نتایج جستجو برای: monozygotic twins

تعداد نتایج: 14593  

Journal: :Behavior genetics 2001
N Jacobs S Van Gestel C Derom E Thiery P Vernon R Derom R Vlietinck

This study investigates the basic assumption of homogeneity of monozygotic (MZ) twins: are there differences according to the timing of the zygotic splitting, early in dichorionic (DC) and later in monochorionic (MC) pairs? We assessed the IQ of 451 same-sexed twin pairs of known zygosity and chorion type with the Wechsler Intelligence Scale for Children-Revised (WISC-R). The variances of withi...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
Mario F Fraga Esteban Ballestar Maria F Paz Santiago Ropero Fernando Setien Maria L Ballestar Damia Heine-Suñer Juan C Cigudosa Miguel Urioste Javier Benitez Manuel Boix-Chornet Abel Sanchez-Aguilera Charlotte Ling Emma Carlsson Pernille Poulsen Allan Vaag Zarko Stephan Tim D Spector Yue-Zhong Wu Christoph Plass Manel Esteller

Monozygous twins share a common genotype. However, most monozygotic twin pairs are not identical; several types of phenotypic discordance may be observed, such as differences in susceptibilities to disease and a wide range of anthropomorphic features. There are several possible explanations for these observations, but one is the existence of epigenetic differences. To address this issue, we exa...

Journal: :Gastroenterology 2004
Carlo Selmi Marlyn J Mayo Nancy Bach Hiromi Ishibashi Pietro Invernizzi Robert G Gish Stuart C Gordon Harlan I Wright Bruce Zweiban Mauro Podda M Eric Gershwin

BACKGROUND & AIMS There is growing evidence that the interplay of genetic susceptibility and environmental factors leads to primary biliary cirrhosis (PBC). In particular, family members of an infected individual have up to a 100-fold higher risk of developing PBC. Although concordant rates for identical twins in other autoimmune diseases range between 25% and 50%, there are no such data on PBC...

Journal: :Forensic science international. Genetics 2014
Jacqueline Weber-Lehmann Elmar Schilling Georg Gradl Daniel C Richter Jens Wiehler Burkhard Rolf

Monozygotic (MZ) twins are considered being genetically identical, therefore they cannot be differentiated using standard forensic DNA testing. Here we describe how identification of extremely rare mutations by ultra-deep next generation sequencing can solve such cases. We sequenced DNA from sperm samples of two twins and from a blood sample of the child of one twin. Bioinformatics analysis rev...

Journal: :Physiological genomics 2005
Anu Sharma Vineet K Sharma Shirley Horn-Saban Doron Lancet Srinivasan Ramachandran Samir K Brahmachari

Quantitative variation in gene expression in humans is the outcome of various factors, including differences in genetic background, gender, age, and environment. However, the extent of the influence of these factors on gene expression is not clear. We attempted to address this issue by carrying out gene expression profiling in blood leukocytes with 13 individuals (including 5 pairs of monozygot...

2014
Pongsathorn Chaiyasap Supasak Kulawonganunchai Chalurmpon Srichomthong Sissades Tongsima Kanya Suphapeetiporn Vorasuk Shotelersuk

Congenital heart defects (CHD) occur in 40% of patients with trisomy 21, while the other 60% have a structurally normal heart. This suggests that the increased dosage of genes on chromosome 21 is a risk factor for abnormal heart development. Interaction of genes on chromosome 21 or their gene products with certain alleles of genes on other chromosomes could contribute to CHD. Here, we identifie...

Journal: :Journal of medical genetics 1994
E Watkiss T Webb G Rysiecki N Girdler E Hewett S Bundey

X inactivation studies have been carried out on 22 pairs of female monozygotic twins, one set of female monozygotic triplets, and their mothers and singleton sisters, using the probe M27 beta. Forty-eight per cent of the twins, 55% of their mothers, and 42% of their singleton sisters showed skewed X inactivation. Two of the triplets and their mother had random X inactivation, while the third tr...

2010
Shigeki Machida Tomomi Takahashi Norimoto Gotoh Nagahisa Yoshimura Takamitsu Fujiwara Dajiro Kurosaka

PURPOSE To present the first findings in the set of monozygotic twins with polypoidal choroidopathy (PCV). METHODS Sixty two-year old monozygotic twin sisters were studied. The concordances and discordances of the clinical features of the twins were determined. Genomic DNA was extracted and genotyped for three established PCV risk-associated single nucleotide polymorphisms, viz CFH I62V, CFH ...

Journal: :Twin research and human genetics : the official journal of the International Society for Twin Studies 2011
Andrew I Spielman Joseph G Brand Yvonne Buischi Walter A Bretz

This study compared the anatomical features of the tongue in nine pairs of twins - six monozygotic and three dizygotic. The aim of the project was to determine if tongues, like any other anatomical structure, could be used to reliably predict relatedness given that tongue shape, presentation and surface can be influenced by environment. Using the method of forced choice, 30 subjects were asked ...

Journal: :British heart journal 1982
J Sehested

The aetiology of coarctation of the aorta is still largely unexplained, and investigations on familial occurrence have given confficting results. -3 Only 10 reports of coarctation of the aorta in monozygotic twins have been published. The lesion has shown discordance1 4-9 in all but one'0 of the cases. In only three of these was there a concordant cardiovascular malformation: atrial septal defe...

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