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BLASTOCYST TRANSFER
BLASTOCYST TRANSFER

... Blastocyst and derivation rate in relation to embryo origin and quality •Sjogren et al, RBM online 2004 •Findikli et al, RBM online 2005 •Mitalipova et al, Stem Cells 2004 (discarded embryos) •Chen et al, Hum Reprod 2005 •Kim et al, Stem Cells 2005 (derivation method depending on blastocyst quality ...
In vitro fertilization (IVF) in mammals: epigenetic and developmental
In vitro fertilization (IVF) in mammals: epigenetic and developmental

... Fertilization of eutherian animals occurs in the maternal oviduct. This is the natural and unique environment to achieve the necessary requirements for embryo life and its early and late development. The embryo conceived in vitro is manipulated and cultured in very different conditions [11, 16]. Con ...
Wnt8 Is Required for Growth-Zone Establishment and Development
Wnt8 Is Required for Growth-Zone Establishment and Development

... The posterior truncation phenotypes resulting from pRNAi against Wnt8 in the spider are at least superficially similar to those observed when Wnt8 and/or Wnt3 are perturbed in vertebrate embryos. Removal or blocking Wnt8 and/or Wnt3 in Xenopus, zebrafish, and mouse results in truncated embryos with ...
Automated sorting of live transgenic embryos
Automated sorting of live transgenic embryos

... Received 7 August 2000; accepted 10 November 2000 ...
Leading The Way in Genetic Fertility Screening
Leading The Way in Genetic Fertility Screening

... in domestic animals) with potential for non-invasive in vitro diagnostics are 1) the secretome: proteins secreted by the embryo that reflect the internal proteomic signature, 2) the metabolome: waste products of energy consumption, and 3) microRNAs: short strands of RNA released into media with a ca ...
Good quality blastocyst from non-/mono
Good quality blastocyst from non-/mono

... findings indicate that embryonic development may be delayed for non- and mono-pronuclear zygotes compared with di-pronuclear zygotes. Another possible explanation for the formation of non-pronuclear zygotes includes the accelerated breakdown of pronuclear membranes and a lack of visualization due to ...
Educational Items Section Prenatal Diagnosis Atlas of Genetics and Cytogenetics
Educational Items Section Prenatal Diagnosis Atlas of Genetics and Cytogenetics

... Neural tube defects have a multifactorial etiology and their incidence is widely variable. They used to be more frequent in the British Isles, Canada, China and other countries like Hungaria with an incidence of 5/1000 births and a recurrence risk of 5%. In France and United States the incidence was ...
A phenotype-based screen for embryonic lethal mutations in the mouse
A phenotype-based screen for embryonic lethal mutations in the mouse

... from Marilyn Fisher (University of Virginia). ENU mutagenesis was performed essentially as described (6). ENU, obtained from Sigma (N-3385) in Isopac bottles containing approximately 1 g of ENU, was dissolved in 10 ml of 95% ethanol. After 1 hr, 90 ml of phosphate– citrate buffer (0.1 M Na2HPO4y0.05 ...
Analysis of the first polar body: preconception genetic
Analysis of the first polar body: preconception genetic

... developing from oocytes whose polar body analysis revealed them to have the normal gene would be transferred in the same cycle. When polar body analysis determines that an oocyte contains the mutant gene, reveals crossing over (heterozygous polar bodies), or fails because of technical difficulties, ...
lecture notes
lecture notes

... Reading: Chapter 17, Molecular Biology of the Gene, 7th Edition. 1. The Drosophila embryo exhibits the most rapid nuclear divisions seen for any animal system, with peak speeds of a division every 5-7 minutes. Following fertilization, the oocyte and sperm pronuclei fuse and undergo a series of divis ...
is in the ndon Care - Guy`s and St Thomas` NHS Foundation Trust
is in the ndon Care - Guy`s and St Thomas` NHS Foundation Trust

... to obtain and fertilise a number of eggs. Once fertilised, the embryos develop for three days and then one cell is removed from each embryo. The genetic material (DNA or chromosomes) within each cell is then tested for the altered gene or chromosome abnormality. Up to two unaffected embryos are then ...
(related to carrier screening and PGD) – March 27th
(related to carrier screening and PGD) – March 27th

... Introduction: Thalassemia has become one of the most prevalent blood disorders around the world and is frequently screened for in PGD. The disease is caused by mutations within the HBA and HBB genes involved in haemoglobin production. In the IVF setting, PGD for thalassemia detection in embryos requ ...
Report of an ad hoc Committee - Georgia Reproductive Specialists
Report of an ad hoc Committee - Georgia Reproductive Specialists

... ICSI, normal embryos have divided into about 4 cells. Three days after insemination or ICSI, normally developing embryos contain about 8 cells. Five days after insemination or ICSI, normally developing embryos have developed to the blastocyst stage, which is typified by an embryo that now has 80 or ...
English - Illumina
English - Illumina

... Partial trisomy + partial monosomy ...
Development of triplet repeat primed PCR (TP
Development of triplet repeat primed PCR (TP

... 14q32.1 (normal alleles - 12 to 44 CAG repeats, mutated alleles - above 52 CAG repeats). This late onset disorder, the most common from its group, presents a high prevalence in the Azores, especially in Flores Island. MJD molecular testing is based on PCR and automated capillary electrophoresis. How ...
Materials and methods for the supplement: Strains and RNAi
Materials and methods for the supplement: Strains and RNAi

... Confocal movies of cortical NMY-2::GFP were acquired at 22-24°C with a spinning disc confocal microscope using a Zeiss C-Apochromat 63X/1.2 NA objective lens, Yokogawa CSU-X1 scan head and an Andor iXon EMCCD camera (512 by 512 pixels). A stack consisting of three z-planes (0.5 µm spacing) with an e ...
Word file
Word file

... Undescended gonads in triple mutant XY embryos. SEM analysis of the genito-urinary system of E18.5 embryos. The left panel shows embryos of XX, and the right panel of XY genotype. Arrows indicate the position of gonads in each panel, narrow arrowheads indicate the uterus, and wide arrowhead the blad ...
Embryo development Lecture 3
Embryo development Lecture 3

... establish the longitudinal axis of the embryo proper • Embryo polarity can be expressed despite abnormal division plane > there is a signal or a gradient defining the apical-basal axis that is independent of the cellular architecture of theembryo. • initial orientation of the signal or gradient depe ...
PowerPoint lecture - Lower Cape May Regional School District
PowerPoint lecture - Lower Cape May Regional School District

... • Changes in chromosome structure can reduce fertility in heterozygotes; but accumulation of multiple changes in homozygotes may result in new species • Certain duplications may allow one copy of a gene to mutate while the other carries out its original function • Example: X and Y chromosomes were o ...
Increasing the denaturation temperature during the first cycles of
Increasing the denaturation temperature during the first cycles of

... are carrying the same mutation, ADO would not cause serious misdiagnosis. For compound heterozygotes or autosomal dominant conditions, however, extensive testing of the amplification protocol with single heterozygous cells and individual calibration of each thermocycler for the effect of denaturatio ...
Reproduction and Fetal Technology
Reproduction and Fetal Technology

... parent’s embryo using an IVF procedure. Some gay male couples use surrogate mothers to have children that are biologically related to at least one of the partners. Surrogate mothers usually receive compensation for carrying the child. There are many ethical and legal concerned with this process sinc ...
Increasing the denaturation temperature during the first cycles of
Increasing the denaturation temperature during the first cycles of

... (190 lysed in ddH2O and 120 in alkaline lysis buffer) and 88 single lymphocytes heterozygous for mutations at both IVS 1 nt 1 and 5 of the p-globin gene were analysed. The efficiency of amplification and frequency of ADO under the different conditions tested are shown in Table I and Figure 2. Amplif ...
SYLABUS
SYLABUS

... The Student should know the basic mechanisms of inheritance, etiology and variation of phenotypic traits (along with dysmorphic features ) of selected genetic disorders to be able to recognize genetic syndromes ; to understand the objectives, principles and stages of genetic counseling and the role ...
Report of an ad hoc Committee
Report of an ad hoc Committee

... divided into about 4 cells. Three days after insemination or ICSI, normally developing embryos contain about 8 cells. Five days after insemination or ICSI, normally developing embryos have developed to the blastocyst stage, which is typified by an embryo that now has 80 or more cells, an inner fluid ...
Proceedings - Applied Reproductive Strategies in Beef Cattle
Proceedings - Applied Reproductive Strategies in Beef Cattle

... populations that have been inbred over a period of time, animals can become so related in general that matings between distant relatives may in fact be matings of closely related individuals at the level of their DNA. The inbreeding coefficient measures the average extent of additional chromosomal h ...
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Preimplantation genetic diagnosis

Pre-implantation genetic diagnosis (PGD or PIGD) refers to genetic profiling of embryos prior to implantation (as a form of embryo profiling), and sometimes even of oocytes prior to fertilization. PGD is considered in a similar fashion to prenatal diagnosis. When used to screen for a specific genetic disease, its main advantage is that it avoids selective pregnancy termination as the method makes it highly likely that the baby will be free of the disease under consideration. PGD thus is an adjunct to assisted reproductive technology, and requires in vitro fertilization (IVF) to obtain oocytes or embryos for evaluation. The term preimplantation genetic screening (PGS) is used to denote procedures that do not look for a specific disease but use PGD techniques to identify embryos at risk. The PGD allows studying the DNA of eggs or embryos to select those that carry certain damaging characteristics. It is useful when there are previous chromosomal or genetic disorders in the family and within the context of in vitro fertilization programs. The procedures may also be called preimplantation genetic profiling to adapt to the fact that they are sometimes used on oocytes or embryos prior to implantation for other reasons than diagnosis or screening.Procedures performed on sex cells before fertilization may instead be referred to as methods of oocyte selection or sperm selection, although the methods and aims partly overlap with PGD.
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