1 - 25 of
139
results
for author:"Bradley A."
in Literature Citations
| High-throughput sequence analysis of variants of human cytomegalovirus strains Towne and AD169. Bradley A.J., Lurain N.S., Ghazal P., Trivedi U., Cunningham C., Baluchova K., Gatherer D., Wilkinson G.W., Dargan D.J., Davison A.J. J. Gen. Virol. 90:2375-2380(2009) · UniProtKB (302) |
| Agouti C57BL/6N embryonic stem cells for mouse genetic resources. Pettitt S.J., Liang Q., Rairdan X.Y., Moran J.L., Prosser H.M., Beier D.R., Lloyd K.C., Bradley A., Skarnes W.C. Nat. Methods 6:493-495(2009) · Mapped (1) |
| Analysis of Pax6 contiguous gene deletions in the mouse, Mus musculus, identifies regions distinct from Pax6 responsible for extreme small-eye and belly-spotting phenotypes. Favor J., Bradley A., Conte N., Janik D., Pretsch W., Reitmeir P., Rosemann M., Schmahl W., Wienberg J., Zaus I. Genetics 182:1077-1088(2009) · Mapped (8) |
| Surfactant protein D and KL-6 as serum biomarkers of interstitial lung disease in patients with scleroderma. Hant F.N., Ludwicka-Bradley A., Wang H.J., Li N., Elashoff R., Tashkin D.P., Silver R.M. J. Rheumatol. 36:773-780(2009) · Mapped (72) |
| Proteomic analysis of CTGF-activated lung fibroblasts: identification of IQGAP1 as a key player in lung fibroblast migration. Bogatkevich G.S., Ludwicka-Bradley A., Singleton C.B., Bethard J.R., Silver R.M. Am. J. Physiol. Lung Cell Mol. Physiol. 295:L603-11(2008) · Mapped (7) |
| Increased insulin action in SKIP heterozygous knockout mice. Ijuin T., Yu Y.E., Mizutani K., Pao A., Tateya S., Tamori Y., Bradley A., Takenawa T. Mol. Cell. Biol. 28:5184-5195(2008) · Mapped (4) |
| Normal germ line establishment in mice carrying a deletion of the Ifitm/Fragilis gene family cluster. Lange U.C., Adams D.J., Lee C., Barton S., Schneider R., Bradley A., Surani M.A. Mol. Cell. Biol. 28:4688-4696(2008) · Mapped (13) |
| Loss of Rassf1a cooperates with Apc(Min) to accelerate intestinal tumourigenesis. van der Weyden L., Arends M.J., Dovey O.M., Harrison H.L., Lefebvre G., Conte N., Gergely F.V., Bradley A., Adams D.J. Oncogene 27:4503-4508(2008) · Mapped (9) |
| Mosaic complementation demonstrates a regulatory role for myosin VIIa in actin dynamics of stereocilia. Prosser H.M., Rzadzinska A.K., Steel K.P., Bradley A. Mol. Cell. Biol. 28:1702-1712(2008) · Mapped (10) |
| Olfactory bulb hypoplasia in Prokr2 null mice stems from defective neuronal progenitor migration and differentiation. Prosser H.M., Bradley A., Caldwell M.A. Eur. J. Neurosci. 26:3339-3344(2007) · Mapped (3) |
| Down-regulation of collagen and connective tissue growth factor expression with hepatocyte growth factor in lung fibroblasts from white scleroderma patients via two signaling pathways. Bogatkevich G.S., Ludwicka-Bradley A., Highland K.B., Hant F., Nietert P.J., Singleton C.B., Silver R.M. Arthritis Rheum. 56:3468-3477(2007) · Mapped (3) |
| Alpha3-integrins are required for hippocampal long-term potentiation and working memory. Chan C.S., Levenson J.M., Mukhopadhyay P.S., Zong L., Bradley A., Sweatt J.D., Davis R.L. Learn. Mem. 14:606-615(2007) · Mapped (4) |
| Impairment of the antifibrotic effect of hepatocyte growth factor in lung fibroblasts from African Americans: possible role in systemic sclerosis. Bogatkevich G.S., Ludwicka-Bradley A., Highland K.B., Hant F., Nietert P.J., Singleton C.B., Feghali-Bostwick C.A., Silver R.M. Arthritis Rheum. 56:2432-2442(2007) · Mapped (3) |
| Requirement of bic/microRNA-155 for normal immune function. Rodriguez A., Vigorito E., Clare S., Warren M.V., Couttet P., Soond D.R., van Dongen S., Grocock R.J., Das P.P., Miska E.A. et al. Science 316:608-611(2007) · Mapped (3) |
| Proteorhodopsin photosystem gene expression enables photophosphorylation in a heterologous host. Martinez A., Bradley A.S., Waldbauer J.R., Summons R.E., DeLong E.F. Proc. Natl. Acad. Sci. U.S.A. 104:5590-5595(2007) · UniProtKB (92) |
| A Sall4 mutant mouse model useful for studying the role of Sall4 in early embryonic development and organogenesis. Warren M., Wang W., Spiden S., Chen-Murchie D., Tannahill D., Steel K.P., Bradley A. Genesis 45:51-58(2007) · Mapped (9) |
| Prokineticin receptor 2 (Prokr2) is essential for the regulation of circadian behavior by the suprachiasmatic nuclei. Prosser H.M., Bradley A., Chesham J.E., Ebling F.J., Hastings M.H., Maywood E.S. Proc. Natl. Acad. Sci. U.S.A. 104:648-653(2007) · Mapped (9) |
| Secretin receptor-deficient mice exhibit impaired synaptic plasticity and social behavior. Nishijima I., Yamagata T., Spencer C.M., Weeber E.J., Alekseyenko O., Sweatt J.D., Momoi M.Y., Ito M., Armstrong D.L., Nelson D.L. et al. Hum. Mol. Genet. 15:3241-3250(2006) · Mapped (1) |
| Functional knockout of the matrilin-3 gene causes premature chondrocyte maturation to hypertrophy and increases bone mineral density and osteoarthritis. van der Weyden L., Wei L., Luo J., Yang X., Birk D.E., Adams D.J., Bradley A., Chen Q. Am. J. Pathol. 169:515-527(2006) · Mapped (45) |
| Geminin is essential to prevent endoreduplication and to form pluripotent cells during mammalian development. Gonzalez M.A., Tachibana K.E., Adams D.J., van der Weyden L., Hemberger M., Coleman N., Bradley A., Laskey R.A. Genes Dev. 20:1880-1884(2006) · Mapped (10) |
| Generation and maintenance of Dmbx1 gene-targeted mutant alleles. Ohtoshi A., Bradley A., Behringer R.R., Nishijima I. Mamm. Genome 17:744-750(2006) · Mapped (1) |
| p63 heterozygous mutant mice are not prone to spontaneous or chemically induced tumors. Keyes W.M., Vogel H., Koster M.I., Guo X., Qi Y., Petherbridge K.M., Roop D.R., Bradley A., Mills A.A. Proc. Natl. Acad. Sci. U.S.A. 103:8435-8440(2006) · Mapped (14) |
| DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage. Zody M.C., Garber M., Adams D.J., Sharpe T., Harrow J., Lupski J.R., Nicholson C., Searle S.M., Wilming L., Young S.K. et al. Nature 440:1045-1049(2006) · UniProtKB (913) |
| Loss of TSLC1 causes male infertility due to a defect at the spermatid stage of spermatogenesis. van der Weyden L., Arends M.J., Chausiaux O.E., Ellis P.J., Lange U.C., Surani M.A., Affara N., Murakami Y., Adams D.J., Bradley A. Mol. Cell. Biol. 26:3595-3609(2006) · UniProtKB (1) · Mapped (4) |
| A deficiency in the region homologous to human 17q21.33-q23.2 causes heart defects in mice. Yu Y.E., Morishima M., Pao A., Wang D.Y., Wen X.Y., Baldini A., Bradley A. Genetics 173:297-307(2006) · Mapped (9) |
