Segmental neurofibromatosis is caused by somatic mutation of the neurofibromatosis type1 (NF1) gene
Tinschert, Sigrid, Naumann, Ilka, Stegmann, Elisabeth, Buske, Annegret, Kaufmann, Dieter, Thiel, Gundula, Jenne, Dieter E
Published in European journal of human genetics : EJHG (01.06.2000)
Published in European journal of human genetics : EJHG (01.06.2000)
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Activation of a Latent Epitope Causing Differential Binding of Anti-Neutrophil Cytoplasmic Antibodies to Proteinase 3
Marta Casal Moura, Thompson, Gwen E, Nelson, Darlene A, Fussner, Lynn A, Hummel, Amber M, Jenne, Dieter E, Emerling, Daniel, Volkmuth, Wayne, Fervenza, Fernando C, Kallenberg, Cees Gm, Langford, Carol A, Mccune, Joseph W, Merkel, Peter A, Monach, Paul A, Seo, Philip, Spiera, Robert F, St Clair, E William, Ytterberg, Steven R, Stone, John H, Robinson, William H, Specks, Ulrich
Published in bioRxiv (25.10.2022)
Published in bioRxiv (25.10.2022)
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Paper
Cell specificity of granzyme gene expression
Garcia-Sanz, JA, MacDonald, HR, Jenne, DE, Tschopp, J, Nabholz, M
Published in The Journal of immunology (1950) (01.11.1990)
Published in The Journal of immunology (1950) (01.11.1990)
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Journal Article
The Humandead ringer/brightHomolog,DRIL1:cDNA Cloning, Gene Structure, and Mapping to D19S886, a Marker on 19p13.3 That Is Strictly Linked to the Peutz–Jeghers Syndrome
Kortschak, R.Daniel, Reimann, Heike, Zimmer, Michael, Eyre, Helen J., Saint, Robert, Jenne, Dieter E.
Published in Genomics (San Diego, Calif.) (15.07.1998)
Published in Genomics (San Diego, Calif.) (15.07.1998)
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The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers syndrome
KORTSCHAK, R. D, REIMANN, H, ZIMMER, M, EYRE, H. J, SAINT, R, JENNE, D. E
Published in Genomics (San Diego, Calif.) (15.07.1998)
Published in Genomics (San Diego, Calif.) (15.07.1998)
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The Human Guanidinoacetate Methyltransferase (GAMT) Gene Maps to a Syntenic Region on 19p13.3, Homologous to Band C of Mouse Chromosome 10, but GAMT Is Not Mutated in Jittery Mice
Jenne, Dieter E., Olsen, Anne S., Zimmer, Michael
Published in Biochemical and biophysical research communications (29.09.1997)
Published in Biochemical and biophysical research communications (29.09.1997)
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Frequent 4-bp deletion in exon 9 of theSMAD4/MADH4 gene in familial juvenile polyposis patients
Friedl, Waltraut, Kruse, Roland, Uhlhaas, Siegfried, Stolte, Manfred, Schartmann, Bettina, Keller, Klaus M., Jungck, Matthias, Stern, Martin, Loff, Steffan, Back, Walter, Propping, Peter, Jenne, Dieter E.
Published in Genes chromosomes & cancer (01.08.1999)
Published in Genes chromosomes & cancer (01.08.1999)
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Journal Article
The Human Met-ase Gene (GZMM): Structure, Sequence, and Close Physical Linkage to the Serine Protease Gene Cluster on 19p13.3
Pilat, Daniel, Fink, Thomas, Obermaier-Skrobanek, Brigitte, Zimmer, Michael, Wekerle, Hartmut, Lichter, Peter, Jenne, Dieter E.
Published in Genomics (San Diego, Calif.) (01.12.1994)
Published in Genomics (San Diego, Calif.) (01.12.1994)
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Structure of the Human Paralemmin Gene (PALM), Mapping to Human Chromosome 19p13.3 and Mouse Chromosome 10, and Exclusion of Coding Mutations ingrizzled, mocha, jittery,andhesitantMice
Burwinkel, Barbara, Miglierini, Giuliana, Jenne, Dieter E., Gilbert, Debra J., Copeland, Neal G., Jenkins, Nancy A., Ring, Huijun Z., Francke, Uta, Kilimann, Manfred W.
Published in Genomics (San Diego, Calif.) (01.05.1998)
Published in Genomics (San Diego, Calif.) (01.05.1998)
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Peutz-Jeghers syndrome: Four novel inactivating germline mutations in theSTK11 gene
Kruse, Roland, Uhlhaas, Siegfried, Lamberti, Christof, Keller, Klaus M., Jackisch, Christian, Steinhard, Johannes, Kn pfle, Gisela, Loff, Steffan, Back, Walter, Stolte, Manfred, Jungck, Matthias, Propping, Peter, Friedl, Waltraut, Jenne, Dieter E.
Published in Human mutation (1999)
Published in Human mutation (1999)
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Journal Article
Structure of the Human Paralemmin Gene ( PALM), Mapping to Human Chromosome 19p13.3 and Mouse Chromosome 10, and Exclusion of Coding Mutations in grizzled, mocha, jittery,and hesitantMice
Burwinkel, Barbara, Miglierini, Giuliana, Jenne, Dieter E., Gilbert, Debra J., Copeland, Neal G., Jenkins, Nancy A., Ring, Huijun Z., Francke, Uta, Kilimann, Manfred W.
Published in Genomics (San Diego, Calif.) (1998)
Published in Genomics (San Diego, Calif.) (1998)
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Journal Article
Human megakaryocytes express clusterin and package it without apolipoprotein A-1 into α-granules
TSCHOPP, J, JENNE, D. E, HERTIG, S, PREISSNER, K. T, MORGENSTERN, H, SAPINO, A.-P, FRENCH, L
Published in Blood (01.07.1993)
Published in Blood (01.07.1993)
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A highly conservative Ile-20 substitution at the dimer-dimer interface selectively reduces stability of the tetrameric transthyretin complex and is associated with familial cardiomyopathy
Jenne, Dieter E., Denzel, Klaus, Blätzinger, Petra, Obermaier-Skrobanek, Brigitte, Linke, Reinhold P., Altland, Klaus
Published in Neuromuscular disorders : NMD (01.02.1996)
Published in Neuromuscular disorders : NMD (01.02.1996)
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Structure of the human paralemmin gene (PALM), mapping to human chromosome 19p13.3 and mouse chromosome 10, and exclusion of coding mutations in grizzled, mocha, jittery, and hesitant mice
BURWINKEL, B, MIGLIERINI, G, JENNE, D. E, GILBERT, D. J, COPELAND, N. G, JENKINS, N. A, RING, H. Z, FRANCKE, U, KILIMANN, M. W
Published in Genomics (San Diego, Calif.) (01.05.1998)
Published in Genomics (San Diego, Calif.) (01.05.1998)
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Structure and evolutionary origin of the human granzyme H gene
Haddad, P, Jenne, D, Tschopp, J, Clément, M V, Mathieu-Mahul, D, Sasportes, M
Published in International immunology (01.01.1991)
Published in International immunology (01.01.1991)
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Three Human Elastase-Like Genes Coordinately Expressed in the Myelomonocyte Lineage are Organized as a Single Genetic Lucus on 19pter
Zimmer, Michael, Medcalf, Robert L., Fink, Thomas M., Mattmann, Chantal, Lichter, Peter, Jenne, Dieter E.
Published in Proceedings of the National Academy of Sciences - PNAS (01.09.1992)
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Published in Proceedings of the National Academy of Sciences - PNAS (01.09.1992)
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