Evidence that MEK1 positively promotes
... We set out to gather evidence on the possibility that Mek1 does positively promote interhomologue strand invasion. Using two different reporter cassettes that contain the recognition sequence for the VMA1-derived homing endonuclease (VDE), we have previously reported on various factors that influence ...
... We set out to gather evidence on the possibility that Mek1 does positively promote interhomologue strand invasion. Using two different reporter cassettes that contain the recognition sequence for the VMA1-derived homing endonuclease (VDE), we have previously reported on various factors that influence ...
alpha-amylase from bacillus licheniformis
... introduced into the chromosome of the SJ5550 host strain using conjugative plasmids carrying the LE399 gene flanked by either xyl, gnt, or amyL B. licheniformis chromosomal DNA sequences. As expected, the integration occurred at the xyl, gnt, and amyL loci by homologous recombination. In a separate ...
... introduced into the chromosome of the SJ5550 host strain using conjugative plasmids carrying the LE399 gene flanked by either xyl, gnt, or amyL B. licheniformis chromosomal DNA sequences. As expected, the integration occurred at the xyl, gnt, and amyL loci by homologous recombination. In a separate ...
PDF
... vertebral column. However, in the axial skeleton of Sd homozygotes, Pax-1 expression stopped abruptly in the thoracic region (Fig. 2C). In three embryos analyzed, only 14, 17 and 18 Pax-1-expressing domains, respectively, were found. In Sd homozygotes no cartilaginous tissues were seen in the more c ...
... vertebral column. However, in the axial skeleton of Sd homozygotes, Pax-1 expression stopped abruptly in the thoracic region (Fig. 2C). In three embryos analyzed, only 14, 17 and 18 Pax-1-expressing domains, respectively, were found. In Sd homozygotes no cartilaginous tissues were seen in the more c ...
Conserved syntenic clusters of protein coding genes are missing in
... basal avian order with a high quality genome assembly, and an oscine passeriform (zebra finch; Taeniopygia guttata; Figure 1). We initially focused on chicken and zebra finch, since these represented the best assembled and curated avian genomes available in Ensembl at the time we began this study. O ...
... basal avian order with a high quality genome assembly, and an oscine passeriform (zebra finch; Taeniopygia guttata; Figure 1). We initially focused on chicken and zebra finch, since these represented the best assembled and curated avian genomes available in Ensembl at the time we began this study. O ...
Duplication 12p and PallisterKillian syndrome
... resulting in tetrasomy 12p, which is often present in a tissue limited mosaic state [Peltom€aki et al., 1987]. The PKS phenotype has also been observed in individuals with complete or partial duplications of 12p (trisomy 12p rather than tetrasomy 12p) as the result of an interstitial duplication or ...
... resulting in tetrasomy 12p, which is often present in a tissue limited mosaic state [Peltom€aki et al., 1987]. The PKS phenotype has also been observed in individuals with complete or partial duplications of 12p (trisomy 12p rather than tetrasomy 12p) as the result of an interstitial duplication or ...
Conserved syntenic clusters of protein coding genes are missing in birds
... basal avian order with a high quality genome assembly, and an oscine passeriform (zebra finch; Taeniopygia guttata; Figure 1). We initially focused on chicken and zebra finch, since these represented the best assembled and curated avian genomes available in Ensembl at the time we began this study. O ...
... basal avian order with a high quality genome assembly, and an oscine passeriform (zebra finch; Taeniopygia guttata; Figure 1). We initially focused on chicken and zebra finch, since these represented the best assembled and curated avian genomes available in Ensembl at the time we began this study. O ...
Electrophoretic karyotypes of clinically isolated yeasts
... directly correlated, but seven C. ufbicms isolates (from six patients) had a common atypical karyotype and shared the same phenotype. These isolates are inferred to be generated by a wide genomic reorganization and mutation and the phenotypic changes may be advantageous for survival. The karyotypes ...
... directly correlated, but seven C. ufbicms isolates (from six patients) had a common atypical karyotype and shared the same phenotype. These isolates are inferred to be generated by a wide genomic reorganization and mutation and the phenotypic changes may be advantageous for survival. The karyotypes ...
Tapanes-Castillo A, Weaver EJ, Smith RP, Kamei Y, Caspary T, Hamilton-Nelson KL, Slifer SH, Martin ER, Bixby JL, Lemmon VP. Neurogenetics. 2012 Feb;11(1):53-71. A modifier locus on chromosome 5 contributes to L1 cell adhesion molecule X-linked hydrocephalus in mice.
... on the reason for the defect in CSF flow. Communicating hydrocephalus arises from problems with CSF secretion or resorption; CSF flows freely between the ventricles and the subarachnoid space. On the other hand, noncommunicating hydrocephalus develops when a physical obstruction blocks CSF flow betw ...
... on the reason for the defect in CSF flow. Communicating hydrocephalus arises from problems with CSF secretion or resorption; CSF flows freely between the ventricles and the subarachnoid space. On the other hand, noncommunicating hydrocephalus develops when a physical obstruction blocks CSF flow betw ...
Coffee B, Ikeda M, Budimirovic DB, Hjelm LN, Kaufmann WE and Warren ST: Mosaic FMR1 Deletion Causes Fragile X Syndrome and Can Lead to Molecular Misdiagnosis: A Case Report and Review of the Literature. American J of Medical Genetics Part A 146A:1358-1367 (2008).
... However, other mutational mechanisms, such as deletions of FMR1, also cause fragile X syndrome. The result is the same for both the expansion mediated silencing and deletion, absence of the gene product, FMRP. We report here on an 11-year-old boy with a cognitive and behavioral profile with features ...
... However, other mutational mechanisms, such as deletions of FMR1, also cause fragile X syndrome. The result is the same for both the expansion mediated silencing and deletion, absence of the gene product, FMRP. We report here on an 11-year-old boy with a cognitive and behavioral profile with features ...
MTHFR C677T and A1298C: Explained In Plain
... Homocysteine is an amino acid linked to a wide range of health problems, and is an independent risk factor for heart disease, stroke and other forms of cardiovascular disease (4, 5, 6). It is naturally formed in the body, but gets broken down (recycled) by Lmethyfolate (active folate). Said another ...
... Homocysteine is an amino acid linked to a wide range of health problems, and is an independent risk factor for heart disease, stroke and other forms of cardiovascular disease (4, 5, 6). It is naturally formed in the body, but gets broken down (recycled) by Lmethyfolate (active folate). Said another ...
THE GENETICS OF CURLY WING IN DROSOPHILA. ANOTHER
... to be present in half of the F1 males which all show the above six recessive first-chromosome characters.Curlythereforeexhibitscompleteindependence of the first or X chromosome (see table 7). If the gene for curly were located in the third chromosome, it would be found to show linkage with other gen ...
... to be present in half of the F1 males which all show the above six recessive first-chromosome characters.Curlythereforeexhibitscompleteindependence of the first or X chromosome (see table 7). If the gene for curly were located in the third chromosome, it would be found to show linkage with other gen ...
- Free Documents
... in the pea plants was . Answer C Topic Concept . B the mechanism controlling the appearance of traits was different between the F and the F plants. Skill Knowledge/Comprehension Which of the following about the law of segregation is false A It states that each of two alleles for a given trait segre ...
... in the pea plants was . Answer C Topic Concept . B the mechanism controlling the appearance of traits was different between the F and the F plants. Skill Knowledge/Comprehension Which of the following about the law of segregation is false A It states that each of two alleles for a given trait segre ...
File
... Step one 3 – Figure out the probability of each Genotype is stillPhenotype. dominant, but it is and This would be GG heterozygous dominant. 13 out of the 4 boxes are out of 4 boxes means it isGG, so that equals 75% ...
... Step one 3 – Figure out the probability of each Genotype is stillPhenotype. dominant, but it is and This would be GG heterozygous dominant. 13 out of the 4 boxes are out of 4 boxes means it isGG, so that equals 75% ...
Deciphering the Galaxy Guppy phenotype
... In point of fact the snakeskin pattern is an example of a trait with continuous variation, meaning it can vary between a coarse pattern and a very fine pattern. When you see a continuous varying trait you can assume it is due to multiple genes, not a single gene. That is why it is so difficult to di ...
... In point of fact the snakeskin pattern is an example of a trait with continuous variation, meaning it can vary between a coarse pattern and a very fine pattern. When you see a continuous varying trait you can assume it is due to multiple genes, not a single gene. That is why it is so difficult to di ...
Network properties of human disease genes with pleiotropic effects
... of a node in a molecular network is often correlated to its centrality [14]. There are different measures that capture the centrality of a node in a network. We constructed a human protein interaction network using a modified version of CRG interactome [15] and investigated for differences in four d ...
... of a node in a molecular network is often correlated to its centrality [14]. There are different measures that capture the centrality of a node in a network. We constructed a human protein interaction network using a modified version of CRG interactome [15] and investigated for differences in four d ...
Package ‘GenomicFeatures’ October 14, 2014
... For asBED, a GRanges, with the columns name, thickStart, thickEnd, blockStarts, blockSizes added. The thick regions correspond to the CDS regions, and the blocks represent the exons. The transcript IDs are stored in the name column. The ranges are the transcript bounds. For asGFF, a GRanges, with co ...
... For asBED, a GRanges, with the columns name, thickStart, thickEnd, blockStarts, blockSizes added. The thick regions correspond to the CDS regions, and the blocks represent the exons. The transcript IDs are stored in the name column. The ranges are the transcript bounds. For asGFF, a GRanges, with co ...
SBI3U0 - Pages
... ____ 51. The term genetic drift is defined as of which of the following? a. any change in gene or allele frequencies in a population b. any random change in gene or allele frequencies in a small population c. a rapid population decrease d. the establishment of a population in a new region e. the mov ...
... ____ 51. The term genetic drift is defined as of which of the following? a. any change in gene or allele frequencies in a population b. any random change in gene or allele frequencies in a small population c. a rapid population decrease d. the establishment of a population in a new region e. the mov ...
RT-PCR Analysis - Shiu Lab - Michigan State University
... the 5 stages of abscission that are shown in Figure 6 and Supplement G. Eight PGs display high levels of expression at anthesis, low levels during the events of cell separation, and high levels post abscission as depicted in Figure 6B. These genes are all from independent subfamilies except two sets ...
... the 5 stages of abscission that are shown in Figure 6 and Supplement G. Eight PGs display high levels of expression at anthesis, low levels during the events of cell separation, and high levels post abscission as depicted in Figure 6B. These genes are all from independent subfamilies except two sets ...
Loss of heterozygosity at D8S262: an early genetic event of
... and nodules of altered hepatocytes (NAHs) described previously by Su et al. [2, 3] are often found in cirrhotic liver tissue. Therefore, mounting evidence suggests that SCC represents precursor lesions that are more advanced than LCC in the course of human hepatocarcinogenesis [4]. Foci of altered h ...
... and nodules of altered hepatocytes (NAHs) described previously by Su et al. [2, 3] are often found in cirrhotic liver tissue. Therefore, mounting evidence suggests that SCC represents precursor lesions that are more advanced than LCC in the course of human hepatocarcinogenesis [4]. Foci of altered h ...
Mendel and Genetics
... State that some genes are present on the X chromosome and absent from the shorter Y chromosome in humans. ...
... State that some genes are present on the X chromosome and absent from the shorter Y chromosome in humans. ...
The universal reagent for genome tailoring
... control that the remaining loxP site does not create a disturbance in the gene function after the selectable marker is removed. Interestingly, this allele without the marker removal (Fig. 3B) can provide a useful tool for learning more about the function of the gene of interest. If the marker was de ...
... control that the remaining loxP site does not create a disturbance in the gene function after the selectable marker is removed. Interestingly, this allele without the marker removal (Fig. 3B) can provide a useful tool for learning more about the function of the gene of interest. If the marker was de ...
Expression of floricaula in single cell layers of
... (Fig. 2). This gave a 9.0 kb band for flo-613 and a 5.5 kb band for wild-type plants that lack the 3.5 kb Tam3 element (Fig. 2A, left two lanes). Most of the chimeras had a 9.0 kb band, showing that they carried Tam3 in the flo gene. In addition, all chimeras had a 5.5 kb band of varying intensity, ...
... (Fig. 2). This gave a 9.0 kb band for flo-613 and a 5.5 kb band for wild-type plants that lack the 3.5 kb Tam3 element (Fig. 2A, left two lanes). Most of the chimeras had a 9.0 kb band, showing that they carried Tam3 in the flo gene. In addition, all chimeras had a 5.5 kb band of varying intensity, ...
William Bateson: a biologist ahead of his time
... species and by his reluctance to accept, in its fullblooded form, the view of chromosomes as the controllers of individual development. Growing evidence suggests that both of these positions have been vindicated. New species are now thought to arise as the result of genetic interactions, chromosomal ...
... species and by his reluctance to accept, in its fullblooded form, the view of chromosomes as the controllers of individual development. Growing evidence suggests that both of these positions have been vindicated. New species are now thought to arise as the result of genetic interactions, chromosomal ...
French 2003 - University of Washington
... cells rapidly transfer their contents into the oocyte (stage 11) then begin to degenerate and undergo apoptosis (stages 12–14). At the same time, two groups of approximately 65– 80 anterior, dorsal follicle cells, one on each side of the dorsal midline of the egg chamber, migrate over the nurse cell ...
... cells rapidly transfer their contents into the oocyte (stage 11) then begin to degenerate and undergo apoptosis (stages 12–14). At the same time, two groups of approximately 65– 80 anterior, dorsal follicle cells, one on each side of the dorsal midline of the egg chamber, migrate over the nurse cell ...
On the mechanism of Wolbachia
... development aborts when sperm from an infected male fertilize an uninfected egg, due to the loss of improperly condensed paternal chromosomes (a notable exception is found in haplo-diploid arthropods species, where the loss of paternal chromosomes is not lethal but leads to haploid embryos that deve ...
... development aborts when sperm from an infected male fertilize an uninfected egg, due to the loss of improperly condensed paternal chromosomes (a notable exception is found in haplo-diploid arthropods species, where the loss of paternal chromosomes is not lethal but leads to haploid embryos that deve ...
X-inactivation
X-inactivation (also called lyonization) is a process by which one of the two copies of the X chromosome present in female mammals is inactivated. The inactive X chromosome is silenced by its being packaged in such a way that it has a transcriptionally inactive structure called heterochromatin. As nearly all female mammals have two X chromosomes, X-inactivation prevents them from having twice as many X chromosome gene products as males, who only possess a single copy of the X chromosome (see dosage compensation). The choice of which X chromosome will be inactivated is random in placental mammals such as humans, but once an X chromosome is inactivated it will remain inactive throughout the lifetime of the cell and its descendants in the organism. Unlike the random X-inactivation in placental mammals, inactivation in marsupials applies exclusively to the paternally derived X chromosome.