Poster presentations: 2. Cytogenetics
Tags: TRISOMY; CYTOGENETICS; POLYMERASE chain reaction
Related Articles
- Malignant Papillary Renal Tumors With Extensive Clear Cell Change. Salama, M. E.; Worsham, M. J.; DePeralta-Venturina, M. // Archives of Pathology & Laboratory Medicine;Sep2003, Vol. 127 Issue 9, p1176
Context.--Histologic subtyping of renal cell carcinomas (RCCs) is based not only on cytoarchitectural pattern but also on distinct cytogenetic abnormalities. Some renal tumors demonstrate overlapping morphologic features, rendering histologic subtyping difficult. One such group of tumors is...
- Poster presentations: 2. Cytogenetics. // Journal of Medical Genetics;Sep2002 Supplement, Vol. 39, pS58
Discusses the abstract of the research paper entitled 'A novel polymorphic imbalance detected by the QF-PCR trisomy assay and implications for result interpretation,' by Kathy Mann, C. Donaghue et al and presented during the British Human Genetics Conference at the University of York in England...
- The use of RT-PCR for the analysis of key loci in acute myeloid leukaemia. Grimwade, David // Journal of Medical Genetics;Sep2003 Supplement, Vol. 40, pS30
Cytogenetic and molecular characterisation of acute myeloid leukaemia (AML) has led to major advances in determining and optimising the treatment approach to patients with this disease. Cases of AML with t(15;17)(q22;q12-21), t(8;21)(q22;q22) and inv (16)(p13q22)/t(16;16)(p13;q22), which lead to...
- Quantitative Fluorescence PCR (QF-PCR): an essential tool for the characterisation of hydatifiform molar pregnancies. Dunlop, Nicola; Shade, M.; Grace, E.; Maher, E.; Porteous, M.; Warner, J. // Journal of Medical Genetics;Sep2003 Supplement, Vol. 40, pS61
Hydatidiform moles occur in approximately 1 in 1000 of all registered pregnancies. Complete hydatidiform moles are usually 46, XX (or rarely 46, XY) with both sets of chromosomes being paternally derived whilst partial hydatidiform moles are often triploid with two paternal contributions. Sample...
- Structural Anomalies in CVS and Amnio Samples Detected by Amnio PCR and CVS PCR. // Journal of Medical Genetics;Sep2004 Supplement, Vol. 41, pS80
Presents an abstract of the study entitled "Structural Anomalies in CVS and Amnio Samples Detected by Amnio PCR and CVS PCR," by Elaine Whitfield, presented during the British Human Genetics Conference held at the University of York in England from September 13 to 15, 2004.
- FISH Analysis of Yq Deletions in Subfertile Men. // Fertility Weekly;9/16/2002, p7
Describes the fluorescence in situ hybridization analysis of Y chromosome long arm deletions in subfertile men considering intracytoplasmic sperm injection in Singapore. Characterization of Yq deletions in infertile men; Use of multiple polymerase chain reaction; Avancement in cytogenetic...
- Novel Functional MAR Elements of Double Minute Chromosomes in Human Ovarian Cells Capable of Enhancing Gene Expression. Yan Jin; Zheng Liu; Wei Cao; Xinying Ma; Yihui Fan; Yang Yu; Jing Bai; Feng Chen; Rosales, Jesusa; Ki-Young Lee; Songbin Fu // PLoS ONE;Feb2012, Vol. 7 Issue 2, p1
Double minute chromosomes or double minutes (DMs) are cytogenetic hallmarks of extrachromosomal genomic amplification and play a critical role in tumorigenesis. Amplified copies of oncogenes in DMs have been associated with increased growth and survival of cancer cells but DNA sequences in DMs...
- Rapid prenatal diagnosis, conventional karyotyping of both? Clarkson, Amanda; Bateman, M. // Journal of Medical Genetics;Sep2003 Supplement, Vol. 40, pS57
The rapid prenatal diagnostic tests, interphase FISH (IFISH) and quantitative fluorescence PCR (QF-PCR), have become increasingly popular in cytogenetic laboratories to test for the common aneuploidies (13,18,21,X and Y). These tests provide reliable, accurate and rapid results and reduce...
- A rare but specific subset of adult AML patients can be defined by the cytogenetically cryptic NUP98-NSD1 fusion gene. Fasan, A; Haferlach, C; Alpermann, T; Kern, W; Haferlach, T; Schnittger, S // Leukemia (08876924);Jan2013, Vol. 27 Issue 1, p245
The article discusses the detection of cytogenetically cryptic NUP98-NSD1 fusion gene in a specific subset of adult acute myeloid leukemia (AML) patients. Cytogenetically detectable chromosomal rearrangement leads to fusion genes in AML cases. The study involved evaluation of NUP98–NSD1 fusion...
