1 - 25 of
184
results
for author:"Stewart A."
in Literature Citations
| Association between vitamin D receptor gene polymorphisms, falls, balance and muscle power: results from two independent studies (APOSS and OPUS). Barr R., Macdonald H., Stewart A., McGuigan F., Rogers A., Eastell R., Felsenberg D., Gluer C., Roux C., Reid D.M. Osteoporos Int 0:0-0(2009) · Mapped (6) |
| A mitotic recombination map proximal to the APC locus on chromosome 5q and assessment of influences on colorectal cancer risk. Howarth K., Ranta S., Winter E., Teixeira A., Schaschl H., Harvey J.J., Rowan A., Jones A., Spain S., Clark S. et al. BMC Med. Genet. 10:54-54(2009) · Mapped (12) |
| Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss. Dai P., Stewart A.K., Chebib F., Hsu A., Rozenfeld J., Huang D., Kang D., Lip V., Fang H., Shao H. et al. Physiol. Genomics 38:281-290(2009) · Mapped (5) |
| New Zealand Ginger mouse: novel model that associates the tyrp1b pigmentation gene locus with regulation of lean body mass. Duchesnes C.E., Naggert J.K., Tatnell M.A., Beckman N., Marnane R.N., Rodrigues J.A., Halim A., Pontre B., Stewart A.W., Wolff G.L. et al. Physiol. Genomics 37:164-174(2009) · Mapped (1) |
| Differential expression and functional characterization of luteinizing hormone receptor splice variants in human luteal cells: implications for luteolysis. Dickinson R.E., Stewart A.J., Myers M., Millar R.P., Duncan W.C. Endocrinology 150:2873-2881(2009) · Mapped (3) |
| Functional characterization of a promoter polymorphism that drives ACSL5 gene expression in skeletal muscle and associates with diet-induced weight loss. Teng A.C., Adamo K., Tesson F., Stewart A.F. FASEB J. 23:1705-1709(2009) · Mapped (3) |
| Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms? Choi B.Y., Stewart A.K., Madeo A.C., Pryor S.P., Lenhard S., Kittles R., Eisenman D., Kim H.J., Niparko J., Thomsen J. et al. |
| Survey of the human pancreatic beta-cell G1/S proteome reveals a potential therapeutic role for cdk-6 and cyclin D1 in enhancing human beta-cell replication and function in vivo. Fiaschi-Taesch N., Bigatel T.A., Sicari B., Takane K.K., Salim F., Velazquez-Garcia S., Harb G., Selk K., Cozar-Castellano I., Stewart A.F. Diabetes 58:882-893(2009) · Mapped (8) |
| Epigenetic downregulation of the DNA repair gene MED1/MBD4 in colorectal and ovarian cancer. Howard J.H., Frolov A., Tzeng C.W., Stewart A., Midzak A., Majmundar A., Godwin A., Heslin M., Bellacosa A., Arnoletti J.P. Cancer Biol. Ther. 8:94-100(2009) · Mapped (3) |
| Putative re-entrant loop 1 of AE2 transmembrane domain has a major role in acute regulation of anion exchange by pH. Stewart A.K., Kurschat C.E., Vaughan-Jones R.D., Alper S.L. J. Biol. Chem. 284:6126-6139(2009) · Mapped (6) |
| Chromatin Central: towards the comparative proteome by accurate mapping of the yeast proteomic environment. Shevchenko A., Roguev A., Schaft D., Buchanan L., Habermann B., Sakalar C., Thomas H., Krogan N.J., Shevchenko A., Stewart A.F. Genome Biol. 9:R167.1-R167.22(2008) · UniProtKB (6) · Mapped (62) |
| A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups. Sulong S., Moorman A.V., Irving J.A., Strefford J.C., Konn Z.J., Case M.C., Minto L., Barber K.E., Parker H., Wright S.L. et al. Blood 113:100-107(2009) · Mapped (7) |
| Hepatocyte growth factor enhances engraftment and function of nonhuman primate islets. Fiaschi-Taesch N.M., Berman D.M., Sicari B.M., Takane K.K., Garcia-Ocana A., Ricordi C., Kenyon N.S., Stewart A.F. Diabetes 57:2745-2754(2008) · Mapped (5) |
| The complex genomic profile of ETV6-RUNX1 positive acute lymphoblastic leukemia highlights a recurrent deletion of TBL1XR1. Parker H., An Q., Barber K., Case M., Davies T., Konn Z., Stewart A., Wright S., Griffiths M., Ross F.M. et al. Genes Chromosomes Cancer 47:1118-1125(2008) · Mapped (11) |
| Effects of NGF, NT-3 and GDNF family members on neurite outgrowth and migration from pelvic ganglia from embryonic and newborn mice. Stewart A.L., Anderson R.B., Kobayashi K., Young H.M. BMC Dev. Biol. 8:73-73(2008) · Mapped (7) |
| The TGM2 gene is associated with schizophrenia in a British population. Bradford M., Law M.H., Stewart A.D., Shaw D.J., Megson I.L., Wei J. Am. J. Med. Genet. B Neuropsychiatr. Genet. 150B:335-340(2009) · Mapped (8) |
| Direct visualization of the trimeric structure of the ASIC1a channel, using AFM imaging. Carnally S.M., Dev H.S., Stewart A.P., Barrera N.P., Van Bemmelen M.X., Schild L., Henderson R.M., Edwardson J.M. Biochem. Biophys. Res. Commun. 372:752-755(2008) · Mapped (4) |
| Mouse Ae1 E699Q mediates SO42-i/anion-o exchange with [SO42-]i-dependent reversal of wild-type pHo sensitivity. Chernova M.N., Stewart A.K., Barry P.N., Jennings M.L., Alper S.L. Am. J. Physiol., Cell Physiol. 295:C302-12(2008) · Mapped (11) |
| Identification of kinetin riboside as a repressor of CCND1 and CCND2 with preclinical antimyeloma activity. Tiedemann R.E., Mao X., Shi C.X., Zhu Y.X., Palmer S.E., Sebag M., Marler R., Chesi M., Fonseca R., Bergsagel P.L. et al. J. Clin. Invest. 118:1750-1764(2008) · Mapped (8) |
| Genetic analysis of the spindle checkpoint genes san-1, mdf-2, bub-3 and the CENP-F homologues hcp-1 and hcp-2 in Caenorhabditis elegans. Hajeri V.A., Stewart A.M., Moore L.L., Padilla P.A. Cell Div 3:6-6(2008) · Mapped (8) |
| AID-dependent activation of a MYC transgene induces multiple myeloma in a conditional mouse model of post-germinal center malignancies. Chesi M., Robbiani D.F., Sebag M., Chng W.J., Affer M., Tiedemann R., Valdez R., Palmer S.E., Haas S.S., Stewart A.K. et al. Cancer Cell 13:167-180(2008) · Mapped (21) |
| Characterisation of a Trichoderma hamatum monooxygenase gene involved in antagonistic activity against fungal plant pathogens. Carpenter M.A., Ridgway H.J., Stringer A.M., Hay A.J., Stewart A. Curr. Genet. 53:193-205(2008) · UniProtKB (2) |
| Mouse strain-specific coding polymorphism in the Slc4a2/Ae2 gene encodes Ae2c2 variants differing in isoform-specific dominant negative activity. Kurschat C.E., Shmukler B.E., Jiang L., Hevi S., Kim E.H., Stewart A.K., Alper S.L. Exp. Physiol. 93:458-467(2008) · Mapped (6) |
| Species differences in Cl- affinity and in electrogenicity of SLC26A6-mediated oxalate/Cl- exchange correlate with the distinct human and mouse susceptibilities to nephrolithiasis. Clark J.S., Vandorpe D.H., Chernova M.N., Heneghan J.F., Stewart A.K., Alper S.L. J. Physiol. (Lond.) 586:1291-1306(2008) · Mapped (16) |
| Zebrafish ae2.2 encodes a second slc4a2 anion exchanger. Shmukler B.E., Clark J.S., Hsu A., Vandorpe D.H., Stewart A.K., Kurschat C.E., Choe S.K., Zhou Y., Amigo J., Paw B.H. et al. Am. J. Physiol. Regul. Integr. Comp. Physiol. 294:R1081-91(2008) · UniProtKB (2) · Mapped (5) |
