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1 - 25 of 34 results for author:"Schroeder J.M." in Literature citations

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Identification of lympho-epithelial Kazal-type inhibitor 2 in human skin as a kallikrein-related peptidase 5-specific protease inhibitor.

Meyer-Hoffert U., Wu Z., Schroeder J.M.

PLoS ONE 4:E4372-E4372(2009) · UniProtKB (2)

Uncovering the evolutionary history of innate immunity: the simple metazoan Hydra uses epithelial cells for host defence.

Bosch T.C.G., Augustin R., Anton-Erxleben F., Fraune S., Hemmrich G., Zill H., Rosenstiel P., Jacobs G., Schreiber S., Leippe M. et al.

Dev. Comp. Immunol. 33:559-569(2009) · UniProtKB (6)

A large German kindred with cold-aggravated myotonia and a heterozygous A1481D mutation in the SCN4A gene.

Schoser B.G.H., Schroeder J.M., Grimm T., Sternberg D., Kress W.

Muscle Nerve 35:599-606(2007) · UniProtKB (1) · Mapped (2)

Gene expression profiling of mice with genetically modified muscle glycogen content.

Parker G.E., Pederson B.A., Obayashi M., Schroeder J.M., Harris R.A., Roach P.J.

Biochem. J. 395:137-145(2006) · Mapped (2)

Glucose metabolism in mice lacking muscle glycogen synthase.

Pederson B.A., Schroeder J.M., Parker G.E., Smith M.W., DePaoli-Roach A.A., Roach P.J.

Diabetes 54:3466-3473(2005) · Mapped (2)

Mutations in SIL1 cause Marinesco-Sjoegren syndrome, a cerebellar ataxia with cataract and myopathy.

Senderek J., Krieger M., Stendel C., Bergmann C., Moser M., Breitbach-Faller N., Rudnik-Schoeneborn S., Blaschek A., Wolf N.I., Harting I. et al.

Nat. Genet. 37:1312-1314(2005) · UniProtKB (2) · Mapped (2)

Role of deadenylation and AUF1 binding in the pH-responsive stabilization of glutaminase mRNA.

Schroeder J.M., Ibrahim H., Taylor L., Curthoys N.P.

Am. J. Physiol. Renal Physiol. 290:F733-40(2006) · Mapped (5)

3'-Untranslated region of phosphoenolpyruvate carboxykinase mRNA contains multiple instability elements that bind AUF1.

Hajarnis S., Schroeder J.M., Curthoys N.P.

J. Biol. Chem. 280:28272-28280(2005) · Mapped (6)

Mice with elevated muscle glycogen stores do not have improved exercise performance.

Pederson B.A., Cope C.R., Irimia J.M., Schroeder J.M., Thurberg B.L., Depaoli-Roach A.A., Roach P.J.

Biochem. Biophys. Res. Commun. 331:491-496(2005) · Mapped (2)

Exercise capacity of mice genetically lacking muscle glycogen synthase: in mice, muscle glycogen is not essential for exercise.

Pederson B.A., Cope C.R., Schroeder J.M., Smith M.W., Irimia J.M., Thurberg B.L., DePaoli-Roach A.A., Roach P.J.

J. Biol. Chem. 280:17260-17265(2005) · Mapped (2)

Abnormal cardiac development in the absence of heart glycogen.

Pederson B.A., Chen H., Schroeder J.M., Shou W., DePaoli-Roach A.A., Roach P.J.

Mol. Cell. Biol. 24:7179-7187(2004) · Mapped (5)

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.

Zuechner S., Mersiyanova I.V., Muglia M., Bissar-Tadmouri N., Rochelle J., Dadali E.L., Zappia M., Nelis E., Patitucci A., Senderek J. et al.

Nat. Genet. 36:449-451(2004) · UniProtKB (1) · Mapped (6)

The novel neurofilament light (NEFL) mutation Glu397Lys is associated with a clinically and morphologically heterogeneous type of Charcot-Marie-Tooth neuropathy.

Zuechner S., Vorgerd M., Sindern E., Schroeder J.M.

Neuromuscul. Disord. 14:147-157(2004) · UniProtKB (1) · Mapped (1)

Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy.

Senderek J., Bergmann C., Stendel C., Kirfel J., Verpoorten N., De Jonghe P., Timmerman V., Chrast R., Verheijen M.H.G., Lemke G. et al.

Am. J. Hum. Genet. 73:1106-1119(2003) · UniProtKB (1) · Mapped (5)

Overexpression of glycogen synthase in mouse muscle results in less branched glycogen.

Pederson B.A., Csitkovits A.G., Simon R., Schroeder J.M., Wang W., Skurat A.V., Roach P.J.

Biochem. Biophys. Res. Commun. 305:826-830(2003) · Mapped (1)

The primary role in biologic activity of the neutrophil chemokines IL-8 and GRO-alpha in cultured nasal epithelial cells.

Rudack C., Maune S., Eble J., Schroeder J.M.

J. Interferon Cytokine Res. 23:113-123(2003) · Mapped (3)

pH-responsive stabilization of glutamate dehydrogenase mRNA in LLC-PK1-F+ cells.

Schroeder J.M., Liu W., Curthoys N.P.

Am. J. Physiol. Renal Physiol. 285:F258-65(2003) · Mapped (4)

Homozygous mutations in caveolin-3 cause a severe form of rippling muscle disease.

Kubisch C., Schoser B.G.H., von Duering M., Betz R.C., Goebel H.-H., Zahn S., Ehrbrecht A., Aasly J., Schroers A., Popovic N. et al.

Ann. Neurol. 53:512-520(2003) · UniProtKB (1)

Mutations in the ganglioside-induced differentiation-associated protein-1 (GDAP1) gene in intermediate type autosomal recessive Charcot-Marie-Tooth neuropathy.

Senderek J., Bergmann C., Ramaekers V.T., Nelis E., Bernert G., Makowski A., Zuechner S., De Jonghe P., Rudnik-Schoeneborn S., Zerres K. et al.

Brain 126:642-649(2003) · UniProtKB (1)

RNase 7, a novel innate immune defense antimicrobial protein of healthy human skin.

Harder J., Schroeder J.M.

J. Biol. Chem. 277:46779-46784(2002) · UniProtKB (1)

Isolation and characterization of human beta-defensin-3, a novel human inducible peptide antibiotic.

Harder J., Bartels J., Christophers E., Schroeder J.-M.

J. Biol. Chem. 276:5707-5713(2001) · UniProtKB (1)

Mucoid Pseudomonas aeruginosa, TNF-alpha, and IL-1beta, but not IL-6, induce human beta-defensin-2 in respiratory epithelia.

Harder J., Meyer-Hoffert U., Teran L.M., Schwichtenberg L., Bartels J., Maune S., Schroeder J.-M.

Am. J. Respir. Cell Mol. Biol. 22:714-721(2000) · UniProtKB (1)

Genomic organization, sequence analysis and transcriptional regulation of the human MCP-4 chemokine gene (SCYA13) in dermal fibroblasts: a comparison to other eosinophilic beta-chemokines.

Hein H., Schluter C., Kulke R., Christophers E., Schroeder J.-M., Bartels J.

Biochem. Biophys. Res. Commun. 255:470-476(1999) · UniProtKB (1)

Delayed production of biologically active O-glycosylated forms of human eotaxin by tumor-necrosis-factor-alpha-stimulated dermal fibroblasts.

Noso N., Bartels J., Mallet A.I., Mochizuki M., Christophers E., Schroeder J.-M.

Eur. J. Biochem. 253:114-122(1998) · UniProtKB (1)

Characterisation of macrophage inflammatory protein-5/human CC cytokine-2, a member of the macrophage-inflammatory-protein family of chemokines.

Coulin F., Power C.A., Alouani S., Peitsch M.C., Schroeder J.M., Moshizuki M., Clark-Lewis I., Wells T.N.

Eur. J. Biochem. 248:507-515(1997)

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