Enrichment of integral membrane proteins from small amounts of brain tissue
Schindler, J, Jung, S, Niedner-Schatteburg, G, Friauf, E, Nothwang, H G
Published in Journal of Neural Transmission (01.08.2006)
Published in Journal of Neural Transmission (01.08.2006)
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Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes
Wirth, J, Nothwang, H-G, van der Maarel, S, Menzel, C, Borck, G, Lopez-Pajares, I, Brøndum-Nielsen, K, Tommerup, N, Bugge, M, Ropers, H-H, Haaf, T
Published in Journal of medical genetics (01.04.1999)
Published in Journal of medical genetics (01.04.1999)
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Retrocochlear function of the peripheral deafness gene Cacna1d
SATHEESH, Somisetty V, KUNERT, Katrin, RÜTTIGER, Lukas, ZUCCOTTI, Annalisa, SCHÖNIG, Kai, FRIAUF, Eckhard, KNIPPER, Marlies, BARTSCH, Dusan, GERD NOTHWANG, Hans
Published in Human molecular genetics (01.09.2012)
Published in Human molecular genetics (01.09.2012)
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cDNA Cloning and Interferon γ Down-Regulation of Proteasomal Subunits X and Y
Akiyama, Kin-Ya, Yokota, Kim-ya, Kagawa, Susumu, Shimbara, Naoki, Tamura, Tomohiro, Akioka, Hiroshi, Nothwang, Hans G., Noda, Chiseko, Tanaka, Keiji, Ichihara, Akira
Published in Science (American Association for the Advancement of Science) (26.08.1994)
Published in Science (American Association for the Advancement of Science) (26.08.1994)
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A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15
WIRTH, Jutta, BACK, Elke, ROPERS, Hans-Hilger, HORSTHEMKE, Bernhard, BUITING, Karin, HÜTTENHOFER, Alexander, NOTHWANG, Hans-Gerd, LICH, Christina, GROSS, Stephanie, MENZEL, Corinna, SCHINZEL, Albert, KIOSCHIS, Petra, TOMMERUP, Niels
Published in Human molecular genetics (01.02.2001)
Published in Human molecular genetics (01.02.2001)
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Molecular cytogenetic characterisation of a complex 46,XY,t(7;8;11;13) chromosome rearrangement in a patient with Moebius syndrome
BORCK, G, WIRTH, J, HARDT, T, TÖNNIES, H, BRØNDUM-NIELSEN, K, BUGGE, M, TOMMERUP, N, NOTHWANG, H-G, ROPERS, H-H, HAAF, T
Published in Journal of medical genetics (01.02.2001)
Published in Journal of medical genetics (01.02.2001)
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Journal Article
Scanning laser optical tomography in a neuropathic mouse model: Visualization of structural changes
Schulze, J., Nolte, L., Lyutenski, S., Tinne, N., Heinemann, D., Ripken, T., Willaredt, M. A., Nothwang, H. G., Lenarz, T., Warnecke, A.
Published in HNO (01.06.2019)
Published in HNO (01.06.2019)
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Scanning laser optical tomography in a neuropathic mouse model : Visualization of structural changes. German version
Schulze, J, Nolte, L, Lyutenski, S, Tinne, N, Heinemann, D, Ripken, T, Willaredt, M A, Nothwang, H G, Lenarz, T, Warnecke, A
Published in HNO (01.08.2019)
Published in HNO (01.08.2019)
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Journal Article
Functional hemizygosity of PAFAH1B3 due to a PAFAH1B3-CLK2 fusion gene in a female with mental retardation, ataxia and atrophy of the brain
NOTHWANG, Hans Gerd, KIM, H. G, ARAI, H, TOMMERUP, N, ROPERS, H. H, WIRTH, J, AOKI, J, GEISTERFER, M, KÜBART, S, WEGNER, R. D, VAN MOERS, A, ASHWORTH, L. K, HAAF, T, BELL, J
Published in Human molecular genetics (01.04.2001)
Published in Human molecular genetics (01.04.2001)
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Journal Article
Isolation of Two Novel Human RhoGEFs, ARHGEF3 and ARHGEF4, in 3p13-21 and 2q22
Thiesen, Signe, Kübart, S., Ropers, H.-H., Nothwang, H.G.
Published in Biochemical and biophysical research communications (24.06.2000)
Published in Biochemical and biophysical research communications (24.06.2000)
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Expression and Function of Chloride Transporters during Development of Inhibitory Neurotransmission in the Auditory Brainstem
Balakrishnan, Veeramuthu, Becker, Michael, Lohrke, Stefan, Nothwang, Hans Gerd, Guresir, Erdem, Friauf, Eckhard
Published in The Journal of neuroscience (15.05.2003)
Published in The Journal of neuroscience (15.05.2003)
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Mutation of CDH23 , encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
Gal, Andreas, Bolz, Hanno, von Brederlow, Benigna, Ramírez, Alfredo, Bryda, Elizabeth C, Kutsche, Kerstin, Nothwang, Hans Gerd, Seeliger, Mathias, Cabrera, Maria del C.-Salcedó, Vila, Manuel Caballeró, Molina, Orfilio Pelaez, Kubisch, Christian
Published in Nature genetics (01.01.2001)
Published in Nature genetics (01.01.2001)
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DXS6673E Encodes a Predominantly Nuclear Protein, and Its Mouse Ortholog DXHXS6673E Is Alternatively Spliced in a Developmental- and Tissue-Specific Manner
Scheer, Maurice P., van der Maarel, S., Kübart, S., Schulz, A., Wirth, J., Schweiger, S., Ropers, H.-H., Nothwang, H.G.
Published in Genomics (San Diego, Calif.) (01.01.2000)
Published in Genomics (San Diego, Calif.) (01.01.2000)
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A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1
Hildebrandt, F, Otto, E, Rensing, C, Nothwang, H G, Vollmer, M, Adolphs, J, Hanusch, H, Brandis, M
Published in Nature genetics (01.10.1997)
Published in Nature genetics (01.10.1997)
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Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epithelium
KUTSCHE, K, GLAUNER, E, ALTHAUS, C, GALA, A, KNAUF, S, POMARINO, A, SCHMIDT, M, SCHRÖDER, B, NOTHWANG, H. G, SCHÜLER, H. M, GOECKE, T. O, KERSTEN, A. J
Published in Cytogenetic and genome research (01.01.2000)
Published in Cytogenetic and genome research (01.01.2000)
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Mutations in ARHGEF6 , encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation
Gal, Andreas, Kutsche, Kerstin, Yntema, Helger, Brandt, Alexander, Jantke, Inka, Gerd Nothwang, Hans, Orth, Ulrike, Boavida, Maria G, David, Dezsö, Chelly, Jamel, Fryns, Jean-Pierre, Moraine, Claude, Ropers, Hans-Hilger, Hamel, Ben C.J, van Bokhoven, Hans
Published in Nature genetics (01.10.2000)
Published in Nature genetics (01.10.2000)
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Journal Article
Identification of a Novel Ran Binding Protein 2 Related Gene (RANBP2L1) and Detection of a Gene Cluster on Human Chromosome 2q11–q12
Nothwang, Hans Gerd, Rensing, Cornelia, Kübler, Matthias, Denich, Dagmar, Brandl, Birgit, Stubanus, Mike, Haaf, Thomas, Kurnit, David, Hildebrandt, Friedhelm
Published in Genomics (San Diego, Calif.) (01.02.1998)
Published in Genomics (San Diego, Calif.) (01.02.1998)
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