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Martin-Luther-Universität Halle-Wittenberg | |||
| Forschungsbericht | Berichtszeitraum: | 01.01.99 - 31.12.00 | ||
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Ballhausen, W.G.(1999)
Erbliches Risiko für Dickdarmkrebs: Genetische Grundlagen des hereditären nicht-polypösen Kolonkarzinoms (HNPCC).
Aktuelle Urologie 30: 184 - 9
Dahse, R., Fiedler, W., Junker, K., Schlichter, A., Schubert, J. und Claussen, U.(1999)
Telomerase activity and telomere lengths:
alterations in renal cell carcinomas.
Kidney International 56: 1289 - 90
Dahse, R., Fiedler, W., von Eggeling, F., Schimmel, B., Koscielny, S., Beleites, E., Claussen, U. und Ernst, G.(1999)
P53 genotyping - an effective concept for
molecular testing of head and neck cancer?
International Journal of Molecular Medicine 4:
279 - 83
Fiedler, W., Junker, K., Schlichter, A., Schubert, J., Ernst, G., Dahse, R. und Claussen, U.(1999)
Determination of telomerase activity for
differential analysis of multifocal renal cell carcinomas.
Kidney International 56: 1286 - 8
Kraus, C., Kastl, S., Günther, K., Klessinger, S., Hohenberger, W. und Ballhausen, W.G.(1999)
A proven de novo germline mutation in HNPCC.
Journal of Medical Genetics 36: 919 - 21
Mayer, K., Ballhausen, W.G. und Rott, H.D.(1999)
Mutation screening of the entire coding regions
of the TSC1 and the TSC2 gene with the protein truncation test (PTT) identifies
frequent splicing defects.
Human Mutation 14: 401 - 11
Riese, U., Dahse, R., Fiedler, W., Theuer, C., Koscielny, S., Ernst, G., Beleites, E., Claussen, U. und von Eggeling, F.(1999)
Tumor suppressor gene p16 (CDKN2A) mutation
status and promoter inactivation in head and neck cancer.
International Journal of Molecular Medicine 4:
61 - 5
Rott, H.D., Ballhausen, W.G. und Mayer, K.(1999)
Klinik und Genetik der tuberösen Sklerose.
Pädiatrische Praxis 56: 233 - 44
Schlichter, A., Fiedler, W., Junker, K., Dahse, R., Claussen, U. und Schubert, J.(1999)
Determination of telomerase activity in
multifocal renal cell carcinoma.
International Journal of Oncology 15: 577 - 81
Starke, H., Schreyer, I., Kahler, C., Fiedler, W., Beensen, V., Heller, A., Nietzel, A., Claussen, U. und Liehr, T.(1999)
Molecular cytogenetic characterization of a
prenatally detected supernumerary minute marker chromosome 8.
Prenatal Diagnosis 19: 1169 - 74
Stonane, E., Fiedler, W., Stonans, I. und von Eggeling, F.(1999)
Identification
of differentially expressed genes in T-lymphocyte subsets of discordant
monozygotic rheumatoid arthritis twins.
Allergologie 2: 119 - 126
Sulekova, Z., Reymond, M., Kockerling, F., Hohenberger, W. und Ballhausen, W.G.(1999)
Exon 14-skipping of the adenomatous polyposis
coli gene in purified epithelial cells of colonic mucosa and tumors.
Anticancer Research 19: 601 - 4
von Eggeling, F., Werner, G., Theuer, C., Riese, U., Dahse, R., Fiedler, W., Schimmel, B., Ernst, G., Karte, K., Claussen, U. und Wollina, U.(1999)
Analysis of the tumor suppressor gene
p16(INK4A) in microdissected melanoma metastases by sequencing, and
microsatellite and methylation screening.
Archieves of Dermatology Research 291: 474 - 7
Ballhausen, W.G.(2000)
Genetic testing for familial adenomatous
polyposis.
Annals of the New York Academy of Sciences 910:
36 - 49
Günther, K., Horbach, T., Hohenberger, W., Kraus, C. und Ballhausen, W.G.(2000)
Colonic late-onset familial adenomatous
polyposis combined with severe duodenal polyposis and familial endometrial
cancer.
American Journal of Medicine 108: 681 – 3
Kastl, S., Günther, K., Merkel, S., Hohenberger, W. und Ballhausen, W.G.(2000)
[Hereditary colonic carcinoma without polyposis
(HNPCC) without satisfying the Amsterdam criteria].
Chirurg 71: 444 - 7
Koscielny, S., Dahse, R., Sonntag, J., Riese, U., Theuer, C., Hofmann, M.E., von Eggeling, F., Claussen, U., Beleites, E., Ernst, G. und Fiedler, W.(2000)
Clinical implications of telomerase activity and inactivation of the tumor suppressor gene p16 (CDKN2A) in head and neck cancer.
Otolaryngol Polska 54: 291 - 5
Koscielny, S., Fiedler, W., Dahse, R. und Beleites, E.(2000)
The Reactivation of telomerase in squamous
epithelial carcinomas in the area of the head and neck.
Laryngorhinootologie 79: 551 – 6
Kraus, C., Braun-Quentin, C., Ballhausen, W.G. und Pfeiffer, R.A.(2000)
RNA-based mutation screening in German families
with Sjogren-Larsson syndrome.
European Journal of Human Genetics 8: 299 - 306
Mayer, K., Ballhausen,
W.G., Leistner, W. und Rott, H.(2000)
Three novel types of splicing aberrations in
the tuberous sclerosis TSC2 gene caused by mutations apart from splice
consensus sequences.
Biochimica et Biophysica Acta 1502: 495 - 507
von Eggeling, F.,
Davies, H., Lomas, L., Fiedler, W., Junker, K., Claussen, U. und Ernst,
G.(2000)
Tissue-specific microdissection coupled with
ProteinChip array technologies: applications in cancer research.
Biotechniques 29: 1066 - 70
Abed, A.A., Vogler, A., Kraus, C., Günther, K. und Ballhausen, W.G.(1999)
Puromycin inhibits nonsense mediated
mRNA decay of STK11 transcripts in
Peutz-Jeghers patients.
Medizinische
Genetik 11: 149
Dahse, R., Fiedler, W., von Eggeling, F., Ernst, G., Koscielny, S., Beleites, E. und Claussen, U.(1999)
Telomerase
activity is not dependent on the p53 status in head and neck cancer.
Medizinische Genetik 11: 151
Dahse, R., Fiedler, W., von Eggeling, F., Koscielny, S., Beleites, E., Ernst, G. und Claussen, U.(1999)
P53
genotyping is not an effective concept for molecular testing head and neck
cancer.
American
Journal of Human Genetics 65:
655
Eberwein, J. und Ballhausen, W.G.(1999)
Distinct compartimentalization in
NIH3T3 cells of p67apc - an isoform encoded by transcripts skipping
exon 14 of the adenomatous polyposis coli (APC) gene.
Medizinische Genetik 11: 151
Ernst, G., Riese, U., Theuer, C., Dahse, R., von Eggeling, F., Koscielny, S., Beleites, E., Claussen, U. und Fiedler, W.(1999)
Different
genomic alterations inactivate the tumor suppressor gene p16 INKA4
(CDKN2A, MTS1) in head and neck cancers.
Medizinische Genetik 11: 152
Fiedler, W., Liehr, T., Hoppe, C., Bereczki, Zs., Schimmel, B., Dahse, R., von Eggeling, F., Koscielny, S., Beleites, E., Gebhart, E., Ernst, G. und Claussen, U. (1999)
Telomerase
(in)activation in head and neck cancers is not caused by genomic alterations of
genes encoding the telomerase complex or the putative telomerase suppressor
gene.
Medizinische Genetik 11: 152
Fiedler, W., Müller, C., Riese, U., Dahse, R., von Eggeling, F., Kosmehl, H., Ernst, G. und Claussen, U.(1999)
Differential
analysis of telomerase activity in microdissected breast cancer samples.
American
Journal of Human Genetics 65:
671
Hoppe, C., Bereczki, Zs., Schimmel, B., Ernst, G., Dahse, R., von Eggeling, F., Koscielny, S., Beleites, E., Claussen, U. und Fiedler, W.(1999)
Microsatellite
analysis of squamous cell carcinomas of the head and neck.
Medizinische Genetik 11: 153
Hühne, K., Park, O., Liehr, T., Fiedler, W. und Rautenstrauss, B.(1999)
Expression
analysis of the PMP22 gene in tumor cell lines with a chromosome 17p11.2
amplification.
Medizinische Genetik 11: 193
Koscielny, S., Dahse, R., Sonntag, J., Riese, U., Theuer, C., Hofmann, S.M.E., von Eggeling, F., Claussen, U., Beleites, E., Ernst, G. und Fiedler, W.(1999)
Clinical
implications of telomerase activity and inactivation of the tumor suppressor
gene p16 (CDKN2A) in head and neck cancer.
Acta
oto-rhino-laryngologica belgica 53: 159
Koscielny, S., Fiedler, W., Beleites, E. und Claussen, U.(1999)
Welche Rolle spielt die Inaktivierung des Promotors p16 bei Plattenepithelkarzinomen im Kopf-Hals-Bereich.
HNO 47: 396
Kraus, C., Landendörfer, W.L., Walden, U., Ballhausen, W.G. und Pfeiffer, R.A.(1999)
A new CFTR gene mutation detected by
TGGE analysis in a child with atypic CF.
Medizinische Genetik 11: 196
Mey, J., Platzer, C., Claussen, U. und Fiedler, W.(1999)
Differential
expressed DNA sequences in PC12 cells obtained by fluorescence DD-RT-PCR and
direct sequencing before and after NGF treatment.
Medizinische Genetik 11: 154
Nietzel, A., Starke, H., Heller, A., Fiedler, W., Senger, G., Gebhart, E., Rocchi, M., Claussen, U. und Liehr, T.(1999)
Characterization
of small marker chromosomes by centromere specific 24-color FISH.
Cytogenetics
and Cell Genetics 85: 40/P142
Schenker, B., Vogler, A., Kraus, C. und Ballhausen, W.G.(1999)
Compound MLH1 mutation in early-onset HNPCC .
Medizinische Genetik 11: 155
Schlichter, S., Junker, K., Fiedler, W., Hindermann, W. und Schubert, J.(1999)
Differentiation
of multifocal renal cell carcinoma (RCC) by comparative genomic hybridization
(CGH) and analysis of telomerase activity.
Journal of
Urology 161: 141
Starke, H., Schreyer, I., Fiedler, W., Beensen, V., Heller, A., Chudoba, I., Claussen, U. und Liehr, T.(1999)
Alternative
strategy for the molecular cytogenetic characterization of small marker
chromosomes in prenatal cases.
Medizinische Genetik 1: 174
Vogler, A., Kraus, C., Günther, K. und Ballhausen, W.G.(1999)
Truncating mutations of the I1307K APC allele occur during DNA synthesis in vitro.
Medizinische Genetik 11: 156-7
von Eggeling, F., Gawriljuk, A., Römer, I., Dahse, R., Fiedler, W., Ernst, G., Klose, J. und Claussen, U.(1999)
Dual-color
differential 2D-proteingelelectrophoresis for the detection of tumor specific
changes of the protein patterns.
Medizinische Genetik 11: 151
von Eggeling, F., Werner, G., Theuer, C., Riese, U., Dahse, R., Fiedler, W., Schimmel, B., Ernst, G., Karte, K., Claussen, U. und Wollina, W.(1999)
Analysis of
the tumor suppressor gene p16(INK4a) in microdissected melanoma
metastases by sequencing, and microsatellite and methylation screening.
International
Journal of Molecular Medicine 4:
S47
Beer, S.,
Gottschalk, P., Bosseckert, H., Ernst, G., Claussen, U. (1), Riese, U., von
Eggeling, F. und Fiedler, W.(2000)
Telomerase
activity in chronic gastritis and the role of H. pylori – Examination based on microdissection of the gastric
mucosa.
Medizinische Genetik 12: 82
Bleichert, A., Fiedler, W., Dahse, R., Claussen, U., Ernst, G., Loncarevic, I.F., Liehr, T. und von Eggeling, F.(2000)
A new FISH
probe for the chromosomal region 9p21 derived from Long Distance (LD)-PCR.
Medizinische Genetik
12: 132
Ernst, G., Werner,
G., Theuer, C., Riese, U., Dahse, R., Fiedler, W., Schimmel, B.,
Claussen, U., Karte, K., Wollina, U. und von Eggeling, F.(2000)
Different inactivating mechanisms of the tumor suppressor gene p16
(CDKN2A, MTS1) in microdissected cutaneous in-transit melanoma metastases.
Medizinische Genetik 12: 126
Fiedler, W., Alves, G., Campos, M.M., von Eggeling, F.,
Ernst, G., Claussen, U. und Ornellas, A.A.(2000)
Determination of telomerase activity in 41 cases of squamous cell
carcinomas of the penis.
Medizinische Genetik
12: 83
Heller, A., Nietzel,
A., Rocchi, M., Starke, H., Fiedler,
W., Claussen, U. und Liehr,
T.(2000)
Centromere-specific multi-color FISH (cenM-FISH) – a new and rapid method
for the identification of marker chromosomes.
European Journal of Human Genetics 8: 87
Heller, A., Nietzel,
A., Rocchi, M., Starke, H., Fiedler,
W., Claussen, U. und Liehr,
T.(2000)
The identification of marker chromosomes with a new multi-color FISH
technique specific for centromeres.
Cellular and Molecular Biology Research 46: Abstract
Band
Hoppe, C., Theuer,
C., Riese, U., Sonntag, J., Hofmann, S.M.E., von Eggeling, F., Koscielny, S.,
Dahse, R., Claussen, U., Beleites, E., Ernst, G. und Fiedler, W.(2000)
Involvement of telomerase and p16 gene in head and neck cancer.
Medizinische Genetik 12: 82
Junker, K., Werner,
W., Kleemann, K., Schubert, J., Fiedler,
W. und Hartmann, A.(2000)
Molecular genetic evaluation of fluorescence diagnosis in bladder cancer.
British Journal of Urology 86
Loncarevic, I.F., Starke, H., Bleck, C., Ziegler, M., Fiedler, W., Liehr, T., Clement, H.J., Kelbova, C. und
Claussen, U.(2000)
Detection of 3´-BCR gene sequences on chromosome der (22)t(t9;22) but not
on der(9)t(9;22) by FISH in 4 patients with a conventional CML.
Medizinische Genetik
12: 132
Mey, J., Müller, C.,
von Eggeling, F., Michel, S., Ernst, G., Claussen, U. und Fiedler, W.(2000)
Towards the detection of telomerase activity in situ.
Medizinische Genetik
12: 81
Starke, S., Henn, W., Reichardt, S., Stumm, M., Behrend, C., Senger, G., Fiedler, W., Claussen, U. und Liehr, T.(2000)
Two
different types of human chromosome 9 pericentric inversions – detected by a
microdissection probe specific for 9p12 and 9q13.
Medizinische Genetik 12: 93
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