Publikationen

1) Eichholz, H. und Schlösser, M, (1978) "Berechnung der Reaktionsgeschwindigkeitskonstanten der Dimerisation von Ethylen und Dimerisierung der Butene an Rhodium-Y- Zeolithen mittels Analogrechners", Bremer Briefe zur Chemie 2, 43-58.
2) Hasnain, S.S., Wardell, E.M., Garner,C.D., Schlösser, M., Beyersmann, D. (1985), "Extended X-ray Absorption fine structure investigations of zinc in 5-aminolaevulinate dehydratase", Biochem. J. 230, 625-633.
3) Schlösser, M. und Beyersmann,D (1987)., "Zinc and Cadmium 5-Amino¬levulinate Dehydratase, Metal-Dependent pH Profiles", Biol. Chem. Hoppe-Seyler 368, 1469-1477.
4) Kolakowski, L.F., Schlösser, M. und Cooperman, B.S.(1988), "Cloning, Molecular Characterization, and Chromosome Localization of the Inorganic Pyrophosphatase (PPA) Gene from S.cerevisiae " Nucleic Acid Res. 16, 10441-10452.
5) Stachel, B., Dougherty, R.C., Lahl, U., Schlösser, M., Zeschmar, B., (1989), "Toxic Environmental Chemicals in Human Semen, Analytical Methods and Case Studies." Andrologica 21, 282-291.
6).Reiss, J., Krawczak, M., Schlösser, M., Wagner, M., Cooper,D.N. (1990)," The effect of replication errors on the mismatch analysis of PCR-amplified DNA." Nucleic Acids Res 18, 973-978.
7) Wagner, M., Schlösser, M., Reiss, J. (1990), "Direct gene diagnosis of cystic fibrosis by allele- specific polymerase chain reactions." Mol Biol and Med 7, 359-364.
8) Reis, A.,Bremer, S., Schlösser, M., Dück, M., Böhm, I., Hundrieser, J., Macek,M., Stuhrmann, M., Wagner, M., Dörk, T., Schnieders, F., Posselt, H.G., Wahn, U., Reiss, J. Trefz, F., Tümmler, B., Krawczak, M., Schmidtke, J., (1990) "Distribution patterns of the delta F508 mutation in the CFTR gene of CF-linked marker haplotypes in the German population." Hum Genet 85, 421-422.
9) Reiss, J., Schlösser, M., Wagner, M., Lenz, U., Krawczak, M.,Ammann, G., Klösser, S., Böwing, B. (1990) "Direkte Gendiagnostik bei Cystischer Fibrose." Monatsschrift Kinderheilkunde 138,434-437.
10) European Working Group on CF Genetics (1990) "Gradient of distribution in Europe of the major CF mutation and of its associated haplotype." Hum Genet 85, 436-445.
11) Berg, L.P., Wieland, K., Millar, D.S.,Schlösser, M., Wagner,M., Kakkar, V.V., Reiss, J., Cooper, D.N.(1990)."Detection of a novel point mutation causing haemophilia A by PCR/direct sequencing of ectopically-transcribed Factor VIII mRNA." Hum Genet 85, 655-658.
12) M. Wagner und M. Schlösser (1990) " Direkte Gendiagnostik der zystischen Fibrose", Niedersächsisches Ärzteblatt 17, 22-24.
13) Schlösser, M., Slomski, R., Wagner, M., Berg, L.P., Kakkar,V.V., Cooper, D.N., Reiss, J.(1990) "Characterization of pathological dystrophin transcripts from the lymphocytes of a muscular dystrophy carrier." Mol Biol Med 7, 519-523.
14) Slomski R, Schlösser M , Chlebowska H, Reiss J and Engel W. (1991) "Detection of human spermatid-specific transcipts in peripheral blood lymphocytes of males and females". Hum Genet 87, 307-310.
15) J. Bal, M. Stuhrmann, M. Schlösser, J. Schmidtke, J. Reiss,(1991), " A cystic fibrosis patient homozygous for the nonsense mutation R553X". J Med Genet 28, 715-717.
16) Schlösser M, Arleth S,Lenz U, Bertele RM, Reiss J, (1991), "A Cystic Fibrosis patient with the nonsense mutation G542X and the splice site mutation 1717-1". J Med Genet,28, 878-880.
17) Dörk T, Schlösser M, Bürger J, Hoffknecht N, Kälin N, Krawczak M, Macek M, Reis A, Will K, Wulbrand U, Wulf B, Reiss J, Tümmler B, Schmidtke J, Stuhrmann M. (1991) " Mutationsanalyse bei deutschen CF-Patienten" Med. Genetik 3, 24-26.
18) Stuhrmann, M., Dörk, T., Krawczak, M., Dueck, M., Banholzer, U., Domagk, J., Hoffknecht, N., Posselt, H.G., Reis, A., Schlösser, M., Trefz, F., Wagner, M., Wahn, U., Wulf, B., Schmidtke, J., Reiss, J., Tümmler, B. "Genotype/phenotype correlations in cystic fibrosis patients" In: Tsui, L.C., et al. (1991) "The identification of the CF (Cystic Fibrosis) gene" Plenum Press, New York, 97-103
19) Plieth J, Rininsland F, Schlösser M, Reiss J, (1992) "Single Strand Conformation Polymorphism (SSCP) Analysis of exon 11 of the CFTR gene reliably detects more than one third of non-delta F508 Mutations in Geman Cystic Fibrosis patients" Hum Genet 88, 283-287.
20) Adham IM, Spitzer U, Schlösser M, Kremling H, Keime S, Engel W. (1992) " A reply, the human proacrosin gene" Eur J Biochem 207, 27-28.
21) Keime S, Heitland K, Kumm S, Schlösser M, Hroch N, Holtz W, Engel W.(1992) " Characterization of Four Genes Encoding Basic Proteins of the Porcine Spermatid Nucleus and Close Linkage of Three of them" Biol Chem Hoppe-Seyler 373,261-270.
22) Kremling H, Reinhardt N, Schlösser M, Engel W. (1992)" The bovine protamine 2 gene, evidence for alternative splicing" Biochimica et Biophysica Acta 1132,133-139.
23) Reiss J, Ellermeyer U, Schloesser M, Fuhrmann W, Drews D, Posselt HG,(1993) " Two Cystic Fibrosis patients with the genotype G542X/G551D" Hum Genet 91,78-79.
24) Reiss J, Ellermeyer U, Rininsland F, Ballhausen P, Lenz U, Wagner S, Schlösser M. ( 1993) " A comprehensive CFTR mutation analysis of German cystic Fibrosis patients". Human Molecular Genetics 2,809-811.
25) Engel W, Adham IM, Keime S, Kremling H, Schlösser M, Nayarnia K. (1993) " The Acrosin Gene, Structure, Regulation and Function" in, Reproductive Immunology Franco Dondero und Peter M. Johnson (Editors), Serono Symposia Publication from Raven Press, New York.
26) Will K, Reiss J, Dean M, Schlösser M, Slomski R, Schmidtke J, Stuhrmann M. (1993) "CFTR transcripts are undetectable in lymphocytes and respiratory epithelial cells of a patient homozygous for the nonsense mutation R553X". J Med Genet 30, 833-837.
27) Knobloch O, Schlösser M, Diedrich U und Kreuz F (1995) "Direkte DNA-Diagnostik einer Form der Spinozerebellären Ataxien jetzt möglich". Deutsches Ärzteblatt 92,821-823.
28) Schloesser M, Hofferbert S, Bartz U, Lutze G, Lämmle B und Engel W (1995) " The novel acceptor splice site mutation 11396(G->A) in the factor XII gene causes a truncated transcript in cross reacting material negative patients" Hum Mol Genet 4, 1235-1237.
29) Diedrich U, Lucius J, Bittermann HJ, Schlösser M, Eckert B, Behnke J, Pabst B (1995) " loss of alleles in brain tumors, distribution and correlations with clinical course" J Neurol 242, 707-711.
30) Gu SM, Orth U, Veske A, Enders H., Klünder K, Schlösser M, Engel W, Schwinger E, Gal A (1996) "Five novel mutations in the L1CAM gene in families with X-linked hydrocphalus" J Med Genet 33, 103-106.
31) Hofferbert S, Müller J, Köstering H, von Ohlen WD, Schlösser M (1996) "A novel 5`-upstream mutation in the factor XII gene is associated with a TaqI restriction site in an Alu repeat in factor XII deficient patients" Hum Genet 97, 838-841.
32.) Pauer HU, Zoll B, Köstering H, Köhler M, Schlösser M (1996) "Thrombophiliegefährdung und Mutation im Faktor V-Gen" Nieders. Ärzteblatt 6, 33-35.
33.)Schlösser M, Engel W. (1997) "Mutationen im Faktor XII-Gen" in "Molekuklargenetik Hereditärer Hämostasedefekte" F.H.Herrmann (Hrsg.), Pabst Science Publishers, Lengerich, Berlin, Düsseldorf, Leipzig, Riga, Scottsdale (USA), Wien , Zagreb.
34). Schlösser M, Vogelsang S, Engel W (1997) „Mikrodeletionen als Ursache männlicher Infertilität?“ Fertilität 13, 95-98.
35.) Schloesser M, Zeerleder S, Lutze G, Halbmayer WM, Hofferbert S, Hinney B, Koestering H, Lammle B, Pindur G, Thies K, Kohler M, Engel W (1997).“ Mutations in the human factor XII gene“: Blood 90(10):3967-77.
36.) Laccone F., Schlösser M.(1997) „A novel point mutation Met1IIe in the X25 gene responsible for Friedreich's Ataxia“. Mutation Research, Mutation and Polymorphism, Report # 2. Online publication
37.) Bartels, I., Schlösser, M., Bartz, U. G., Pauer, H.-U.(1998) Paternal origin of trisomy 21 following intracytoplasmic sperm injection (ICSI). Human Reproduction 13, 3345-3346.
38.) Adham, I. M., Schlösser, M., Engel, W. (1998) „Acrosin“. In "Handbook of proteolytic enzymes"; Barrett, A. J., Rawlings, N. D., Woessner, J. F. (Eds.) Academic Press, London, pp. 90-93.
39.) Zeerleder, S., Schloesser, M., Redondo, M., Wuillemin, W. A., Engel, W., Furlan, M., Lämmle, B. (1999) „Reevaluation of the incidence of thromboembolic complications in congenital factor XII deficiency“. Thromb. Haemost. 82, 1240-1246.
40.) Pauer, H.-U., Neesen, J., Schloesser, M., Hinney, B., Rauskolb, R. (2000) „Homozygous factor V Leiden mutation in a woman with multiple adverse pregnancy outcomes“. Arch. Gynecol Obstet. 264, 164-165.
41.) Brüchert V., Jørgensen B. B., Neumann K., Riechmann D., Schlösser M., and Schulz H. (2003) Regulation of bacterial sulfate reduction and hydrogen sulfide fluxes in the central Namibian coastal upwelling zone. Geochimica et Cosmochimica Acta 67, 4505-4518.
42.) Adham, I.M., Schlösser, M., Engel, W. (2004) „Acrosin“ Barrett. A.,Rawlings, N.,Woessner, J.(Editors) Handbook of Proteolytic Enzymes, 2nd ed., Vol. 2, 1562-1565.
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