A conserved blueprint for the eye? - treisman lab
... sine oculis (so), a homeodomain protein,(5,6) while eyes absent (eya)(7) and dachshund (dac)(8) encode novel nuclear proteins. No mutations in toy are available, but mutations in any of the other genes can result in the absence of the eye due to the lack of any photoreceptor differentiation. so is a ...
... sine oculis (so), a homeodomain protein,(5,6) while eyes absent (eya)(7) and dachshund (dac)(8) encode novel nuclear proteins. No mutations in toy are available, but mutations in any of the other genes can result in the absence of the eye due to the lack of any photoreceptor differentiation. so is a ...
ppt
... – Homologous chromosomes come together as pairs by synapsis – Each pair, with four chromatids, is called a tetrad – Nonsister chromatids exchange genetic material by crossing over ...
... – Homologous chromosomes come together as pairs by synapsis – Each pair, with four chromatids, is called a tetrad – Nonsister chromatids exchange genetic material by crossing over ...
Coc - ARVO Journals
... Purpose. To characterize the mouse cataract mutation Coc. Methods. Coc is an X-radiation-induced autosomal dominant cataract mutation maintained on a murine C3H inbred strain. The affected heterozygotes were outcrossed to C57BL/6, and (C3H Coc/+ X C57BL/6) mice that were Coc/+ were then backcrossed ...
... Purpose. To characterize the mouse cataract mutation Coc. Methods. Coc is an X-radiation-induced autosomal dominant cataract mutation maintained on a murine C3H inbred strain. The affected heterozygotes were outcrossed to C57BL/6, and (C3H Coc/+ X C57BL/6) mice that were Coc/+ were then backcrossed ...
The gene responsible for Clouston hidrotic
... explain all types of ectodermal dysplasias, including HED, where the disease is caused by a disturbed mesoderm–ectoderm interaction during morphogenesis of the ectodermal tissues (27,28). Given this hypothesis, it may be significant that two forms of non-syndromic neurosensory deafness, recessive DF ...
... explain all types of ectodermal dysplasias, including HED, where the disease is caused by a disturbed mesoderm–ectoderm interaction during morphogenesis of the ectodermal tissues (27,28). Given this hypothesis, it may be significant that two forms of non-syndromic neurosensory deafness, recessive DF ...
Population Differences in Transcript
... genome, respectively. Although it has been suggested that SNPs residing in transcription factors (TFs) have no significant attributable effect on gene expression variation [11], it is unknown whether a variant that affects the genes regulated by a TF operates through a system of regulated pathways. ...
... genome, respectively. Although it has been suggested that SNPs residing in transcription factors (TFs) have no significant attributable effect on gene expression variation [11], it is unknown whether a variant that affects the genes regulated by a TF operates through a system of regulated pathways. ...
Analyzing human variation with Galaxy
... Part 1: Filtering out SNPs found in genomes of healthy individuals Uploading files Using Galaxy libraries Basic filtering ...
... Part 1: Filtering out SNPs found in genomes of healthy individuals Uploading files Using Galaxy libraries Basic filtering ...
CHAPTER 5 General discussion - UvA-DARE
... bleble gene is lost. Therefore this step should be omitted in future experiments. When colony formationn was uniform and the ble gene was still present after single spore isolation and repeatedd subcultivation on both selective and non-selective media, fusion products were mitoticallyy stable. Stabl ...
... bleble gene is lost. Therefore this step should be omitted in future experiments. When colony formationn was uniform and the ble gene was still present after single spore isolation and repeatedd subcultivation on both selective and non-selective media, fusion products were mitoticallyy stable. Stabl ...
Enlis Genome Research - Release Notes
... - Main Application: Added Homozygous Regions Detector tool. Find regions of the genome with "runs" of consecutive homozygous variants. For rare disease analysis, these regions may indicate a consanguineous union, and provide a starting point for finding recessive disease. In tumor samples, these reg ...
... - Main Application: Added Homozygous Regions Detector tool. Find regions of the genome with "runs" of consecutive homozygous variants. For rare disease analysis, these regions may indicate a consanguineous union, and provide a starting point for finding recessive disease. In tumor samples, these reg ...
Fig. 4 - Cambridge University Press
... this was not due to a primer failure, as indicated by a validation of the assay. Discriminant analysis showed a significant shift of gene expression upon CLA feeding, allowing for clear group assignment (Fig. 3 and Fig. 4 (a)). From this model we determined which genes were preferentially targeted a ...
... this was not due to a primer failure, as indicated by a validation of the assay. Discriminant analysis showed a significant shift of gene expression upon CLA feeding, allowing for clear group assignment (Fig. 3 and Fig. 4 (a)). From this model we determined which genes were preferentially targeted a ...
GATA factor function in heart development
... pnr gene affects heart development. (A-D) Expression of pnr results in overexpression of a D-mef2 heart enhancer and cardiac hyperplasia. Stage 11 (A,B) and 16 (C,D) embryos stained for lacZ expression under the control of a D-mef2 cardial cell enhancer are shown. (A,C) WT, wild-type embryos; (B,D) ...
... pnr gene affects heart development. (A-D) Expression of pnr results in overexpression of a D-mef2 heart enhancer and cardiac hyperplasia. Stage 11 (A,B) and 16 (C,D) embryos stained for lacZ expression under the control of a D-mef2 cardial cell enhancer are shown. (A,C) WT, wild-type embryos; (B,D) ...
CHARACTER CHANGES CAUSED BY MUTATION OF AN ENTIRE
... was due to a physical loss or a total inactivation of an entire region of a chromosome. These alternatives, loss or inactivation, can hardly be maintained as an explanation of the case of deficiency here described. This deficiency is shown to have a striking general effect on all mutant genes in the ...
... was due to a physical loss or a total inactivation of an entire region of a chromosome. These alternatives, loss or inactivation, can hardly be maintained as an explanation of the case of deficiency here described. This deficiency is shown to have a striking general effect on all mutant genes in the ...
Meiosis and Mendel
... chromosomes are two chromosomes—one inherited from the mother, one from the father—that have the same length and general appearance. More importantly, these chromosomes have copies of the same genes, although the two copies may differ. For example, if you have a gene that influences blood cholestero ...
... chromosomes are two chromosomes—one inherited from the mother, one from the father—that have the same length and general appearance. More importantly, these chromosomes have copies of the same genes, although the two copies may differ. For example, if you have a gene that influences blood cholestero ...
The Chloroplast trnT–trnF Region in the Seed Plant
... that resembled the ‘‘)35’’ and ‘‘)10’’ promoter regions of bacterial genes, probably because of the bacterial origin of the chloroplast (see also HanleyBowdoin and Chua 1987; Bogorad 1991; Inokuchi and Yamao 1995). Analysis of these conserved regions together with ones seen in other plastid genes yi ...
... that resembled the ‘‘)35’’ and ‘‘)10’’ promoter regions of bacterial genes, probably because of the bacterial origin of the chloroplast (see also HanleyBowdoin and Chua 1987; Bogorad 1991; Inokuchi and Yamao 1995). Analysis of these conserved regions together with ones seen in other plastid genes yi ...
Krebs, RA and AG Fasolo.
... homozygous for one or more recessive traits to one that is wild-type (normal in expression for all traits and homozygous for the wild-type allele). Each cross requires two weeks for offspring to emerge. Lab 3. Chromosome mapping Goal: To use genetically designed strains that control patterns of inhe ...
... homozygous for one or more recessive traits to one that is wild-type (normal in expression for all traits and homozygous for the wild-type allele). Each cross requires two weeks for offspring to emerge. Lab 3. Chromosome mapping Goal: To use genetically designed strains that control patterns of inhe ...
Genetics of Down Syndrome
... with an improvement of the investigation methods. The direct preparation of meristematic somatic cells was followed by long-term and shortterm cell cultures of differentiated somatic cells removed postpartum, by the culture of amniotic fluid specimen and biopsy of chorionic villi, as well as the ana ...
... with an improvement of the investigation methods. The direct preparation of meristematic somatic cells was followed by long-term and shortterm cell cultures of differentiated somatic cells removed postpartum, by the culture of amniotic fluid specimen and biopsy of chorionic villi, as well as the ana ...
Recombination
... past. Without recombination, in a strictly asexual population, every gene shares the same ancestor. In sexually reproducing populations, however, gene genealogies will differ, as they are being shuffled by recombination. This can be well illustrated with parts of the human genome differing in their ...
... past. Without recombination, in a strictly asexual population, every gene shares the same ancestor. In sexually reproducing populations, however, gene genealogies will differ, as they are being shuffled by recombination. This can be well illustrated with parts of the human genome differing in their ...
Epigenetic Effects of Psychological Stressors in Humans
... the last decade, 2003-2013, in the relevant field of interest. ...
... the last decade, 2003-2013, in the relevant field of interest. ...
Diploidization of meiosis in autotetraploids
... diploidization. In a cytologically diploidized organism, only bivalents are formed during meiosis, even though there are sets of four completely homologous chromosomes. In many autopolyploids, the chromosomes show no preference for pairing partner. These species have “tetrasomic” inheritance which m ...
... diploidization. In a cytologically diploidized organism, only bivalents are formed during meiosis, even though there are sets of four completely homologous chromosomes. In many autopolyploids, the chromosomes show no preference for pairing partner. These species have “tetrasomic” inheritance which m ...
How pupils use a model for abstract concepts in genetics
... resemble their parents. That is, to probe for knowledge of related mechanisms such as genes and DNA. The aim of the third part of the interview was to determine the interviewee’s conception of the means of genetic inheritance. If the pupil had either mentioned or heard of genes or DNA, they were ask ...
... resemble their parents. That is, to probe for knowledge of related mechanisms such as genes and DNA. The aim of the third part of the interview was to determine the interviewee’s conception of the means of genetic inheritance. If the pupil had either mentioned or heard of genes or DNA, they were ask ...
Shedding Genomic Ballast: Extensive Parallel Loss of Ancestral
... in which each of 3507 families present in at least two of the genomes was treated as a cladistic character (scored ‘‘present’’ or ‘‘absent’’). Three hundred seventy-one of these families were present in all genomes analyzed, 187 other families were parsimony-uninformative, and 2949 were parsimony-in ...
... in which each of 3507 families present in at least two of the genomes was treated as a cladistic character (scored ‘‘present’’ or ‘‘absent’’). Three hundred seventy-one of these families were present in all genomes analyzed, 187 other families were parsimony-uninformative, and 2949 were parsimony-in ...
Evaluation of existing motif detection tools on their
... effect of vitD3 - Human and mouse cell lines treated with vitD3 versus no vitD3 (Control) - Measured the expression of all genes in the human and mouse cells using microarrays for both conditions over different time points - Select differentially expressed genes (vitD3 versus Control) -> phenotype ...
... effect of vitD3 - Human and mouse cell lines treated with vitD3 versus no vitD3 (Control) - Measured the expression of all genes in the human and mouse cells using microarrays for both conditions over different time points - Select differentially expressed genes (vitD3 versus Control) -> phenotype ...
Differential Gene Expression in the Gastrula of Xenopus Laevis
... Confirmed the presence of Differential Gastrula mRNA separate from Maternal mRNA Gradually disappear after Gastrula; Implication that it has little preceding stages. Some increase in concentration. ...
... Confirmed the presence of Differential Gastrula mRNA separate from Maternal mRNA Gradually disappear after Gastrula; Implication that it has little preceding stages. Some increase in concentration. ...
Meiotic DSBs and the control of mammalian recombination
... years we learned that hotspots, as well as being present in mice, are found in humans, dogs, yeast, and Arabidopsis, but curiously are thought not to be present in C. elegans or Drosophila species, although definitive, high-resolution molecular studies have yet to be carried out in these latter exce ...
... years we learned that hotspots, as well as being present in mice, are found in humans, dogs, yeast, and Arabidopsis, but curiously are thought not to be present in C. elegans or Drosophila species, although definitive, high-resolution molecular studies have yet to be carried out in these latter exce ...