Pathway/Genome Navigator - Bioinformatics Research Group at SRI
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... If you create a web account, you can define a favorite database that will be opened by default when you login ...
Structural Domains and Matrix Attachment Regions
... the highest matrix affinity to be identified. Here, binding assays were performed with saturating amounts of matrix proteins. These have been established empirically by testing increasing amounts of isolated matrices, until a point was reached at which all of a labeled MAR fragment was matrix bound. ...
... the highest matrix affinity to be identified. Here, binding assays were performed with saturating amounts of matrix proteins. These have been established empirically by testing increasing amounts of isolated matrices, until a point was reached at which all of a labeled MAR fragment was matrix bound. ...
Acetylglutamate kinase is required for both gametophyte function
... targeted to plastid (Bannai et al. 2002). To confirm NAGK localization, plants co-expressing 35S::NAGK-GFP and the plastid marker 35S::Plastid-RFP were produced by crossing and examined with confocal laser scanning microscopy. In root cells, NAGK-GFP was found to colocalize with the plastid-localized ...
... targeted to plastid (Bannai et al. 2002). To confirm NAGK localization, plants co-expressing 35S::NAGK-GFP and the plastid marker 35S::Plastid-RFP were produced by crossing and examined with confocal laser scanning microscopy. In root cells, NAGK-GFP was found to colocalize with the plastid-localized ...
Imprinting evolution and the price of silence
... DNA methylation and imprint marks Other than typical sequence polymorphisms that do not correlate with imprint status, the nucleotide sequence of the two alleles of imprinted genes are identical. Therefore, the imprint marks that distinguish the two parental alleles must be epigenetic in nature. Epi ...
... DNA methylation and imprint marks Other than typical sequence polymorphisms that do not correlate with imprint status, the nucleotide sequence of the two alleles of imprinted genes are identical. Therefore, the imprint marks that distinguish the two parental alleles must be epigenetic in nature. Epi ...
Flowering Newsletter bibliography for 2007
... Coneva V, Zhu T, Colasanti J. 2007. Expression differences between normal and indeterminate1 maize suggest downstream targets of ID1, a floral transition regulator in maize. Journal of Experimental Botany 58, 3679–3693. Cookson SJ, Chenu K, Granier C. 2007. Day length affects the dynamics of leaf ex ...
... Coneva V, Zhu T, Colasanti J. 2007. Expression differences between normal and indeterminate1 maize suggest downstream targets of ID1, a floral transition regulator in maize. Journal of Experimental Botany 58, 3679–3693. Cookson SJ, Chenu K, Granier C. 2007. Day length affects the dynamics of leaf ex ...
BREAST CANCER RISK ASSESSMENT, RACHEL C. JANKOWITZ
... Here is another risk evaluator called the Tyrer-Cusick model. So the Tyrer-Cusick Risk Evaluator is a little bit more cumbersome to do. I think it's less easy to do in a busy primary care setting because it takes me at least 10 minutes to do for each patient. I can show you some of the things that g ...
... Here is another risk evaluator called the Tyrer-Cusick model. So the Tyrer-Cusick Risk Evaluator is a little bit more cumbersome to do. I think it's less easy to do in a busy primary care setting because it takes me at least 10 minutes to do for each patient. I can show you some of the things that g ...
Identifying genetic susceptibility factors for
... which has been designated tt, was significantly underrepresented in the tuberculosis cases compared with the controls (P l 0.01) (Table 2 ; [21]). The odds ratio for subjects of genotype tt having tuberculosis compared with those of genotypes TT\Tt combined was 0.53 (95 % confidence interval 0.31–0. ...
... which has been designated tt, was significantly underrepresented in the tuberculosis cases compared with the controls (P l 0.01) (Table 2 ; [21]). The odds ratio for subjects of genotype tt having tuberculosis compared with those of genotypes TT\Tt combined was 0.53 (95 % confidence interval 0.31–0. ...
The genetic causes of male factor infertility: A review
... Chromosomal abnormalities account for approximately 5% of infertility in males, and the prevalence increases to 15% in the population of azoospermic males (2). Abnormalities of the Y chromosome, such as microdeletions, are the major cause of azoospermia (the complete absence of sperm in the ejaculat ...
... Chromosomal abnormalities account for approximately 5% of infertility in males, and the prevalence increases to 15% in the population of azoospermic males (2). Abnormalities of the Y chromosome, such as microdeletions, are the major cause of azoospermia (the complete absence of sperm in the ejaculat ...
Access Presentation
... - G/G mutation enhances binding of transcriptional activator Sp1 to P2 resulting in increase in Mdm2 transcription ...
... - G/G mutation enhances binding of transcriptional activator Sp1 to P2 resulting in increase in Mdm2 transcription ...
Biological Natural Kinds
... whose variation from one another is a natural part of what it is to be a member of those kinds. In the physical sciences, this heterogeneity amongst individuals is abstracted away from or otherwise ignored in treating those individuals as members of a physical kind (a proton, a chemical element, an ...
... whose variation from one another is a natural part of what it is to be a member of those kinds. In the physical sciences, this heterogeneity amongst individuals is abstracted away from or otherwise ignored in treating those individuals as members of a physical kind (a proton, a chemical element, an ...
Recombinant Human Epidermal Growth Factor EPICULT®
... Epidermal growth factor (EGF) is prototypic of a family of growth factors that are derived from membrane-anchored precursors. All members of this family are characterized by the presence of at least one EGF structural unit in their extracellular domain. The EGF structural unit is defined by the pres ...
... Epidermal growth factor (EGF) is prototypic of a family of growth factors that are derived from membrane-anchored precursors. All members of this family are characterized by the presence of at least one EGF structural unit in their extracellular domain. The EGF structural unit is defined by the pres ...
IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS) e-ISSN: 2278-3008, p-ISSN:2319-7676.
... The ERβ gene is located on chromosome 14q22-24 [22]. Systemic mutation screening of the coding region and part of the 50 and 30 regions of the ERβ gene revealed two common single nucleotide polymorphisms: G/A exchange at nucleotide 1730 in the 30 untranslated region in exon 8, and a silent 1082 G/A ...
... The ERβ gene is located on chromosome 14q22-24 [22]. Systemic mutation screening of the coding region and part of the 50 and 30 regions of the ERβ gene revealed two common single nucleotide polymorphisms: G/A exchange at nucleotide 1730 in the 30 untranslated region in exon 8, and a silent 1082 G/A ...
Introduction - bei DuEPublico
... 2) evasion of apoptosis 3) insensitivity to antigrowth signals 4) sustained angiogenesis 5) limitless replicative potential and 6) capacity to invade tissue and grow at metastatic sites The number of mutations required to gain these abilities varies. For example, in some cells mutation of the TP53 g ...
... 2) evasion of apoptosis 3) insensitivity to antigrowth signals 4) sustained angiogenesis 5) limitless replicative potential and 6) capacity to invade tissue and grow at metastatic sites The number of mutations required to gain these abilities varies. For example, in some cells mutation of the TP53 g ...
1 Title: Evidence for large domains of similarly expressed genes in
... restricted to specific target genes. Several examples of insulators, sequences that prevent neighboring modules from affecting transcription have been identified (reviewed in [2]). These insulators seem to function, not by deactivating cis-modules, but by preventing their influence from being propag ...
... restricted to specific target genes. Several examples of insulators, sequences that prevent neighboring modules from affecting transcription have been identified (reviewed in [2]). These insulators seem to function, not by deactivating cis-modules, but by preventing their influence from being propag ...
Gene Conversion as a Source of Nucleotide Diversity in
... both, all except possibly one are consistent with an origin by gene conversion. This result is supported not only by the identity of the polymorphic nucleotides but also by the significant clustering of polymorphic nucleotides within each gene. Positioning of the polymorphisms within derived three-d ...
... both, all except possibly one are consistent with an origin by gene conversion. This result is supported not only by the identity of the polymorphic nucleotides but also by the significant clustering of polymorphic nucleotides within each gene. Positioning of the polymorphisms within derived three-d ...
Title Page Pages to read in ... before coming to lab, fair
... 1. TITLE AND AUTHORS - This includes the title that indicates what the study is about and the names of all of the report authors. 2. ABSTRACT - The results should be summarized. Background is stated in one or two sentences. There is a clear statement of the questions addressed. Methods are summarize ...
... 1. TITLE AND AUTHORS - This includes the title that indicates what the study is about and the names of all of the report authors. 2. ABSTRACT - The results should be summarized. Background is stated in one or two sentences. There is a clear statement of the questions addressed. Methods are summarize ...
Meiosis
... Abnormal numbers of sex chromosomes do not usually affect survival Sex chromosome abnormalities tend to be less severe as a result of – Small size of the Y chromosome – X-chromosome inactivation – In each cell of a human female, one of the two X chromosomes becomes tightly coiled and inactive – ...
... Abnormal numbers of sex chromosomes do not usually affect survival Sex chromosome abnormalities tend to be less severe as a result of – Small size of the Y chromosome – X-chromosome inactivation – In each cell of a human female, one of the two X chromosomes becomes tightly coiled and inactive – ...
Spatially ordered transcription of regulatory DNA in
... show expression (Fig. 4C,E). Later, the signal is particularly strong in the ventral nerve cord, although the ectoderm is also labelled (Fig. 4D,F). We can attribute no function to these transcripts, as chromosome breaks in the iab region have no apparent effect on the development of PS13-15 (Karch ...
... show expression (Fig. 4C,E). Later, the signal is particularly strong in the ventral nerve cord, although the ectoderm is also labelled (Fig. 4D,F). We can attribute no function to these transcripts, as chromosome breaks in the iab region have no apparent effect on the development of PS13-15 (Karch ...
Involvement of Sox1, 2 and 3 in the early and subsequent molecular
... 2522 Y. Kamachi and others hours). Because of this early response, we have anticipated that the mechanism of δ1-crystallin gene activation is highly relevant to the lens induction process, reflecting the second state being met within the ectoderm. We have found that δ1-crystallin gene is regulated ...
... 2522 Y. Kamachi and others hours). Because of this early response, we have anticipated that the mechanism of δ1-crystallin gene activation is highly relevant to the lens induction process, reflecting the second state being met within the ectoderm. We have found that δ1-crystallin gene is regulated ...
Variation 3.3
... The sophomore class at Roosevelt High School in Metropolitan City is one of five high schools that conduct two community service projects each year, one in the fall and one in the spring. This fall, 150 students from Roosevelt High signed up to help. The same number signed up in the spring, but 30 o ...
... The sophomore class at Roosevelt High School in Metropolitan City is one of five high schools that conduct two community service projects each year, one in the fall and one in the spring. This fall, 150 students from Roosevelt High signed up to help. The same number signed up in the spring, but 30 o ...
Leukaemia Section del(17p) in non-Hodgkin's lymphoma (NHL) Atlas of Genetics and Cytogenetics
... classification and to the different sensitivity of the detection methods. 10 to 15% of follicle centre cell lymphoma (FCCL) and mantle cell lymphomas (MCL) may carry a 17pchromosome; minority of marginal zone B-cell lymphomas may be associated with 17p deletion. This anomaly is rarely found in T-cel ...
... classification and to the different sensitivity of the detection methods. 10 to 15% of follicle centre cell lymphoma (FCCL) and mantle cell lymphomas (MCL) may carry a 17pchromosome; minority of marginal zone B-cell lymphomas may be associated with 17p deletion. This anomaly is rarely found in T-cel ...
View Full PDF - Biochemical Society Transactions
... certain legume hosts [2]. Although not completely elucidated, several mechanisms have been postulated to explain the beneficial effect associated with the symbiotic hydrogenase activity. Among them, hydrogenase reaction might protect nitrogenase from the detrimental effect of oxygen, prevent inhibit ...
... certain legume hosts [2]. Although not completely elucidated, several mechanisms have been postulated to explain the beneficial effect associated with the symbiotic hydrogenase activity. Among them, hydrogenase reaction might protect nitrogenase from the detrimental effect of oxygen, prevent inhibit ...
p16INK4a immunocytochemical analysis is an
... 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, the results of gene deletion studies and protein expression analyses by ICC may differ. Indeed, several studies have shown that p16INK4a pro ...
... 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, the results of gene deletion studies and protein expression analyses by ICC may differ. Indeed, several studies have shown that p16INK4a pro ...
Single nucleotide polymorphism in coronary
... with glutation peroxidase (GPx-1 rs1050450) 599C/T SNP and both of them were found to play role in ISR significantly.9 eNOS CAD patients studied in other project were proven that carriers of the 298Asp allele of the eNOS (rs1799983) polymorphism showed a higher frequency of restenosis compared to 29 ...
... with glutation peroxidase (GPx-1 rs1050450) 599C/T SNP and both of them were found to play role in ISR significantly.9 eNOS CAD patients studied in other project were proven that carriers of the 298Asp allele of the eNOS (rs1799983) polymorphism showed a higher frequency of restenosis compared to 29 ...