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Neonatal diabetes mellitus: A model for personalized medicine
Neonatal diabetes mellitus: A model for personalized medicine

... uncertain percentage could result from an unknown cause. Whenever possible, the specific gene names causing the disease should be used; however, the term MODY is useful for facilitating recognition of patients suitable for genetic screening by clinicians familiar with this phenotypic description. ND ...
Multiple Routes to Subfunctionalization and Gene Duplicate
Multiple Routes to Subfunctionalization and Gene Duplicate

... the same selection pressures that operate at a pair of duplicate loci. If a change in the environmental circumstances of the species is posited, it would be very unlikely that this shift would happen at precisely the same time as the fixation of a duplication by drift. The set of mutationally access ...
Simulating Natural Selection
Simulating Natural Selection

... 7. Add the number of remaining lima and kidney beans together. Record this information in the appropriate place in the Table 2. 8. To find the frequencies of lima beans and kidney beans that remain in the paper bag, divide the numbers of each of the remaining beans by the total number of remaining ...
Mothers against dpp participates in a DPP/TGF
Mothers against dpp participates in a DPP/TGF

... To clarify Mad’s function in DPP-responsive cells, we have continued to focus on the embryonic midgut. Here we are able to utilize genotypes that are null for Mad to examine the relationship between Mad and dpp. In the midgut, dpp is expressed in the visceral mesoderm of parasegments (ps) 3 and 7 (F ...
Consulta: subjectFacets:"16S rRNA" Registros recuperados: 43
Consulta: subjectFacets:"16S rRNA" Registros recuperados: 43

... Sugarcane is an important agricultural product of Brazil, with a total production of more than 500 million tons. Knowledge of the bacterial community associated with agricultural crops and the soil status is a decisive step towards understanding how microorganisms influence crop productivity. Howeve ...
Human mutations in glucose 6-phosphate dehydrogenase reflect
Human mutations in glucose 6-phosphate dehydrogenase reflect

... produce NADPH, a key electron donor in the defense against oxidizing agents and in reductive biosynthetic reactions. Inherited G6PD deficiency is associated with either episodic hemolytic anemia (triggered by fava beans or other agents) or life-long hemolytic anemia. We show here that an evolutionar ...
PH4 of Petunia Is an R2R3 MYB Protein That Activates
PH4 of Petunia Is an R2R3 MYB Protein That Activates

... derived lines) and the 3-rutinosides show little or no fading (de Vlaming et al., 1982). When we crossed the unstable ph4-V2166 allele into a genetic background that allows the synthesis of 3RGac5G-substituted anthocyanins, the flowers displayed upon opening a blue-violet color and were dotted with ...
Copyright © The McGraw-Hill Companies, Inc. Permission
Copyright © The McGraw-Hill Companies, Inc. Permission

... Autosomal dominant inheritance. When one parent has an autosomal dominant condition and the other does not, each offspring has a 50 percent probability of inheriting the mutant allele and the condition. The affected parent is Aa here, and not AA, because for many dominant disorders, the homozygous d ...
Inference of homologous recombination in bacteria using whole
Inference of homologous recombination in bacteria using whole

... Graph model since two recombinant branches affecting different regions may coalesce with each other. Thus inference when T , θ, ρ and δ are known can be done even for a large genomic alignment by parallelization of the inference of the recombination events for each alignment region. Alignment regio ...
Chromosomal Aberration of the 11q23 Locus in Acute Leukemia
Chromosomal Aberration of the 11q23 Locus in Acute Leukemia

... the clinical outcome of 11q23+/MLL+ AML is more heterogeneous. 14-16 The Medical Research Council 14 and the Southwest Oncology Group15 classify the risk for patients with AML with t(9;11) as intermediate and poor, respectively. Even more disagreement surrounds the prognostic relevance of classic t( ...
Available as a free here - European Cystic Fibrosis Society
Available as a free here - European Cystic Fibrosis Society

... tion and an abnormal NPD or 2 identified CFTR mutations), it would be overly cautious not to consider this person a CF patient, even in an atypical form [15]. Thus, we stress the importance of the clinical picture in addition to test results to interpret fully a patient’s condition. In infants identi ...
Human mitochondrial transfer RNAs: Role of pathogenic
Human mitochondrial transfer RNAs: Role of pathogenic

... Most of the observed mtDNA changes represent neutral polymorphisms and have been used to track human migrations.70 The large prevalence of variations in tRNA genes calls for the elucidation of their pathogenicity. In addition, clinical misattribution of pathogenicity is an important issue due to the ...
hirota - Genetics
hirota - Genetics

... The order of cistrons involved in gefietic transfer has been determined by the method of overlapping deletions; they can be arranged on F, with the galactose -A-Bgenes in the following order: gal (operator-epimerase-transferase-kinase) C-D-E-F.One group of cistrons ( Aand B ) containing mutations th ...
Gene Section WWC1 (WW and C2 domain containing 1)
Gene Section WWC1 (WW and C2 domain containing 1)

... (isoform 1), with a predicted molecular weight of 125kDa. It was first cloned and identified as a protein that interacts with the postsynaptic protein dendrin (Kremerskothen et al., 2003). KIBRA is constituted by two N-terminal WW domains, a C2 domain, a glutamic acid-rich domain and a PDZ binding m ...
PDF
PDF

... a trithorax group regulator. We propose that Utx is needed in the early embryo to prevent inappropriate instalment of long-term Polycomb repression at HOX genes in cells in which these genes must be kept active. In contrast to PRC2, which is essential for, and continuously required during, germ cell ...
Maintenance of genomic integrity by p53: complementary
Maintenance of genomic integrity by p53: complementary

... are far less clear. Furthermore, it is still not known, whether and how p53 directly participates in DNA repair processes, despite some evidence pointing to this possibility. Last but not least, a possible role of p53 in the control of genomic integrity in its non-induced state, i.e., in the absence ...
PDF
PDF

... lens formation without the formation of the retina has been reported (Mencl, 1903; Spemann, 1912). How the lens develops in these species in the absence of the retina is not understood. The nature of this problem can best be demonstrated by the example of lens formation in the zebrafish retinal home ...
Transcriptional Attenuation
Transcriptional Attenuation

... phenomenon that reduces the extent or rate of transcription. In studies of bacterial gene regulation, however, it has acquired a more restricted definition and is used to describe a mechanism in which the level of transcriptional termination at a single, specific site within an operon, called an att ...
Charge Transport in DNA - Insights from
Charge Transport in DNA - Insights from

... The state of knowledge of DNA stretching in 2000 was summarized in two reviews. [24, 25] At that time, a dispute on the nature of the overstretched state of dsDNA started, and it is in fact still going on. In contrast to the proposal of S-DNA, the overstretching profile of DNA was attributed to force ...
Mutations at the Darkener of apricot Locus Modulate Transcript
Mutations at the Darkener of apricot Locus Modulate Transcript

... role in the expression of the mutation-causing transposable element, and in modifying its activity, result in an alteration of the mutant phenotype. We are seeking to understand the functions these modifiers serve in retrotransposon and gene expression. Modifiers of wa comprise the most extensive se ...
Quantitative trait loci associated with maximal exercise endurance in
Quantitative trait loci associated with maximal exercise endurance in

... linked with aerobic running capacity on rat chromosome 16 and suggestive linkage on chromosome 3. Given the health implications of understanding the genetic regulation of a complex trait such as maximal exercise endurance, it is important that additional research be conducted in species that will al ...
C57BL/6 - Envigo
C57BL/6 - Envigo

BIOLOGY 3 Lab Manual - Los Angeles Mission College
BIOLOGY 3 Lab Manual - Los Angeles Mission College

... If the independent variable is discontinuous or discrete (i.e., there are very limited or finite values for the independent variable), then a bar graph would be appropriate. For example, if you wanted to graph the average GPA of students at each of the nine LACCD community colleges, the independent ...
Array-based sequencing of filaggrin gene for
Array-based sequencing of filaggrin gene for

... with a conserved exon structure and likely shared functions in epithelial biology (Gan et al. 1990; Henry et al. 2012; Strasser et al. 2014). FLG transcription is initiated in exon 2 with the majority of the profilaggrin polyprotein produced from the extremely long (>12Kb) and highly repetitive exon ...
Genetics Practice Test
Genetics Practice Test

... ____ 31. Animal breeders maintain cat and dog breeds by the process of hybridization. _________________________ ____ 32. Native Americans took teosine and used selective breeding to make corn, a more productive and nutritious plant. _________________________ ____ 33. Exposing bacteria to radiation o ...
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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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