Mef2 gene expression marks the cardiac and skeletal muscle
... MEF2 DNA-binding activity is also present in neonatal cardiac myocytes, indicating that MEF2 expression can be controlled independently of the skeletal muscle bHLH proteins (Zhu et al., 1991; Yu et al., 1992; Navankasattusas et al., 1992; Ianello et al., 1991). The majority of cardiac gene control r ...
... MEF2 DNA-binding activity is also present in neonatal cardiac myocytes, indicating that MEF2 expression can be controlled independently of the skeletal muscle bHLH proteins (Zhu et al., 1991; Yu et al., 1992; Navankasattusas et al., 1992; Ianello et al., 1991). The majority of cardiac gene control r ...
Activation of the Interleukin-3 Gene by Chromosome
... IL-3 gene. The two chromosome 5 breakpoints were separated by less than 500 bp. The genomic structure in Cases 1 and 2 suggested that a normal IL-3 gene product was over-expressed as a result of the altered promotor structure. This would predict that the IL-3 gene on the translocated chromosome was ...
... IL-3 gene. The two chromosome 5 breakpoints were separated by less than 500 bp. The genomic structure in Cases 1 and 2 suggested that a normal IL-3 gene product was over-expressed as a result of the altered promotor structure. This would predict that the IL-3 gene on the translocated chromosome was ...
Ray-tracing Method for Estimating Radio Propagation Using Genetic
... approach to increasing the processing speed for ray tracing. There are three main approaches used to increase processing speed for ray tracing: 1) optimization of compu- ...
... approach to increasing the processing speed for ray tracing. There are three main approaches used to increase processing speed for ray tracing: 1) optimization of compu- ...
Leukaemia Section del(17p) in myeloïd malignancies Atlas of Genetics and Cytogenetics
... Alias: 17p syndrome in myeloïd malignancies Note: Recently, we and others reported in ANLL and MDS a strong correlation between 17p deletion (a clonal cytogenetic anomaly consisting of a deletion of the short arm of chromosome 17), and a particular form of morphological dysgranulopoiesis, we also fo ...
... Alias: 17p syndrome in myeloïd malignancies Note: Recently, we and others reported in ANLL and MDS a strong correlation between 17p deletion (a clonal cytogenetic anomaly consisting of a deletion of the short arm of chromosome 17), and a particular form of morphological dysgranulopoiesis, we also fo ...
A Guide for Patients
... have failed prior IVF attempts. Although AH may improve embryo implantation and pregnancy rates in these circumstances, there is no clear benefit in younger IVF patients. Preimplantation genetic diagnosis (PGD) is performed at some centers to screen for inherited diseases. In PGD, one or two cells a ...
... have failed prior IVF attempts. Although AH may improve embryo implantation and pregnancy rates in these circumstances, there is no clear benefit in younger IVF patients. Preimplantation genetic diagnosis (PGD) is performed at some centers to screen for inherited diseases. In PGD, one or two cells a ...
Aberrant replication timing induces defective chromosome
... As ORC is not required for the activation of origins in yeast and Xenopus once Cdc6 and MCM proteins have bound [22,23], ORC may only be necessary for the recruitment of these proteins to origins. ORC’s role in transcriptional regulation suggests that it may also provide a ‘landing pad’ for other pr ...
... As ORC is not required for the activation of origins in yeast and Xenopus once Cdc6 and MCM proteins have bound [22,23], ORC may only be necessary for the recruitment of these proteins to origins. ORC’s role in transcriptional regulation suggests that it may also provide a ‘landing pad’ for other pr ...
A small region on the X chromosome of Drosophila regulates a key
... region existed, then hemizygosity for this region, achieved as explained in Figure lc, should shift the sexual phenotype of developing tissue from female to intersexual or to male. The results obtained with a series of twelve distal deficiencies are given in Figure 4a. In nine of the genotypes teste ...
... region existed, then hemizygosity for this region, achieved as explained in Figure lc, should shift the sexual phenotype of developing tissue from female to intersexual or to male. The results obtained with a series of twelve distal deficiencies are given in Figure 4a. In nine of the genotypes teste ...
Preparation of recombinant proteins in milk to improve human and
... additional possibilities for farm animal selection. The best alleles of the major milk protein genes can now be selected using genetic markers. This approach is being more and more used. Yet, it remains that a number of modifications of milk composition can be obtained only via transgenesis. The pro ...
... additional possibilities for farm animal selection. The best alleles of the major milk protein genes can now be selected using genetic markers. This approach is being more and more used. Yet, it remains that a number of modifications of milk composition can be obtained only via transgenesis. The pro ...
GAs
... • A Steady-State GA usually will select two parents, create 1-2 offspring which will replace the 1-2 worst individuals in the current population even if the offspring are worse than the individuals they replace. • This slightly different than (+1) or (+2) replacement. ...
... • A Steady-State GA usually will select two parents, create 1-2 offspring which will replace the 1-2 worst individuals in the current population even if the offspring are worse than the individuals they replace. • This slightly different than (+1) or (+2) replacement. ...
RecA maintains the integrity of chloroplast DNA molecules in
... Wt plants and plants homozygous for a T-DNA insertion near the 3# end (drt100-1) or in the middle (drt100-2) of the single exon in the DRT100 gene were selected from SALK lines 021479 and 102492, respectively, using PCR-based genotyping. Primers to distinguish wt alleles from those containing the T- ...
... Wt plants and plants homozygous for a T-DNA insertion near the 3# end (drt100-1) or in the middle (drt100-2) of the single exon in the DRT100 gene were selected from SALK lines 021479 and 102492, respectively, using PCR-based genotyping. Primers to distinguish wt alleles from those containing the T- ...
Genotype–phenotype correlations in nemaline myopathy caused by
... rare causes of nemaline myopathy. Mutations in the gene for tropomyosin 3 (TPM3) have been identified in four kindreds [11 –15], and mutations in the gene for tropomyosin 2 (TPM2) in three patients in two unrelated families [16]. A severe form of nemaline myopathy with unusual associated features du ...
... rare causes of nemaline myopathy. Mutations in the gene for tropomyosin 3 (TPM3) have been identified in four kindreds [11 –15], and mutations in the gene for tropomyosin 2 (TPM2) in three patients in two unrelated families [16]. A severe form of nemaline myopathy with unusual associated features du ...
Genetics of Colorectal Cancer - Scioto County Medical Society
... Attenuated FAP APC mutation in Ashkenazi Jews ...
... Attenuated FAP APC mutation in Ashkenazi Jews ...
Adventitious root formation in rice requires OsGNOM1 and
... with impaired root formation have been discovered [69]. However, due to the complex structure and intricate regulation of their root systems, the mechanism of AR development is still far from clear. Phytohormone is required for the establishment of appropriate root architecture. It affects the numbe ...
... with impaired root formation have been discovered [69]. However, due to the complex structure and intricate regulation of their root systems, the mechanism of AR development is still far from clear. Phytohormone is required for the establishment of appropriate root architecture. It affects the numbe ...
Gibberellin Signaling: Biosynthesis, Catabolism, and
... and catabolism that relate to signaling. Then, we discuss components of the GA response pathway that have been identified primarily through the analysis of mutants exhibiting altered GA responses. We conclude with a summary of the cereal aleurone, which has proven to be an excellent model system for ...
... and catabolism that relate to signaling. Then, we discuss components of the GA response pathway that have been identified primarily through the analysis of mutants exhibiting altered GA responses. We conclude with a summary of the cereal aleurone, which has proven to be an excellent model system for ...
Genetic Algorithms (GA)
... Explores an area somewhere “in between” two parent areas in the solution space. It combines information from two parents. Tries to maintain the good characteristics of both parents. ...
... Explores an area somewhere “in between” two parent areas in the solution space. It combines information from two parents. Tries to maintain the good characteristics of both parents. ...
Oncomedicine Base Excision Repair Manipulation in Breast
... Genomic instability, Radiation therapy ...
... Genomic instability, Radiation therapy ...
Genetics of Primary ciliary dyskinesia - HAL
... have always been found in association with ODA defects and account for about 14% of those patients 32. Thanks to a genetic linkage analysis performed in one large consanguineous multiplex family, mutations have been identified in a second gene encoding a dynein heavy chain, DNAH5 33 34. DNAH5, loca ...
... have always been found in association with ODA defects and account for about 14% of those patients 32. Thanks to a genetic linkage analysis performed in one large consanguineous multiplex family, mutations have been identified in a second gene encoding a dynein heavy chain, DNAH5 33 34. DNAH5, loca ...
What stay-green mutants tell us about nitrogen remobilization in leaf
... options and close in on the region of the genome that the stay-green locus occupies. As well as promiscuous alien recombination, there is a further experimental benefit of Lolium and Festuca for genetic analysis: a high degree of molecular polymorphism between the species and genera. This is reflect ...
... options and close in on the region of the genome that the stay-green locus occupies. As well as promiscuous alien recombination, there is a further experimental benefit of Lolium and Festuca for genetic analysis: a high degree of molecular polymorphism between the species and genera. This is reflect ...
1 Epistasis Underlying a Fitness Trait within a Natural
... populations within a 200 m radius of each other (Bradshaw et al. 2003): "Stream side," from along the stream itself; "Backwater," from a backwater of the stream about 100 m north of the first collection site; "Sandy bog," a sandy bog about 300 m to the west of the stream and separated from it by dry ...
... populations within a 200 m radius of each other (Bradshaw et al. 2003): "Stream side," from along the stream itself; "Backwater," from a backwater of the stream about 100 m north of the first collection site; "Sandy bog," a sandy bog about 300 m to the west of the stream and separated from it by dry ...
Role of HPC2/ELAC2 in Hereditary Prostate
... (⬎4 ng/ml), a sextant biopsy (three cores from each side) of the prostate was TaqAmpliGold DNA polymerase, and 50 ng of template DNA. PCR was performed. An abnormal DRE or TRUS result, regardless of the serum PSA performed using a Tetrad thermal cycler (MJ Research, Cambridge, MA) with the following ...
... (⬎4 ng/ml), a sextant biopsy (three cores from each side) of the prostate was TaqAmpliGold DNA polymerase, and 50 ng of template DNA. PCR was performed. An abnormal DRE or TRUS result, regardless of the serum PSA performed using a Tetrad thermal cycler (MJ Research, Cambridge, MA) with the following ...
International Journal of Antimicrobial Agents Prevalence of
... amino acid at 83 (Ser) with a large hydrophobic amino acid (Phe), or substitution of the negatively charged Asp at position 87. In this study, mutations in the QRDR of gyrA were found either in codon 83 or 87, as reported from other countries [13]. The fact that different mutation types appeared dur ...
... amino acid at 83 (Ser) with a large hydrophobic amino acid (Phe), or substitution of the negatively charged Asp at position 87. In this study, mutations in the QRDR of gyrA were found either in codon 83 or 87, as reported from other countries [13]. The fact that different mutation types appeared dur ...
