Features and phylogeny of the six compared Plasmodium genomes
... sequence similarity, which we considered as positional orthologs. It should be mentioned that although we excluded positional orthologs in this analysis because we did not consider them as strictly parasitespecific, we think that divergent positional orthologs are themselves interesting genes for fo ...
... sequence similarity, which we considered as positional orthologs. It should be mentioned that although we excluded positional orthologs in this analysis because we did not consider them as strictly parasitespecific, we think that divergent positional orthologs are themselves interesting genes for fo ...
miRNA - apctp
... ts in about 30% of colonies displaying a white phenotype, which is identical to the one of al-1 mutants. • This phenomenon was termed quelling. ...
... ts in about 30% of colonies displaying a white phenotype, which is identical to the one of al-1 mutants. • This phenomenon was termed quelling. ...
Jump to Terms beginning with: A B Ca-Cn Co
... At meiosis in a reciprocal translocation heterozygote, the passage (segregation) of both normal chromosomes to one pole and both translocated chromosomes to the other pole, giving genetically balanced gametes. Segregation of centromeres during meiosis in a reciprocal translocation heterozygote such ...
... At meiosis in a reciprocal translocation heterozygote, the passage (segregation) of both normal chromosomes to one pole and both translocated chromosomes to the other pole, giving genetically balanced gametes. Segregation of centromeres during meiosis in a reciprocal translocation heterozygote such ...
Review A model for chromosome structure during the mitotic
... core/matrix strand via MARS (green dots) with closely associated replication origins (included in green dots). Probable attachments to transcription complexes are not illustrated for simplicity (Jackson et al. 1996). The DNA loops are present on only one side of the matrix strand. For diagrammatic p ...
... core/matrix strand via MARS (green dots) with closely associated replication origins (included in green dots). Probable attachments to transcription complexes are not illustrated for simplicity (Jackson et al. 1996). The DNA loops are present on only one side of the matrix strand. For diagrammatic p ...
Supplementary Material (doc 236K)
... Phenotype search, Location search, and Other parameters. The minimum requirement is to specify at least one trait (phenoTrait) or one of the three location specifications. Both a trait and a location can be specified. A parameter named tab must be specified in order for any search to be performed. T ...
... Phenotype search, Location search, and Other parameters. The minimum requirement is to specify at least one trait (phenoTrait) or one of the three location specifications. Both a trait and a location can be specified. A parameter named tab must be specified in order for any search to be performed. T ...
Leukaemia Section 1q translocations (unbalanced) in myeloid malignancies Atlas of Genetics and Cytogenetics
... mutagenic exposure. The balanced t(1;5)(q23;q33) involving the PDGFRB gene is associated with a myeloproliferative disorder and eosinophilia (Johansson et al., 1997). der(6)t(1;6)(q21-23;p21.3). Found in chronic myeloproliferative disorders and less frequently in AML/MDS. DNA sequences may be overre ...
... mutagenic exposure. The balanced t(1;5)(q23;q33) involving the PDGFRB gene is associated with a myeloproliferative disorder and eosinophilia (Johansson et al., 1997). der(6)t(1;6)(q21-23;p21.3). Found in chronic myeloproliferative disorders and less frequently in AML/MDS. DNA sequences may be overre ...
Design and Operation of Large Scale RNA production v2
... • RNA has many reactive groups that must be protected during synthesis, and then removed afterwards to generate biologically active RNA ...
... • RNA has many reactive groups that must be protected during synthesis, and then removed afterwards to generate biologically active RNA ...
1 Supplemental Table 1. FACS-isolated, SSEA-4
... -encodes the human homolog of the protooncogene c-kit, -the protein is a type 3 transmembrane receptor for mast cell growth factor, also known as stem cell factor and KIT ligand, -promotion of primordial follicle activation, oocyte growth, and follicle survival 35, -mutations in this gene are asso ...
... -encodes the human homolog of the protooncogene c-kit, -the protein is a type 3 transmembrane receptor for mast cell growth factor, also known as stem cell factor and KIT ligand, -promotion of primordial follicle activation, oocyte growth, and follicle survival 35, -mutations in this gene are asso ...
Gene Prediction - Compgenomics2010
... Ribosome binding site model was also added to augment accuracy in the prediction of translational start sites. ...
... Ribosome binding site model was also added to augment accuracy in the prediction of translational start sites. ...
Chapter 8 - Lamar County School District
... (Remember, haploid or half plus haploid or half gives diploid or whole?) ...
... (Remember, haploid or half plus haploid or half gives diploid or whole?) ...
N. crassa et al. However, despite the speed and
... Increasing the efficiency of random isolates by using multiply marked testers: Rather that testing an unknown by crossing it to markers in the seven linkage groups one or two at a time, it is more efficient to use multiply marked strains. Testers have been developed that incorporate markers tagging ...
... Increasing the efficiency of random isolates by using multiply marked testers: Rather that testing an unknown by crossing it to markers in the seven linkage groups one or two at a time, it is more efficient to use multiply marked strains. Testers have been developed that incorporate markers tagging ...
Q - gst boces
... Traits are controlled by genes. Genes are found on chromosomes Chromosomes are wound up DNA ...
... Traits are controlled by genes. Genes are found on chromosomes Chromosomes are wound up DNA ...
Full text
... give rise to spermatogonia (Hardy et al., 1979), failure of cytokinesis during stem cell divisions should result in the permanent inactivation of these cells. Oogenesis phenotype In trans to a chromosomal deficiency or a null allele such as dia2, the dia1 allele exhibits an oogenesis phenotype. Alth ...
... give rise to spermatogonia (Hardy et al., 1979), failure of cytokinesis during stem cell divisions should result in the permanent inactivation of these cells. Oogenesis phenotype In trans to a chromosomal deficiency or a null allele such as dia2, the dia1 allele exhibits an oogenesis phenotype. Alth ...
Vectors - Rajshahi University
... advantage of the phage vector is its high transformation efficiency, about 1000 times more efficient than the plasmid vector. ...
... advantage of the phage vector is its high transformation efficiency, about 1000 times more efficient than the plasmid vector. ...
Gene Prediction - Compgenomics2010
... Ribosome binding site model was also added to augment accuracy in the prediction of translational start sites. ...
... Ribosome binding site model was also added to augment accuracy in the prediction of translational start sites. ...
Leukaemia Section t(6;14)(p25;q32) IRF4/IGH / t(2;6)(p12;p25) IRF4/IGK / t(6;22)(p25;q11) IRF4/IGL
... MUM1/IRF4 in multiple myeloma and in a subtype of mature B-cell lymphomas (Iida et al., 1997; Salaverria et al., 2011). The translocation leads to the overexpression of the MUM1/IRF4 gene. In multiple myeloma, IRF4 is similarly juxtaposed by an illegitimate IG switch recombination to the IG loci (Ii ...
... MUM1/IRF4 in multiple myeloma and in a subtype of mature B-cell lymphomas (Iida et al., 1997; Salaverria et al., 2011). The translocation leads to the overexpression of the MUM1/IRF4 gene. In multiple myeloma, IRF4 is similarly juxtaposed by an illegitimate IG switch recombination to the IG loci (Ii ...
Inquiry into Life Twelfth Edition
... • These are position- and orientationindependent DNA elements that stimulate or depress, respectively, transcription of associated genes • Are often tissue-specific in that they rely on tissue-specific DNA-binding proteins for their activities • Some DNA elements can act either as enhancer or silenc ...
... • These are position- and orientationindependent DNA elements that stimulate or depress, respectively, transcription of associated genes • Are often tissue-specific in that they rely on tissue-specific DNA-binding proteins for their activities • Some DNA elements can act either as enhancer or silenc ...
BMC Genomics - Gene Quantification
... In a complex mRNA population with small absolute numbers of individual transcripts, such as that from a single eukaryotic cell, sampling effects can result in only a subset of the population of starting RNA molecules being represented in the final amplified population. This is particularly problemat ...
... In a complex mRNA population with small absolute numbers of individual transcripts, such as that from a single eukaryotic cell, sampling effects can result in only a subset of the population of starting RNA molecules being represented in the final amplified population. This is particularly problemat ...
ASC-169: Beef Sire Selection Manual
... For the purposes of this manual, the focus will be on the genetic component of the phenotype. The genetic component of all living things is expressed through the production of proteins at the cellular level. Cells can turn on or turn off the production of proteins through signals from other cells, ...
... For the purposes of this manual, the focus will be on the genetic component of the phenotype. The genetic component of all living things is expressed through the production of proteins at the cellular level. Cells can turn on or turn off the production of proteins through signals from other cells, ...
Genetic Analysis: the Terminology *
... If limbless phenotype, then nls phenotype does NOT depend on wild type gene product of xlb, so xlb is NOT downstream of nls. The epistasis result is consistent with xlb --------l nls xlb could also function in parallel to nls If ectopic limbs, then xlb phenotype does NOT depend on nls, thus nls is N ...
... If limbless phenotype, then nls phenotype does NOT depend on wild type gene product of xlb, so xlb is NOT downstream of nls. The epistasis result is consistent with xlb --------l nls xlb could also function in parallel to nls If ectopic limbs, then xlb phenotype does NOT depend on nls, thus nls is N ...
Punnet Square Lab
... The normal female condition is a result of the chromosomal pairing XX, while the normal male condition is XY. Certain genes located on the X chromosome, not associated with female sex characteristics, cause sex-linked recessive traits. As a result, females must receive two recessive alleles to exhib ...
... The normal female condition is a result of the chromosomal pairing XX, while the normal male condition is XY. Certain genes located on the X chromosome, not associated with female sex characteristics, cause sex-linked recessive traits. As a result, females must receive two recessive alleles to exhib ...
Identifying Genes Required for Cell Division in the Early C. elegans
... cell division and subsequent development of the zygote. The spindle facilitates chromosome segregation to properly distribute genetic information to newly formed daughter cells. Four C. elegans temperature-sensitive mutants are examined in this paper that have defects in spindle formation or functio ...
... cell division and subsequent development of the zygote. The spindle facilitates chromosome segregation to properly distribute genetic information to newly formed daughter cells. Four C. elegans temperature-sensitive mutants are examined in this paper that have defects in spindle formation or functio ...
Structure and Transcription of the singed Locus of Drosophila
... transcription of singed in the ovary is from middle to late stages of oogenesis. Analysis of RNA in embryos from the reciprocal crosses between wild type and singed-3 showed that all three RNAs are maternally inherited with very little zygotic transcription in embryos. The mutation singed3 appears t ...
... transcription of singed in the ovary is from middle to late stages of oogenesis. Analysis of RNA in embryos from the reciprocal crosses between wild type and singed-3 showed that all three RNAs are maternally inherited with very little zygotic transcription in embryos. The mutation singed3 appears t ...
2015 JUNIOR GENETICS EASY 4455 (easy) HIH1040-1/ES94
... Q: What is the dense center of a cell that contains the genetic material? A: Nucleus 4461 (easy) TH447/HIH1060-1 Q: 2 part question: How many pairs of chromosomes are there in a horse & are these pairs always identical in nature? A: 32 pairs; not always identical 4462 (easy) HIH1060-1/HS19/TH458-9/E ...
... Q: What is the dense center of a cell that contains the genetic material? A: Nucleus 4461 (easy) TH447/HIH1060-1 Q: 2 part question: How many pairs of chromosomes are there in a horse & are these pairs always identical in nature? A: 32 pairs; not always identical 4462 (easy) HIH1060-1/HS19/TH458-9/E ...
PDF - American Society of Mammalogists
... mitochondrial DNA. Recently, a class of mammalian autosomal genes has emerged that shows expression of only 1 parental allele. This phenomenon has been termed ‘‘genomic imprinting.’’ Genomic imprinting is an epigenetic effect resulting from chromosomal marks established during gametogenesis. Such im ...
... mitochondrial DNA. Recently, a class of mammalian autosomal genes has emerged that shows expression of only 1 parental allele. This phenomenon has been termed ‘‘genomic imprinting.’’ Genomic imprinting is an epigenetic effect resulting from chromosomal marks established during gametogenesis. Such im ...
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.