232 related articles for article (PubMed ID: 33905568)
1. Germline Saturation Mutagenesis Induces Skeletal Phenotypes in Mice.
Rios JJ; Denton K; Russell J; Kozlitina J; Ferreira CR; Lewanda AF; Mayfield JE; Moresco E; Ludwig S; Tang M; Li X; Lyon S; Khanshour A; Paria N; Khalid A; Li Y; Xie X; Feng JQ; Xu Q; Lu Y; Hammer RE; Wise CA; Beutler B
J Bone Miner Res; 2021 Aug; 36(8):1548-1565. PubMed ID: 33905568
[TBL] [Abstract][Full Text] [Related]
2. Saturation mutagenesis defines novel mouse models of severe spine deformity.
Rios JJ; Denton K; Yu H; Manickam K; Garner S; Russell J; Ludwig S; Rosenfeld JA; Liu P; Munch J; Sucato DJ; Beutler B; Wise CA
Dis Model Mech; 2021 Jun; 14(6):. PubMed ID: 34142127
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Mouse mutagenesis with the chemical supermutagen ENU.
Probst FJ; Justice MJ
Methods Enzymol; 2010; 477():297-312. PubMed ID: 20699147
[TBL] [Abstract][Full Text] [Related]
5. ENU-induced phenovariance in mice: inferences from 587 mutations.
Arnold CN; Barnes MJ; Berger M; Blasius AL; Brandl K; Croker B; Crozat K; Du X; Eidenschenk C; Georgel P; Hoebe K; Huang H; Jiang Z; Krebs P; La Vine D; Li X; Lyon S; Moresco EM; Murray AR; Popkin DL; Rutschmann S; Siggs OM; Smart NG; Sun L; Tabeta K; Webster V; Tomisato W; Won S; Xia Y; Xiao N; Beutler B
BMC Res Notes; 2012 Oct; 5():577. PubMed ID: 23095377
[TBL] [Abstract][Full Text] [Related]
6. Simulation and estimation of gene number in a biological pathway using almost complete saturation mutagenesis screening of haploid mouse cells.
Tokunaga M; Kokubu C; Maeda Y; Sese J; Horie K; Sugimoto N; Kinoshita T; Yusa K; Takeda J
BMC Genomics; 2014 Nov; 15(1):1016. PubMed ID: 25418962
[TBL] [Abstract][Full Text] [Related]
7. Probability of phenotypically detectable protein damage by ENU-induced mutations in the Mutagenetix database.
Wang T; Bu CH; Hildebrand S; Jia G; Siggs OM; Lyon S; Pratt D; Scott L; Russell J; Ludwig S; Murray AR; Moresco EMY; Beutler B
Nat Commun; 2018 Jan; 9(1):441. PubMed ID: 29382827
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. An ENU-induced mutation of Nrg1 causes dilated pupils and a reduction in muscarinic receptors in the sphincter pupillae.
Chen B; Li K; Zhang F; Zhai G; Gong W; Qiang S; Xue Z
PLoS One; 2011; 6(9):e25176. PubMed ID: 21949880
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. A phenotype-driven ENU mutagenesis screen for the identification of dominant mutations involved in alcohol consumption.
Pawlak CR; Sanchis-Segura C; Soewarto D; Wagner S; Hrabé de Angelis M; Spanagel R
Mamm Genome; 2008 Feb; 19(2):77-84. PubMed ID: 18213483
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. An N-ethyl-N-nitrosourea mutagenesis screen for epigenetic mutations in the mouse.
Percec I; Thorvaldsen JL; Plenge RM; Krapp CJ; Nadeau JH; Willard HF; Bartolomei MS
Genetics; 2003 Aug; 164(4):1481-94. PubMed ID: 12930754
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Large-scale N-ethyl-N-nitrosourea mutagenesis of mice--from phenotypes to genes.
Rathkolb B; Fuchs E; Kolb HJ; Renner-Müller I; Krebs O; Balling R; Hrabé de Angelis M; Wolf E
Exp Physiol; 2000 Nov; 85(6):635-44. PubMed ID: 11187959
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. ENU-induced missense mutation in the C-propeptide coding region of Col2a1 creates a mouse model of platyspondylic lethal skeletal dysplasia, Torrance type.
Furuichi T; Masuya H; Murakami T; Nishida K; Nishimura G; Suzuki T; Imaizumi K; Kudo T; Ohkawa K; Wakana S; Ikegawa S
Mamm Genome; 2011 Jun; 22(5-6):318-28. PubMed ID: 21538020
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Dose-dependent induction of recessive mutations with N-ethyl-N-nitrosourea in primordial germ cells of male mice.
Shibuya T; Horiya N; Matsuda H; Sakamoto K; Hara T
Mutat Res; 1996 Oct; 357(1-2):219-24. PubMed ID: 8876697
[TBL] [Abstract][Full Text] [Related]
20. ENU mutagenesis as a tool for understanding lung development and disease.
Yates L; McMurray F; Zhang Y; Greenfield A; Moffatt M; Cookson W; Dean C
Biochem Soc Trans; 2009 Aug; 37(Pt 4):838-42. PubMed ID: 19614604
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]