Jenkins NA - Search Results

1

Transposon mutagenesis identifies genetic drivers of Braf(V600E) melanoma.

Mann MB, Black MA, Jones DJ, Ward JM, Yew CC, Newberg JY, Dupuy AJ, Rust AG, Bosenberg MW, McMahon M, Print CG, Copeland NG, Jenkins NA. Mann MB, et al. Among authors: jenkins na. Nat Genet. 2015 May;47(5):486-95. doi: 10.1038/ng.3275. Epub 2015 Apr 13. Nat Genet. 2015. PMID: 25848750 Free PMC article.

2

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region.

Leff SE, Brannan CI, Reed ML, Ozçelik T, Francke U, Copeland NG, Jenkins NA. Leff SE, et al. Among authors: jenkins na. Nat Genet. 1992 Dec;2(4):259-64. doi: 10.1038/ng1292-259. Nat Genet. 1992. PMID: 1303276

3

A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression.

Cattanach BM, Barr JA, Evans EP, Burtenshaw M, Beechey CV, Leff SE, Brannan CI, Copeland NG, Jenkins NA, Jones J. Cattanach BM, et al. Among authors: jenkins na. Nat Genet. 1992 Dec;2(4):270-4. doi: 10.1038/ng1292-270. Nat Genet. 1992. PMID: 1303278

4

The mouse short ear skeletal morphogenesis locus is associated with defects in a bone morphogenetic member of the TGF beta superfamily.

Kingsley DM, Bland AE, Grubber JM, Marker PC, Russell LB, Copeland NG, Jenkins NA. Kingsley DM, et al. Among authors: jenkins na. Cell. 1992 Oct 30;71(3):399-410. doi: 10.1016/0092-8674(92)90510-j. Cell. 1992. PMID: 1339316 Free article.

5

Structure of the mouse IL-10 gene and chromosomal localization of the mouse and human genes.

Kim JM, Brannan CI, Copeland NG, Jenkins NA, Khan TA, Moore KW. Kim JM, et al. Among authors: jenkins na. J Immunol. 1992 Jun 1;148(11):3618-23. J Immunol. 1992. PMID: 1350294

6

Regional localization of three convertases, PC1 (Nec-1), PC2 (Nec-2), and furin (Fur), on mouse chromosomes.

Copeland NG, Gilbert DJ, Chrétien M, Seidah NG, Jenkins NA. Copeland NG, et al. Among authors: jenkins na. Genomics. 1992 Aug;13(4):1356-8. doi: 10.1016/0888-7543(92)90069-5. Genomics. 1992. PMID: 1354647

7

The human pseudoautosomal GM-CSF receptor alpha subunit gene is autosomal in mouse.

Disteche CM, Brannan CI, Larsen A, Adler DA, Schorderet DF, Gearing D, Copeland NG, Jenkins NA, Park LS. Disteche CM, et al. Among authors: jenkins na. Nat Genet. 1992 Aug;1(5):333-6. doi: 10.1038/ng0892-333. Nat Genet. 1992. PMID: 1363815

8

Recombinant inbred mouse strains: models for disease study.

Justice MJ, Jenkins NA, Copeland NG. Justice MJ, et al. Among authors: jenkins na. Trends Biotechnol. 1992 Apr;10(4):120-6. doi: 10.1016/0167-7799(92)90193-y. Trends Biotechnol. 1992. PMID: 1368097 Review.

9

Four novel members of the connexin family of gap junction proteins. Molecular cloning, expression, and chromosome mapping.

Haefliger JA, Bruzzone R, Jenkins NA, Gilbert DJ, Copeland NG, Paul DL. Haefliger JA, et al. Among authors: jenkins na. J Biol Chem. 1992 Jan 25;267(3):2057-64. J Biol Chem. 1992. PMID: 1370487 Free article.

10

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: jenkins na. Nature. 1992 Mar 26;356(6367):314-7. doi: 10.1038/356314a0. Nature. 1992. PMID: 1372394

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