BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

191 related articles for article (PubMed ID: 17986521)

  • 1. An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda.
    Barbaric I; Perry MJ; Dear TN; Rodrigues Da Costa A; Salopek D; Marusic A; Hough T; Wells S; Hunter AJ; Cheeseman M; Brown SD
    Physiol Genomics; 2008 Feb; 32(3):311-21. PubMed ID: 17986521
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Characterization of two ENU-induced mutations affecting mouse skeletal morphology.
    Dauphinee SM; Eva MM; Yuki KE; Herman M; Vidal SM; Malo D
    G3 (Bethesda); 2013 Oct; 3(10):1753-8. PubMed ID: 23979929
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Signaling Pathway.
    Esapa CT; Piret SE; Nesbit MA; Loh NY; Thomas G; Croucher PI; Brown MA; Brown SD; Cox RD; Thakker RV
    PLoS One; 2016; 11(12):e0167916. PubMed ID: 27959934
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mouse mutants from chemically mutagenized embryonic stem cells.
    Munroe RJ; Bergstrom RA; Zheng QY; Libby B; Smith R; John SW; Schimenti KJ; Browning VL; Schimenti JC
    Nat Genet; 2000 Mar; 24(3):318-21. PubMed ID: 10700192
    [TBL] [Abstract][Full Text] [Related]  

  • 5. New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.
    Sabrautzki S; Rubio-Aliaga I; Hans W; Fuchs H; Rathkolb B; Calzada-Wack J; Cohrs CM; Klaften M; Seedorf H; Eck S; Benet-Pagès A; Favor J; Esposito I; Strom TM; Wolf E; Lorenz-Depiereux B; Hrabě de Angelis M
    Mamm Genome; 2012 Aug; 23(7-8):416-30. PubMed ID: 22527485
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
    Flenniken AM; Osborne LR; Anderson N; Ciliberti N; Fleming C; Gittens JE; Gong XQ; Kelsey LB; Lounsbury C; Moreno L; Nieman BJ; Peterson K; Qu D; Roscoe W; Shao Q; Tong D; Veitch GI; Voronina I; Vukobradovic I; Wood GA; Zhu Y; Zirngibl RA; Aubin JE; Bai D; Bruneau BG; Grynpas M; Henderson JE; Henkelman RM; McKerlie C; Sled JG; Stanford WL; Laird DW; Kidder GM; Adamson SL; Rossant J
    Development; 2005 Oct; 132(19):4375-86. PubMed ID: 16155213
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Wa5 is a novel ENU-induced antimorphic allele of the epidermal growth factor receptor.
    Lee D; Cross SH; Strunk KE; Morgan JE; Bailey CL; Jackson IJ; Threadgill DW
    Mamm Genome; 2004 Jul; 15(7):525-36. PubMed ID: 15366372
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Functional analysis of a novel ENU-induced PHD finger 11 (Phf11) mouse mutant.
    Zhang Y; Dean C; Chessum L; Nguyen D; Stewart M; Taylor M; Cookson WO; Moffatt MF
    Mamm Genome; 2014 Dec; 25(11-12):573-82. PubMed ID: 25091723
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Three ENU-induced neurological mutations in the pore loop of sodium channel Scn8a (Na(v)1.6) and a genetically linked retinal mutation, rd13.
    Buchner DA; Seburn KL; Frankel WN; Meisler MH
    Mamm Genome; 2004 May; 15(5):344-51. PubMed ID: 15170223
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of a novel missense mutation on murine Pax3 through ENU mutagenesis.
    Xiao Y; Zhang L; He K; Gao X; Yang L; He L; Ma G; Guo X
    J Genet Genomics; 2011 Aug; 38(8):333-9. PubMed ID: 21867959
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A Sox10 expression screen identifies an amino acid essential for Erbb3 function.
    Buac K; Watkins-Chow DE; Loftus SK; Larson DM; Incao A; Gibney G; Pavan WJ
    PLoS Genet; 2008 Sep; 4(9):e1000177. PubMed ID: 18773073
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A new mouse model of type 2 diabetes, produced by N-ethyl-nitrosourea mutagenesis, is the result of a missense mutation in the glucokinase gene.
    Toye AA; Moir L; Hugill A; Bentley L; Quarterman J; Mijat V; Hough T; Goldsworthy M; Haynes A; Hunter AJ; Browne M; Spurr N; Cox RD
    Diabetes; 2004 Jun; 53(6):1577-83. PubMed ID: 15161764
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An ENU-induced point mutation in the mouse Btaf1 gene causes post-gastrulation embryonic lethality and protein instability.
    Wansleeben C; van Gurp L; de Graaf P; Mousson F; Marc Timmers HT; Meijlink F
    Mech Dev; 2011; 128(5-6):279-88. PubMed ID: 21419221
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Ethylnitrosourea-induced mutation and molecular analysis of transgenic mice containing the gpt shuttle vector.
    Yamada T; Yamamoto R; Kaneko H; Yoshitake A
    Mutat Res; 1999 Apr; 441(1):59-72. PubMed ID: 10224323
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A phenotype-driven ENU mutagenesis screen identifies novel alleles with functional roles in early mouse craniofacial development.
    Sandell LL; Iulianella A; Melton KR; Lynn M; Walker M; Inman KE; Bhatt S; Leroux-Berger M; Crawford M; Jones NC; Dennis JF; Trainor PA
    Genesis; 2011 Apr; 49(4):342-59. PubMed ID: 21305688
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.