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1 - 25 of 45 results for author:"Langmann T." in Literature citations

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The retinitis pigmentosa 28 protein FAM161A is a novel ciliary protein involved in intermolecular protein interaction and microtubule association.

Zach F., Grassmann F., Langmann T., Sorusch N., Wolfrum U., Stohr H.

Hum. Mol. Genet. 21:4573-4586(2012) · UniProtKB (3) · Mapped (5)

Postzygotic HRAS and KRAS mutations cause nevus sebaceous and Schimmelpenning syndrome.

Groesser L., Herschberger E., Ruetten A., Ruivenkamp C., Lopriore E., Zutt M., Langmann T., Singer S., Klingseisen L., Schneider-Brachert W. et al.

Nat. Genet. 44:783-787(2012) · UniProtKB (1) · Mapped (12)

Retinal expression of the X-linked juvenile retinoschisis (RS1) gene is controlled by an upstream CpG island and two opposing CRX-bound regions.

Kraus D., Karlstetter M., Walczak Y., Hilfinger D., Langmann T., Weber B.H.

Biochim. Biophys. Acta 1809:245-254(2011) · Mapped (3)

The Na/K-ATPase is obligatory for membrane anchorage of retinoschisin, the protein involved in the pathogenesis of X-linked juvenile retinoschisis.

Friedrich U., Stohr H., Hilfinger D., Loenhardt T., Schachner M., Langmann T., Weber B.H.

Hum. Mol. Genet. 20:1132-1142(2011) · Mapped (22)

The novel activated microglia/macrophage WAP domain protein, AMWAP, acts as a counter-regulator of proinflammatory response.

Karlstetter M., Walczak Y., Weigelt K., Ebert S., Van den Brulle J., Schwer H., Fuchshofer R., Langmann T.

J. Immunol. 185:3379-3390(2010) · UniProtKB (1) · Mapped (3)

Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa.

Langmann T., Di Gioia S.A., Rau I., Stohr H., Maksimovic N.S., Corbo J.C., Renner A.B., Zrenner E., Kumaramanickavel G., Karlstetter M. et al.

Am. J. Hum. Genet. 87:376-381(2010) · UniProtKB (2) · Mapped (9)

CRX ChIP-seq reveals the cis-regulatory architecture of mouse photoreceptors.

Corbo J.C., Lawrence K.A., Karlstetter M., Myers C.A., Abdelaziz M., Dirkes W., Weigelt K., Seifert M., Benes V., Fritsche L.G. et al.

Genome Res. 20:1512-1525(2010) · Mapped (8)

HIF-1beta determines ABCA1 expression under hypoxia in human macrophages.

Ugocsai P., Hohenstatt A., Paragh G., Liebisch G., Langmann T., Wolf Z., Weiss T., Groitl P., Dobner T., Kasprzak P. et al.

Int. J. Biochem. Cell Biol. 42:241-252(2010) · Mapped (8)

Docosahexaenoic acid attenuates microglial activation and delays early retinal degeneration.

Ebert S., Weigelt K., Walczak Y., Drobnik W., Mauerer R., Hume D.A., Weber B.H., Langmann T.

J. Neurochem. 110:1863-1875(2009) · Mapped (3)

Induction of early growth response-1 mediates microglia activation in vitro but is dispensable in vivo.

Langmann T., Ebert S., Walczak Y., Weigelt K., Ehrengruber M.U., Stiewe T., Weber B.H.

Neuromolecular Med. 11:87-96(2009) · Mapped (6)

Induction of STAP-1 promotes neurotoxic activation of microglia.

Stoecker K., Weigelt K., Ebert S., Karlstetter M., Walczak Y., Langmann T.

Biochem. Biophys. Res. Commun. 379:121-126(2009) · Mapped (3)

CRX controls retinal expression of the X-linked juvenile retinoschisis (RS1) gene.

Langmann T., Lai C.C., Weigelt K., Tam B.M., Warneke-Wittstock R., Moritz O.L., Weber B.H.

Nucleic Acids Res. 36:6523-6534(2008) · Mapped (5)

A novel solid phase technology for high-throughput gene synthesis.

Van den Brulle J., Fischer M., Langmann T., Horn G., Waldmann T., Arnold S., Fuhrmann M., Schatz O., O'Connell T., O'Connell D. et al.

BioTechniques 45:340-343(2008) · Mapped (1)

Dap12 expression in activated microglia from retinoschisin-deficient retina and its PU.1-dependent promoter regulation.

Weigelt K., Ernst W., Walczak Y., Ebert S., Loenhardt T., Klug M., Rehli M., Weber B.H., Langmann T.

J. Leukoc. Biol. 82:1564-1574(2007) · Mapped (3)

The satiety factor apolipoprotein A-IV modulates intestinal epithelial permeability through its interaction with alpha-catenin: implications for inflammatory bowel diseases.

Orso E., Moehle C., Boettcher A., Szakszon K., Werner T., Langmann T., Liebisch G., Buechler C., Ritter M., Kronenberg F. et al.

Horm. Metab. Res. 39:601-611(2007) · Mapped (2)

Aquaporin-8 expression is reduced in ileum and induced in colon of patients with ulcerative colitis.

Zahn A., Moehle C., Langmann T., Ehehalt R., Autschbach F., Stremmel W., Schmitz G.

World J. Gastroenterol. 13:1687-1695(2007) · Mapped (2)

Genome-wide expression profiling of the retinoschisin-deficient retina in early postnatal mouse development.

Gehrig A., Langmann T., Horling F., Janssen A., Bonin M., Walter M., Poths S., Weber B.H.

Invest. Ophthalmol. Vis. Sci. 48:891-900(2007) · Mapped (9)

Isomer specific effects of Conjugated Linoleic Acid on macrophage ABCG1 transcription by a SREBP-1c dependent mechanism.

Ecker J., Langmann T., Moehle C., Schmitz G.

Biochem. Biophys. Res. Commun. 352:805-811(2007) · Mapped (9)

High molecular weight adiponectin reduces apolipoprotein B and E release in human hepatocytes.

Neumeier M., Sigruener A., Eggenhofer E., Weigert J., Weiss T.S., Schaeffler A., Schlitt H.J., Aslanidis C., Piso P., Langmann T. et al.

Biochem. Biophys. Res. Commun. 352:543-548(2007) · Mapped (17)

Aberrant intestinal expression and allelic variants of mucin genes associated with inflammatory bowel disease.

Moehle C., Ackermann N., Langmann T., Aslanidis C., Kel A., Kel-Margoulis O., Schmitz-Madry A., Zahn A., Stremmel W., Schmitz G.

J. Mol. Med. 84:1055-1066(2006) · UniProtKB (1) · Mapped (10)

Induction of Raf kinase inhibitor protein contributes to macrophage differentiation.

Schuierer M.M., Heilmeier U., Boettcher A., Ugocsai P., Bosserhoff A.K., Schmitz G., Langmann T.

Biochem. Biophys. Res. Commun. 342:1083-1087(2006) · Mapped (3)

Ephrin-B2 is differentially expressed in the intestinal epithelium in Crohn's disease and contributes to accelerated epithelial wound healing in vitro.

Hafner C., Meyer S., Langmann T., Schmitz G., Bataille F., Hagen I., Becker B., Roesch A., Rogler G., Landthaler M. et al.

World J. Gastroenterol. 11:4024-4031(2005) · Mapped (2)

Transcriptional regulatory networks in lipid metabolism control ABCA1 expression.

Schmitz G., Langmann T.

Biochim. Biophys. Acta 1735:1-19(2005) · Mapped (2)

Screening for functional sequence variations and mutations in ABCA1.

Probst M.C., Thumann H., Aslanidis C., Langmann T., Buechler C., Patsch W., Baralle F.E., Dallinga-Thie G.M., Geisel J., Keller C. et al.

Atherosclerosis 175:269-279(2004) · UniProtKB (1) · Mapped (7)

Expression pattern and raft association of NIPSNAP3 and NIPSNAP4, highly homologous proteins encoded by genes in close proximity to the ATP-binding cassette transporter A1.

Buechler C., Bodzioch M., Bared S.M., Sigruener A., Boettcher A., Lapicka-Bodzioch K., Aslanidis C., Duong C.Q., Grandl M., Langmann T. et al.

Genomics 83:1116-1124(2004) · Mapped (2)

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