse M; Isaacs A; Davies K; Browne M; Fisher EM; Martin J; Rastan S; Brown SD; Hunter J
Nat Genet; 2000 Aug; 25(4):440-3. PubMed ID: 10932191
[TBL] [Abstract][Full Text] [Related]
10. Focusing forward genetics: a tripartite ENU screen for neurodevelopmental mutations in the mouse.
Stottmann RW; Moran JL; Turbe-Doan A; Driver E; Kelley M; Beier DR
Genetics; 2011 Jul; 188(3):615-24. PubMed ID: 21515572
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Functional genomics the old-fashioned way: chemical mutagenesis in mice.
Inamdar MS
Bioessays; 2001 Feb; 23(2):116-20. PubMed ID: 11169583
[TBL] [Abstract][Full Text] [Related]
13. Dominant cataract mutations and specific-locus mutations in mice induced by radiation or ethylnitrosourea.
Ehling UH; Favor J; Kratochvilova J; Neuhäuser-Klaus A
Mutat Res; 1982 Feb; 92(1-2):181-92. PubMed ID: 7088001
[TBL] [Abstract][Full Text] [Related]
14. Identification of 17 hearing impaired mouse strains in the TMGC ENU-mutagenesis screen.
Kermany MH; Parker LL; Guo YK; Miller D; Swanson DJ; Yoo TJ; Goldowitz D; Zuo J
Hear Res; 2006 Oct; 220(1-2):76-86. PubMed ID: 16949226
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. A genomewide screening of N-ethyl-N-nitrosourea-mutagenized mice for musculoskeletal phenotypes.
Srivastava AK; Mohan S; Wergedal JE; Baylink DJ
Bone; 2003 Aug; 33(2):179-91. PubMed ID: 14499351
[TBL] [Abstract][Full Text] [Related]
17. An allelic series of mutations in Smad2 and Smad4 identified in a genotype-based screen of N-ethyl-N- nitrosourea-mutagenized mouse embryonic stem cells.
Vivian JL; Chen Y; Yee D; Schneider E; Magnuson T
Proc Natl Acad Sci U S A; 2002 Nov; 99(24):15542-7. PubMed ID: 12432092
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in plasma enzyme activities as novel organ-specific disease models.
Aigner B; Rathkolb B; Klaften M; Sedlmeier R; Klempt M; Wagner S; Michel D; Mayer U; Klopstock T; de Angelis MH; Wolf E
Exp Physiol; 2009 Apr; 94(4):412-21. PubMed ID: 19151073
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
