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mgm1, the earliest sex-specific germline marker in Drosophila
mgm1, the earliest sex-specific germline marker in Drosophila

... Somatic follicle cells also undergo some rounds of endoreplication (Calvi et al., 1998). To test whether ectopic esg expression prevents endoreplication either in nurse cells or in follicle cells in female gonads, we analyzed females carrying a hs::esg construct (a kind gift from S. Hayashi) that we ...
Parallels between UNUSUAL FLORAL ORGANS and FIMBRIATA
Parallels between UNUSUAL FLORAL ORGANS and FIMBRIATA

... of both species can therefore be considered to cause a loss of both apical and lateral determinacy in lateral meristems. The UFO gene of Arabidopsis has a mutant phenotype that shows severa1 features of both meristem and organ identity mutants (Levin and Meyerowitz, 1995; Wilkinson and Haughn, 1995) ...
Set 2: Mutations
Set 2: Mutations

... Genes mutate at known rates, but the rate varies depending on the gene involved - some genes have high spontaneous mutation rates. Calculation of the average number of mutant genes in a human: 1. There are thought to be about 100,000 genes making up the human genome. 2. Since there are two copies of ...
Localization of a blood pressure QTL on rat chromosome 1 using
Localization of a blood pressure QTL on rat chromosome 1 using

... heterozygous for the original introgressed chromosomal segment. F1 rats were intercrossed to obtain F2 rats that were genotyped for markers in the congenic segment to look for recombinants. Rats with appropriate recombinant chromosomes were crossed to S again to duplicate the recombinant chromosome. ...
Text S1.
Text S1.

... Criteria to define trans-specifically shared S-alleles Based on the mismatch distribution for interspecific pairs of SRK sequences between A. lyrata and A. halleri (Fig. 2), we defined "trans-specifically shared S-alleles", i.e. alleles assumed to have evolved from a single S-allele in the direct an ...
characterizing the genetic bases of autosomal recessive disorders
characterizing the genetic bases of autosomal recessive disorders

... Autosomal recessive disorders have devastating effects on patients and their families. Elucidating the genetic bases of such disorders is essential to improve their clinical outcome and for implementing effective prevention programs. In this dissertation, the genetic bases of seven autosomal recessi ...
Narcolepsy (HLA-DQB1) Genotyping - Lab Test Directory
Narcolepsy (HLA-DQB1) Genotyping - Lab Test Directory

...  Supportive of a clinical diagnosis of narcolepsy  Does not by itself establish a diagnosis • Negative o HLA-DQB1*06:02 allele not detected  Diagnosis of narcolepsy is less likely but not eliminated Limitations • Does not differentiate between heterozygosity and homozygosity of the HLA-DQB1*06:02 ...
Development and Evaluation of Chromosome Segment
Development and Evaluation of Chromosome Segment

... Given the rapid increase in world population, the next century may witness serious global food shortage problems. Consequently, the need to increase grain yield is critical. Meanwhile, rice is one of the most important crops in the world, and in order to meet the growing demand for food driven by po ...
A Neurology patient`s best friend: not letting sleeping dogs lie or
A Neurology patient`s best friend: not letting sleeping dogs lie or

... detecting changes in respiratory rate, heart rate, odors, or other such features. This area has been fraught with controversy however and there have only been a few limitedstudies. It remains to be seen if seizure alert dogs are practical. It is often beneficial,!:ohaveanimalmodelsof disease both fo ...
cDNA cloning, expression and chromosomal localization of the
cDNA cloning, expression and chromosomal localization of the

... compared this location with the locations of other genes that have been mapped in the region and show that the position of the human txl gene can be assigned to chromosome 18q21 (Figure 2). This region of chromosome 18 has been extensively studied because its involvement in different types of tumors ...
The genetic basis of inherited anomalies of the teeth: Part 1: Clinical
The genetic basis of inherited anomalies of the teeth: Part 1: Clinical

... These include dental diseases affecting enamel and dentin formation and anomalies in teeth number. Genetic diseases affecting tooth structure have been classified by the affected tissue (enamel versus dentin), by their specificity (syndromic versus non-syndromic) and their pattern of inheritance: au ...
Erp, an extracellular protein family specific to
Erp, an extracellular protein family specific to

... domains : a highly conserved amino-terminal domain which includes a signal sequence, a central variable region containing repeats based on the motif PGLTS, and a conserved carboxy-terminal domain rich in proline and alanine. The number and fidelity of PGLTS repeats of the central region differ consi ...
Cell Division Studies of Escherichia Coli: Expression and Protein
Cell Division Studies of Escherichia Coli: Expression and Protein

... eventual cell death at the nonpermissive temperaturedl,77,94,120). The ftsZ(sulB) gene and two neighboring cell division genes, ftsQ and ftsA in this 2 min region(94,96,109,129,130) are part of a large cell envelope-cell division gene cluster (Fig. 1). ...
A Century of Hardy–Weinberg Equilibrium
A Century of Hardy–Weinberg Equilibrium

... workers, though there was uncertainty about degrees of freedom. (In this case, there are three classes, yielding two degrees of freedom, but one is associated with estimation of gene frequency in order to estimate genotypic expectations). It is immediately clear that, on the assumption of HWE, the o ...
A genome-wide association scan in pig identifies novel regions
A genome-wide association scan in pig identifies novel regions

... linkage information can be used only for within-family selection, and the linkage QTL intervals are generally wide and therefore are not suitable for candidate gene searches. However, association mapping (also known as linkage disequilibrium mapping) with dense SNP markers can map QTL segregating in ...
localization of histone gene transcripts in newt lampbrush
localization of histone gene transcripts in newt lampbrush

... chromosomes' lateral loops depends on sequence purity of the labelled probe. The recent availability of short DNA sequences cloned in plasmid or bacteriophage vectors has made possible the production, by nick-translation, of labelled probes of great sequence purity. Such probes, after denaturation, ...
A Century of Hardy–Weinberg Equilibrium
A Century of Hardy–Weinberg Equilibrium

... workers, though there was uncertainty about degrees of freedom. (In this case, there are three classes, yielding two degrees of freedom, but one is associated with estimation of gene frequency in order to estimate genotypic expectations). It is immediately clear that, on the assumption of HWE, the o ...
Molecular Genetic Testing For BRAF Mutations
Molecular Genetic Testing For BRAF Mutations

... positive tumors have overall improved response rates and progression-free survival with kinase inhibitor-directed therapy. Testing whether BRAF mutation exists in melanoma is therefore of critical therapeutic importance. Full sequencing of BRAF may be indicated as a follow-up test in patients with m ...
Single Nucleotide Polymorphism (SNP) 分析與應用
Single Nucleotide Polymorphism (SNP) 分析與應用

... are estimated to occur at a frequency of approximately one per 1000 nucleotides. • SNPs are biallelic polymorphisms, that is, the nucleotide identity at these polymorphic positions is generally constrained to one of two possibilities in humans, humans rather than the four nucleotide possibilities th ...
Alu repeat analysis in the complete human genome: trends and
Alu repeat analysis in the complete human genome: trends and

... subfamily, Alu J (genomic coverage ∼2.5%). Members of younger Alu subfamily, known as Alu Y, are extremely less represented (genomic coverage ∼1.5%) compared with older subfamilies. A very small contribution (genomic coverage ∼0.4%) comes from Alu elements that do not belong to any ...
Two groups of human herpesvirus 6 identified by sequence
Two groups of human herpesvirus 6 identified by sequence

... (Martin et al., 1991; Lindquester & Pellett, 1991). In this study we investigated the molecular basis for differences between HH¥-6 strain groups by PCR and sequence analysis of 15 variants, including laboratory reference strains from both groups. We also studied, by PCR, strains in two potential pa ...
Homework: Karyotyping Activity
Homework: Karyotyping Activity

... Karyotype - ____________________________________________________ ...
Chapter 1 - College Test bank - get test bank and solution manual
Chapter 1 - College Test bank - get test bank and solution manual

... At 8 months of age was your child an easy, slow-to-warm-up, or difficult baby in terms of Thomas and Chess’s classic temperamental categories? On what do you base this judgment? ...
early RNs, crossing over initiates, then synapsis begins Chiasmata
early RNs, crossing over initiates, then synapsis begins Chiasmata

... A--------------- b Recombinant gamete a --------------- B Recombinant gamete a --------------- b Parental gamete ...
CNS.Biomarker.template - College of American Pathologists
CNS.Biomarker.template - College of American Pathologists

... Isocitrate dehydrogenase (IDH) is an enzyme that exists in 5 isoforms, each of which catalyzes the reaction of isocitrate to α-ketoglutarate.7 The finding of mutations in IDH1 and IDH2 in diffuse gliomas has dramatically changed the practice of neuropathology and neurooncology. Mutations in IDH1 are ...
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Designer baby

Designer baby is a term that refers to the product of a genetically engineered baby. These babies are ""designed"" (fixed/changed) while still in the womb to achieve more desired looks, skills, or talents.
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