1 - 25 of
117
results
for author:"Mueller J."
in Literature Citations
| Inflammasome-mediated disease animal models reveal roles for innate but not adaptive immunity. Brydges S.D., Mueller J.L., McGeough M.D., Pena C.A., Misaghi A., Gandhi C., Putnam C.D., Boyle D.L., Firestein G.S., Horner A.A. et al. Immunity 30:875-887(2009) · Mapped (12) |
| Association of transcription factor polymorphisms PITX3 and EN1 with Parkinson's disease. Haubenberger D., Reinthaler E., Mueller J.C., Pirker W., Katzenschlager R., Froehlich R., Bruecke T., Daniel G., Auff E., Zimprich A. Neurobiol. Aging 0:0-0(2009) · Mapped (2) |
| A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures. Schlachter K., Gruber-Sedlmayr U., Stogmann E., Lausecker M., Hotzy C., Balzar J., Schuh E., Baumgartner C., Mueller J.C., Illig T. et al. Neurology 72:974-978(2009) · Mapped (4) |
| Genetic factors influencing age at onset in LRRK2-linked Parkinson disease. Golub Y., Berg D., Calne D.B., Pfeiffer R.F., Uitti R.J., Stoessl A.J., Wszolek Z.K., Farrer M.J., Mueller J.C., Gasser T. et al. Parkinsonism Relat. Disord. 15:539-541(2009) · Mapped (4) |
| Lack of support for association between common variation in TNFSF4 and myocardial infarction in a German population. Koch W., Hoppmann P., Mueller J.C., Schomig A., Kastrati A. Nat. Genet. 40:1386-7; author reply 2008:1387-8(2008) · Mapped (3) |
| Search for informative polymorphisms in candidate genes: clock genes and circadian behaviour in blue tits. Steinmeyer C., Mueller J.C., Kempenaers B. Genetica 136:109-117(2009) · UniProtKB (1) |
| Initial description of the human NLRP3 promoter. Anderson J.P., Mueller J.L., Misaghi A., Anderson S., Sivagnanam M., Kolodner R.D., Hoffman H.M. Genes Immun. 9:721-726(2008) · Mapped (6) |
| Identification of EpCAM as the gene for congenital tufting enteropathy. Sivagnanam M., Mueller J.L., Lee H., Chen Z., Nelson S.F., Turner D., Zlotkin S.H., Pencharz P.B., Ngan B.Y., Libiger O. et al. Gastroenterology 135:429-437(2008) · Mapped (1) |
| A functional polymorphism in the SCN1A gene is not associated with carbamazepine dosages in Austrian patients with epilepsy. Zimprich F., Stogmann E., Bonelli S., Baumgartner C., Mueller J.C., Meitinger T., Zimprich A., Strom T.M. Epilepsia 49:1108-1109(2008) · Mapped (4) |
| The mouse X chromosome is enriched for multicopy testis genes showing postmeiotic expression. Mueller J.L., Mahadevaiah S.K., Park P.J., Warburton P.E., Page D.C., Turner J.M. Nat. Genet. 40:794-799(2008) · UniProtKB (1) |
| An increase in mitochondrial DNA promotes nuclear DNA replication in yeast. Blank H.M., Li C., Mueller J.E., Bogomolnaya L.M., Bryk M., Polymenis M. PLoS Genet. 4:e1000047-e1000047(2008) · Mapped (5) |
| Targeted gene deletion and phenotypic analysis of the Drosophila melanogaster seminal fluid protease inhibitor Acp62F. Mueller J.L., Linklater J.R., Ravi Ram K., Chapman T., Wolfner M.F. Genetics 178:1605-1614(2008) · Mapped (12) |
| Fibrinogen genes and myocardial infarction: a haplotype analysis. Koch W., Hoppmann P., Biele J., Mueller J.C., Schomig A., Kastrati A. Arterioscler. Thromb. Vasc. Biol. 28:758-763(2008) · Mapped (13) |
| Linker histone H1 represses recombination at the ribosomal DNA locus in the budding yeast Saccharomyces cerevisiae. Li C., Mueller J.E., Elfline M., Bryk M. Mol. Microbiol. 67:906-919(2008) · Mapped (3) |
| Genetic variability in the SNCA gene influences alpha-synuclein levels in the blood and brain. Fuchs J., Tichopad A., Golub Y., Munz M., Schweitzer K.J., Wolf B., Berg D., Mueller J.C., Gasser T. FASEB J. 22:1327-1334(2008) · Mapped (3) |
| The transcription factor PITX3 is associated with sporadic Parkinson's disease. Fuchs J., Mueller J.C., Lichtner P., Schulte C., Munz M., Berg D., Wullner U., Illig T., Sharma M., Gasser T. Neurobiol. Aging 30:731-738(2009) · Mapped (7) |
| The DNA binding parvulin Par17 is targeted to the mitochondrial matrix by a recently evolved prepeptide uniquely present in Hominidae. Kessler D., Papatheodorou P., Stratmann T., Dian E.A., Hartmann-Fatu C., Rassow J., Bayer P., Mueller J.W. BMC Biol. 5:37-37(2007) · UniProtKB (14) |
| Isw2 regulates gene silencing at the ribosomal DNA locus in Saccharomyces cerevisiae. Mueller J.E., Li C., Bryk M. Biochem. Biophys. Res. Commun. 361:1017-1021(2007) · Mapped (1) |
| No association of common VCP variants with sporadic frontotemporal dementia. Schumacher A., Friedrich P., Diehl J., Ibach B., Schoepfer-Wendels A., Mueller J.C., Konta L., Laws S.M., Kurz A., Foerstl H. et al. Neurobiol. Aging 30:333-335(2009) · Mapped (6) |
| Isw1 acts independently of the Isw1a and Isw1b complexes in regulating transcriptional silencing at the ribosomal DNA locus in Saccharomyces cerevisiae. Mueller J.E., Bryk M. J. Mol. Biol. 371:1-10(2007) · Mapped (6) |
| Association of variants in the BAT1-NFKBIL1-LTA genomic region with protection against myocardial infarction in Europeans. Koch W., Hoppmann P., Michou E., Jung V., Pfeufer A., Mueller J.C., Gieger C., Wichmann H.E., Meitinger T., Schomig A. et al. Hum. Mol. Genet. 16:1821-1827(2007) · Mapped (55) |
| Lymphotoxin-alpha and galectin-2 SNPs are not associated with myocardial infarction in two different German populations. Sedlacek K., Neureuther K., Mueller J.C., Stark K., Fischer M., Baessler A., Reinhard W., Broeckel U., Lieb W., Erdmann J. et al. J. Mol. Med. 85:997-1004(2007) · Mapped (19) |
| Drd4 gene polymorphisms are associated with personality variation in a passerine bird. Fidler A.E., van Oers K., Drent P.J., Kuhn S., Mueller J.C., Kempenaers B. Proc. Biol. Sci. 274:1685-1691(2007) · UniProtKB (1) |
| The clinical continuum of cryopyrinopathies: novel CIAS1 mutations in North American patients and a new cryopyrin model. Aksentijevich I., D Putnam C., Remmers E.F., Mueller J.L., Le J., Kolodner R.D., Moak Z., Chuang M., Austin F., Goldbach-Mansky R. et al. Arthritis Rheum. 56:1273-1285(2007) · Mapped (6) |
| No association of polymorphisms in the gene encoding 5-lipoxygenase-activating protein and myocardial infarction in a large central European population. Koch W., Hoppmann P., Mueller J.C., Schomig A., Kastrati A. Genet. Med. 9:123-129(2007) · Mapped (1) |
