Translational control of regA, a key gene controlling
... produced by each of the modified constructs, by setting the frequency with which the control construct (pVcRegA1, shortend A1) restored the WT phenotype equal to 100%. Mutational ablation of AUG1, AUG2 or ORF2 causes a marked reduction of regA expression Here, we use RNA nomenclature (AUG, etc) when ...
... produced by each of the modified constructs, by setting the frequency with which the control construct (pVcRegA1, shortend A1) restored the WT phenotype equal to 100%. Mutational ablation of AUG1, AUG2 or ORF2 causes a marked reduction of regA expression Here, we use RNA nomenclature (AUG, etc) when ...
Congenital hereditary cataracts
... congenital, human cataracts with the corresponding mouse models. First, early events will be influenced by genes coding for transcription factors like Pax6, Pitx3, Maf or Sox. If the lens is maturing, mutations affecting the lens membranes (aquaporins/Mip, Lim-2 or connexins) or the structural prote ...
... congenital, human cataracts with the corresponding mouse models. First, early events will be influenced by genes coding for transcription factors like Pax6, Pitx3, Maf or Sox. If the lens is maturing, mutations affecting the lens membranes (aquaporins/Mip, Lim-2 or connexins) or the structural prote ...
the genetics of the budgerigar
... factors" exist, and that they exert their action and produce visible results by influencing developmental processes. But since it is impossible to tell how many such factors are related to any one developmental process, we shall not assigp particular functions to particular genes; we shall not speak ...
... factors" exist, and that they exert their action and produce visible results by influencing developmental processes. But since it is impossible to tell how many such factors are related to any one developmental process, we shall not assigp particular functions to particular genes; we shall not speak ...
Telomereled bouquet formation facilitates homologous chromosome
... doublet signals near the tip of the nuclei where rDNA was also closely located, while probes from centromereproximal regions or interstitial regions were located away from the tip and were not always paired. With respect to the bouquet arrangement of the chromosomes, we examined whether each of thes ...
... doublet signals near the tip of the nuclei where rDNA was also closely located, while probes from centromereproximal regions or interstitial regions were located away from the tip and were not always paired. With respect to the bouquet arrangement of the chromosomes, we examined whether each of thes ...
Root Hairs as a Model System for Studying Plant
... the tip-focused [Ca2 ]c gradient. In root hairs, an arti®cial [Ca2 ]c causes transient reorientation of growth only if applied across the apical, cytoplasm-rich region of the tip where growth is already occurring. In root hairs in which microtubules have been stabilized by treatment with taxol, a ...
... the tip-focused [Ca2 ]c gradient. In root hairs, an arti®cial [Ca2 ]c causes transient reorientation of growth only if applied across the apical, cytoplasm-rich region of the tip where growth is already occurring. In root hairs in which microtubules have been stabilized by treatment with taxol, a ...
Multiple domain structure in a chitinase gene (chic)
... 1992; Kuranda & Robbins, 1991), but these sequences are not always homologous. This suggests that chitinase genes have spread through various organisms in the process of evolution and have formed several gene families. Streptomyces spp. are typical soil inhabitants, and produce various carbohydrases ...
... 1992; Kuranda & Robbins, 1991), but these sequences are not always homologous. This suggests that chitinase genes have spread through various organisms in the process of evolution and have formed several gene families. Streptomyces spp. are typical soil inhabitants, and produce various carbohydrases ...
by Vanessa Di Gioacchino A thesis submitted to the Department of Biology
... Goα47A is a candidate gene in a putative haloperidol-affected pathway that is highly expressed in the nervous system. The gene encodes nine transcripts and two isoforms, which are 98% identical and differ only in the N-terminal region. However, the individual roles for each of the two different prot ...
... Goα47A is a candidate gene in a putative haloperidol-affected pathway that is highly expressed in the nervous system. The gene encodes nine transcripts and two isoforms, which are 98% identical and differ only in the N-terminal region. However, the individual roles for each of the two different prot ...
Wnt signaling
... proteins (see www.stanford.edu/~rnusse/pathways/cell2.html). Due to this complexity, this review will focus only on well-established, core components of the pathway (for review, see Wodarz and Nusse, 1998; Peifer and Polakis, 2000). A major effector of the canonical Wnt signaling pathway is the tran ...
... proteins (see www.stanford.edu/~rnusse/pathways/cell2.html). Due to this complexity, this review will focus only on well-established, core components of the pathway (for review, see Wodarz and Nusse, 1998; Peifer and Polakis, 2000). A major effector of the canonical Wnt signaling pathway is the tran ...
Azza Ahmed Ibrahim Abo senna_GST paper
... Acute leukemia is a frequent malignancy affecting both adults and children. The etiology of acute leukemia is unknown, although many conditions may influence its development. Like many other cancers, acute leukemia is considered to be a complex disease, which is determined by combination of genetic ...
... Acute leukemia is a frequent malignancy affecting both adults and children. The etiology of acute leukemia is unknown, although many conditions may influence its development. Like many other cancers, acute leukemia is considered to be a complex disease, which is determined by combination of genetic ...
- Zurich Open Repository and Archive
... Type C stay-green mutants are defined as being defective in the pathway of chlorophyll breakdown, which involves pheophorbide a oxygenase (PAO), required for loss of green color. By analyzing senescence parameters, such as protein degradation, expression of senescence-associated genes and loss of ph ...
... Type C stay-green mutants are defined as being defective in the pathway of chlorophyll breakdown, which involves pheophorbide a oxygenase (PAO), required for loss of green color. By analyzing senescence parameters, such as protein degradation, expression of senescence-associated genes and loss of ph ...
Understanding the Scurred condition in Polled Cattle
... Most calves that are horned can be identified at birth or shortly after, and almost always by weaning time. Distinguishing between smooth-polled and scurred-polled is more difficult. Scurs, a rudimentary horn growth, are often not seen until cattle are nearly a year old or sometimes even older. Scur ...
... Most calves that are horned can be identified at birth or shortly after, and almost always by weaning time. Distinguishing between smooth-polled and scurred-polled is more difficult. Scurs, a rudimentary horn growth, are often not seen until cattle are nearly a year old or sometimes even older. Scur ...
Stem Cell Therapy In Pediatric Neurological Disorders
... pediatricians since they are the primary caregivers to all the children with pediatric neurological disorders. Nowadays with availability of information on the internet, parents of these children obtain a lot of knowledge about newer treatment options and then ask their doctors about it. It's import ...
... pediatricians since they are the primary caregivers to all the children with pediatric neurological disorders. Nowadays with availability of information on the internet, parents of these children obtain a lot of knowledge about newer treatment options and then ask their doctors about it. It's import ...
Genomic Databases for Tomato
... this library were used to generate fingerprints at the Arizona Genome Institute (Mueller et al. 2005b; http://www.sgn.cornell.edu/cview/map.pl?map_id9& physical1). The fingerprints are used in selecting subsequent BACs for BAC-by-BAC sequencing. To anchor BACs to the linkage map “Tomato-EXPEN 2000 ...
... this library were used to generate fingerprints at the Arizona Genome Institute (Mueller et al. 2005b; http://www.sgn.cornell.edu/cview/map.pl?map_id9& physical1). The fingerprints are used in selecting subsequent BACs for BAC-by-BAC sequencing. To anchor BACs to the linkage map “Tomato-EXPEN 2000 ...
for growth. fermentation end products and genes required growth of
... constructed by the following procedure. Strain LAB1955, which has a plasmid (erythromycin resistant) integration mutation in narG was previously isolated (15). Chromosomal DNA prepared from LAB1955 cells was digested with BamHI or HindIII, the recognition sites of which flank the narG insert. The di ...
... constructed by the following procedure. Strain LAB1955, which has a plasmid (erythromycin resistant) integration mutation in narG was previously isolated (15). Chromosomal DNA prepared from LAB1955 cells was digested with BamHI or HindIII, the recognition sites of which flank the narG insert. The di ...
Chromosome Aberrations
... results in an inversion loop • Problems arise when a crossover occurs within the loop • Paracentric inversion crossover results in dicentric and acentric chromosomes • Two normal and two abnormal gametes • Dicentric chromosome is pulled in opposite directions and parts are lost • Acentric chromosome ...
... results in an inversion loop • Problems arise when a crossover occurs within the loop • Paracentric inversion crossover results in dicentric and acentric chromosomes • Two normal and two abnormal gametes • Dicentric chromosome is pulled in opposite directions and parts are lost • Acentric chromosome ...
Xq28 duplications
... How common are Xq28 duplications? Duplications of Xq28 are considered quite rare but now that more specific laboratory techniques are available, the frequency of diagnoses is increasing. At the time of updating this booklet in 2015, over 100 male and almost 100 female cases of Xq28 duplication had b ...
... How common are Xq28 duplications? Duplications of Xq28 are considered quite rare but now that more specific laboratory techniques are available, the frequency of diagnoses is increasing. At the time of updating this booklet in 2015, over 100 male and almost 100 female cases of Xq28 duplication had b ...
Cloning and Sequence Analysis of the xylL Gene Responsible for
... restriction endonuclease and ligation of DNA fragments by T4 DNA ligase were performed by standard procedures as recommended by the supplier (Posco Co., Seoul, Korea). The pCS1 and pCSP21 carrying the xylL gene were previously cloned from the chromosomal DNA of Pseudomonas sp. S-47 (9). In this stud ...
... restriction endonuclease and ligation of DNA fragments by T4 DNA ligase were performed by standard procedures as recommended by the supplier (Posco Co., Seoul, Korea). The pCS1 and pCSP21 carrying the xylL gene were previously cloned from the chromosomal DNA of Pseudomonas sp. S-47 (9). In this stud ...
and Athletic Performance - Department of Mechanical Engineering
... and the process by which the information gets out of the nucleus into the cytoplasm, where the protein will be made, starts with transcription. It occurs in the nucleus when a gene’s information (encoded in DNA) is copied into a molecule called messenger RNA. The mRNA then carries this information o ...
... and the process by which the information gets out of the nucleus into the cytoplasm, where the protein will be made, starts with transcription. It occurs in the nucleus when a gene’s information (encoded in DNA) is copied into a molecule called messenger RNA. The mRNA then carries this information o ...
Inhibition of the Particle-associated RNA
... every test as a standard reference compound. For accurate quantitative comparisons, various compounds were tested in parallel in the same experiment using a single virus preparation. Unless otherwise stated, inhibitory compounds at a range of different concentrations from o-I to o.ooi mM were added ...
... every test as a standard reference compound. For accurate quantitative comparisons, various compounds were tested in parallel in the same experiment using a single virus preparation. Unless otherwise stated, inhibitory compounds at a range of different concentrations from o-I to o.ooi mM were added ...
Schwann Cell-Specific Ablation of Laminin 1 Causes Apoptosis and
... Laminins are heterotrimeric glycoproteins composed of an ␣-, -, and ␥-chain. Five ␣-chains, four -chains, and three ␥-chains have been identified, and 15 isoforms have been observed (Yin et al., 2003). Laminin ␥1 is one of the most abundant chains and is present in 11 isoforms, including all known ...
... Laminins are heterotrimeric glycoproteins composed of an ␣-, -, and ␥-chain. Five ␣-chains, four -chains, and three ␥-chains have been identified, and 15 isoforms have been observed (Yin et al., 2003). Laminin ␥1 is one of the most abundant chains and is present in 11 isoforms, including all known ...
earth science - Augusta County Public Schools
... Lipids insulate, store energy, and make up cell membranes. Proteins may be structural or may function in transport, movement, defense, or cell regulations. Nucleic acids (DNA and RNA) control cell activities by directing protein synthesis. ...
... Lipids insulate, store energy, and make up cell membranes. Proteins may be structural or may function in transport, movement, defense, or cell regulations. Nucleic acids (DNA and RNA) control cell activities by directing protein synthesis. ...
Julio`s MCB - Digital Access to Scholarship at Harvard
... importers for heme and Fe/S cluster biogenesis. A genetic deficiency of Mfrn1 results in a profound hypochromic anemia in vertebrate species. To map the cis-regulatory modules (CRMs) that control expression of the Mfrn genes, we utilized genome-wide chromatin immunoprecipitation (ChIP) datasets for ...
... importers for heme and Fe/S cluster biogenesis. A genetic deficiency of Mfrn1 results in a profound hypochromic anemia in vertebrate species. To map the cis-regulatory modules (CRMs) that control expression of the Mfrn genes, we utilized genome-wide chromatin immunoprecipitation (ChIP) datasets for ...
CIBI3031-070 Midterm Examination III November 2005
... ____ 23. Which of the following is NOT associated with meiosis? a. sperm and egg b. somatic cells c. reduction of the chromosome number ____ 24. If a daughter expresses an X-linked recessive gene, she inherited the trait from a. her mother. b. both parents. c. her father. ____ 25. If two genes are ...
... ____ 23. Which of the following is NOT associated with meiosis? a. sperm and egg b. somatic cells c. reduction of the chromosome number ____ 24. If a daughter expresses an X-linked recessive gene, she inherited the trait from a. her mother. b. both parents. c. her father. ____ 25. If two genes are ...
Sample pages 2 PDF
... mutations at the microphthalmia (mi) locus (23,24). This locus was originally described more than 50 yrs earlier with a single mutant allele, mi (25). Meanwhile, more than 30 additional alleles—many of them spontaneous, and some induced chemically, by irradiation or by targeted mutagenesis—have been ...
... mutations at the microphthalmia (mi) locus (23,24). This locus was originally described more than 50 yrs earlier with a single mutant allele, mi (25). Meanwhile, more than 30 additional alleles—many of them spontaneous, and some induced chemically, by irradiation or by targeted mutagenesis—have been ...