Recent Publications (1994-97)

Welter, C., Theisinger, B., Rio, M.C., Seitz, G., Schueder, G. and Blin, N. (1994). Expression pattern of breast cancer-associated protein pS2/BCEI in colorectal tumors. Int J Cancer 56: 52-55

Muellenbach, R., Tisborn, S. and Blin, N. (1994). Sequence patterns and hybridisation analysis of clones generated by Alu-PCR. DNA Sequence 4: 249-252

Dooley, S., Wundrack, I., Welter, C. and Blin, N. (1994). Constitutive c-myc overexpression and P2/P1 promoter shift in a small cell lung cancer cell line. Int J Oncol 5: 65-68

Blin, N., Wundrack, I., Holzmann, K., Suijkerbuijk, R., Schmitt, H. and Muellenbach, R. (1994). Topography of a new repetitve DNA family on hominoid acrocentric chromosomes. Bullet Pol Acad Sci , 41: 353-361

Schmitt, H., Blin, N., Zankl, H. and Scherthan, H. (1994). Telomere length variation in normal and malignant human tissues. Genes Chromosomes & Cancer 11: 171-177

Wundrack, I., Meese, E., Muellenbach, R. and Blin, N. (1994). Debrisoquine hydroxylase gene polymorphism in meningioma. Acta Neuropathol. 88: 472-474

Schmitt, H., Kehrer, H., Enders, H., Latos-Bielenska, A., Lamour, V., Lipinski, M. and Blin, N. (1994). Involvement of 22q13.3 in chromosomal anomalies. Oncology Reports 1: 881-884

Wundrack, I., Muellenbach, R., Seitz, G., Welter, C. and Blin, N. (1994). PCR expression analysis of the estrogen-inducible gene BCEI in gastrointestinal tumors. Disease Markers 12: 63-69

Blin, N., Schneider, G., Janka, M., Subke, F., Zang, K.D. and Meese, E. (1995). Lack of isodisomy for chromosome 22 in disomic meningiomas. Cytogenet Cell Genet 71: 139-141

Dooley, S., Wundrack, I., Blin, N. and Welter, C. (1995). Coexpression pattern of c-myc associated genes in a small cell lung cancer cell line with high steady state c-myc transcription. Biochem Biophys Res Commun 213: 789-795

Meese, E., Mueller, H.W., Brass, N., Trent, J.M. and Blin, N. (1995). Assignment of Alu-repetitive sequences to large restriction fragments from human chromosomes 6 and 22. Mol Biol Rep 21: 81-84

Blin, N., Welter, C. and Seitz, G. (1996). Genetische Aspekte bei Tumoren des Gastrointestinaltraktes. In: Klinische Gastroenterologie, Eds. E.G. Hahn, J.F. Riemann, pp. 310-316, Thieme Verlag, Stuttgart

Schmitt, H., Wundrack, I., Beck, S., Goett, P., Welter, C., Shizuya, H., Simon, M. and Blin, N. (1996a). A third P-domain peptide gene (TFF3), human intestinal trefoil factor, maps to 21q22.3. Cytogenet Cell Genet , 72: 299-302 [Abstract]

Wundrack, I., Reichert, J., Langer, H., Leicht, E., Herrmann, M., Subke, F., Meese, E. and Blin N. (1996). A family with a germline mutation of the RET proto-oncogene with multiple endocrine neoplasia type 2A (MEN2A). Endocrin Pathol 7: 71-76 [Abstract]

Machado, J.-C., Carneiro, F., Ribeiro, P., Blin, N. and Sobrinho-Simoes, M. (1996). pS2 protein expression in gastric carcinoma: an immunohistochemical and immunoradiometric study. Eur J Cancer 32A: 1585-1590 [Abstract]

Muellenbach, R., Pusch, C., Holzmann, K., Suijkerbuijk, R. and Blin, N. (1996). Distribution and linkage of repetitive clusters from the heterochromatic region of human chromosome 22. Chromos Res 4: 282-287 [Abstract]

Schmitt, H., Kim, U.-J., Slepak, T., Blin, N., Simon, M. and Shizuya, H. (1996b). Framework for a physical map of the human 22q13 region using Bacterial Artificial Chromosomes (BACs). Genomics 33: 9-20 [Abstract]

Beck, S., Schmitt, H., Shizuya, H., Blin, N. and Goett, P. (1996). Cloning of contiguous genomic fragments from human chromosome 21 harbouring three trefoil peptide genes. Hum Genet 98: 233-235 [Abstract]

Pusch, C., Wang, Z., Roe, B. and Blin, N. (1996a). Genomic structure of RNA polymerase II small subunit (hRPB14.4.) locus (POLR2F) and mapping to 22q13.1 by sequence identity. Genomics 34: 440-442

Goett, P. and Blin, N. (1996). Molecular carcinogenesis of the upper digestive tract: multistep models without sure foothold yet. Cancer J 9: 124-128

Dooley, S., Seib, T., Welter, C. and Blin, N. (1996). c-myb intron I protein binding and association with transcriptional activity in leukemic cells. Leukemia Res 20: 429-439

Reichert, J. and Blin, N. (1996). Human and rodent expression pattern of a fusion gene isolated from a MCF7 cDNA library. Int J Oncol 9: 29-32

Pusch, C., Muellenbach, R., Goett, P., Schmitt, H., Wang, Z., Roe, B. and Blin, N. (1996b). Cosmid-derived transcripts and sequence tags mapped to three subregions of human chromosome 22. Gene 183: 29-33 [Abstract]

Machado, J.-C., Carneiro, F., Blin, N. and Sobrinho-Simoes, M. (1996). Pattern of expression of pS2 protein in premalignant and malignant lesions of gastric epithelium. Eur J Cancer Prev 5: 169-179 [Abstract]

Goett, P., Beck, S., Machado, J.-C., Carneiro, F., Schmitt, H. and Blin, N. (1996). Human trefoil peptides: Genomic structure in 21q22.3 and coordinated expression. Eur J Hum Genet 161: 308-315 [Abstract]

Pusch, C., Schmitt, H. and Blin, N. (1997). Increased cloning efficiency by cycle restricted ligation (CRL). Trends Genet (Techn Tips Online), in press

Schmitt, H., Sasiadek, M., Jagielski, J. and Blin, N. (1997). Correction of the cytogenetic diagnosis of a rare translocation t(3;21) by fluorescence in situ hybridization. submitted

Schroeder, K., Bartsch, O., Schuffenhauer, S., Blin, N. and Schmitt, H. (1997). Determination of breakpoints in region q13.1 by BAC mapping in 22q-deletion patients. in preparation

Simon M.-P., Pedeutour F., Sirvent N., Grosgeorge J., Minoletti F., Coindre J.-M., Terrier-Lacombe M.-J., Mandahl N., Craver R., Blin N., Sozzi G., Turc-Carel C., O'Brien K., Kedra D., Fransson I., Guilbaud C., Dumanski J. (1997). Deregulation of the platelet-derived growth factor B-chain gene (PDGFB) via its fusion with the collagen gene (COL1A1) in dermatofibrosarcoma protuberans and giant-cell fibroblastoma. Nature Genet. 15:95-98

Machado J.-C., Blin N., G÷tt P. (1997). Ordering the multitude of molecular events in stomach carcinogenesis. Gastroenterol. Pol ., in press

Seib T., Blin N., Hilgert K., Seifert M., Theisinger B., Dooley S., Zang K-D., Welter C. (1997) Mapping of the trefoil peptide gene region on 21q22.3. Genomics 40:200-202

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