Search Results - "Strissel, P. L."

Regulation of the NRSF/REST gene by methylation and CREB affects the cellular phenotype of small-cell lung cancer by Kreisler, A, Strissel, P L, Strick, R, Neumann, S B, Schumacher, U, Becker, C-M

“…The neuron-restrictive silencer factor/RE1-silencing transcription factor (NRSF/REST) is a negative regulator of gene expression restricting the expression of…”
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Hypermethylation and loss of retinoic acid receptor responder 1 expression in human choriocarcinoma by Huebner, H, Strick, R, Wachter, D L, Kehl, S, Strissel, P L, Schneider-Stock, R, Hartner, A, Rascher, W, Horn, L C, Beckmann, M W, Ruebner, M, Fahlbusch, F B

“…Human placental development resembles tumorigenesis, due to the invasive and fusogenic potential of trophoblasts. However, these features are tightly…”
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Polymorphisms in the novel serotonin receptor subunit gene HTR3C show different risks for acute chemotherapy-induced vomiting after anthracycline chemotherapy by Fasching, P. A., Kollmannsberger, B., Strissel, P. L., Niesler, B., Engel, J., Kreis, H., Lux, M. P., Weihbrecht, S., Lausen, B., Bani, M. R., Beckmann, M. W., Strick, R.

“…The aim of this study was to correlate chemotherapy-induced nausea and vomiting (CINV) with commonly occurring single nucleotide polymorphisms (SNP) in the…”
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Contribution of different placental cells to the expression and stimulation of antimicrobial proteins (AMPs) by Klaffenbach, D, Friedrich, D, Strick, R, Strissel, P.L, Beckmann, M.W, Rascher, W, Gessner, A, Dötsch, J, Meißner, U, Schnare, M

“…Abstract The placenta is a major barrier that prevents potentially infectious agents from causing fetal diseases or related complications during pregnancy…”
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Single nucleotide polymorphism D1853N of the ATM gene may alter the risk for breast cancer by Schrauder, M., Frank, S., Strissel, P. L., Lux, M. P., Bani, M. R., Rauh, C., Sieber, C. C., Heusinger, K., Hartmann, A., Schulz-Wendtland, R., Strick, R., Beckmann, M. W., Fasching, Peter A.

“…Purpose Various ATM (ataxia telangiectasia-mutated) mutations and polymorphisms have been reported to be associated with an increased breast cancer risk…”
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DNA structural properties of AF9 are similar to MLL and could act as recombination hot spots resulting in MLL/AF9 translocations and leukemogenesis by STRISSEL, P. L, STRICK, R, TOMEK, R. J, ROE, B. A, ROWLEY, J. D, ZELEZNIK-LE, N. J

“…The human AF9 gene at 9p22 is one of the most common fusion partner genes with the MLL gene at 11q23, resulting in the t(9;11)(p22;q23). The MLL-AF9 fusion…”
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Evaluation of clinical parameters and estrogen receptor alpha gene polymorphisms for patients with endometriosis by Renner, S P, Strick, R, Oppelt, P, Fasching, P A, Engel, S, Baumann, R, Beckmann, M W, Strissel, P L

“…Endometriosis is a chronic inflammatory disease, which is especially found in women with subfertility problems with an incidence of up to 30%. The disease is…”
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DNA sequence variations of the entire anti-Müllerian hormone (AMH) gene promoter and AMH protein expression in patients with the Mayer–Rokitanski–Küster–Hauser syndrome by Oppelt, P., Strissel, P.L., Kellermann, A., Seeber, S., Humeny, A., Beckmann, M.W., Strick, R.

“…BACKGROUND: The etiology of the Mayer–Rokitanski–Küster–Hauser (MRKH) syndrome, where congenitally the Müllerian ducts fail to develop into the uterus, cervix…”
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An In vivo topoisomerase II cleavage site and a DNase I hypersensitive site colocalize near exon 9 in the MLL breakpoint cluster region by STRISSEL, P. L, STRICK, R, ROWLEY, J. D, ZELEZNIK-LE, N. J

“…The human myeloid-lymphoid leukemia gene, MLL (also called ALL-1, Htrx, or HRX ), maps to chromosomal band 11q23. MLL is involved in translocations that result…”
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Specific Mg2+ binding to AT-rich regions of chromatin in the evolution of eukaryotes by STRISSEL, P. L, GAVRILOV, K. L, LEVI-SETTI, R, STRICK, R

“…At SIMS XIV, we reported SIMS evidence of specific Mg2+ binding to the AT-rich regions of human metaphase chromosomes represented by G-bands. Subsequent…”
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Cation-Chromatin Binding as Shown by Ion Microscopy Is Essential for the Structural Integrity of Chromosomes by Strick, Reiner, Strissel, Pamela L., Gavrilov, Konstantin, Levi-Setti, Riccardo

“…Mammalian interphase and mitotic cells were analyzed for their cation composition using a three-dimensional high resolution scanning ion microprobe. This…”
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Higher incidence of linked malformations in siblings of Mayer–Rokitansky–Küster–Hauser-syndrome patients by Wottgen, M., Brucker, S., Renner, S.P., Strissel, P.L., Strick, R., Kellermann, A., Wallwiener, D., Beckmann, M.W., Oppelt, P.

“…BACKGROUND Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome is a malformation of the female genital tract (vaginal aplasia, rudimentary uterus, normal fallopian…”
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Dietary Bioflavonoids Induce Cleavage in the MLL Gene and May Contribute to Infant Leukemia by Strick, Reiner, Strissel, Pamela L., Borgers, Susanne, Smith, Steve L., Rowley, Janet D.

“…Chromosomal translocations involving the MLL gene occur in about 80% of infant leukemia. In the search for possible agents inducing infant leukemia, we…”
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Assessment of pituitary and steroid hormones and members of the TGF-beta superfamily for ovarian function in patients with congenital uterus and vaginal aplasia (MRKH syndrome) by Strissel, P L, Oppelt, P, Cupisti, S, Stiegler, E, Beckmann, M W, Strick, R

“…Patients with Mayer-Rokitanski-Kuster-Hauser (MRKH) syndrome have congenital uterine and vaginal aplasia. The main question of this study was, if the absence…”
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Risk Factors for Endometriosis in a German Case-Control Study by Burghaus, S, Klingsiek, P, Fasching, P A, Engel, A, Häberle, L, Strissel, P L, Schmidt, M, Jonas, K, Strehl, J D, Hartmann, A, Lermann, J, Boosz, A, Thiel, F C, Müller, A, Beckmann, M W, Renner, S P

“…The etiology of endometriosis is still a research field in which few consistent data are available. Large case-control studies or even cohort studies are rare,…”
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Scaffold-Associated Regions in the Human Type I Interferon Gene Cluster on the Short Arm of Chromosome 9 by Strissel, Pamela L., Dann, Hadas Arad, Pomykala, Helen M., Diaz, Manuel O., Rowley, Janet D., Olopade, Olufunmilayo I.

“…Scaffold-associated regions (SARs) function at the level of modeling or shaping the chromatin of DNA into loop domains. We have mapped 36 SARs in the human…”
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Polymorphisms in estrogen metabolism and estrogen pathway genes and the risk of miscarriage by Cupisti, S., Fasching, Peter A., Ekici, A. B., Strissel, P. L., Loehberg, C. R., Strick, R., Engel, J., Dittrich, R., Beckmann, M. W., Goecke, T. W.

“…Purpose This study investigated genetic variations in the estrogen pathway and their association with miscarriages. Methods A total of 483 patients were…”
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AF10 Is Split by MLL and HEAB, a Human Homolog to a Putative Caenorhabditis elegans ATP/GTP-Binding Protein in an Invins(10; 11)(p12;q23q12) by Tanabe, Satoru, Bohlander, Stefan K., Vignon, Christine V., III, Rafael Espinosa, Zhao, Nanding, Strissel, Pamela L., Zeleznik-Le, Nancy J., Rowley, Janet D.

“…Invins(10;11)(p12;q23q12) is one of the rare but recurring chromosome rearrangements seen in acute monoblastic leukemia. We cloned the proximal 10p breakpoint…”
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Common chromatin structures at breakpoint cluster regions may lead to chromosomal translocations found in chronic and acute leukemias by STRICK, Reiner, YANMING ZHANG, EMMANUEL, Neelmini, STRISSEL, Pamela L

“…The t(9;22) BCR/ABL fusion is associated with over 90% of chronic myelogenous and 25% of acute lymphocytic leukemia. Chromosome 11q23 translocations in acute…”
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High resolution SIMS imaging of cations in mammalian cell mitosis, and in Drosophila polytene chromosomes by Levi-Setti, R., Gavrilov, K.L., Neilly, M.E., Strick, R., Strissel, P.L.

“…The University of Chicago high resolution scanning ion microprobe (UC-SIM) was used to image, by Secondary Ion Mass Spectrometry (SIMS), the distribution of Ca…”
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