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The full-length HIV-1 molecular clone pLAI 61 was used to produce
The full-length HIV-1 molecular clone pLAI 61 was used to produce

... capped G residue. Supplementary Table 1 lists all oligonucleotides used in this study. The tat exon 1 was amplified by PCR on pLAI with primers NotI-WdV005 and WdV002; tat exon 2 with primers WdV007 and NotI-WdV004; rev exon 1 with primers NotI-WdV001 and WdV002; rev exon 2 with primers WdV003 and N ...
Pitx1 and Pitx2 are required for development of hindlimb buds
Pitx1 and Pitx2 are required for development of hindlimb buds

... specify limb bud segments, for example, the proximal segment from which the stylopod (femur) develops. As this proximal segment is marked by expression of Meis genes, we investigated Meis gene expression in embryos mutant for Pitx1 or for Pitx1 and Pitx2. In both, Meis2 expression was similar to tha ...
Triplet repeat primed PCR assay for the screening and diagnosis of
Triplet repeat primed PCR assay for the screening and diagnosis of

... neurodegenerative diseases caused by dynamic expansions of trinucleotide repeats in different genes (Table 1). These diseases are characterized by progressive incoordination of gait, poor coordination of hands, speech, and eye movements. They are either inherited recessively (FA) or dominantly (SCA) ...
2014 Nuclear Medicine curriculum
2014 Nuclear Medicine curriculum

... Clinical Radiology throughout the 6 year period. We would recommend that at ST3 the content of the training should comprise 80% Clinical Radiology and 20% Nuclear Medicine. This may be done on a sessional basis or as a series of training blocks. By ST6 the ratios should be reversed so that 20% of th ...
Embryonic Development following Somatic Cell
Embryonic Development following Somatic Cell

... therapeutics (Hochedlinger and Jaenisch, 2003). Following the recent successful derivation of the first human nuclear transfer embryonic stem cells (ntESCs) (Tachibana et al., 2013) and the generation of human ntESCs from aged adult or patient cells (Chung et al., 2014; Yamada et al., 2014), this pr ...
Wnt Signaling and an APC-Related Gene Specify Endoderm in
Wnt Signaling and an APC-Related Gene Specify Endoderm in

... First, E does not produce endoderm and instead produces pharyngeal tissue and body wall muscles, which are mesodermal tissues normally produced by MS. Second, the E blastomere adopts an accelerated cleavage rate similar to MS; for example, the E daughters divide prematurely at about the same time as ...
In-class assignment: Fukuda et al. (2016) paper
In-class assignment: Fukuda et al. (2016) paper

... knocked out, both transcript levels drop, suggesting that Oct4 is a positive regulator of expression of both genes. It is surprising for two genes with antagonistic functions to have the same positive regulator. Usually, the cell will express two antagonistic genes differentially, so the results are ...
Different Effects of PCR Inhibitors on Multiplex STR Assays
Different Effects of PCR Inhibitors on Multiplex STR Assays

... wood from interior crime scenes can also contain inhibitors that interfere with the DNA polymerase’s activity. The impact of these contaminants on the multiplex STR assays can vary from attenuation to complete inhibition of the amplification process, resulting in partial STR profiles or profiles wit ...
emboj7601705-sup
emboj7601705-sup

... increasing amounts of Gsc MO (as indicated on the abscissa). Dorsal marginal zone (DMZ) explants were excised at stage 10 and cultured until sibling embryos reached stage 13. For RNA extraction and cDNA synthesis, 8 DMZs were used per sample. To study the responses in gene expression upon increasing ...
Article Mitochondrial DNA turnover occurs during preimplantation
Article Mitochondrial DNA turnover occurs during preimplantation

... (GV) were isolated from ovaries, unfertilized eggs (UF) were collected 12 h after HCG injection, and fertilized eggs (FE), 2-, 4-, 8-cell and blastocyst stage embryos were collected after successful mating at 24, 36, 48, 60 and 72 h post-HCG (a–g). MtDNA copy number was measured in groups of embryos ...
Educational Items Section Chromosomal Disorders - Karyotype Indications in Oncology and Haematology
Educational Items Section Chromosomal Disorders - Karyotype Indications in Oncology and Haematology

... Sterility workup once gynaecological or endocrine causes have been ruled out (Klinefelter, Turner, Testicular feminization). If more than two spontaneous miscarriages cytogenetic studies are indicated on the parents to rule out a translocation carrier; a foetal karyotype is recommended if at all pos ...
Karyotype Indications - Atlas of Genetics and Cytogenetics in
Karyotype Indications - Atlas of Genetics and Cytogenetics in

... However some chromosomal disorders are not linked to maternal age ( Turner syndrome, trisomy 16) Causes of meiotic non disjunction related to maternal age are not well defined: ...
The role of free radicals and antioxidants in
The role of free radicals and antioxidants in

... ROS are essential and are indicative of metabolic activity within the follicle. High ROS levels in the culture media, however, on the morning after oocyte retrieval correlated with lower blastocyst development, poor fertilization and cleavage rates, and higher embryonic fragmentation following ICSI ...
Genetic and epigenetic risks of intracytoplasmic sperm injection
Genetic and epigenetic risks of intracytoplasmic sperm injection

... function (i.e. myotonic dystrophy, Nooman syndrome, sickle cell anemia, β-thalassemia, Kartagener syndrome, primary ciliary dyskinesia, Fanconi anemia or ataxia telangiectasia) and endocrinopathies lead to human male infertility. In addition, numerical/structural chromosomal abnormalities result in ...
Health outcomes of children born after IVF/ICSI: a review of current
Health outcomes of children born after IVF/ICSI: a review of current

... Of particular concern is the possibility of genomic imprinting disorders in assisted-conception children due to disturbances in the establishment and maintenance of imprinting during gametogenesis, fertilization and embryonic development (Amor and Halliday, 2008; Owen and Segars, 2009). According to ...
Chapter 5
Chapter 5

... or the newborn, an alternative is to remove the baby surgically through an incision in the uterine wall. For example, in long labor, breech position, and anoxia – Today there is debate if Caesarean sections are too widely used by physicians ...
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PDF

... genetic material (haploid and 'anucleate' embryos obtained by inactivation of one or both of the gametes with X-rays). It was with loach embryos that morphogenetic function of nuclei was studied for the first time using the method of radiation-induced inactivation of nuclei; it was shown that the nu ...
Tetraploid rescue - Development
Tetraploid rescue - Development

... counterstained with eosin. ...
Real time PCR and it`s role in diagnosis
Real time PCR and it`s role in diagnosis

... falciparum parasite is of extreme importance if we are to combat human malaria.This parasite uses the process of antigenic variation to expose the human immune system to continually changing antigens on the surface of infected red blood cells. Real-time PCR assays have the potential to detect low le ...
DpnII - Inv. PCR of miniMos for distribution
DpnII - Inv. PCR of miniMos for distribution

... Protocol 2 - Inverse PCR individual inserts There is a very nice and comprehensive protocol that covers how to map Mos1 insertions by Boulin & Bessereau (2007) in Nature Protocols. This protocol is meant as a complement to their protocol because we changed and optimized several parameters which in o ...
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View PDF

... cataract to lethal cardiorespiratory disorder. Therefore molecular analysis is very helpful especially for those who are asymptomatic or exhibit equivocal symptoms and has an immense value as a screening procedure to identify mutations in DM1 families and to reduce the birth rate of DM1 infants. ...
Insulin-like growth factor (IGF) signalling is required for early dorso
Insulin-like growth factor (IGF) signalling is required for early dorso

... resulted in a greatly expanded development of anterior structures at the expense of trunk and tail. IGF-1R knockdown caused a significant decrease in the expression of Otx2, Rx3, FGF8, Pax6.2 and Ntl, while excess IGF signalling expanded Otx2 expression in presumptive forebrain tissue and widened th ...
Ophthalmic Pathology Specialty Conference USCAP 2015
Ophthalmic Pathology Specialty Conference USCAP 2015

... • Oral lesions similar to HBID may occur in the context of other genetic disorders (Darier-White disease and the white sponge nevus of Canon) • Ocular involvement appears to be unique to HBID ...
Discover Debate Decide_exploring ethical
Discover Debate Decide_exploring ethical

... Dominant Allele: Expressed in the characteristics of an individual even if there is only one copy. It will overshadow the recessive allele. Egg cell: A female sex cell or gamete. Embryo: An organism at any time before full development, birth, or hatching. Gamete: A mature sex cell that usually has o ...
chapt21_HumanBiology14e_lecture
chapt21_HumanBiology14e_lecture

... • Cystic fibrosis – Cl- ions do not pass normally through a cell membrane, resulting in thick mucus in lungs ...
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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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