Search Results - "Rommel, Birgit"
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Factors targeting MED12 to drive tumorigenesis? [version 2; peer review: 2 approved, 1 approved with reservations]
Published in F1000 research (2018)“…Mediator Complex Subunit 12 (MED12) is part of the transcriptional preinitiation machinery. Mutations of its gene predominantly occur in two types of highly…”
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Activation of the two microRNA clusters C19MC and miR-371-3 does not play prominent role in thyroid cancer
Published in Molecular cytogenetics (15-10-2012)“…Chromosomal rearrangements of band 19q13.4 are frequent cytogenetic alterations in benign thyroid adenomas. Apparently, these alterations lead to the…”
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ABO blood groups and the risk of SARS-CoV-2 infection
Published in Protoplasma (01-11-2022)“…There is no doubt that genetic factors of the host play a role in susceptibility to infectious diseases. An association between ABO blood groups and SARS-CoV-2…”
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Factors targeting MED12 to drive tumorigenesis?
Published in F1000 research (2018)“…Mediator Complex Subunit 12 (MED12) is part of the transcriptional preinitiation machinery. Mutations of its gene predominantly occur in two types of highly…”
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Reasons to Reconsider Risk Associated With Power Morcellation of Uterine Fibroids
Published in In vivo (Athens) (01-01-2020)“…Our insights into the molecular pathogenesis of uterine smooth muscle tumors have improved significantly. Accordingly, in the present review, we advocate a…”
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Case Report: A Low-grade Uterine Leiomyosarcoma Showing Multiple Genetic Aberrations Including a Bi-allelic Loss of the Retinoblastoma Gene Locus, as well as Germ-line Uniparental Disomy for Part of the Long Arm of Chromosome 22
Published in Anticancer research (01-05-2017)“…Uterine leiomyosarcomas are rare tumors with adverse prognosis. Recently, it has been suggested that a possible genetic subgroup of these tumors might be…”
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Comment re: HMGA2 is a negative regulator of DNA-PK pathway
Published in Cancer research (Chicago, Ill.) (15-02-2010)Get full text
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Malignant mesenchymal tumors of the uterus - time to advocate a genetic classification
Published in Expert review of anticancer therapy (01-11-2016)“…Introduction: Sarcomas are rare uterine tumors with leiomyosarcomas and endometrial stromal sarcomas constituting the predominant entities often making their…”
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HMGI-C, a Member of the High Mobility Group Family of Proteins, is Expressed in Hematopoietic Stem Cells and in Leukemic Cells
Published in Leukemia & lymphoma (1997)“…The human HMGI-C gene encoding a member of the high mobility group protein family normally is expressed only during embryonic/fetal development hut in none of…”
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Interphase fluorescence in situ hybridization analysis detects a much higher rate of thyroid tumors with clonal cytogenetic deviations of the main cytogenetic subgroups than conventional cytogenetics
Published in Cancer genetics (01-07-2011)“…In benign thyroid lesions, three main cytogenetic subgroups, characterized by trisomy 7 or structural aberrations involving either chromosomal region 19q13.4…”
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A Highly Complex Chromosomal Rearrangement between Five Chromosomes in a Healthy Female Diagnosed in Preparation for Intracytoplasmatic Sperm Injection
Published in The journal of histochemistry and cytochemistry (01-03-2005)“…We report a case of a de novo complex chromosomal rearrangement among five chromosomes found in a clinically healthy woman. The only indication for chromosome…”
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Ten Pulmonary Chondroid Hamartomas With Chromosome 6p21 Breakpoints Within the HMG-I(Y) Gene or Its Immediate Surroundings
Published in JNCI : Journal of the National Cancer Institute (04-09-1996)“…To determine whether the HMG-I(Y) gene is rearranged in 6p21 translocations, Kazmierczak et al designed a primer pair specific for intron 3 of the gene to…”
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An unbalanced t(15;18)(q21-q22;p11) as the sole cytogenetic aberration in a patient with B-cell chronic lymphocytic leukemia
Published in Cancer genetics and cytogenetics (01-07-2010)Get full text
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Interstitial deletion of 5q33.3q35.1 in a girl with mild mental retardation
Published in American journal of medical genetics (17-07-2000)“…Constitutional interstitial deletions of 5q are uncommon. The corresponding phenotype is not well defined. But severe mental retardation seems to be a…”
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No rearrangement of c-mos in salivary gland pleomorphic adenomas with 8q12 aberrations
Published in Cancer genetics and cytogenetics (15-10-1990)“…The frequent occurrence of salivary gland pleomorphic adenomas characterized by clonal structural chromosome abnormalities involving 8q12 raises the question…”
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Failure to detect human papillomavirus sequences at the 3p21 rearrangement site in pleomorphic adenomas
Published in Cancer genetics and cytogenetics (01-04-1991)“…Eighteen salivary gland pleomorphic adenomas, including nine with a t(3;8)(p21;q12) as the sole chromosome abnormality, were tested for the presence of human…”
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Leiomyoma cells with 12q15 aberrations can be transformed in vitro and show a relatively stable karyotype during precrisis period
Published in Cancer genetics and cytogenetics (15-07-1991)“…Tumor cells from three uterine leiomyomas showing translocations involving 12q14-15 were transformed by transfection using the "early regions" of the SV40…”
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