1 - 25 of 34 results for author:"Wilkinson J.E." in Literature citations
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| Neurodegeneration and early lethality in superoxide dismutase 2-deficient mice: a comprehensive analysis of the central and peripheral nervous systems. Oh S.S., Sullivan K.A., Wilkinson J.E., Backus C., Hayes J.M., Sakowski S.A., Feldman E.L. Neuroscience 212:201-213(2012) · Mapped (10) |
| RASA1 maintains the lymphatic vasculature in a quiescent functional state in mice. Lapinski P.E., Kwon S., Lubeck B.A., Wilkinson J.E., Srinivasan R.S., Sevick-Muraca E., King P.D. J. Clin. Invest. 122:733-747(2012) · Mapped (5) |
| Pioglitazone induces a proadipogenic antitumor response in mice with PAX8-PPARgamma fusion protein thyroid carcinoma. Dobson M.E., Diallo-Krou E., Grachtchouk V., Yu J., Colby L.A., Wilkinson J.E., Giordano T.J., Koenig R.J. Endocrinology 152:4455-4465(2011) · Mapped (5) |
| Development of severe skeletal defects in induced SHP-2-deficient adult mice: a model of skeletal malformation in humans with SHP-2 mutations. Bauler T.J., Kamiya N., Lapinski P.E., Langewisch E., Mishina Y., Wilkinson J.E., Feng G.S., King P.D. Dis Model Mech 4:228-239(2011) · Mapped (10) |
| Macrophage migration inhibitory factor-knockout mice are long lived and respond to caloric restriction. Harper J.M., Wilkinson J.E., Miller R.A. FASEB J. 24:2436-2442(2010) · Mapped (2) |
| Paired box gene 8-peroxisome proliferator-activated receptor-gamma fusion protein and loss of phosphatase and tensin homolog synergistically cause thyroid hyperplasia in transgenic mice. Diallo-Krou E., Yu J., Colby L.A., Inoki K., Wilkinson J.E., Thomas D.G., Giordano T.J., Koenig R.J. Endocrinology 150:5181-5190(2009) · Mapped (14) |
| Expression and sub-cellular localization of the CCAAT/enhancer binding protein alpha in relation to postnatal development and malignancy of the prostate. Zhang J., Wilkinson J.E., Gonit M., Keck R., Selman S., Ratnam M. Prostate 68:1206-1214(2008) · Mapped (4) |
| The DNA sequence and biological annotation of human chromosome 1. Gregory S.G., Barlow K.F., McLay K.E., Kaul R., Swarbreck D., Dunham A., Scott C.E., Howe K.L., Woodfine K., Spencer C.C.A. et al. Nature 441:315-321(2006) · UniProtKB (5,143) |
| The DNA sequence of the human X chromosome. Ross M.T., Grafham D.V., Coffey A.J., Scherer S., McLay K., Muzny D., Platzer M., Howell G.R., Burrows C., Bird C.P. et al. Nature 434:325-337(2005) · UniProtKB (1,805) |
| Nucleotide sequence based characterizations of two cryptic plasmids from the marine bacterium Ruegeria isolate PR1b. Zhong Z., Caspi R., Helinski D., Knauf V., Sykes S., O'Byrne C., Shea T.P., Wilkinson J.E., DeLoughery C., Toukdarian A. Plasmid 49:233-252(2003) · UniProtKB (185) |
| A transgenic mouse strain with antigen-specific T cells (RAG1KO/sf/OVA) demonstrates that the scurfy (sf) mutation causes a defect in T-cell tolerization. Zahorsky-Reeves J.L., Wilkinson J.E. Comp. Med. 52:58-62(2002) · Mapped (16) |
| Phenotypic variations of orpk mutation and chromosomal localization of modifiers influencing kidney phenotype. Sommardahl C., Cottrell M., Wilkinson J.E., Woychik R.P., Johnson D.K. Physiol. Genomics 7:127-134(2001) · Mapped (5) |
| Sequence analysis of a 101-kilobase plasmid required for agar degradation by a Microscilla isolate. Zhong Z., Toukdarian A., Helinski D., Knauf V., Sykes S., Wilkinson J.E., O'Bryne C., Shea T., DeLoughery C., Caspi R. Appl. Environ. Microbiol. 67:5771-5779(2001) · UniProtKB (64) |
| The murine mutation scurfy (sf) results in an antigen-dependent lymphoproliferative disease with altered T cell sensitivity. Zahorsky-Reeves J.L., Wilkinson J.E. Eur. J. Immunol. 31:196-204(2001) · Mapped (2) |
| Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse. Brunkow M.E., Jeffery E.W., Hjerrild K.A., Paeper B., Clark L.B., Yasayko S.-A., Wilkinson J.E., Galas D., Ziegler S.F., Ramsdell F. |
| Cellular and molecular characterization of the scurfy mouse mutant. Clark L.B., Appleby M.W., Brunkow M.E., Wilkinson J.E., Ziegler S.F., Ramsdell F. J. Immunol. 162:2546-2554(1999) · Mapped (5) |
| Effect of the viable-yellow (A(vy)) agouti allele on skin tumorigenesis and humoral hypercalcemia in v-Ha-ras transgenic TGxAC mice. Hansen L.A., Malarkey D.E., Wilkinson J.E., Rosenberg M., Woychik R.E., Tennant R.W. Carcinogenesis 19:1837-1845(1998) · Mapped (3) |
| Epidermal growth factor receptor activity mediates renal cyst formation in polycystic kidney disease. Richards W.G., Sweeney W.E., Yoder B.K., Wilkinson J.E., Woychik R.P., Avner E.D. J. Clin. Invest. 101:935-939(1998) · Mapped (11) |
| Efficacy of taxol in the orpk mouse model of polycystic kidney disease. Sommardahl C.S., Woychik R.P., Sweeney W.E., Avner E.D., Wilkinson J.E. Pediatr. Nephrol. 11:728-733(1997) · Mapped (5) |
| Role of the agouti gene in obesity. Michaud E.J., Mynatt R.L., Miltenberger R.J., Klebig M.L., Wilkinson J.E., Zemel M.B., Wilkison W.O., Woychik R.P. J. Endocrinol. 155:207-209(1997) · Mapped (3) |
| The role of the agouti gene in the yellow obese syndrome. Miltenberger R.J., Mynatt R.L., Wilkinson J.E., Woychik R.P. J. Nutr. 127:1902S-1907S(1997) · Mapped (3) |
| Differential rescue of the renal and hepatic disease in an autosomal recessive polycystic kidney disease mouse mutant. A new model to study the liver lesion. Yoder B.K., Richards W.G., Sommardahl C., Sweeney W.E., Michaud E.J., Wilkinson J.E., Avner E.D., Woychik R.P. Am. J. Pathol. 150:2231-2241(1997) · Mapped (5) |
| Combined effects of insulin treatment and adipose tissue-specific agouti expression on the development of obesity. Mynatt R.L., Miltenberger R.J., Klebig M.L., Zemel M.B., Wilkinson J.E., Wilkinson W.O., Woychik R.P. Proc. Natl. Acad. Sci. U.S.A. 94:919-922(1997) · Mapped (3) |
| Oval cell proliferation associated with the murine insertional mutation TgN737Rpw. Richards W.G., Yoder B.K., Isfort R.J., Detilleux P.G., Foster C., Neilsen N., Woychik R.P., Wilkinson J.E. Am. J. Pathol. 149:1919-1930(1996) · Mapped (9) |
| The mouse homolog of the Wiskott-Aldrich syndrome protein (WASP) gene is highly conserved and maps near the scurfy (sf) mutation on the X chromosome. Derry J.M.J., Wiedemann P., Blair P., Wang Y., Kerns J.A., Lemahieu V., Godfrey V.L., Wilkinson J.E., Francke U. |