Structural recovery of the retina in a retinoschisin-deficient mouse after gene replacement therapy by solid lipid nanoparticles
Apaolaza, P.S, del Pozo-Rodríguez, A, Solinís, M.A, Rodríguez, J.M, Friedrich, U, Torrecilla, J, Weber, B.H.F, Rodríguez-Gascón, A
Published in Biomaterials (01.06.2016)
Published in Biomaterials (01.06.2016)
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The role of caspases in photoreceptor cell death of the retinoschisin-deficient mouse
Gehrig, A., Janssen, A., Horling, F., Grimm, C., Weber, B.H.F.
Published in Cytogenetic and genome research (01.01.2006)
Published in Cytogenetic and genome research (01.01.2006)
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Comparative mapping of human claudin-1 (CLDN1) in great apes
Nanda, I., Krämer, F., Weber, B.H.F., Schempp, W., Schmid, M.
Published in Cytogenetic and genome research (01.01.2005)
Published in Cytogenetic and genome research (01.01.2005)
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Identifying differentially expressed genes in the mammalian retina and the retinal pigment epithelium by suppression subtractive hybridization
Schulz, H.L., Rahman, F.A., Fadl El Moula, F.M., Stojic, J., Gehrig, A., Weber, B.H.F.
Published in Cytogenetic and genome research (01.01.2004)
Published in Cytogenetic and genome research (01.01.2004)
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Solid lipid nanoparticle-based vectors intended for the treatment of X-linked juvenile retinoschisis by gene therapy: In vivo approaches in Rs1h-deficient mouse model
Apaolaza, P.S., del Pozo-Rodríguez, A., Torrecilla, J., Rodríguez-Gascón, A., Rodríguez, J.M., Friedrich, U., Weber, B.H.F., Solinís, M.A.
Published in Journal of controlled release (10.11.2015)
Published in Journal of controlled release (10.11.2015)
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EST mining of the UniGene dataset to identify retina-specific genes
STÖHR, H, MAH, N, SCHULZ, H. L, GEHRIG, A, FRÖHLICH, S, WEBER, B. H. F
Published in Cytogenetic and genome research (01.01.2000)
Published in Cytogenetic and genome research (01.01.2000)
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Differential diagnosis of primary failure of eruption (PFE) with and without evidence of pathogenic mutations in the PTHR1 gene
Pilz, P., Meyer-Marcotty, P., Eigenthaler, M., Roth, H., Weber, B.H.F., Stellzig-Eisenhauer, A.
Published in Journal of orofacial orthopedics (01.05.2014)
Published in Journal of orofacial orthopedics (01.05.2014)
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Identification of an oncostatin M receptor mutation associated with familial primary cutaneous amyloidosis
Babilas, P., Fiebig, B.S., Aslanidis, C., Hansen, J., Röcken, C., Schroeder, J., Schmitz, G., Weber, B.H.F., Landthaler, M., Vogt, T.
Published in British journal of dermatology (1951) (01.10.2009)
Published in British journal of dermatology (1951) (01.10.2009)
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Wie groß sind die kleinen genetischen Risiken?
Heid, I.M., Winkler, T.W., Grassmann, F., Weber, B.H.F.
Published in Medizinische Genetik (23.11.2011)
Published in Medizinische Genetik (23.11.2011)
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Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk
Rivera, A., Fisher, S.A., Fritsch, L.G., Keilhauer, C.N., Lichtner, P., Meitinger, T., Weber, B.H.F.
Published in American journal of ophthalmology (2006)
Published in American journal of ophthalmology (2006)
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Journal Article
PTEN mutations do not cause nuclear [beta]-catenin accumulation in endometrial carcinomas
Wappenschmidt, B, Wardelmann, E, Gehrig, A, Schöndorf, T, Maass, N, Bonatz, G, Gassel, A.-M, Pietsch, T, Mallmann, P, Weber, B.H.F, Schmutzler, R.K
Published in Human pathology (01.10.2004)
Published in Human pathology (01.10.2004)
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Journal Article
PTEN mutations do not cause nuclear β-catenin accumulation in endometrial carcinomas
Wappenschmidt, B., Wardelmann, E., Gehrig, A., Schöndorf, T., Maass, N., Bonatz, G., Gassel, A.-M., Pietsch, T., Mallmann, P., Weber, B.H.F., Schmutzler, R.K.
Published in Human pathology (01.10.2004)
Published in Human pathology (01.10.2004)
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Journal Article
Wie groß sind die kleinen genetischen Risiken?
Heid, I.M., Winkler, T.W., Grassmann, F., Weber, B.H.F.
Published in Medizinische Genetik (01.09.2011)
Published in Medizinische Genetik (01.09.2011)
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Journal Article
cDNA cloning and genomic structure of a novel gene (C11orf9) localized to chromosome 11q12-->q13.1 which encodes a highly conserved, potential membrane-associated protein
Stöhr, H, Marquardt, A, White, K, Weber, B H
Published in Cytogenetic and genome research (01.01.2000)
Published in Cytogenetic and genome research (01.01.2000)
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Isolation of a Drosophila T-box gene closely related to human TBX1
Porsch, Matthias, Hofmeyer, Kerstin, Bausenwein, Burkhard S, Grimm, Stefan, Weber, Bernhard H.F, Miassod, Raimond, Pflugfelder, Gert O
Published in Gene (08.06.1998)
Published in Gene (08.06.1998)
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