1 - 25 of 36 results for author:"Bonin M." in Literature citations
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| A 15q24 microdeletion in transient myeloproliferative disease (TMD) and acute megakaryoblastic leukaemia (AMKL) implicates PML and SUMO3 in the leukaemogenesis of TMD/AMKL. Haemmerling S., Behnisch W., Doerks T., Korbel J.O., Bork P., Moog U., Hentze S., Grasshoff U., Bonin M., Riess O. et al. Br. J. Haematol. 157:180-187(2012) · Mapped (13) |
| Long-term follow-up of the human phenotype in three siblings with cone dystrophy associated with a homozygous p.G461R mutation of KCNV2. Friedburg C., Wissinger B., Schambeck M., Bonin M., Kohl S., Lorenz B. Invest. Ophthalmol. Vis. Sci. 52:8621-8629(2011) · Mapped (2) |
| Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response. Wissinger B., Schaich S., Baumann B., Bonin M., Jagle H., Friedburg C., Varsanyi B., Hoyng C.B., Dollfus H., Heckenlively J.R. et al. Hum. Mutat. 32:1398-1406(2011) · Mapped (2) |
| Spinocerebellar ataxia type 15: diagnostic assessment, frequency, and phenotypic features. Synofzik M., Beetz C., Bauer C., Bonin M., Sanchez-Ferrero E., Schmitz-Hubsch T., Wullner U., Nagele T., Riess O., Schols L. et al. J. Med. Genet. 48:407-412(2011) · Mapped (8) |
| De novo MECP2 duplication in two females with random X-inactivation and moderate mental retardation. Grasshoff U., Bonin M., Goehring I., Ekici A., Dufke A., Cremer K., Wagner N., Rossier E., Jauch A., Walter M. et al. Eur. J. Hum. Genet. 19:507-512(2011) · Mapped (15) |
| Differential expression of invasion promoting genes in childhood rhabdomyosarcoma. Armeanu-Ebinger S., Bonin M., Habig K., Poremba C., Koscielniak E., Godzinski J., Warmann S.W., Fuchs J., Seitz G. Int. J. Oncol. 38:993-1000(2011) · Mapped (3) |
| Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1. Jensen L.R., Chen W., Moser B., Lipkowitz B., Schroeder C., Musante L., Tzschach A., Kalscheuer V.M., Meloni I., Raynaud M. et al. Eur. J. Hum. Genet. 19:717-720(2011) · Mapped (5) |
| ARHGEF7 (Beta-PIX) acts as guanine nucleotide exchange factor for leucine-rich repeat kinase 2. Haebig K., Gloeckner C.J., Miralles M.G., Gillardon F., Schulte C., Riess O., Ueffing M., Biskup S., Bonin M. PLoS ONE 5:e13762-e13762(2010) · Mapped (19) |
| Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Horn D., Kapeller J., Rivera-Brugues N., Moog U., Lorenz-Depiereux B., Eck S., Hempel M., Wagenstaller J., Gawthrope A., Monaco A.P. et al. Hum. Mutat. 31:E1851-E1860(2010) · UniProtKB (1) · Mapped (11) |
| Alpha-synuclein deficiency leads to increased glyoxalase I expression and glycation stress. Kurz A., Rabbani N., Walter M., Bonin M., Thornalley P., Auburger G., Gispert S. Cell. Mol. Life Sci. 68:721-733(2011) · Mapped (3) |
| A53T-alpha-synuclein overexpression impairs dopamine signaling and striatal synaptic plasticity in old mice. Kurz A., Double K.L., Lastres-Becker I., Tozzi A., Tantucci M., Bockhart V., Bonin M., Garcia-Arencibia M., Nuber S., Schlaudraff F. et al. PLoS ONE 5:e11464-e11464(2010) · Mapped (1) |
| Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation. Berkel S., Marshall C.R., Weiss B., Howe J., Roeth R., Moog U., Endris V., Roberts W., Szatmari P., Pinto D. et al. |
| Structural and functional phenotyping in the cone-specific photoreceptor function loss 1 (cpfl1) mouse mutant - a model of cone dystrophies. Fischer M.D., Tanimoto N., Beck S.C., Huber G., Schaeferhoff K., Michalakis S., Riess O., Wissinger B., Biel M., Bonin M. et al. Adv. Exp. Med. Biol. 664:593-599(2010) · Mapped (1) |
| Alpha-synuclein deficiency affects brain Foxp1 expression and ultrasonic vocalization. Kurz A., Wohr M., Walter M., Bonin M., Auburger G., Gispert S., Schwarting R.K. Neuroscience 166:785-795(2010) · Mapped (6) |
| Toll-like receptor 3 has no critical role during early immune response of human monocyte-derived dendritic cells after infection with the human cytomegalovirus strain TB40E. Mezger M., Bonin M., Kessler T., Gebhardt F., Einsele H., Loeffler J. Viral Immunol. 22:343-351(2009) · Mapped (9) |
| Genome-wide association study reveals genetic risk underlying Parkinson's disease. Simon-Sanchez J., Schulte C., Bras J.M., Sharma M., Gibbs J.R., Berg D., Paisan-Ruiz C., Lichtner P., Scholz S.W., Hernandez D.G. et al. Nat. Genet. 41:1308-1312(2009) · Mapped (51) |
| Knockdown of transactive response DNA-binding protein (TDP-43) downregulates histone deacetylase 6. Fiesel F.C., Voigt A., Weber S.S., Van den Haute C., Waldenmaier A., Gorner K., Walter M., Anderson M.L., Kern J.V., Rasse T.M. et al. EMBO J. 29:209-221(2010) · Mapped (43) |
| In vivo analysis of cone survival in mice. Beck S.C., Schaeferhoff K., Michalakis S., Fischer M.D., Huber G., Rieger N., Riess O., Wissinger B., Biel M., Bonin M. et al. Invest. Ophthalmol. Vis. Sci. 51:493-497(2010) · Mapped (5) |
| New insights into the expanding complexity of the tumor suppressor ASPP2. Kampa K.M., Bonin M., Lopez C.D. Cell Cycle 8:2871-2876(2009) · Mapped (3) |
| Periphilin is strongly expressed in the murine nervous system and is indispensable for murine development. Soehn A.S., Pham T.T., Schaeferhoff K., Floss T., Weisenhorn D.M., Wurst W., Bonin M., Riess O. Genesis 47:697-707(2009) · Mapped (33) |
| Microarray expression analysis of human dopaminergic neuroblastoma cells after RNA interference of SNCA--a key player in the pathogenesis of Parkinson's disease. Habig K., Walter M., Stappert H., Riess O., Bonin M. Brain Res. 1256:19-33(2009) · Mapped (8) |
| TREM2 is upregulated in amyloid plaque-associated microglia in aged APP23 transgenic mice. Frank S., Burbach G.J., Bonin M., Walter M., Streit W., Bechmann I., Deller T. Glia 56:1438-1447(2008) · Mapped (3) |
| Microarray expression analysis reveals genetic pathways implicated in C621 synphilin-1-mediated toxicity. Bonin M., Marx F.P., Kautzmann S., Riess O., Kruger R. J Neural Transm 115:941-958(2008) · Mapped (10) |
| Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2. Wissinger B., Dangel S., Jagle H., Hansen L., Baumann B., Rudolph G., Wolf C., Bonin M., Koeppen K., Ladewig T. et al. Invest. Ophthalmol. Vis. Sci. 49:751-757(2008) · Mapped (2) |
| RNA interference of LRRK2-microarray expression analysis of a Parkinson's disease key player. Habig K., Walter M., Poths S., Riess O., Bonin M. Neurogenetics 9:83-94(2008) · Mapped (4) |