نتایج جستجو برای: karyotyping

تعداد نتایج: 1991  

Journal: :Cell Biochemistry and Biophysics 2011

Journal: :Applied optics 2001
J J Scherer J B Paul H Jiao A O'Keefe

A new technique that enables frequency-resolved cavity ringdown absorption spectra to be obtained over a large optical bandwidth by a single laser shot is described. The technique, ringdown spectral photography (RSP), simultaneously employs two key principles to record the time and frequency response of an optical cavity along orthogonal axes of a CCD array detector. Previously, the principles ...

Journal: :Genetics 2007
Weichang Yu Jonathan C Lamb Fangpu Han James A Birchler

Global genomic analysis of transposable element distributions of both natural (En/Spm, Ac-Ds, and MuDR/Mu) and modified (RescueMu) types was performed by fluorescence in situ hybridization (FISH) on somatic chromosomes coupled with karyotyping of each chromosome. In lines without an active transposable element, the locations of silent En/Spm, Ac-Ds, and MuDR/Mu elements were visualized, reveali...

Journal: :The New England journal of medicine 2012
Ronald J Wapner Christa Lese Martin Brynn Levy Blake C Ballif Christine M Eng Julia M Zachary Melissa Savage Lawrence D Platt Daniel Saltzman William A Grobman Susan Klugman Thomas Scholl Joe Leigh Simpson Kimberly McCall Vimla S Aggarwal Brian Bunke Odelia Nahum Ankita Patel Allen N Lamb Elizabeth A Thom Arthur L Beaudet David H Ledbetter Lisa G Shaffer Laird Jackson

BACKGROUND Chromosomal microarray analysis has emerged as a primary diagnostic tool for the evaluation of developmental delay and structural malformations in children. We aimed to evaluate the accuracy, efficacy, and incremental yield of chromosomal microarray analysis as compared with karyotyping for routine prenatal diagnosis. METHODS Samples from women undergoing prenatal diagnosis at 29 c...

2009
Neelam Saba Saba Irshad

Turner’s syndrome is a disorder in human females characterized by the presence of one normal X chromosome and the complete or partial loss of the second X chromosome. Turner’s syndrome is usually diagnosed by karyotyping which is time-consuming, expensive and unfeasible for population screening. The present method of molecular detection was based on the ability of HpaII, a methylation sensitive...

Journal: :Hong Kong medical journal = Xianggang yi xue za zhi 2014
Justin D Y Tien L C Lau S L Tien M H Tan

OBJECTIVES To assess the clinical utility of conventional karyotyping as a diagnostic tool in soft tissue tumours amidst the increasing use of molecular cytogenetics. DESIGN Case series. SETTING Singapore General Hospital, an Asian institution. PARTICIPANTS A total of 35 participants (18 male and 17 female) aged 15 to 81 years were included in this study. Conventional karyotyping of 35 co...

2015
Kaan Savasoglu Kadriye Bahriye Payzin Fusun Ozdemirkiran Belgin Berber

Objective: To determine the use of the Quantitative Real Time PCR (RQ-PCR) assay follow-up with Chronic Myeloid Leukemia (CML) patients. Study Design: Cross-sectional observational. Place and Duration of Study: Izmir Ataturk Education and Research Hospital, Izmir, Turkey, from 2009 to 2013. Methodology: Cytogenetic, FISH, RQ-PCR test results from 177 CML patients' materials selected between 200...

Journal: :Annals of the Academy of Medicine, Singapore 2010
J L Heng Y C Chen T C Quah T C Liu A E J Yeoh

INTRODUCTION Childhood leukaemia accounts for more than 40% of new childhood cancer cases. Karyotyping of cytogenetic abnormalities in such cases continues to provide critical prognostic information which allows the delivery of an appropriate intensity of treatment. Unfortunately, karyotyping of childhood leukaemia is difficult, laborious and often unsuccessful. Banding resolution tends to be p...

Journal: :Cytometry 2002
Zhenzhen Kou Liang Ji Xuegong Zhang

BACKGROUND Comparative genomic hybridization (CGH) is a relatively new molecular cytogenetic method for detecting chromosomal imbalance. Karyotyping of human metaphases is an important step to assign each chromosome to one of 23 or 24 classes (22 autosomes and two sex chromosomes). Automatic karyotyping in CGH analysis is needed. However, conventional karyotyping approaches based on DAPI images...

Journal: :G3 2016
Aiko Iwata-Otsubo Brittany Radke Seth Findley Brian Abernathy C Eduardo Vallejos Scott A Jackson

Fluorescence in situ hybridization (FISH)-based karyotyping is a powerful cytogenetics tool to study chromosome organization, behavior, and chromosome evolution. Here, we developed a FISH-based karyotyping system using a probe mixture comprised of centromeric and subtelomeric satellite repeats, 5S rDNA, and chromosome-specific BAC clones in common bean, which enables one to unambiguously distin...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید