Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome
Meins, M, Lehmann, J, Gerresheim, F, Herchenbach, J, Hagedorn, M, Hameister, K, Epplen, J T
Published in Journal of medical genetics (01.02.2005)
Published in Journal of medical genetics (01.02.2005)
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Influence of graphite edge crystallographic orientation on the first lithium intercalation in Li-ion battery
Bernardo, Ph, Le Meins, J.-M., Vidal, L., Dentzer, J., Gadiou, R., Märkle, W., Novák, P., Spahr, M.E., Vix-Guterl, C.
Published in Carbon (New York) (01.09.2015)
Published in Carbon (New York) (01.09.2015)
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Journal Article
MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin
Trappe, R., Laccone, F., Cobilanschi, J., Meins, M., Huppke, P., Hanefeld, F., Engel, W.
Published in American journal of human genetics (01.05.2001)
Published in American journal of human genetics (01.05.2001)
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Journal Article
Synthesis of polymer nanocomposites by UV-curing of organoclay–acrylic resins
Keller, L., Decker, C., Zahouily, K., Benfarhi, S., Le Meins, J.M., Miehe-Brendle, J.
Published in Polymer (Guilford) (13.10.2004)
Published in Polymer (Guilford) (13.10.2004)
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Journal Article
Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome
Vega, H, Trainer, A H, Gordillo, M, Crosier, M, Kayserili, H, Skovby, F, Uzielli, M L Giovannucci, Schnur, R E, Manouvrier, S, Blair, E, Hurst, J A, Forzano, F, Meins, M, Simola, K O J, Raas-Rothschild, A, Hennekam, R C M, Jabs, E Wang
Published in Journal of medical genetics (01.01.2010)
Published in Journal of medical genetics (01.01.2010)
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Journal Article
Five Novel Locations of Neocentromeres in Human: 18q22.1, Xq27.1 similar to 27.2, Acro p13, Acro p12, and Heterochromatin of Unknown Origin
Klein, E, Rocchi, M, Ovens-Raeder, A, Kosyakova, N, Weise, A, Ziegler, M, Meins, M, Morlot, S, Fischer, W, Volleth, M, Polityko, A, Ogilvie, CMackie, Kraus, C, Liehr, T
Published in Cytogenetic and genome research (01.04.2012)
Published in Cytogenetic and genome research (01.04.2012)
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Journal Article
Five Novel Locations of Neocentromeres in Human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and Heterochromatin of Unknown Origin
Klein, E., Rocchi, M., Ovens-Raeder, A., Kosyakova, N., Weise, A., Ziegler, M., Meins, M., Morlot, S., Fischer, W., Volleth, M., Polityko, A., Ogilvie, C. Mackie, Kraus, C., Liehr, T.
Published in Cytogenetic and genome research (01.04.2012)
Published in Cytogenetic and genome research (01.04.2012)
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Journal Article
10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences
Liehr, T., Stumm, M., Wegner, R.D., Bhatt, S., Hickmann, P., Patsalis, P.C., Meins, M., Morlot, S., Klaschka, V., Ewers, E., Hinreiner, S., Mrasek, K., Kosyakova, N., Cai, W.W., Cheung, S.W., Weise, A.
Published in Cytogenetic and genome research (01.01.2009)
Published in Cytogenetic and genome research (01.01.2009)
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Journal Article
Partial trisomy of chromosome 22 resulting from an interstitial duplication of 22q11.2 in a child with typical cat eye syndrome
Meins, M, Burfeind, P, Motsch, S, Trappe, R, Bartmus, D, Langer, S, Speicher, M R, Mühlendyck, H, Bartels, I, Zoll, B
Published in Journal of medical genetics (01.05.2003)
Published in Journal of medical genetics (01.05.2003)
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Journal Article
Characterisation of hydroclimatological trends and variability in the Lake Naivasha basin, Kenya
Odongo, Vincent Omondi, van der Tol, Christiaan, van Oel, Pieter R., Meins, Frank M., Becht, Robert, Onyando, Japheth, Su, Zhongbo
Published in Hydrological processes (15.07.2015)
Published in Hydrological processes (15.07.2015)
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Journal Article
Coupling socio-economic factors and eco-hydrological processes using a cascade-modeling approach
Odongo, V.O., Mulatu, D.W., Muthoni, F.K., van Oel, P.R., Meins, F.M., van der Tol, C., Skidmore, A.K., Groen, T.A., Becht, R., Onyando, J.O., van der Veen, A.
Published in Journal of hydrology (Amsterdam) (01.10.2014)
Published in Journal of hydrology (Amsterdam) (01.10.2014)
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Journal Article
Novel mutations in exon 6 of the GFAP gene affect a highly conserved if motif in the rod domain 2B and are associated with early onset infantile Alexander disease
Hartmann, H, Herchenbach, J, Stephani, U, Ledaal, P, Donnerstag, F, Lücke, T, Das, A M, Christen, H J, Hagedorn, M, Meins, M
Published in Neuropediatrics (01.06.2007)
Published in Neuropediatrics (01.06.2007)
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Journal Article
Variable and multiple expression of Protease Nexin-1 during mouse organogenesis and nervous system development
MANSUY, I. M, VAN DER PUTTEN, H, SCHMID, P, MAINS, M, BOTTERI, F. M, MONARD, D
Published in Development (Cambridge) (01.12.1993)
Published in Development (Cambridge) (01.12.1993)
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Journal Article
Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patients
Meins, M, Brockmann, K, Yadav, S, Haupt, M, Sperner, J, Stephani, U, Hanefeld, F
Published in Neuropediatrics (01.08.2002)
Published in Neuropediatrics (01.08.2002)
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Journal Article
The Effects of Groundwater and Surface Water Use on Total Water Availability and Implications for Water Management: The Case of Lake Naivasha, Kenya
van Oel, Pieter R., Mulatu, Dawit W., Odongo, Vincent O., Meins, Frank M., Hogeboom, Rick J., Becht, Robert, Stein, Alfred, Onyando, Japheth O., van der Veen, Anne
Published in Water resources management (01.07.2013)
Published in Water resources management (01.07.2013)
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A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis
Trappe, R., Böhm, D., Kohlhase, J., Weise, A., Liehr, T., Essers, G., Meins, M., Zoll, B., Bartels, I., Burfeind, P.
Published in Cytogenetic and genome research (01.01.2002)
Published in Cytogenetic and genome research (01.01.2002)
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