نتایج جستجو برای: tetrasomy

تعداد نتایج: 240  

2015
Venkata Padmalatha

Supernumerary Marker Chromosomes (SMC) follow non mendelian fashion in their inheritance, and are reported in variety of phenotypes. Although markers that contain satellites/bi-satellite variations of short arms do not confer any phenotypic alterations, it affects the fertility, vigour and interferes at non-disjunction during cell division and proves lethal to foetus. We report a couple wherein...

Journal: :American journal of medical genetics. Part A 2012
Anna Kostanecka Lindsey B Close Kosuke Izumi Ian D Krantz Mary Pipan

Pallister-Killian syndrome is a sporadic disorder caused by the presence of mosaic tetrasomy of the short arms of chromosome 12. Case reports of children with Pallister-Killian syndrome have described a range of developmental and behavioral outcomes, but no systematic studies of these outcomes exist. The objective of this study was to describe developmental and behavioral characteristics of ind...

2011
Jie Hu Suneeta Madan-Khetarpal Alvaro H. Serrano Russi Sally Kochmar Stephanie J. DeWard Malini Sathanoori Urvashi Surti

We characterized three supernumerary marker chromosomes (SMCs) simultaneously present in a 2-year- and 10-month-old male patient with mental retardation and dysmorphic features. Peripheral blood chromosome analysis revealed two to three SMCs in 25/26 cells analyzed. The remaining one cell had one SMC. Microarray comparative genomic hybridization (aCGH) showed mosaicism for gains of 5q35.3, 15q1...

Journal: :Journal of medical genetics 1998
H Rivera L Bobadilla A Rolon J Kunz J A Crolla

A female infant who died at 2 years of age with growth and psychomotor retardation, wide anterior fontanelle, downward slanting palpebral fissures, large, simple ears, joint dislocation/contractures, recurrent infections, and severe pulmonary hypertension was found to have a de novo 7p+ chromosome. The G banding pattern was suggestive of a triplication of 7p21.3 and 7p22; results of fluorescenc...

Journal: :International journal of oncology 2007
Julia Rosenhahn Anja Weise Susanne Michel Katrin Hennig Isabell Hartmann Jana Schiefner Katrin Schubert Thomas Liehr Ferdinand von Eggeling Ivan F Loncarevic

Approximately 30% of chronic myeloid leukemia patients show initially no response to Imatinib, a potent inhibitor of BCR-ABL. This intrinsic resistance may be due to BCR-ABL-independent cell growth. Here we analysed the cytogenetic anomalies and the proteomic profiling in KCL22-S and KCL22-R, two Imatinib-sensitive and -resistant derivative cell lines of KCL22. A tetrasomy 8 and a non-reciproca...

Journal: :Carcinogenesis 2015
Qing Lan Martyn T Smith Xiaojiang Tang Weihong Guo Roel Vermeulen Zhiying Ji Wei Hu Alan E Hubbard Min Shen Cliona M McHale Chuangyi Qiu Songwang Liu Boris Reiss Laura Beane-Freeman Aaron Blair Yichen Ge Jun Xiong Laiyu Li Stephen M Rappaport Hanlin Huang Nathaniel Rothman Luoping Zhang

Formaldehyde (FA) is an economically important industrial chemical to which millions of people worldwide are exposed environmentally and occupationally. Recently, the International Agency for Cancer Research concluded that there is sufficient evidence that FA causes leukemia, particularly myeloid leukemia. To evaluate the biological plausibility of this association, we employed a chromosome-wid...

Journal: :Carcinogenesis 1998
L Zhang N Rothman Y Wang R B Hayes G Li M Dosemeci S Yin P Kolachana N Titenko-Holland M T Smith

Two of the most common cytogenetic changes in therapy- and chemical-related leukemia are the loss and long (q) arm deletion of chromosomes 5 and 7. The detection of these aberrations in lymphocytes of individuals exposed to potential leukemogens may serve as useful biomarkers of increased leukemia risk. We have used a novel fluorescence in situ hybridization (FISH) procedure to determine if spe...

2018
Cathryn Poulton Gareth Baynam Clarissa Yates Hamid Alinejad-Rokny Simon Williams Helen Wright Karen J Woodward Soruba Sivamoorthy Joanne Peverall Peter Shipman David Ravine John Beilby Julian Ik-Tsen Heng

BACKGROUND Pallister-Killian syndrome (PKS) is a rare multisystem developmental syndrome usually caused by mosaic tetrasomy of chromosome 12p that is known to be associated with neurological defects. METHODS We describe two patients with PKS, one of whom has bilateral perisylvian polymicrogyria (PMG), the other with macrocephaly, enlarged lateral ventricles and hypogenesis of the corpus callo...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2012
Michael Chester Joseph P Gallagher V Vaughan Symonds Ana Veruska Cruz da Silva Evgeny V Mavrodiev Andrew R Leitch Pamela S Soltis Douglas E Soltis

Polyploidy, or whole genome duplication, has played a major role in the evolution of many eukaryotic lineages. Although the prevalence of polyploidy in plants is well documented, the molecular and cytological consequences are understood largely from newly formed polyploids (neopolyploids) that have been grown experimentally. Classical cytological and molecular cytogenetic studies both have show...

Journal: :Cancer research 1989
B U Holecek R Kerler H M Rabes

A chromosomal analysis was performed on two cell lines which were derived from the liver of two rats exposed to diethylnitrosamine in vivo. The cells were obtained by collagenase perfusion of the liver at an early stage of development of ATPase-deficient putative preneoplastic populations, and propagated from foci of epithelial cells which started growth in vitro. Cell line CL 38 proved to be t...

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