THE GENETICS OF CURLY WING IN DROSOPHILA. ANOTHER
... are found t o be equallydistributedbetweencurlyand same holds true in a cross of a curly maleand an “Xple”2female; that is, a female which is homozygous for the first-chromosome characters, scute, echinus, cut, vermilion, garnet and forked. Here also the curly is found to be present in half of the F ...
... are found t o be equallydistributedbetweencurlyand same holds true in a cross of a curly maleand an “Xple”2female; that is, a female which is homozygous for the first-chromosome characters, scute, echinus, cut, vermilion, garnet and forked. Here also the curly is found to be present in half of the F ...
Product description P018-G1 SHOX-v03 - MRC
... Intended use: The SALSA® MLPA® probemix P018 SHOX is an in vitro diagnostic (IVD)1 or research use only (RUO) assay for the detection of deletions or duplications in the human short stature homeobox (SHOX) gene and its regulatory regions located on Xp22.33/Yp11.32 as a cause for disorders associated ...
... Intended use: The SALSA® MLPA® probemix P018 SHOX is an in vitro diagnostic (IVD)1 or research use only (RUO) assay for the detection of deletions or duplications in the human short stature homeobox (SHOX) gene and its regulatory regions located on Xp22.33/Yp11.32 as a cause for disorders associated ...
Teeth Common Concerns FTNW
... Extra teeth Words Extra teeth Supernumerary teeth Supplemental teeth Hyperdontia Many extra teeth Mesiodens Extra top front tooth Paramolar Extra top molar usually on the cheek side of the gum, rather than the mouth side It’s not uncommon to have an extra tooth. At least 1 to 3 people in every 100 h ...
... Extra teeth Words Extra teeth Supernumerary teeth Supplemental teeth Hyperdontia Many extra teeth Mesiodens Extra top front tooth Paramolar Extra top molar usually on the cheek side of the gum, rather than the mouth side It’s not uncommon to have an extra tooth. At least 1 to 3 people in every 100 h ...
Regular Papers - Fungal Genetics Stock Center
... In Neurospora crassa the comple x translo cation, T(IIIR -> X; IIIR; VIL) D305 (also referred to as T(D305)) translocates a LG IIIR segment into another unide ntified chromosome (P erkins 1 997 Adv . Gen et. 36: 239 -397 ). W hen this translocation is crossed by normal sequence some of the progeny a ...
... In Neurospora crassa the comple x translo cation, T(IIIR -> X; IIIR; VIL) D305 (also referred to as T(D305)) translocates a LG IIIR segment into another unide ntified chromosome (P erkins 1 997 Adv . Gen et. 36: 239 -397 ). W hen this translocation is crossed by normal sequence some of the progeny a ...
SALSA MLPA probemix P018-F1 SHOX - MRC
... within the PAR1 region (pseudoautosomal region 1) which covers the 3000 kb of the X and Y chromosomes next to the p-telomere. This P018-F1 SHOX probemix contains probes for each exon of the human SHOX gene, as well as a probe just before the SHOX promoter region. In addition, several probes are pres ...
... within the PAR1 region (pseudoautosomal region 1) which covers the 3000 kb of the X and Y chromosomes next to the p-telomere. This P018-F1 SHOX probemix contains probes for each exon of the human SHOX gene, as well as a probe just before the SHOX promoter region. In addition, several probes are pres ...
The female-killing chromosome of the silkworm, Bombyx mori, was
... Bombyx mori is a female-heterogametic organism (female, ZW; male, ZZ) that appears to have a putative feminizing gene (Fem) on the W chromosome. The paternally transmitted mutant W chromosome, Df(pSa+pW+od)Fem, derived from the translocation-carrying W chromosome (pSa+pW+od), is inert as femaleness ...
... Bombyx mori is a female-heterogametic organism (female, ZW; male, ZZ) that appears to have a putative feminizing gene (Fem) on the W chromosome. The paternally transmitted mutant W chromosome, Df(pSa+pW+od)Fem, derived from the translocation-carrying W chromosome (pSa+pW+od), is inert as femaleness ...
Mapping of QTL for body conformation and behavior in cattle
... The genetic marker map covered 3155.5 cM of the bovine genome across all autosomes and the pseudoautosomal region of the sex chromosomes. The average marker interval was 13.9 cM and ranged from 6.0 cM (chromosome 23) to 23.2 cM (chromosome 9) on individual chromosomes (Table 2). A total of 60 QTL wi ...
... The genetic marker map covered 3155.5 cM of the bovine genome across all autosomes and the pseudoautosomal region of the sex chromosomes. The average marker interval was 13.9 cM and ranged from 6.0 cM (chromosome 23) to 23.2 cM (chromosome 9) on individual chromosomes (Table 2). A total of 60 QTL wi ...
Parallel Evolution of Copy-Number Variation across Continents in
... The differentiated CNVs have a median length of 1,500 bp; the length distribution is shown in figure 1. There is little evidence that these differentiated CNVs are heterogeneously distributed across chromosome arms (P ¼ 0.096, v2 test), and they are not enriched within large chromosomal inversions ( ...
... The differentiated CNVs have a median length of 1,500 bp; the length distribution is shown in figure 1. There is little evidence that these differentiated CNVs are heterogeneously distributed across chromosome arms (P ¼ 0.096, v2 test), and they are not enriched within large chromosomal inversions ( ...
Multiple Routes to Subfunctionalization and Gene Duplicate
... a duplication by drift. The set of mutationally accessible alleles determines the opportunity for neofunctionalization; it is not the fixation of a duplication that creates opportunities for beneficial mutations. Models of neofunctionalization artificially restrict the question of when mutation and sel ...
... a duplication by drift. The set of mutationally accessible alleles determines the opportunity for neofunctionalization; it is not the fixation of a duplication that creates opportunities for beneficial mutations. Models of neofunctionalization artificially restrict the question of when mutation and sel ...
SVPaper050711
... Table 1 classifies SVs greater than 100 bp into two groups: 99.4% are simple and 0.6% are complex. Simple SVs include those whose structural interpretation is straightforward: insertions, deletions and inversions. We separately identify one type of insertion, a copy number gain, consisting of non-re ...
... Table 1 classifies SVs greater than 100 bp into two groups: 99.4% are simple and 0.6% are complex. Simple SVs include those whose structural interpretation is straightforward: insertions, deletions and inversions. We separately identify one type of insertion, a copy number gain, consisting of non-re ...
TRANSLOCATIONS INVOLVING T H E THIRD AND THE FOURTH
... I n the case of the “Pale” translocation described by BRIDGES(1919, 1923), a section of the second chromosome carrying the genes from plexus to speck was broken off and became permanently attached to the third chromosome near the gene ebony. Flies heterozygous for the translocation, that is, carryin ...
... I n the case of the “Pale” translocation described by BRIDGES(1919, 1923), a section of the second chromosome carrying the genes from plexus to speck was broken off and became permanently attached to the third chromosome near the gene ebony. Flies heterozygous for the translocation, that is, carryin ...
Polyploidy
... …essential genes do not tolerate mutation, …duplications of essential genes, then subsequent mutations, confers adaptive potential to the organism, ...
... …essential genes do not tolerate mutation, …duplications of essential genes, then subsequent mutations, confers adaptive potential to the organism, ...
Phylogenetic analysis of three complete gap
... S.D. Eastman et al. / Genomics 87 (2006) 265 – 274 Connexin genes are arranged in clades identifiable by similar colors used on phylogram tree (Fig. 1). Zebrafish connexin genes are subsequently organized by ascending molecular weight within a clade. ‘‘Previous name’’ indicates previous publication ...
... S.D. Eastman et al. / Genomics 87 (2006) 265 – 274 Connexin genes are arranged in clades identifiable by similar colors used on phylogram tree (Fig. 1). Zebrafish connexin genes are subsequently organized by ascending molecular weight within a clade. ‘‘Previous name’’ indicates previous publication ...
Imposition of Crossover Interference through the
... Our study provides strong evidence that synapsis initiation and crossing over occur at the same sites on chromosomes. First, and most compelling, we have found that SICs display interference, just like COs. In addition, SICs tend to be reduced in frequency near centromeres, and they are found at hig ...
... Our study provides strong evidence that synapsis initiation and crossing over occur at the same sites on chromosomes. First, and most compelling, we have found that SICs display interference, just like COs. In addition, SICs tend to be reduced in frequency near centromeres, and they are found at hig ...
mei-38 Is Required for Chromosome Segregation During Meiosis in
... without kinetochore capture of microtubules that grow from the poles. We have characterized the mei-38 gene in Drosophila and found it may be required for chromosome organization within the karyosome. Nondisjunction of homologous chromosomes occurs in mei-38 mutants primarily at the first meiotic di ...
... without kinetochore capture of microtubules that grow from the poles. We have characterized the mei-38 gene in Drosophila and found it may be required for chromosome organization within the karyosome. Nondisjunction of homologous chromosomes occurs in mei-38 mutants primarily at the first meiotic di ...
Polyploidy
... • A change in gene regulation brought about without a change in DNA sequence, – often to the structure of the chromosome, – or through modification of the nucleotide bases, ...
... • A change in gene regulation brought about without a change in DNA sequence, – often to the structure of the chromosome, – or through modification of the nucleotide bases, ...
by Attila Mokanszki Supervisor: Prof. Dr. Eva Olah
... spinal and bulbular muscular athrophy (SBMA). The expansion of poliglutamin repeat relates to male infertility and insufficient masculinisation (MAIS). Cystic fibrosis is one of the most common autosomal recessive disease, affecting one in 2500 live births. Insufficient functioning of the CFTR prot ...
... spinal and bulbular muscular athrophy (SBMA). The expansion of poliglutamin repeat relates to male infertility and insufficient masculinisation (MAIS). Cystic fibrosis is one of the most common autosomal recessive disease, affecting one in 2500 live births. Insufficient functioning of the CFTR prot ...
genomebiology.com
... exons/introns from previously intronic/exonic sequences, respectively), and insertion into first and last exons. However, no extensive analysis has compared the effects of TEs on the transcriptomes of mammals, non-mammalian vertebrates and invertebrates. Results: We analyzed the influence of TEs on ...
... exons/introns from previously intronic/exonic sequences, respectively), and insertion into first and last exons. However, no extensive analysis has compared the effects of TEs on the transcriptomes of mammals, non-mammalian vertebrates and invertebrates. Results: We analyzed the influence of TEs on ...
Genetic balancers
... Lethals were balanced because of the short genetic distances. In all cases, recombination was easily detected by the presence of Dpy, Unc, or DpyUnc recombinant animals among the self progeny of a heterozygote. The types and numbers of recombinant progeny gave distance and gene order relative to the ...
... Lethals were balanced because of the short genetic distances. In all cases, recombination was easily detected by the presence of Dpy, Unc, or DpyUnc recombinant animals among the self progeny of a heterozygote. The types and numbers of recombinant progeny gave distance and gene order relative to the ...
LINKAGE AND MAPPING IN EUKARYOTES
... However, at meiosis, crossing over allows the alleles of associated loci to show some measure of independence. A geneticist can use crossing over between loci to determine how close one locus actually is to another on a chromosome and thus to map an entire chromosome and eventually the entire genome ...
... However, at meiosis, crossing over allows the alleles of associated loci to show some measure of independence. A geneticist can use crossing over between loci to determine how close one locus actually is to another on a chromosome and thus to map an entire chromosome and eventually the entire genome ...
Analyzing Loss of Heterozygosity in in Partek Genomics Suite™ v6.6
... important to emphasize that the unpaired design does not actually detect LOH in strict sense, but rather runs of homozygosity in regions that are expected to be heterozygous. As SNPs are known to be population specific, the interpretation of the data should be performed with caution in cases when ba ...
... important to emphasize that the unpaired design does not actually detect LOH in strict sense, but rather runs of homozygosity in regions that are expected to be heterozygous. As SNPs are known to be population specific, the interpretation of the data should be performed with caution in cases when ba ...
Two Linked Blood Pressure Quantitative Trait Loci on
... humans. Because RNO10 and mouse chromosome 11 (MMU11) are well conserved and because the mouse map contains many more known loci than the rat map, the mouse map serves as a good bridge for comparisons between rats and humans. Although there certainly are many loci common to MMU11 and HSA17, the orde ...
... humans. Because RNO10 and mouse chromosome 11 (MMU11) are well conserved and because the mouse map contains many more known loci than the rat map, the mouse map serves as a good bridge for comparisons between rats and humans. Although there certainly are many loci common to MMU11 and HSA17, the orde ...
chromosomal
... Sex chromosome aneuploids is less devastating than in autosomal aneupoilds. This is because of X-inactivation mechanisms and the fact that Y carries very few genes that determine male sex. *Ivana FELLNEROVÁ, PřF UP Olomouc* ...
... Sex chromosome aneuploids is less devastating than in autosomal aneupoilds. This is because of X-inactivation mechanisms and the fact that Y carries very few genes that determine male sex. *Ivana FELLNEROVÁ, PřF UP Olomouc* ...
Unraveling the Genetic Mysteries of the Corneal Dystrophies
... Epithelial Basement Membrane Dystrophy Meesman’s Dystrophy Band-shaped/Whorled Microcystic Dystrophy (Lisch dystrophy) ...
... Epithelial Basement Membrane Dystrophy Meesman’s Dystrophy Band-shaped/Whorled Microcystic Dystrophy (Lisch dystrophy) ...
Analysis of Cross Sequence Similarities for Multiple - PolyU
... I-frame since the redundancy found between two consecutive frames is always significant when comparing with that found within the frame itself. In the field of DNA compression, current algorithms are analogous to intra-frame compression as redundant information is exploited only within one chromosom ...
... I-frame since the redundancy found between two consecutive frames is always significant when comparing with that found within the frame itself. In the field of DNA compression, current algorithms are analogous to intra-frame compression as redundant information is exploited only within one chromosom ...