19. - 21. März 2014 in Essen - Deutsche Gesellschaft für
... Prof. Dr. med. Klaus Zerres, Aachen Prof. Dr. rer. nat. Kerstin Kutsche, Hamburg Prof. Dr. med. Jürgen Kohlhase, Freiburg Prof. Dr. med. Michael Speicher, Graz Prof. Dr. med. Wolfgang Berger, Zürich Prof. Dr. med. Gerd Utermann, Innsbruck Dr. rer. nat. Michael Bonin, Tübingen Prof. Dr. med. Gabriele ...
... Prof. Dr. med. Klaus Zerres, Aachen Prof. Dr. rer. nat. Kerstin Kutsche, Hamburg Prof. Dr. med. Jürgen Kohlhase, Freiburg Prof. Dr. med. Michael Speicher, Graz Prof. Dr. med. Wolfgang Berger, Zürich Prof. Dr. med. Gerd Utermann, Innsbruck Dr. rer. nat. Michael Bonin, Tübingen Prof. Dr. med. Gabriele ...
chicken.db - Bioconductor
... the ncbi2ensembl table in the appropriate organism package. Users who wish to only use mappings from ensembl are encouraged to see the ensembl2ncbi table which is also found in the appropriate organism packages. These mappings are based upon the ensembl table which is contains data from BOTH of thes ...
... the ncbi2ensembl table in the appropriate organism package. Users who wish to only use mappings from ensembl are encouraged to see the ensembl2ncbi table which is also found in the appropriate organism packages. These mappings are based upon the ensembl table which is contains data from BOTH of thes ...
An Introduction to RNA Interference (RNAi)
... systems when their early work was performed. Short double-stranded RNAs (dsRNAs) mediate RNAi in human cells Shortly after Fire and Mello’s discovery, dsRNAs were found to induce similar gene silencing in a variety of other organisms. However, it was still not believed that RNAi could also work in h ...
... systems when their early work was performed. Short double-stranded RNAs (dsRNAs) mediate RNAi in human cells Shortly after Fire and Mello’s discovery, dsRNAs were found to induce similar gene silencing in a variety of other organisms. However, it was still not believed that RNAi could also work in h ...
Marfan syndrome. Part 1: pathophysiology and diagnosis
... cardiovascular features seen in patients with Marfan syndrome, but lacked others such as lens dislocation.10 this connective-tissue disorder was inherited also as a autosomal dominant trait, but no mutations in the fibrillin-1 gene were found.10 the gene responsible for this Marfan-like syndrome (re ...
... cardiovascular features seen in patients with Marfan syndrome, but lacked others such as lens dislocation.10 this connective-tissue disorder was inherited also as a autosomal dominant trait, but no mutations in the fibrillin-1 gene were found.10 the gene responsible for this Marfan-like syndrome (re ...
Single Nucleotide Polymorphism (SNP) of the Endothelial Nitric
... package (SAS Institute, Cary, North Carolina). The Kolmogorov-Smirnov goodness-of-fit test was used to determine if the data were normally distributed. For each biallelic marker, allele frequencies were calculated from the genotypes in the patients and control groups using the Hardy-Weinberg ...
... package (SAS Institute, Cary, North Carolina). The Kolmogorov-Smirnov goodness-of-fit test was used to determine if the data were normally distributed. For each biallelic marker, allele frequencies were calculated from the genotypes in the patients and control groups using the Hardy-Weinberg ...
BRIEF COMMUNICATION Glutathione S transferase theta 1
... in controls and in MDS cases previously exposed to any substance, but tended to be higher in unexposed MDS patients (40%, P 5 0.07). Our results do not confirm the higher incidence of GSTT 1 null genotype observed in MDS. The lower incidence of GSTT 1 null genotype in MDS cases exposed to some compo ...
... in controls and in MDS cases previously exposed to any substance, but tended to be higher in unexposed MDS patients (40%, P 5 0.07). Our results do not confirm the higher incidence of GSTT 1 null genotype observed in MDS. The lower incidence of GSTT 1 null genotype in MDS cases exposed to some compo ...
PART 16 - PTools.ir
... pulsatile manner and exhibits a diurnal rhythm; its highest levels occur at night. However, these TSH excursions are modest in comparison to those of other pituitary hormones, in part, because TSH has a relatively long plasma half-life (50 min). Consequently, single measurements of TSH are adequate ...
... pulsatile manner and exhibits a diurnal rhythm; its highest levels occur at night. However, these TSH excursions are modest in comparison to those of other pituitary hormones, in part, because TSH has a relatively long plasma half-life (50 min). Consequently, single measurements of TSH are adequate ...
Escherichia coli rpoB Mutants Have Increased
... Note that these population genetic simulations capture the important effects of clonal interference. Multiple mutational events generating each category of mutant can occur in a single simulation, and multiple subpopulations with different beneficial mutations typically compete before one marker sta ...
... Note that these population genetic simulations capture the important effects of clonal interference. Multiple mutational events generating each category of mutant can occur in a single simulation, and multiple subpopulations with different beneficial mutations typically compete before one marker sta ...
Molecular Plant-Microbio Interactions
... coding for an aminotransferase. Because the Tn5lacZ is inserted downstream of the stop codon of this ORF, the insertion does not affect the transcription of the bioA homolog. The second ORF has 57% identity and 75% similarity at the amino acid level with the potF gene from E. coli (Pistocchi et al. ...
... coding for an aminotransferase. Because the Tn5lacZ is inserted downstream of the stop codon of this ORF, the insertion does not affect the transcription of the bioA homolog. The second ORF has 57% identity and 75% similarity at the amino acid level with the potF gene from E. coli (Pistocchi et al. ...
Multiplex PCR for specific identification and determination of mating
... Gramaje et al., 2009, 2012). Phaeoacremonium spp. occurring on grapevines have been extensively studied. Since the description of Phaeoacremonium, the number of species in this genus has increased to 36 (www.mycobank.org), of which 25 were described from grapevines with esca or Petri disease symptom ...
... Gramaje et al., 2009, 2012). Phaeoacremonium spp. occurring on grapevines have been extensively studied. Since the description of Phaeoacremonium, the number of species in this genus has increased to 36 (www.mycobank.org), of which 25 were described from grapevines with esca or Petri disease symptom ...
Chapter_005 - IHMC Public Cmaps (2)
... If a woman has a first-degree relative with breast cancer, her risk doubles Recurrence risk increases if age of onset in the affected relative is early and if the cancer is bilateral An autosomal dominant form (5%) has been linked to chromosomes 13 and 17 Other genes are implicated Mosby items and d ...
... If a woman has a first-degree relative with breast cancer, her risk doubles Recurrence risk increases if age of onset in the affected relative is early and if the cancer is bilateral An autosomal dominant form (5%) has been linked to chromosomes 13 and 17 Other genes are implicated Mosby items and d ...
Implementing array comparative genomic hybridization in male
... reproduction begins years before the interaction of the sperm and the oocycte, and requires careful coordination and development of multiple systems, including the germline lineage, formation of future gonads, genital tracts, etc. [7]. Up to 50% of male infertility may have a genetic etiology. These ...
... reproduction begins years before the interaction of the sperm and the oocycte, and requires careful coordination and development of multiple systems, including the germline lineage, formation of future gonads, genital tracts, etc. [7]. Up to 50% of male infertility may have a genetic etiology. These ...
EPHX1 polymorphisms, COPD and asthma in 47,000 individuals and in meta-analysis
... to chronic obstructive pulmonary disease (COPD) and asthma. We genotyped participants from the Copenhagen City Heart Study (n510,038) and the Copenhagen General Population Study (n537,022) for the T113C and A139G variants in the EPHX1 gene and measured lung function and recorded COPD hospitalisation ...
... to chronic obstructive pulmonary disease (COPD) and asthma. We genotyped participants from the Copenhagen City Heart Study (n510,038) and the Copenhagen General Population Study (n537,022) for the T113C and A139G variants in the EPHX1 gene and measured lung function and recorded COPD hospitalisation ...
Introduction
... Geneticists illustrate the inheritance of a gene within a family by using a pedigree chart. In a pedigree chart, males are symbolized by a square (□) and females are symbolized by a circle (○). People who are affected by a condition or disease are symbolized by a dark square or circle. This pedigree ...
... Geneticists illustrate the inheritance of a gene within a family by using a pedigree chart. In a pedigree chart, males are symbolized by a square (□) and females are symbolized by a circle (○). People who are affected by a condition or disease are symbolized by a dark square or circle. This pedigree ...
Gene Section MLL (myeloid/lymphoid or mixed lineage leukemia) Atlas of Genetics and Cytogenetics
... Hess JL, Huret JL. MLL (myeloid/lymphoid or mixed lineage leukemia). Atlas Genet Cytogenet Oncol Haematol.2001;5(1):11-13. Huret JL. MLL (myeloid/lymphoid or mixed lineage leukemia). Atlas Genet Cytogenet Oncol Haematol.1997;1(2):68-69. This work is licensed under a Creative Commons Attribution-Nonc ...
... Hess JL, Huret JL. MLL (myeloid/lymphoid or mixed lineage leukemia). Atlas Genet Cytogenet Oncol Haematol.2001;5(1):11-13. Huret JL. MLL (myeloid/lymphoid or mixed lineage leukemia). Atlas Genet Cytogenet Oncol Haematol.1997;1(2):68-69. This work is licensed under a Creative Commons Attribution-Nonc ...
Gene Technology Regulation 2002
... (1) For section 71(7) of the Act, the regulator must vary the licence, or refuse to vary the licence, within 90 days after the day an application for a variation of the licence is received by the regulator. (2) For the period mentioned in subsection (1), the following days are not counted— (a) ...
... (1) For section 71(7) of the Act, the regulator must vary the licence, or refuse to vary the licence, within 90 days after the day an application for a variation of the licence is received by the regulator. (2) For the period mentioned in subsection (1), the following days are not counted— (a) ...
p16INK4a immunocytochemical analysis is an
... modify the results. It has been suggested in previous studies that the significance of p16INK4a gene deletions would disappear within the subgroups of T-ALL and B-precursor ALL.16,17 Our data show that T phenotype does not account for the poorer outcome of p16INK4a ICC–negative patients. However, th ...
... modify the results. It has been suggested in previous studies that the significance of p16INK4a gene deletions would disappear within the subgroups of T-ALL and B-precursor ALL.16,17 Our data show that T phenotype does not account for the poorer outcome of p16INK4a ICC–negative patients. However, th ...
Application of Pedigree Analysis
... guide to go along with this section. Just remember to determine the genotypes of those possessing the sexlinked trait first. From there, using Punnett squares, you should be able to determine the genotypes of most, if not all of the family. Neither Grandma or Grandpa Flipnob are colourblind. All of ...
... guide to go along with this section. Just remember to determine the genotypes of those possessing the sexlinked trait first. From there, using Punnett squares, you should be able to determine the genotypes of most, if not all of the family. Neither Grandma or Grandpa Flipnob are colourblind. All of ...
Document
... available from the families Cervidae and Bovidae alone. All currently available species PrP gene sequences add up to a total of about 155. This number increases to about 300 when all allelic variants based on amino acid polymorphisms are counted. This dataset is an important source of information un ...
... available from the families Cervidae and Bovidae alone. All currently available species PrP gene sequences add up to a total of about 155. This number increases to about 300 when all allelic variants based on amino acid polymorphisms are counted. This dataset is an important source of information un ...
Exclusion of known corneal dystrophy genes in an autosomal
... families with Fleck dystrophy [8], although incomplete penetrance was documented in some families. PIP5K3 encodes for a member of the phosphoinositide 3-kinase family and is involved in the regulation of endosomal transport. However, it must be noted that in addition to being dystrophic, corneal fle ...
... families with Fleck dystrophy [8], although incomplete penetrance was documented in some families. PIP5K3 encodes for a member of the phosphoinositide 3-kinase family and is involved in the regulation of endosomal transport. However, it must be noted that in addition to being dystrophic, corneal fle ...
text only - Sweet Corn Disease Nursery
... race. None of the Rp genes currently used in sweet corn are overcome by the avirulent race (i.e., the “old race”). Hybrids with certain combinations of Rp genes (e.g., Rp1-D+Rp-G, Rp1-D+Rp1-I, RpDGJ, or RpJFC) are resistant to all three races used in the UI nurseries. In commercial production, hybri ...
... race. None of the Rp genes currently used in sweet corn are overcome by the avirulent race (i.e., the “old race”). Hybrids with certain combinations of Rp genes (e.g., Rp1-D+Rp-G, Rp1-D+Rp1-I, RpDGJ, or RpJFC) are resistant to all three races used in the UI nurseries. In commercial production, hybri ...
Identifying Common Genetic Variants by High
... screened at each exon of ACVRL1 and ENG by highresolution melting, the most common result was a single melting curve cluster, indicating that all 20 alleles were identical (observed in 17 of 24 exons). In 5 exons, 1 aberrant melting curve revealed a single common variant, and in ACVRL1, exon 3, 2 va ...
... screened at each exon of ACVRL1 and ENG by highresolution melting, the most common result was a single melting curve cluster, indicating that all 20 alleles were identical (observed in 17 of 24 exons). In 5 exons, 1 aberrant melting curve revealed a single common variant, and in ACVRL1, exon 3, 2 va ...
Detection and identification of bacteria in clinical samples by 16S
... 598 bp PCRs detected and identified the bacterial 16S rRNA gene in 23 (31 %) and 38 (51 %) of the 75 samples, respectively. The 1343 bp PCR identified 19 of 23 (83 %) PCR-positive samples to species level while the 762/598 bp PCR identified 14 of 38 (37 %) bacterial 16S rRNA gene fragments to specie ...
... 598 bp PCRs detected and identified the bacterial 16S rRNA gene in 23 (31 %) and 38 (51 %) of the 75 samples, respectively. The 1343 bp PCR identified 19 of 23 (83 %) PCR-positive samples to species level while the 762/598 bp PCR identified 14 of 38 (37 %) bacterial 16S rRNA gene fragments to specie ...
A Mutation in LTBP2 Causes Congenital Glaucoma in
... dynamic relationship between aqueous humor production and outflow. Obstruction of aqueous humor outflow leads to elevated IOP, which is an important risk factor for the development of glaucoma [2]. Although glaucoma is generally considered a disease of older adults, it is an important and devastatin ...
... dynamic relationship between aqueous humor production and outflow. Obstruction of aqueous humor outflow leads to elevated IOP, which is an important risk factor for the development of glaucoma [2]. Although glaucoma is generally considered a disease of older adults, it is an important and devastatin ...
Exam Questions from Exam 1 – Basic Genetic Tests
... Next you isolate a mutant strain of yeast that cannot grow on medium lacking leucine. This strain contains a single mutation you call leu1–. The leu1– mutation is near to drk1– on the same chromosome. When the leu1– mutant is mated to wild-type yeast, the resulting diploids cannot grow on medium lac ...
... Next you isolate a mutant strain of yeast that cannot grow on medium lacking leucine. This strain contains a single mutation you call leu1–. The leu1– mutation is near to drk1– on the same chromosome. When the leu1– mutant is mated to wild-type yeast, the resulting diploids cannot grow on medium lac ...