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793 results
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Lymphoproliferation disorder in mice explained by defects in Fas antigen that mediates apoptosis.
Watanabe-Fukunaga R, Brannan CI, Copeland NG, Jenkins NA, Nagata S. Watanabe-Fukunaga R, et al. Among authors: copeland ng. Nature. 1992 Mar 26;356(6367):314-7. doi: 10.1038/356314a0. Nature. 1992. PMID: 1372394
The cDNA structure, expression, and chromosomal assignment of the mouse Fas antigen.
Watanabe-Fukunaga R, Brannan CI, Itoh N, Yonehara S, Copeland NG, Jenkins NA, Nagata S. Watanabe-Fukunaga R, et al. Among authors: copeland ng. J Immunol. 1992 Feb 15;148(4):1274-9. J Immunol. 1992. PMID: 1371136
Molecular cloning of the murine ST2 gene. Characterization and chromosomal mapping.
Tominaga S, Jenkins NA, Gilbert DJ, Copeland NG, Tetsuka T. Tominaga S, et al. Among authors: copeland ng. Biochim Biophys Acta. 1991 Aug 27;1090(1):1-8. doi: 10.1016/0167-4781(91)90029-l. Biochim Biophys Acta. 1991. PMID: 1832015
Novel myosin heavy chain encoded by murine dilute coat colour locus.
Mercer JA, Seperack PK, Strobel MC, Copeland NG, Jenkins NA. Mercer JA, et al. Among authors: copeland ng. Nature. 1991 Feb 21;349(6311):709-13. doi: 10.1038/349709a0. Nature. 1991. PMID: 1996138
Sequence homology shared by neurofibromatosis type-1 gene and IRA-1 and IRA-2 negative regulators of the RAS cyclic AMP pathway.
Buchberg AM, Cleveland LS, Jenkins NA, Copeland NG. Buchberg AM, et al. Among authors: copeland ng. Nature. 1990 Sep 20;347(6290):291-4. doi: 10.1038/347291a0. Nature. 1990. PMID: 2169593
Dilute (d) coat colour mutation of DBA/2J mice is associated with the site of integration of an ecotropic MuLV genome.
Jenkins NA, Copeland NG, Taylor BA, Lee BK. Jenkins NA, et al. Among authors: copeland ng. Nature. 1981 Oct 1;293(5831):370-4. doi: 10.1038/293370a0. Nature. 1981. PMID: 6268990
The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells.
Avraham KB, Hasson T, Steel KP, Kingsley DM, Russell LB, Mooseker MS, Copeland NG, Jenkins NA. Avraham KB, et al. Among authors: copeland ng. Nat Genet. 1995 Dec;11(4):369-75. doi: 10.1038/ng1295-369. Nat Genet. 1995. PMID: 7493015
Generalized lymphoproliferative disease in mice, caused by a point mutation in the Fas ligand.
Takahashi T, Tanaka M, Brannan CI, Jenkins NA, Copeland NG, Suda T, Nagata S. Takahashi T, et al. Among authors: copeland ng. Cell. 1994 Mar 25;76(6):969-76. doi: 10.1016/0092-8674(94)90375-1. Cell. 1994. PMID: 7511063
A novel cytokine-inducible gene CIS encodes an SH2-containing protein that binds to tyrosine-phosphorylated interleukin 3 and erythropoietin receptors.
Yoshimura A, Ohkubo T, Kiguchi T, Jenkins NA, Gilbert DJ, Copeland NG, Hara T, Miyajima A. Yoshimura A, et al. Among authors: copeland ng. EMBO J. 1995 Jun 15;14(12):2816-26. EMBO J. 1995. PMID: 7796808 Free PMC article.
Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences.
Steingrímsson E, Moore KJ, Lamoreux ML, Ferré-D'Amaré AR, Burley SK, Zimring DC, Skow LC, Hodgkinson CA, Arnheiter H, Copeland NG, et al. Steingrímsson E, et al. Among authors: copeland ng. Nat Genet. 1994 Nov;8(3):256-63. doi: 10.1038/ng1194-256. Nat Genet. 1994. PMID: 7874168
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