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mart
mart

... • more frequent updates  possibly different result when repeating analyses • more information • one needs to know about the structure of the database, the API of the webservice etc. ...
the Liver - Saudi Medical Journal
the Liver - Saudi Medical Journal

... Saud University (No. E-10-132). The study group comprised of 65 women (mean age 34.1 ±6.2 years, range 15-45 years) with unexplained RSA, consecutively referred. The reference population (controls) consisted of 65 women who had at least two children and were without known pregnancy losses or any kno ...
138-142-Smad6 and TGF-b expression in obesity linked cardiac
138-142-Smad6 and TGF-b expression in obesity linked cardiac

... progress with hypertension increase stroke volume and it generate wall stress23,24. As the obesity progress or prolonged many changes happened in a cardiac system which includes dilation, hypertrophy, progressive dysfunction and finally ends up with cardiac failure25,26. The gene expression associat ...
Identical mutations in RAG1 or RAG2 genes leading
Identical mutations in RAG1 or RAG2 genes leading

... The diversity of immunoglobulins and T-cell receptors (TCRs) is mediated by the somatic recombination of genes encoding variable (V), diversity (D), and joining (J) segments by a mechanism known as V(D)J recombination.1 The RAG1 and RAG2 proteins, the expression of which is restricted to immature ly ...
PDF - WashU Epigenome Browser
PDF - WashU Epigenome Browser

... Supports pairwise chromatin interaction results from Hi-C, 5C, and ChIA-PET. ...
Set 2: Mutations
Set 2: Mutations

... mutations that result from alterations to the DNA base sequence. Examples include: – Sickle-cell disease – Cystic fibrosis – Thalassemias These mutations are harmful because they alter the DNA sequence, thereby upsetting the structure and function of the protein they code for. Neutral Mutations: Bec ...
Estimating lethal allele frequencies in complex pedigrees via gene
Estimating lethal allele frequencies in complex pedigrees via gene

... expected lethal allele frequency from known individual genotypes (carriers) among a set of relevant ancestors. Here we used a Fortran program written by LIDAUER and ESSL (1994) based on a concept developed by ALLAIRE et al. (1982). With this program, only six generations of each reference animal are ...
TregouetD_EGEE3-presentation
TregouetD_EGEE3-presentation

... • 8.1 millions of combinations tested in less than 45 days (instead of more than 10 years on a single Pentium 4) • 29 regions where haplotypes could be better predictors than SNPs alone were identified • To control for false positives , replication was investigated in about 7000 CAD patients and 700 ...
Gene Mutations Caused by Radiation
Gene Mutations Caused by Radiation

... spontaneously, are similarly rare (although they were carefully looked for) in the irradiated material. At the same time, we must acknowledge that even in untreated material, as in the comparisons of "highmutation-rate lines" with other lines reported by Neel (60) and by Ives (29), the rates for one ...
Patterns of gene action in plant development revealed by enhancer
Patterns of gene action in plant development revealed by enhancer

... development. We describe here the development of an efficient insertional mutagenesis system in Arabidopsis that permits identification of genes by their patterns of expression during development. Transposable elements of the Ac/Ds system carrying the GUS reporter gene have been designed to act as e ...
Mouse Strain and Genetic Nomenclature
Mouse Strain and Genetic Nomenclature

... always begin with an uppercase letter b. use American or British spelling c. be specific and brief d. include the word mouse True or False. Gene symbols should include tissue specificity or molecular weight designations. Give an example of a gene name and symbol. Provide an example of a genetic mark ...
Leukaemia Section 12p abnormalities in myeloid malignancies Atlas of Genetics and Cytogenetics
Leukaemia Section 12p abnormalities in myeloid malignancies Atlas of Genetics and Cytogenetics

... generally associated with a poor prognosis; however, different clinical courses are defined concerning the magnitude of 12p; a group with small deletions has a better prognosis than patients with 12p abnormalities in general and a lower tendency to additional chromosomal rearrangements; submicroscop ...
fliD operon of Salmonella typhimurium
fliD operon of Salmonella typhimurium

... onto the hooks of JiD-mutant cells, the method described by Kagawa e t al. (1981, 1983) was adopted. The purified flagellin monomers were added to cells suspended in PBS (0.145 M NaCl; 0-15 M sodium phosphate) and incubated at 26 "C for 12 h. Formation of filaments was examined by electron microscop ...
Mendelian Genetics
Mendelian Genetics

... Mendelian Genetics 11.3 Solving genetics problems ...
RNA-Mediated Programming of Developmental
RNA-Mediated Programming of Developmental

... the cultures were starved to induce autogamy, a self-fertilization process. To check for deletions in new macronuclei, 20 postautogamous cells from each clone were grown together. Pre- and postautogamous DNA samples were analyzed on Southern blots, and relative A gene copy numbers were determined by ...
Of mice and men – are mice relevant models for human disease
Of mice and men – are mice relevant models for human disease

... diseases which are rarely included into clinical trials. Furthermore, Dr. Johnson added that there are question marks over the doses given to mice. 'We often see publications where drug exposures are so far off what we would use in the clinic that it's not translatable,' she said, adding that 'mice ...
Restless Legs Syndrome
Restless Legs Syndrome

... Putting this into perspective: • A PAR of 0.5 for BTBD9 implies that it is causative in 50% of RLS cases – this is a level unprecedented for a common disease. • The genetic contribution of BTBD9 to RLS approximates that of the ApoE4 allele association to Alzheimer’s disease. • The results are extre ...
From DNA to Disorder - Liberty Union High School District
From DNA to Disorder - Liberty Union High School District

... paper three-dimensional of the protein called fibroblast growth factor receptor 3 (FGFR3), which, when mutated, causes the disorder achondroplasia. Achondroplasia comes from Greek roots meaning “without cartilage formation” and is one of the most common forms of dwarfism, a genetic condition that us ...
Gene tree reconstruction and orthology analysis based on
Gene tree reconstruction and orthology analysis based on

... to the total number of visits, is the stationary probability. In practice, frequencies are collected after a period of burn in, i.e., the time it takes for the chain to “forget” its starting state, and up to an estimated stopping time, sufficiently late to make the estimation of the stationary distr ...
Cloning and functional analysis of the chitinase gene promoter in
Cloning and functional analysis of the chitinase gene promoter in

... The successful creation of transgenic plants with the required level and pattern of expression of the transferred exogenous gene is largely determined by the gene promoter sequences, which are important transcription regulatory elements. Constitutive expression promoters such as cauliflower mosaic v ...
Hemophilia A
Hemophilia A

... mortality due to ischemic heart disease is lower in hemophilia patients than in the general male population. ...
Hemophilia
Hemophilia

... but rather the Y chromosome (responsible for male characteristics), but all their daughters will be carriers. ...
- Iranian Journal of Basic Medical Sciences
- Iranian Journal of Basic Medical Sciences

... strains, have caused a major health problem in global community (18). Rapid detection of MDR strains would help efficient treatment of patients and prevents widespread distribution of these isolates (1-5). This study aimed to survey the use of PCR-RFLP in comparison with proportional method for rapi ...
apbio ch 14 study guide
apbio ch 14 study guide

... o In the flower-color example, the F1 plants inherited a purple-flower allele from one parent and a white-flower allele from the other. o The plants had purple flowers because the allele for that trait is dominant. 4. Mendel’s law of segregation states that the two alleles for a heritable character ...
MEDICAL BIOLOGY
MEDICAL BIOLOGY

... Genotype - refers to the sum total of genes inherited from both the parents which provides individual development (ontogenesis) and formation of phenotype. Phenotype – refers to the detectable or observable structural and functional characters by the genes interactions and factors of environment. It ...
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Neuronal ceroid lipofuscinosis

Neuronal ceroid lipofuscinoses (NCL) is the general name for a family of at least eight genetically separate neurodegenerative disorders that result from excessive accumulation of lipopigments (lipofuscin) in the body's tissues. These lipopigments are made up of fats and proteins. Their name comes from the word stem lipo-, which is a variation on ""lipid"" or ""fat"", and from the term pigment, used because the substances take on a greenish-yellow color when viewed under an ultraviolet light microscope. These lipofuscin materials build up in neuronal cells and many organs, including the liver, spleen, myocardium, and kidneys.
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