1 - 25 of
26
results
for author:"Rolfs A."
in Literature Citations
| Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. Sidransky E., Nalls M.A., Aasly J.O., Aharon-Peretz J., Annesi G., Barbosa E.R., Bar-Shira A., Berg D., Bras J., Brice A. et al. N. Engl. J. Med. 361:1651-1661(2009) · Mapped (11) |
| Interferon-beta modulates protein synthesis in the central nervous system. Beyer S., Raether G., Stadler K., Hoffrogge R., Scharf C., Rolfs A., Mix E., Strauss U. J. Neuroimmunol. 213:31-38(2009) · Mapped (1) |
| High-resolution DNA-binding specificity analysis of yeast transcription factors. Zhu C., Byers K.J., McCord R.P., Shi Z., Berger M.F., Newburger D.E., Saulrieta K., Smith Z., Shah M.V., Radhakrishnan M. et al. |
| Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia. Hehr U., Bauer P., Winner B., Schule R., Olmez A., Koehler W., Uyanik G., Engel A., Lenz D., Seibel A. et al. Ann. Neurol. 62:656-665(2007) · Mapped (6) |
| Eye movement abnormalities in spinocerebellar ataxia type 17 (SCA17). Hubner J., Sprenger A., Klein C., Hagenah J., Rambold H., Zuhlke C., Kompf D., Rolfs A., Kimmig H., Helmchen C. Neurology 69:1160-1168(2007) · Mapped (10) |
| Approaching a complete repository of sequence-verified protein-encoding clones for Saccharomyces cerevisiae. Hu Y., Rolfs A., Bhullar B., Murthy T.V.S., Zhu C., Berger M.F., Camargo A.A., Kelley F., McCarron S., Jepson D. et al. Genome Res. 17:536-543(2007) · UniProtKB (1,727) |
| Functional properties of multiple isoforms of human divalent metal-ion transporter 1 (DMT1). Mackenzie B., Takanaga H., Hubert N., Rolfs A., Hediger M.A. |
| 3-Hydroxy-3-methylglutaryl coenzyme A reductase inhibitor Atorvastatin mediated effects depend on the activation status of target cells in PLP-EAE. Mix E., Ibrahim S.M., Pahnke J., Glass A., Mazon-Pelaez I., Lemcke S., Koczan D., Gimsa U., Bansemer S., Scheel T. et al. J. Autoimmun. 27:251-265(2006) · Mapped (7) |
| Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approach. Tomiuk J., Bachmann L., Bauer C., Rolfs A., Schols L., Roos C., Zischler H., Schuler M.M., Bruntner S., Riess O. et al. Eur. J. Hum. Genet. 15:81-87(2007) · Mapped (10) |
| Functional significance of HCN2/3-mediated I(h) in striatal cells at early developmental stages. Bajorat R., Brauer A.U., Wasner U., Rolfs A., Strauss U. J. Neurosci. Res. 82:206-213(2005) · Mapped (2) |
| Identification of quantitative trait loci controlling cortical motor evoked potentials in experimental autoimmune encephalomyelitis: correlation with incidence, onset and severity of disease. Mazon Pelaez I., Vogler S., Strauss U., Wernhoff P., Pahnke J., Brockmann G., Moch H., Thiesen H.J., Rolfs A., Ibrahim S.M. Hum. Mol. Genet. 14:1977-1989(2005) · Mapped (28) |
| Wnt-5a expression in the rat neuronal progenitor cell line ST14A. Peters S., Mix E., Bauer P., Weinelt S., Schubert B., Knoblich R., Boettcher T., Strauss U., Pahnke J., Cattaneo E. et al. Exp. Brain Res. 158:189-195(2004) · UniProtKB (1) |
| Overexpression of glial cell line-derived neurotrophic factor induces genes regulating migration and differentiation of neuronal progenitor cells. Pahnke J., Mix E., Knoblich R., Muller J., Zschiesche M., Schubert B., Koczan D., Bauer P., Bottcher T., Thiesen H.J. et al. Exp. Cell Res. 297:484-494(2004) · Mapped (1) |
| Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotype. Bauer P., Laccone F., Rolfs A., Wullner U., Bosch S., Peters H., Liebscher S., Scheible M., Epplen J.T., Weber B.H. et al. J. Med. Genet. 41:230-232(2004) · Mapped (10) |
| Intestinal expression of genes involved in iron absorption in humans. Rolfs A., Bonkovsky H.L., Kohlroser J.G., McNeal K., Sharma A., Berger U.V., Hediger M.A. Am. J. Physiol. Gastrointest. Liver Physiol. 282:G598-607(2002) · Mapped (11) |
| Residual galactosylsphingosine (psychosine) beta-galactosidase activities and associated GALC mutations in late and very late onset Krabbe disease. Harzer K., Knoblich R., Rolfs A., Bauer P., Eggers J. Clin. Chim. Acta 317:77-84(2002) · Mapped (2) |
| NPC1: complete genomic sequence, mutation analysis, and characterization of haplotypes. Bauer P., Knoblich R., Bauer C., Finckh U., Hufen A., Kropp J., Braun S., Kustermann-Kuhn B., Schmidt D., Harzer K. et al. |
| An iron-regulated ferric reductase associated with the absorption of dietary iron. McKie A.T., Barrow D., Latunde-Dada G.O., Rolfs A., Sager G., Mudaly E., Mudaly M., Richardson C., Barlow D., Bomford A. et al. |
| Clozapine-induced agranulocytosis and hereditary polymorphisms of clozapine metabolizing enzymes: no association with myeloperoxidase and cytochrome P4502D6. Dettling M., Sachse C., Muller-Oerlinghausen B., Roots I., Brockmoller J., Rolfs A., Cascorbi I. Pharmacopsychiatry 33:218-220(2000) · Mapped (20) |
| A novel duodenal iron-regulated transporter, IREG1, implicated in the basolateral transfer of iron to the circulation. McKie A.T., Marciani P., Rolfs A., Brennan K., Wehr K., Barrow D., Miret S., Bomford A., Peters T.J., Farzaneh F. et al. |
| Mouse hypoxia-inducible factor-1alpha is encoded by two different mRNA isoforms: expression from a tissue-specific and a housekeeping-type promoter. Wenger R.H., Rolfs A., Spielmann P., Zimmermann D.R., Gassmann M. Blood 91:3471-3480(1998) · Mapped (3) |
| Man9-mannosidase from pig liver is a type-II membrane protein that resides in the endoplasmic reticulum. cDNA cloning and expression of the enzyme in COS 1 cells. Bieberich E., Treml K., Volker C., Rolfs A., Kalz-Fueller B., Bause E. Eur. J. Biochem. 246:681-689(1997) · UniProtKB (1) |
| The mouse gene for hypoxia-inducible factor-1alpha. Genomic organization, expression and characterization of an alternative first exon and 5' flanking sequence. Wenger R.H., Rolfs A., Kvietikova I., Spielmann P., Zimmermann D.R., Gassmann M. Eur. J. Biochem. 246:155-165(1997) · UniProtKB (1) · Mapped (2) |
| Two new missense mutations in a non-Jewish Caucasian family with type 3 Gaucher disease. Seeman P.J.V., Finckh U., Hoeppner J., Lakner V., Liebisch I., Grau G., Rolfs A. Neurology 46:1102-1107(1996) · UniProtKB (1) |
| Nucleotide sequence, chromosomal assignment and mRNA expression of mouse hypoxia-inducible factor-1 alpha. Wenger R.H., Rolfs A., Marti H.H., Guenet J.-L., Gassmann M. Biochem. Biophys. Res. Commun. 223:54-59(1996) · UniProtKB (1) · Mapped (2) |
